-
1
-
-
33749444308
-
Incidence and prevalence of idiopathic pulmonary fibrosis
-
Raghu, G., Weycker, D., Edelsberg, J., Bradford, W. Z. & Oster, G. Incidence and prevalence of idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 174, 810-816 (2006).
-
(2006)
Am. J. Respir. Crit. Care Med.
, vol.174
, pp. 810-816
-
-
Raghu, G.1
Weycker, D.2
Edelsberg, J.3
Bradford, W.Z.4
Oster, G.5
-
2
-
-
34547597339
-
Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003
-
Olson, A. L. et al. Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003. Am. J. Respir. Crit. Care Med. 176, 277-284 (2007).
-
(2007)
Am. J. Respir. Crit. Care Med.
, vol.176
, pp. 277-284
-
-
Olson, A.L.1
-
3
-
-
84865692752
-
Stromedix acquisition signals growing interest in fibrosis
-
Allison, M. Stromedix acquisition signals growing interest in fibrosis. Nat. Biotechnol. 30, 375-376 (2012).
-
(2012)
Nat. Biotechnol.
, vol.30
, pp. 375-376
-
-
Allison, M.1
-
4
-
-
84901759236
-
A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis
-
King, T. E. Jr. et al. A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N. Engl. J. Med. 370, 2083-2092 (2014).
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 2083-2092
-
-
King, T.E.1
-
5
-
-
79953728756
-
Novel therapeutic approaches for pulmonary fibrosis
-
Datta, A., Scotton, C. J. & Chambers, R. C. Novel therapeutic approaches for pulmonary fibrosis. Br. J. Pharmacol. 163, 141-172 (2011).
-
(2011)
Br. J. Pharmacol.
, vol.163
, pp. 141-172
-
-
Datta, A.1
Scotton, C.J.2
Chambers, R.C.3
-
6
-
-
84942985200
-
Predictors of mortality and progression in scleroderma-associated interstitial lung disease: A systematic review
-
Winstone, T. et al. Predictors of mortality and progression in scleroderma-associated interstitial lung disease: a systematic review. Chest 13, 2626 (2014).
-
(2014)
Chest
, vol.13
, pp. 2626
-
-
Winstone, T.1
-
7
-
-
33748201695
-
Interstitial lung disease in rheumatoid arthritis: Recent advances
-
Kim, D. Interstitial lung disease in rheumatoid arthritis: recent advances. Curr. Opin. Pulm. Med. 12, 346-353 (2006).
-
(2006)
Curr. Opin. Pulm. Med.
, vol.12
, pp. 346-353
-
-
Kim, D.1
-
8
-
-
84897961068
-
Understanding CT patterns in idiopathic pulmonary fibrosis
-
Hart, S. P. Understanding CT patterns in idiopathic pulmonary fibrosis. Lancet Respir. Med. 2, 249-250 (2014).
-
(2014)
Lancet Respir. Med.
, vol.2
, pp. 249-250
-
-
Hart, S.P.1
-
9
-
-
0032477553
-
Effect of diagnosis on survival benefit of lung transplantation for end-stage lung disease
-
Hosenpud, J. D., Bennett, L. E., Keck, B. M., Edwards, E. B. & Novick, R. J. Effect of diagnosis on survival benefit of lung transplantation for end-stage lung disease. Lancet 351, 24-27 (1998).
-
(1998)
Lancet
, vol.351
, pp. 24-27
-
-
Hosenpud, J.D.1
Bennett, L.E.2
Keck, B.M.3
Edwards, E.B.4
Novick, R.J.5
-
10
-
-
84861394764
-
Prednisone azathioprine and N acetylcysteine for pulmonary fibrosis
-
Raghu, G., Anstrom, K. J., King, T. E. Jr., Lasky, J. A. & Martinez, F. J. Prednisone, azathioprine and N acetylcysteine for pulmonary fibrosis. N. Engl. J. Med. 366, 1968-1977 (2012).
-
(2012)
N. Engl. J. Med.
, vol.366
, pp. 1968-1977
-
-
Raghu, G.1
Anstrom, K.J.2
King, T.E.3
Lasky, J.A.4
Martinez, F.J.5
-
11
-
-
79957670746
-
Pirfenidone for diabetic nephropathy
-
Sharma, K. et al. Pirfenidone for diabetic nephropathy. J. Am. Soc. Nephrol. 22, 1144-1151 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 1144-1151
-
-
Sharma, K.1
-
12
-
-
84891490618
-
Synthesis and biological evaluation of the pirfenidone derivatives as antifibrotic agents
-
Ma, Z. et al. Synthesis and biological evaluation of the pirfenidone derivatives as antifibrotic agents. Bioorg. Med. Chem. Lett. 24, 220-223 (2014).
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 220-223
-
-
Ma, Z.1
-
13
-
-
0037061867
-
Nephropathy in patients with type 2 diabetes
-
Remuzzi, G., Schieppati, A. & Ruggenenti, P. Nephropathy in patients with type 2 diabetes. N. Engl. J. Med. 346, 1145-1151 (2002).
-
(2002)
N. Engl. J. Med.
, vol.346
, pp. 1145-1151
-
-
Remuzzi, G.1
Schieppati, A.2
Ruggenenti, P.3
-
14
-
-
12344250764
-
Chronic kidney disease: The global challenge
-
Meguid El Nahas, A. & Bello, A. K. Chronic kidney disease: the global challenge. Lancet 365, 331-340 (2005).
-
(2005)
Lancet
, vol.365
, pp. 331-340
-
-
Meguid El Nahas, A.1
Bello, A.K.2
-
15
-
-
44849114597
-
Aliskiren combined with losartan in type 2 diabetes and nephropathy
-
Parving, H., Persson, F., Lewis, J. B., Lewis, E. J. & Hollenberg, N. K. Aliskiren combined with losartan in type 2 diabetes and nephropathy. N. Engl. J. Med. 358, 2433-2446 (2008).
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 2433-2446
-
-
Parving, H.1
Persson, F.2
Lewis, J.B.3
Lewis, E.J.4
Hollenberg, N.K.5
-
16
-
-
70349756901
-
Effects of losartan on hepatic expression of nonphagocytic NADPH oxidase and fibrogenic genes in patients with chronic hepatitis C
-
Colmenero, J. et al. Effects of losartan on hepatic expression of nonphagocytic NADPH oxidase and fibrogenic genes in patients with chronic hepatitis C. Am. J. Physiol. Gastrointest. Liver Physiol. 297, G726-G734 (2009).
-
(2009)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.297
, pp. G726-G734
-
-
Colmenero, J.1
-
17
-
-
80051566676
-
A randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis
-
Talmadge, E. et al. A randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 184, 92-99 (2011).
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.184
, pp. 92-99
-
-
Talmadge, E.1
-
18
-
-
40049097359
-
Liver cirrhosis
-
Schuppan, D. & Afdhal, N. H. Liver cirrhosis. Lancet 371, 838-851 (2008).
-
(2008)
Lancet
, vol.371
, pp. 838-851
-
-
Schuppan, D.1
Afdhal, N.H.2
-
19
-
-
84891489391
-
Strategic management of keloid disease in ethnic skin: A structured approach supported by emerging literature
-
Ud Din, S. & Bayat, A. Strategic management of keloid disease in ethnic skin: a structured approach supported by emerging literature. Br. J. Dermatol. 169, 71-81 (2013).
-
(2013)
Br. J. Dermatol.
, vol.169
, pp. 71-81
-
-
Ud Din, S.1
Bayat, A.2
-
20
-
-
84870328390
-
Urinary proteomics for early diagnosis in diabetic nephropathy
-
Zurbig, P. et al. Urinary proteomics for early diagnosis in diabetic nephropathy. Diabetes 61, 3304-3313 (2012).
-
(2012)
Diabetes
, vol.61
, pp. 3304-3313
-
-
Zurbig, P.1
-
21
-
-
77955881563
-
Diminished prostaglandin E2 contributes to the apoptosis paradox in idiopathic pulmonary fibrosis
-
Maher, T. M. et al. Diminished prostaglandin E2 contributes to the apoptosis paradox in idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 182, 73-82 (2010).
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.182
, pp. 73-82
-
-
Maher, T.M.1
-
22
-
-
84859589441
-
A systems approach identifies HIPK2 as a key regulator of kidney fibrosis
-
Jin, Y. et al. A systems approach identifies HIPK2 as a key regulator of kidney fibrosis. Nat. Med. 18, 580-589 (2012).
-
(2012)
Nat. Med.
, vol.18
, pp. 580-589
-
-
Jin, Y.1
-
23
-
-
84894593599
-
Molecular mechanisms of epithelial-mesenchymal transition
-
Lamouille, S., Xu, J. & Derynck, R. Molecular mechanisms of epithelial-mesenchymal transition. Nat. Rev. Mol. Cell Biol. 15, 178-196 (2014).
-
(2014)
Nat. Rev. Mol. Cell Biol.
, vol.15
, pp. 178-196
-
-
Lamouille, S.1
Xu, J.2
Derynck, R.3
-
24
-
-
47749101725
-
Functional Wnt signalling is increased in idiopathic pulmonary fibrosis
-
Konigshoff, M. et al. Functional Wnt signalling is increased in idiopathic pulmonary fibrosis. PLoS ONE 3, e2142 (2008).
-
(2008)
PLoS ONE
, vol.3
, pp. e2142
-
-
Konigshoff, M.1
-
25
-
-
84882289111
-
Origin and function of myofibroblasts in kidney fibrosis
-
LeBleu, V. S. et al. Origin and function of myofibroblasts in kidney fibrosis. Nat. Med. 19, 1047-1054 (2013).
-
(2013)
Nat. Med.
, vol.19
, pp. 1047-1054
-
-
LeBleu, V.S.1
-
26
-
-
73949096744
-
Fate tracing reveals the pericyte and not epithelial origin of myofibroblasts in kidney fibrosis
-
Humphreys, B. D. et al. Fate tracing reveals the pericyte and not epithelial origin of myofibroblasts in kidney fibrosis. Am. J. Pathol. 176, 85-97 (2010).
-
(2010)
Am. J. Pathol.
, vol.176
, pp. 85-97
-
-
Humphreys, B.D.1
-
27
-
-
84855511323
-
Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition
-
Rock, J. R. et al. Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition. Proc. Natl Acad. Sci. USA 108, E1475-E1483 (2011).
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. E1475-E1483
-
-
Rock, J.R.1
-
28
-
-
84901746607
-
The idiopathic pulmonary fibrosis clinical research network. Randomized trial of acetylcysteine in idiopathic pulmonary fibrosis
-
The idiopathic pulmonary fibrosis clinical research network. Randomized trial of acetylcysteine in idiopathic pulmonary fibrosis. N. Engl. J. Med. 370, 2093-2101 (2014).
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 2093-2101
-
-
-
29
-
-
84890946148
-
Bardoxolone methyl in type 2 diabetes and stage 4 chronic kidney disease
-
De Zeeuw, D. et al. Bardoxolone methyl in type 2 diabetes and stage 4 chronic kidney disease. N. Engl. J. Med. 369, 2492-2503 (2013).
-
(2013)
N. Engl. J. Med.
, vol.369
, pp. 2492-2503
-
-
De Zeeuw, D.1
-
30
-
-
44649083783
-
Superoxide scavenging activity of pirfenidone-iron complex
-
Mitani, Y. et al. Superoxide scavenging activity of pirfenidone-iron complex. Biochem. Biophys. Res. Commun. 372, 19-23 (2008).
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.372
, pp. 19-23
-
-
Mitani, Y.1
-
31
-
-
0031842059
-
Colchicine, D penicillamine and prednisone in the treatment of idiopathic pulmonary fibrosis: A controlled clinical trial
-
Selman, M. et al. Colchicine, D penicillamine and prednisone in the treatment of idiopathic pulmonary fibrosis: a controlled clinical trial. Chest 114, 507-512 (1998).
-
(1998)
Chest
, vol.114
, pp. 507-512
-
-
Selman, M.1
-
32
-
-
2942699911
-
Combined corticosteroid and cyclophosphamide therapy does not alter survival in idiopathic pulmonary fibrosis
-
Collard, H. R. et al. Combined corticosteroid and cyclophosphamide therapy does not alter survival in idiopathic pulmonary fibrosis. Chest 125, 2169-2174 (2004).
-
(2004)
Chest
, vol.125
, pp. 2169-2174
-
-
Collard, H.R.1
-
33
-
-
84879555016
-
Identification of steroid sensitive responders versus non-responders in the treatment of keloid disease
-
Ud Din, S., Bowring, A., Derbyshire, A., Morris, J. & Bayat, A. Identification of steroid sensitive responders versus non-responders in the treatment of keloid disease. Arch. Dermatol. Res. 305, 423-432 (2013).
-
(2013)
Arch. Dermatol. Res.
, vol.305
, pp. 423-432
-
-
Ud Din, S.1
Bowring, A.2
Derbyshire, A.3
Morris, J.4
Bayat, A.5
-
34
-
-
84864219469
-
Corticosteroid plus pentoxifylline is not better than corticosteroid alone for improving survival in severe alcoholic hepatitis (COPE Trial)
-
Sidhu, S. S. et al. Corticosteroid plus pentoxifylline is not better than corticosteroid alone for improving survival in severe alcoholic hepatitis (COPE Trial). Dig. Dis. Sci. 57, 1664-1674 (2012).
-
(2012)
Dig. Dis. Sci.
, vol.57
, pp. 1664-1674
-
-
Sidhu, S.S.1
-
35
-
-
36348994975
-
Influence of ursodeoxycholic acid on the mortality and malignancy associated with primary biliary cirrhosis: A population-based cohort study
-
Jackson, H. et al. Influence of ursodeoxycholic acid on the mortality and malignancy associated with primary biliary cirrhosis: a population-based cohort study. Hepatology 46, 1131-1137 (2007).
-
(2007)
Hepatology
, vol.46
, pp. 1131-1137
-
-
Jackson, H.1
-
36
-
-
68849118799
-
CCR1 and CCR5 promote hepatic fibrosis in mice
-
Seki, E. et al. CCR1 and CCR5 promote hepatic fibrosis in mice. J. Clin. Invest. 119, 1858-1870 (2009).
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 1858-1870
-
-
Seki, E.1
-
37
-
-
67651156353
-
CCR2 promotes hepatic fibrosis in mice
-
Seki, E. et al. CCR2 promotes hepatic fibrosis in mice. Hepatology 50, 185-197 (2009).
-
(2009)
Hepatology
, vol.50
, pp. 185-197
-
-
Seki, E.1
-
38
-
-
0037099161
-
The relationship between individual histologic features and disease progression in idiopathic pulmonary fibrosis
-
Nicholson, A. G. et al. The relationship between individual histologic features and disease progression in idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 166, 173-177 (2002).
-
(2002)
Am. J. Respir. Crit. Care Med.
, vol.166
, pp. 173-177
-
-
Nicholson, A.G.1
-
39
-
-
84899547894
-
Identification of a cell of origin for fibroblasts comprising the fibrotic reticulum in idiopathic pulmonary fibrosis
-
Xia, H. et al. Identification of a cell of origin for fibroblasts comprising the fibrotic reticulum in idiopathic pulmonary fibrosis. Am. J. Pathol. 184, 1369-1383 (2014).
-
(2014)
Am. J. Pathol.
, vol.184
, pp. 1369-1383
-
-
Xia, H.1
-
40
-
-
48949117344
-
Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis
-
Andersson-Sjoland, A. et al. Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis. Int. J. Biochem. Cell Biol. 40, 2129-2140 (2008).
-
(2008)
Int. J. Biochem. Cell Biol.
, vol.40
, pp. 2129-2140
-
-
Andersson-Sjoland, A.1
-
41
-
-
84886304100
-
Role of lung pericytes and resident fibroblasts in the pathogenesis of pulmonary fibrosis
-
Hung, C. et al. Role of lung pericytes and resident fibroblasts in the pathogenesis of pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 188, 820-830 (2013).
-
(2013)
Am. J. Respir. Crit. Care Med.
, vol.188
, pp. 820-830
-
-
Hung, C.1
-
42
-
-
42949163491
-
Mechanisms of hepatic fibrogenesis
-
Friedman, S. L. Mechanisms of hepatic fibrogenesis. Gastroenterology 134, 1655-1669 (2008).
-
(2008)
Gastroenterology
, vol.134
, pp. 1655-1669
-
-
Friedman, S.L.1
-
43
-
-
0035070056
-
Cyclooxygenase 2 deficiency results in a loss of the anti-proliferative response to transforming growth factor-β in human fibrotic lung fibroblasts and promotes bleomycin-induced pulmonary fibrosis in mice
-
Keerthisingam, C. B. et al. Cyclooxygenase 2 deficiency results in a loss of the anti-proliferative response to transforming growth factor-β in human fibrotic lung fibroblasts and promotes bleomycin-induced pulmonary fibrosis in mice. Am. J. Pathol. 158, 1411-1422 (2001).
-
(2001)
Am. J. Pathol.
, vol.158
, pp. 1411-1422
-
-
Keerthisingam, C.B.1
-
44
-
-
0030883273
-
Scleroderma lung fibroblasts exhibit elevated and dysregulated type i collagen biosynthesis
-
Shi-Wen, X. et al. Scleroderma lung fibroblasts exhibit elevated and dysregulated type I collagen biosynthesis. Arthritis Rheum. 40, 1237-1244 (1997).
-
(1997)
Arthritis Rheum.
, vol.40
, pp. 1237-1244
-
-
Shi-Wen, X.1
-
45
-
-
55349144194
-
Adenoviral overexpression and small interfering RNA suppression demonstrate that plasminogen activator inhibitor 1 produces elevated collagen accumulation in normal and keloid fibroblasts
-
Tuan, T.-L. et al. Adenoviral overexpression and small interfering RNA suppression demonstrate that plasminogen activator inhibitor 1 produces elevated collagen accumulation in normal and keloid fibroblasts. Am. J. Pathol. 173, 1311-1325 (2008).
-
(2008)
Am. J. Pathol.
, vol.173
, pp. 1311-1325
-
-
Tuan, T.-L.1
-
46
-
-
78149329845
-
Hypermethylation of PTGER2 confers prostaglandin E2 resistance in fibrotic fibroblasts from humans and mice
-
Huang, S. K. et al. Hypermethylation of PTGER2 confers prostaglandin E2 resistance in fibrotic fibroblasts from humans and mice. Am. J. Pathol. 177, 2245-2255 (2010).
-
(2010)
Am. J. Pathol.
, vol.177
, pp. 2245-2255
-
-
Huang, S.K.1
-
47
-
-
77952116121
-
Methylation determines fibroblast activation and fibrogenesis in the kidney
-
Bechtel, W. et al. Methylation determines fibroblast activation and fibrogenesis in the kidney. Nat. Med. 16, 544-550 (2010).
-
(2010)
Nat. Med.
, vol.16
, pp. 544-550
-
-
Bechtel, W.1
-
48
-
-
80055106592
-
Delayed stress fiber formation mediates pulmonary myofibroblast differentiation in response to TGF-β
-
Sandbo, N. et al. Delayed stress fiber formation mediates pulmonary myofibroblast differentiation in response to TGF-β. Am. J. Physiol. Lung Cell. Mol. Physiol. 301, L656-L666 (2011).
-
(2011)
Am. J. Physiol. Lung Cell. Mol. Physiol.
, vol.301
, pp. L656-L666
-
-
Sandbo, N.1
-
49
-
-
0038823614
-
Myofibroblast differentiation by transforming growth factor-β1 is dependent on cell adhesion and integrin signalling via focal adhesion kinase
-
Thannickal, V. J. et al. Myofibroblast differentiation by transforming growth factor-β1 is dependent on cell adhesion and integrin signalling via focal adhesion kinase. J. Biol. Chem. 278, 12384-12389 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 12384-12389
-
-
Thannickal, V.J.1
-
50
-
-
84861437351
-
Protection from liver fibrosis by a peroxisome proliferator-activated receptor γ agonist
-
Iwaisako, K. et al. Protection from liver fibrosis by a peroxisome proliferator-activated receptor γ agonist. Proc. Natl Acad. Sci. USA 109, E1369-E1376 (2012).
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. E1369-E1376
-
-
Iwaisako, K.1
-
51
-
-
84868646303
-
Multigenerational epigenetic adaption of the hepatic wound-healing response
-
Zeybel, M. et al. Multigenerational epigenetic adaption of the hepatic wound-healing response. Nat. Med. 18, 1369-1377 (2012).
-
(2012)
Nat. Med.
, vol.18
, pp. 1369-1377
-
-
Zeybel, M.1
-
52
-
-
75149141045
-
MeCP2 controls an epigenetic pathway that promotes myofibroblast transdifferentiation and fibrosis
-
Mann, J. et al. MeCP2 controls an epigenetic pathway that promotes myofibroblast transdifferentiation and fibrosis. Gastroenterology 138, 705-714 (2010).
-
(2010)
Gastroenterology
, vol.138
, pp. 705-714
-
-
Mann, J.1
-
53
-
-
79251563128
-
PPAR-γ ligands repress TGF-β-induced myofibroblast differentiation by targeting the PI3k/Akt pathway: Implications for therapy of fibrosis
-
Kulkarni, A. A., Thatcher, T. H., Olsen, K. C., Maggirwar, S. B. & Phipps, R. P. PPAR-γ ligands repress TGF-β-induced myofibroblast differentiation by targeting the PI3k/Akt pathway: implications for therapy of fibrosis. PLoS ONE 6, 1-11 (2011).
-
(2011)
PLoS ONE
, vol.6
, pp. 1-11
-
-
Kulkarni, A.A.1
Thatcher, T.H.2
Olsen, K.C.3
Maggirwar, S.B.4
Phipps, R.P.5
-
54
-
-
78349281192
-
PPARγ downregulation by TGF β in fibroblast and impaired expression and function in systemic sclerosis: A novel mechanism for progressive fibrogenesis
-
Wei, J. et al. PPARγ downregulation by TGF β in fibroblast and impaired expression and function in systemic sclerosis: a novel mechanism for progressive fibrogenesis. PLoS ONE 5, 1-13 (2010).
-
(2010)
PLoS ONE
, vol.5
, pp. 1-13
-
-
Wei, J.1
-
55
-
-
75449116707
-
Long-term efficacy of rosiglitazone in non-alcoholic steatohepatitis: Results of the fatty liver improvement by rosiglitazone therapy (FLIRT 2) extension trial
-
Ratziu, V. et al. Long-term efficacy of rosiglitazone in non-alcoholic steatohepatitis: results of the fatty liver improvement by rosiglitazone therapy (FLIRT 2) extension trial. Hepatology 51, 445-453 (2010).
-
(2010)
Hepatology
, vol.51
, pp. 445-453
-
-
Ratziu, V.1
-
56
-
-
33751545838
-
A placebo-controlled trial of pioglitazone in subjects with non-alcoholic steatohepatitis
-
Belfort, R. et al. A placebo-controlled trial of pioglitazone in subjects with non-alcoholic steatohepatitis. N. Engl. J. Med. 355, 2297-2307 (2006).
-
(2006)
N. Engl. J. Med.
, vol.355
, pp. 2297-2307
-
-
Belfort, R.1
-
57
-
-
77954638677
-
Discovery of GSK21246458, a highly potent inhibitor of PI3K and the mammalian target of rapamycin
-
Knight, S. D. et al. Discovery of GSK21246458, a highly potent inhibitor of PI3K and the mammalian target of rapamycin. Am. Chem. Soc. Chem. Lett. 1, 39-43 (2010).
-
(2010)
Am. Chem. Soc. Chem. Lett.
, vol.1
, pp. 39-43
-
-
Knight, S.D.1
-
58
-
-
33747819801
-
MTOR and cancer: Insights into a complex relationship
-
Sabatini, D. M. mTOR and cancer: insights into a complex relationship. Nat. Rev. Cancer 6, 729-734 (2006).
-
(2006)
Nat. Rev. Cancer
, vol.6
, pp. 729-734
-
-
Sabatini, D.M.1
-
59
-
-
0036753494
-
Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control
-
Loewith, R. et al. Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control. Mol. Cell 10, 457-468 (2002).
-
(2002)
Mol. Cell
, vol.10
, pp. 457-468
-
-
Loewith, R.1
-
60
-
-
79959886642
-
An investigator-driven study of everolimus in surgical lung biopsy confirmed idiopathic pulmonary fibrosis
-
Malouf, M. A., Hopkins, P. & Glanville, A. R. Everolimus in IPF study investigators. An investigator-driven study of everolimus in surgical lung biopsy confirmed idiopathic pulmonary fibrosis. Respirology 16, 776-783 (2011).
-
(2011)
Respirology
, vol.16
, pp. 776-783
-
-
Malouf, M.A.1
Hopkins, P.2
Glanville, A.R.3
-
61
-
-
0036769168
-
Imatinib: A selective tyrosine kinase inhibitor
-
Manley, P. W. et al. Imatinib: a selective tyrosine kinase inhibitor. Eur. J. Cancer 38, S19-S27 (2002).
-
(2002)
Eur. J. Cancer
, vol.38
, pp. S19-S27
-
-
Manley, P.W.1
-
62
-
-
19644385336
-
Imatinib as a novel antifibrotic agent in bleomycin-induced pulmonary fibrosis in mice
-
Aono, Y. et al. Imatinib as a novel antifibrotic agent in bleomycin-induced pulmonary fibrosis in mice. Am. J. Respir. Crit. Care Med. 1 71, 1279-1285 (2005).
-
(2005)
Am. J. Respir. Crit. Care Med.
, vol.171
, pp. 1279-1285
-
-
Aono, Y.1
-
63
-
-
77749324295
-
Imatinib treatment for idiopathic pulmonary fibrosis: Randomized placebo-controlled trial results
-
Daniels, C. E. et al. Imatinib treatment for idiopathic pulmonary fibrosis: randomized placebo-controlled trial results. Am. J. Respir. Crit. Care Med. 181, 604-610 (2010).
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.181
, pp. 604-610
-
-
Daniels, C.E.1
-
64
-
-
84868214290
-
Imatinib mesylate in scleroderma-associated diffuse skin fibrosis: A phase II multicentre randomized double-blinded controlled trial
-
Prey, S. et al. Imatinib mesylate in scleroderma-associated diffuse skin fibrosis: a phase II multicentre randomized double-blinded controlled trial. Br. J. Dermatol. 167, 1138-1144 (2012).
-
(2012)
Br. J. Dermatol.
, vol.167
, pp. 1138-1144
-
-
Prey, S.1
-
65
-
-
84901810710
-
Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis
-
Richeldi, L. et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N. Engl. J. Med. 370, 2071-2082 (2014).
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 2071-2082
-
-
Richeldi, L.1
-
66
-
-
84901689853
-
Therapeutic approaches to diabetic nephropathy-beyond the RAS
-
Fernandez-Fernandez, B., Ortiz, A., Gomez-Guerro, C. & Egido, J. Therapeutic approaches to diabetic nephropathy-beyond the RAS. Nat. Rev. Nephrol. 10, 325-346 (2014).
-
(2014)
Nat. Rev. Nephrol.
, vol.10
, pp. 325-346
-
-
Fernandez-Fernandez, B.1
Ortiz, A.2
Gomez-Guerro, C.3
Egido, J.4
-
67
-
-
63349085077
-
C Jun N terminal kinase 1 is required for the development of pulmonary fibrosis
-
Alcorn, J. F. et al. C Jun N terminal kinase 1 is required for the development of pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol. 40, 422-432 (2009).
-
(2009)
Am. J. Respir. Cell. Mol. Biol.
, vol.40
, pp. 422-432
-
-
Alcorn, J.F.1
-
68
-
-
0037186459
-
Identification of novel inhibitors of the transforming growth factor β1 (TGF-β1) type i receptor (ALK5)
-
Callahan, J. F. et al. Identification of novel inhibitors of the transforming growth factor β1 (TGF-β1) type I receptor (ALK5). J. Med. Chem. 45, 999-1001 (2002).
-
(2002)
J. Med. Chem.
, vol.45
, pp. 999-1001
-
-
Callahan, J.F.1
-
69
-
-
0036085920
-
SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type 1 activin receptor-like kinase (ALK) receptors ALK4, ALK5 and ALK7
-
Inman, G. J. SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type 1 activin receptor-like kinase (ALK) receptors ALK4, ALK5 and ALK7. Mol. Pharmacol. 62, 65-74 (2002).
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 65-74
-
-
Inman, G.J.1
-
70
-
-
80053585761
-
Induction of heart valve lesions by small-molecule ALK5 inhibitors
-
Anderton, M. J. et al. Induction of heart valve lesions by small-molecule ALK5 inhibitors. Toxicol. Pathol. 39, 916-924 (2011).
-
(2011)
Toxicol. Pathol.
, vol.39
, pp. 916-924
-
-
Anderton, M.J.1
-
71
-
-
84866985855
-
Targeting the TGF-β signalling pathway in disease
-
Akhurst, R. J. & Hata, A. Targeting the TGF-β signalling pathway in disease. Nat. Rev. Drug Discov. 11, 790-811 (2012).
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 790-811
-
-
Akhurst, R.J.1
Hata, A.2
-
72
-
-
3242799550
-
Smad3 null mice develop airspace enlargement and are resistant to TGF-β-mediated pulmonary fibrosis
-
Bonniaud, P. Smad3 null mice develop airspace enlargement and are resistant to TGF-β-mediated pulmonary fibrosis. J. Immunol. 173, 2099-2108 (2004).
-
(2004)
J. Immunol.
, vol.173
, pp. 2099-2108
-
-
Bonniaud, P.1
-
73
-
-
0346727324
-
Targeted disruption of TGF-β1/Smad3 signalling protects against renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction
-
Sato, M., Muragaki, Y., Saika, S., Roberts, A. & Ooshima, A. Targeted disruption of TGF-β1/Smad3 signalling protects against renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction. J. Clin. Invest. 112, 1486-1494 (2003).
-
(2003)
J. Clin. Invest.
, vol.112
, pp. 1486-1494
-
-
Sato, M.1
Muragaki, Y.2
Saika, S.3
Roberts, A.4
Ooshima, A.5
-
74
-
-
0033524949
-
The integrin αvβ6 binds and activates latent TGF-β1: A mechanism for regulating pulmonary fibrosis
-
Munger, J. A. Huang, X. et al. The integrin αvβ6 binds and activates latent TGF-β1: a mechanism for regulating pulmonary fibrosis. Cell 96, 319-328 (1999).
-
(1999)
Cell
, vol.96
, pp. 319-328
-
-
Munger, J.A.1
Huang, X.2
-
75
-
-
48549103201
-
Inhibition of integrin αvβ6 on cholangiocytes blocks transforming growth factor b activation and retards biliary fibrosis progression
-
Patsenker, E. et al. Inhibition of integrin αvβ6 on cholangiocytes blocks transforming growth factor b activation and retards biliary fibrosis progression. Gastroenterology 135, 660-670 (2008).
-
(2008)
Gastroenterology
, vol.135
, pp. 660-670
-
-
Patsenker, E.1
-
76
-
-
84889886646
-
Targeting of av integrin identifies a core molecular pathway that regulates fibrosis in several organs
-
Henderson, N. C. et al. Targeting of av integrin identifies a core molecular pathway that regulates fibrosis in several organs. Nat. Med. 19, 1617-1624 (2013).
-
(2013)
Nat. Med.
, vol.19
, pp. 1617-1624
-
-
Henderson, N.C.1
-
77
-
-
77956425361
-
Allosteric inhibition of lysyl oxidase like 2 impedes the development of a pathologic microenvironment
-
Barry-Hamilton, V. et al. Allosteric inhibition of lysyl oxidase like 2 impedes the development of a pathologic microenvironment. Nat. Med. 16, 1009-1017 (2010).
-
(2010)
Nat. Med.
, vol.16
, pp. 1009-1017
-
-
Barry-Hamilton, V.1
-
78
-
-
77954233028
-
Modulation of lysyl oxidase like 2 enzymatic activity by an allosteric antibody inhibitor
-
Rodriguez, H. M. et al. Modulation of lysyl oxidase like 2 enzymatic activity by an allosteric antibody inhibitor. J. Biol. Chem. 285, 20964-20974 (2010).
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 20964-20974
-
-
Rodriguez, H.M.1
-
79
-
-
80052941457
-
Transglutaminase 2 and its role in pulmonary fibrosis
-
Olsen, K. C. et al. Transglutaminase 2 and its role in pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 184, 699-707 (2011).
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.184
, pp. 699-707
-
-
Olsen, K.C.1
-
80
-
-
0041342003
-
Tissue transglutaminase and the progression of human renal scarring
-
Johnson, T. S. et al. Tissue transglutaminase and the progression of human renal scarring. J. Am. Soc. Nephrol. 14, 2052-2062 (2003).
-
(2003)
J. Am. Soc. Nephrol.
, vol.14
, pp. 2052-2062
-
-
Johnson, T.S.1
-
81
-
-
70350380992
-
Increased TG2 expression can result in induction of transforming growth factor 1, causing increased synthesis and deposition of matrix proteins, which can be regulated by nitric oxide
-
Telci, D., Collighan, R. J., Basaga, H. & Griffin, M. Increased TG2 expression can result in induction of transforming growth factor 1, causing increased synthesis and deposition of matrix proteins, which can be regulated by nitric oxide. J. Biol. Chem. 284, 29547-29558 (2009).
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 29547-29558
-
-
Telci, D.1
Collighan, R.J.2
Basaga, H.3
Griffin, M.4
-
82
-
-
84878661078
-
Always cleave up your mess: Targeting collagen degradation to treat tissue fibrosis
-
McKleroy, W., Lee, T.-H. & Atabai, K. Always cleave up your mess: targeting collagen degradation to treat tissue fibrosis. Am. J. Physiol. Lung Cell. Mol. Physiol. 304, L709-L721 (2013).
-
(2013)
Am. J. Physiol. Lung Cell. Mol. Physiol.
, vol.304
, pp. L709-L721
-
-
McKleroy, W.1
Lee, T.-H.2
Atabai, K.3
-
83
-
-
84880588126
-
Assessment of Brd4 inhibition in idiopathic pulmonary fibrosis lung fibroblasts and in vivo models of lung fibrosis
-
Tang, X. et al. Assessment of Brd4 inhibition in idiopathic pulmonary fibrosis lung fibroblasts and in vivo models of lung fibrosis. Am. J. Pathol. 183, 470-479 (2013).
-
(2013)
Am. J. Pathol.
, vol.183
, pp. 470-479
-
-
Tang, X.1
-
84
-
-
37548998589
-
Pirfenidone inhibits the expression of HSP47 in TGF-β1-stimulated human lung fibroblasts
-
Nakayama, S. et al. Pirfenidone inhibits the expression of HSP47 in TGF-β1-stimulated human lung fibroblasts. Life Sci. 82, 210-217 (2008).
-
(2008)
Life Sci.
, vol.82
, pp. 210-217
-
-
Nakayama, S.1
-
85
-
-
11144328418
-
Noninvasive assessment of liver fibrosis by measurement of stiffness in patients with chronic hepatitis C
-
Ziol, M. et al. Noninvasive assessment of liver fibrosis by measurement of stiffness in patients with chronic hepatitis C. Hepatology 41, 48-54 (2005).
-
(2005)
Hepatology
, vol.41
, pp. 48-54
-
-
Ziol, M.1
-
86
-
-
65549160523
-
Tissue stiffness, latent TGF-β1 activation and mechanical signal transduction: Implications for the pathogenesis and treatment of fibrosis
-
Hinz, B. Tissue stiffness, latent TGF-β1 activation and mechanical signal transduction: implications for the pathogenesis and treatment of fibrosis. Curr. Rheumatol. Rep. 11, 120-126 (2009).
-
(2009)
Curr. Rheumatol. Rep.
, vol.11
, pp. 120-126
-
-
Hinz, B.1
-
87
-
-
84942990573
-
A multiwall platform for studying stiffness dependant cell biology
-
Mih, J. D. et al. A multiwall platform for studying stiffness dependant cell biology. PLoS ONE 6, 1-10 (2011).
-
(2011)
PLoS ONE
, vol.6
, pp. 1-10
-
-
Mih, J.D.1
-
88
-
-
77955914547
-
Feedback amplification of fibrosis through matrix stiffening and COX 2 suppression
-
Liu, F. et al. Feedback amplification of fibrosis through matrix stiffening and COX 2 suppression. J. Cell Biol. 190, 693-706 (2010).
-
(2010)
J. Cell Biol.
, vol.190
, pp. 693-706
-
-
Liu, F.1
-
89
-
-
79959893918
-
Hepatitic stellate cells require a stiff environment for myofibroblastic differentiation
-
Olsen, A. L. et al. Hepatitic stellate cells require a stiff environment for myofibroblastic differentiation. Am. J. Physiol. Lung Cell. Mol. Physiol. 301, G110-G118 (2011).
-
(2011)
Am. J. Physiol. Lung Cell. Mol. Physiol.
, vol.301
, pp. G110-G118
-
-
Olsen, A.L.1
-
90
-
-
84883175889
-
Peptide-mediated inhibition of mitogen-activated protein kinase 2 ameliorates bleomycin-induced pulmonary fibrosis
-
Vittal, R. et al. Peptide-mediated inhibition of mitogen-activated protein kinase 2 ameliorates bleomycin-induced pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol. 49, 47-57 (2013).
-
(2013)
Am. J. Respir. Cell. Mol. Biol.
, vol.49
, pp. 47-57
-
-
Vittal, R.1
-
91
-
-
39149103740
-
The bleomycin animal model: A useful tool to investigate treatment options for idiopathic pulmonary fibrosis?
-
Moeller, A., Ask, K., Warburton, D., Gauldie, J. & Kolb, M. The bleomycin animal model: a useful tool to investigate treatment options for idiopathic pulmonary fibrosis? Int. J. Biochem. Cell Biol. 40, 362-382 (2008).
-
(2008)
Int. J. Biochem. Cell Biol.
, vol.40
, pp. 362-382
-
-
Moeller, A.1
Ask, K.2
Warburton, D.3
Gauldie, J.4
Kolb, M.5
-
92
-
-
67650506936
-
Open access chemical and clinical probes to support drug discovery
-
Edwards, A. M., Bountra, C, Kerr, D. J. & Willson, T. M. Open access chemical and clinical probes to support drug discovery. Nat. Chem. Biol. 5, 436-440 (2009).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 436-440
-
-
Edwards, A.M.1
Bountra, C.2
Kerr, D.J.3
Willson, T.M.4
-
95
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
Morphy, R. & Rankovic, Z. Designed multiple ligands. An emerging drug discovery paradigm. J. Med. Chem. 48, 6523-6543 (2005).
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
96
-
-
49649123154
-
BIBF-1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumour efficacy
-
Hilberg, F., Roth, G. J., Krssak, M., Kautschitsch, S. & Sommergruber, W. BIBF-1120: triple angiokinase inhibitor with sustained receptor blockade and good antitumour efficacy. Cancer Res. 68, 4774-4782 (2008).
-
(2008)
Cancer Res.
, vol.68
, pp. 4774-4782
-
-
Hilberg, F.1
Roth, G.J.2
Krssak, M.3
Kautschitsch, S.4
Sommergruber, W.5
-
97
-
-
54249155522
-
Network pharmacology: The next paradigm in drug discovery
-
Hopkins, A. L. Network pharmacology: the next paradigm in drug discovery. Nat. Chem. Biol. 4, 682-690 (2008).
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 682-690
-
-
Hopkins, A.L.1
-
98
-
-
84861943484
-
L Chemical genetic discovery of targets and anti-targets for cancer polypharmacology
-
Dar, A. C, Das, T. K., Shokat, K. M. & Cagan, R. L Chemical genetic discovery of targets and anti-targets for cancer polypharmacology. Nature 486, 80-84 (2012).
-
(2012)
Nature
, vol.486
, pp. 80-84
-
-
Dar, A.C.1
Das, T.K.2
Shokat, K.M.3
Cagan, R.4
-
99
-
-
84870987376
-
Automated design of ligands to polypharmacological ligands
-
Besnard, J. Automated design of ligands to polypharmacological ligands. Nature 492, 215-220 (2011).
-
(2011)
Nature
, vol.492
, pp. 215-220
-
-
Besnard, J.1
-
100
-
-
84905496728
-
Phenotypic screening in cancer drug discovery-past, present and future
-
Moffat, J. G., Rudolph, J. & Bailey, D. Phenotypic screening in cancer drug discovery-past, present and future. Nat. Rev. Drug Discov. 13, 588-602 (2014).
-
(2014)
Nat. Rev. Drug Discov.
, vol.13
, pp. 588-602
-
-
Moffat, J.G.1
Rudolph, J.2
Bailey, D.3
-
101
-
-
84875457503
-
The why and how of phenotypic small molecule screens
-
Eggert, U. S. The why and how of phenotypic small molecule screens. Nat. Chem. Biol. 9, 206-209 (2013).
-
(2013)
Nat. Chem. Biol.
, vol.9
, pp. 206-209
-
-
Eggert, U.S.1
-
102
-
-
79959929769
-
How were new medicines discovered? Nat
-
Swinney, D. C. & Anthony, J. How were new medicines discovered? Nat. Review Drug Discov. 10, 507-519 (2011).
-
(2011)
Review Drug Discov.
, vol.10
, pp. 507-519
-
-
Swinney, D.C.1
Anthony, J.2
-
103
-
-
0020660817
-
4 an adequate model of human cirrhosis?
-
4 an adequate model of human cirrhosis? Hepatology 3, 112-120 (1983).
-
(1983)
Hepatology
, vol.3
, pp. 112-120
-
-
Tamayo, R.P.1
-
104
-
-
24944437926
-
Modeling liver fibrosis in rodents
-
Constandinou, C, Henderson, N. & Iredale, J. P. Modeling liver fibrosis in rodents. Methods Mol. Med. 117, 237-250 (2005).
-
(2005)
Methods Mol. Med.
, vol.117
, pp. 237-250
-
-
Constandinou, C.1
Henderson, N.2
Iredale, J.P.3
-
105
-
-
0017172219
-
Idiopathic pulmonary fibrosis. Clinical, histologic, radiographic, physiologic, scintigraphic, cytologic and biochemical aspects
-
Crystal, R. G. et al. Idiopathic pulmonary fibrosis. Clinical, histologic, radiographic, physiologic, scintigraphic, cytologic and biochemical aspects. Ann. Intern. Med. 85, 769-788 (1976).
-
(1976)
Ann. Intern. Med.
, vol.85
, pp. 769-788
-
-
Crystal, R.G.1
-
106
-
-
0347996179
-
Pirfenidone treatment decreases transforming growth factor-p 1 and matrix proteins and ameliorates fibrosis in chronic cyclosporine nephrotoxicity
-
Shihab, F S., Bennett, W. M., Yi, H. & Andoh, T F. Pirfenidone treatment decreases transforming growth factor-p 1 and matrix proteins and ameliorates fibrosis in chronic cyclosporine nephrotoxicity. Am. J. Transplant. 2, 111-119 (2002).
-
(2002)
Am. J. Transplant.
, vol.2
, pp. 111-119
-
-
Shihab, F.S.1
Bennett, W.M.2
Yi, H.3
Andoh, T.F.4
-
107
-
-
0032842405
-
Effects of pirfenidone on transforming growth factor-p gene expression at the transcriptional level in bleomycin hamster model of lung fibrosis
-
Iyer, S. N., Gurujeyalakshmi, G. & Giri, S. N. Effects of pirfenidone on transforming growth factor-p gene expression at the transcriptional level in bleomycin hamster model of lung fibrosis. J. Pharmacol. Exp. Ther. 291, 367-373 (1999).
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.291
, pp. 367-373
-
-
Iyer, S.N.1
Gurujeyalakshmi, G.2
Giri, S.N.3
-
108
-
-
0037141774
-
A novel anti-fibrotic agent pirfenidone suppresses tumor necrosis factor-a at the translational level
-
Nakazato, H., Oku, H., Yamane, S., Tsuruta, Y & Suzuki, R. A novel anti-fibrotic agent pirfenidone suppresses tumor necrosis factor-a at the translational level. Eur. J. Pharmacol. 446, 177-185 (2002).
-
(2002)
Eur. J. Pharmacol.
, vol.446
, pp. 177-185
-
-
Nakazato, H.1
Oku, H.2
Yamane, S.3
Tsuruta, Y.4
Suzuki, R.5
-
109
-
-
0037141772
-
Pirfenidone suppresses tumor necrosis factor-a, enhances interleukin 10 and protects mice from endotoxic shock
-
Oku, H., Nakazato, H., Horikawa, T., Tsuruta, Y. & Suzuki, R. Pirfenidone suppresses tumor necrosis factor-a, enhances interleukin 10 and protects mice from endotoxic shock. Eur. J. Pharmacol. 446, 167-176 (2002).
-
(2002)
Eur. J. Pharmacol.
, vol.446
, pp. 167-176
-
-
Oku, H.1
Nakazato, H.2
Horikawa, T.3
Tsuruta, Y.4
Suzuki, R.5
-
111
-
-
79958297487
-
Antifibrotic activities of pirfenidone in animal models
-
Schaefer, C. J., Ruhrmund, D. W, Pan, L, Seiwert, S. D. & Kossen, K. Antifibrotic activities of pirfenidone in animal models. Eur. Respir. Rev. 20, 85-97 (2011).
-
(2011)
Eur. Respir. Rev.
, vol.20
, pp. 85-97
-
-
Schaefer, C.J.1
Ruhrmund, D.W.2
Pan, L.3
Seiwert, S.D.4
Kossen, K.5
-
112
-
-
79956341531
-
Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): Two randomised trials
-
Noble, P. W. et al. Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials. Lancet 377, 1760-1769 (2011).
-
(2011)
Lancet
, vol.377
, pp. 1760-1769
-
-
Noble, P.W.1
-
113
-
-
84898792564
-
Anti-fibrotic and anti-inflammatory activity of the tyrosine kinase inhibitor, nintedanib, in experimental models of lung fibrosis
-
Wollin, L, Maillet, I., Quesniaux, V., Holweg, A. & Ryffel, B. Anti-fibrotic and anti-inflammatory activity of the tyrosine kinase inhibitor, nintedanib, in experimental models of lung fibrosis. J. Pharmacol. Exp. Ther. 349, 209-220 (2014).
-
(2014)
J. Pharmacol. Exp. Ther.
, vol.349
, pp. 209-220
-
-
Wollin, L.1
Maillet, I.2
Quesniaux, V.3
Holweg, A.4
Ryffel, B.5
-
116
-
-
0035852724
-
Angiotensin II type 1 receptor blockers
-
Burnier, M. Angiotensin II type 1 receptor blockers. Circulation 103, 904-912 (2001).
-
(2001)
Circulation
, vol.103
, pp. 904-912
-
-
Burnier, M.1
-
118
-
-
0030077247
-
Pharmacological characterization of A-127722: An orally active and highly potent ETA-selective receptor antagonist
-
Opgenorth, T. J. et al. Pharmacological characterization of A-127722: an orally active and highly potent ETA-selective receptor antagonist. J. Pharmacol. Exp. Ther. 276, 473-481 (1996).
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.276
, pp. 473-481
-
-
Opgenorth, T.J.1
-
119
-
-
67650034626
-
Endothelin antagonism in portal hypertensive mice: Implications for endothelin receptor-specific signaling in liver disease
-
Feng, H. Q., Weymouth, N. D. & Rockey, D. C. Endothelin antagonism in portal hypertensive mice: implications for endothelin receptor-specific signaling in liver disease. Am. J. Physiol. Gastrointest. Liver Physiol. 297, G27-G33 (2009).
-
(2009)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.297
, pp. G27-G33
-
-
Feng, H.Q.1
Weymouth, N.D.2
Rockey, D.C.3
-
120
-
-
79953295959
-
Addition of atrasentan to renin-angiotensin system blockade reduces albuminuria in diabetic nephropathy
-
Kohan, D. E. et al. Addition of atrasentan to renin-angiotensin system blockade reduces albuminuria in diabetic nephropathy. J. Am. Soc. Nephrol. 22, 763-772 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 763-772
-
-
Kohan, D.E.1
-
121
-
-
84942997901
-
-
US Patent US20100204163A1
-
Melvin Jr., L. S., Ullrich, M., Hege, H. G. & Weymann, J. Metabolites and derivatives of ambrisentan. US Patent US20100204163A1 (2008).
-
(2008)
Metabolites and Derivatives of Ambrisentan
-
-
Melvin, L.S.1
Ullrich, M.2
Hege, H.G.3
Weymann, J.4
-
122
-
-
0028946351
-
Endothelin 1 in idiopathic pulmonary fibrosis
-
Uguccioni, M. et al. Endothelin 1 in idiopathic pulmonary fibrosis. J. Clin. Pathol. 48, 330-334 (1995).
-
(1995)
J. Clin. Pathol.
, vol.48
, pp. 330-334
-
-
Uguccioni, M.1
-
123
-
-
34347228684
-
Endothelin 1 Induces alveolar epithelial-mesenchymal transition through endothelin type A receptor-mediated production of TGF-β1
-
Jain, R., Shaul, P. W., Borok, Z. & Willis, B. C. Endothelin 1 Induces alveolar epithelial-mesenchymal transition through endothelin type A receptor-mediated production of TGF-β1. Am. J. Respir. Cell. Mol. Biol. 37, 38-47 (2007).
-
(2007)
Am. J. Respir. Cell. Mol. Biol.
, vol.37
, pp. 38-47
-
-
Jain, R.1
Shaul, P.W.2
Borok, Z.3
Willis, B.C.4
-
124
-
-
84877297353
-
Treatment of idiopathic pulmonary fibrosis with ambrisentan
-
Raghu, G. et al. Treatment of idiopathic pulmonary fibrosis with ambrisentan. Ann. Intern. Med. 158, 641-649 (2013).
-
(2013)
Ann. Intern. Med.
, vol.158
, pp. 641-649
-
-
Raghu, G.1
-
125
-
-
0028292620
-
Pharmacological characterization of bosentan, a new potent orally active nonpeptide endothelin receptor antagonist
-
Clozel, M. et al. Pharmacological characterization of bosentan, a new potent orally active nonpeptide endothelin receptor antagonist. J. Pharmacol. Exp. Ther. 270, 228-235 (1994).
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.270
, pp. 228-235
-
-
Clozel, M.1
-
126
-
-
0030755489
-
Increased endothelin 1 in bleomycin-induced pulmonary fibrosis and the effect of an endothelin receptor antagonist
-
Park, S. H., Saleh, D., Giaid, A. & Michel, R. P. Increased endothelin 1 in bleomycin-induced pulmonary fibrosis and the effect of an endothelin receptor antagonist. Am. J. Respir. Crit. Care Med. 156, 600-608 (1997).
-
(1997)
Am. J. Respir. Crit. Care Med.
, vol.156
, pp. 600-608
-
-
Park, S.H.1
Saleh, D.2
Giaid, A.3
Michel, R.P.4
-
127
-
-
10444270963
-
Digital ulcers in systemic sclerosis: Prevention by treatment with bosentan, an oral endothelin receptor antagonist
-
Korn, J. H. et al. Digital ulcers in systemic sclerosis: prevention by treatment with bosentan, an oral endothelin receptor antagonist. Arthritis Rheum. 50, 3985-3993 (2004).
-
(2004)
Arthritis Rheum.
, vol.50
, pp. 3985-3993
-
-
Korn, J.H.1
-
128
-
-
77954222367
-
Randomized, prospective, placebo-controlled trial of bosentan in interstitial lung disease secondary to systemic sclerosis
-
Seibold, J. R. et al. Randomized, prospective, placebo-controlled trial of bosentan in interstitial lung disease secondary to systemic sclerosis. Arthritis Rheum. 62, 2101-2108 (2010).
-
(2010)
Arthritis Rheum.
, vol.62
, pp. 2101-2108
-
-
Seibold, J.R.1
-
129
-
-
84877828545
-
The chemistry and biological activities of N-acetylcysteine
-
Samuni, Y., Goldstein, S., Dean, O. M. & Berk, M. The chemistry and biological activities of N-acetylcysteine. Biochim. Biophys. Acta 1830, 4117-4129 (2013).
-
(2013)
Biochim. Biophys. Acta
, pp. 4117-4129
-
-
Samuni, Y.1
Goldstein, S.2
Dean, O.M.3
Berk, M.4
-
130
-
-
0037278466
-
Molecular mechanisms of N-acetylcysteine actions
-
Zafarullaha, M., Li, W. Q., Sylvestera, J. & Ahmad, M. Molecular mechanisms of N-acetylcysteine actions. Cell. Mol. Life Sci. 60, 6-20 (2003).
-
(2003)
Cell. Mol. Life Sci.
, vol.60
, pp. 6-20
-
-
Zafarullaha, M.1
Li, W.Q.2
Sylvestera, J.3
Ahmad, M.4
-
131
-
-
84862290446
-
Liver fibrosis and hepatocyte apoptosis are attenuated by GKT137831, a novel NOX4/NOX1 inhibitor in vivo
-
Jiang, J. X. et al. Liver fibrosis and hepatocyte apoptosis are attenuated by GKT137831, a novel NOX4/NOX1 inhibitor in vivo. Free Radic. Biol. Med. 53, 289-296 (2012).
-
(2012)
Free Radic. Biol. Med.
, vol.53
, pp. 289-296
-
-
Jiang, J.X.1
-
132
-
-
78149268561
-
First in class, potent, and orally bioavailable NADPH oxidase isoform 4 (Nox4) inhibitors for the treatment of idiopathic pulmonary fibrosis
-
Laleu, B. et al. First in class, potent, and orally bioavailable NADPH oxidase isoform 4 (Nox4) inhibitors for the treatment of idiopathic pulmonary fibrosis. J. Med. Chem. 53, 7715-7730 (2010).
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7715-7730
-
-
Laleu, B.1
-
133
-
-
84901835198
-
Genetic targeting or pharmacologic inhibition of NADPH oxidase Nox4 provides renoprotection in long-term diabetic nephropathy
-
Jha, J. C. et al. Genetic targeting or pharmacologic inhibition of NADPH oxidase Nox4 provides renoprotection in long-term diabetic nephropathy. J. Am. Soc. Nephrol. 25, 1237-1254 (2014).
-
(2014)
J. Am. Soc. Nephrol.
, vol.25
, pp. 1237-1254
-
-
Jha, J.C.1
-
134
-
-
84899103689
-
Reversal of persistent fibrosis in aging by targeting Nox4-Nrf2 redox imbalance
-
Hecker, L. et al. Reversal of persistent fibrosis in aging by targeting Nox4-Nrf2 redox imbalance. Sci. Transl. Med. 6, 231ra47 (2014).
-
(2014)
Sci. Transl. Med.
, vol.6
, pp. 231ra47
-
-
Hecker, L.1
-
135
-
-
84866950669
-
Nicotinamide adenine dinucleotide phosphate oxidase in experimental liver fibrosis: GKT137831 as a novel potential therapeutic agent
-
Aoyama, T. et al. Nicotinamide adenine dinucleotide phosphate oxidase in experimental liver fibrosis: GKT137831 as a novel potential therapeutic agent. Hepatology 56, 2316-2327 (2012).
-
(2012)
Hepatology
, vol.56
, pp. 2316-2327
-
-
Aoyama, T.1
-
136
-
-
84867160764
-
Bardoxolone methyl decreases megalin and activates Nrf2 in the kidney
-
Reisman, S. A. et al. Bardoxolone methyl decreases megalin and activates Nrf2 in the kidney. J. Am. Soc. Nephrol. 23, 1663-1673 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 1663-1673
-
-
Reisman, S.A.1
-
137
-
-
33845976705
-
Triterpenoid CDDO-Me blocks the NF-κB pathway by direct inhibition of IKKβ on Cys179
-
Ahmad, R., Raina, D., Meyer, C., Kharbanda, S. & Kufe, D. Triterpenoid CDDO-Me blocks the NF-κB pathway by direct inhibition of IKKβ on Cys179. J. Biol. Chem. 281, 35764-35769 (2006).
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 35764-35769
-
-
Ahmad, R.1
Raina, D.2
Meyer, C.3
Kharbanda, S.4
Kufe, D.5
-
138
-
-
79960855656
-
Bardoxolone methyl and kidney function in CKD with type 2 diabetes
-
Pergola, P. E. et al. Bardoxolone methyl and kidney function in CKD with type 2 diabetes. N. Engl. J. Med. 365, 327-336 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 327-336
-
-
Pergola, P.E.1
-
139
-
-
0034705588
-
Functional probing of the human glucocorticoid receptor steroid-interacting surface by site-directed mutagenesis
-
Lind, U. et al. Functional probing of the human glucocorticoid receptor steroid-interacting surface by site-directed mutagenesis. J. Biol. Chem. 275, 19041-19049 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 19041-19049
-
-
Lind, U.1
-
140
-
-
0032387850
-
Involution of keloid implants in athymic mice treated with pirfenidone or with triamcinolone
-
Shetlar, M.R., Shetlar, D.J., Bloom, R.F., Shetlar, C.L & Margolin, S.B. Involution of keloid implants in athymic mice treated with pirfenidone or with triamcinolone. J. Lab. Clin. Med. 132, 491-496 (1998).
-
(1998)
J. Lab. Clin. Med.
, vol.132
, pp. 491-496
-
-
Shetlar, M.R.1
Shetlar, D.J.2
Bloom, R.F.3
Shetlar, C.L.4
Margolin, S.B.5
-
141
-
-
14444281382
-
Identification of high-affinity binding sites for the insulin sensitizer rosiglitazone (BRL 49653) in rodent and human adipocytes using a radioiodinated ligand for peroxisomal proliferator-activated receptor y
-
Young, P. W. et al. Identification of high-affinity binding sites for the insulin sensitizer rosiglitazone (BRL 49653) in rodent and human adipocytes using a radioiodinated ligand for peroxisomal proliferator-activated receptor y. J. Pharmacol. Exp. Ther. 284, 751-759 (1998).
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.284
, pp. 751-759
-
-
Young, P.W.1
-
142
-
-
84864287438
-
Evaluation of the antifibrotic effect of fenofibrate and rosiglitazone on bleomycin-induced pulmonary fibrosis in rats
-
Samah, M., El Aidy, Ael-R., Tawfik, M. K. &Ewais, M. M. S. Evaluation of the antifibrotic effect of fenofibrate and rosiglitazone on bleomycin-induced pulmonary fibrosis in rats. Eur. J. Pharmacol. 689, 186-193 (2012).
-
(2012)
Eur. J. Pharmacol.
, vol.689
, pp. 186-193
-
-
Samah, M.1
El Aidy Ael, R.2
Tawfik, M.K.3
Ewais, M.M.S.4
-
143
-
-
84885405205
-
Dual peroxisome proliferator-activated receptor a/5 agonist GFT505 improves hepatic and peripheral insulin sensitivity in abdominally obese subjects
-
Cariou, B. et al. Dual peroxisome proliferator-activated receptor a/5 agonist GFT505 improves hepatic and peripheral insulin sensitivity in abdominally obese subjects. Diabetes Care 36, 2923-2930 (2013).
-
(2013)
Diabetes Care
, vol.36
, pp. 2923-2930
-
-
Cariou, B.1
-
144
-
-
84888285959
-
Hepatoprotective effects of the dual peroxisome proliferator-activated receptor a/S agonist, GFT505, in rodent models of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis
-
Staels, B. et al. Hepatoprotective effects of the dual peroxisome proliferator-activated receptor a/S agonist, GFT505, in rodent models of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis. Hepatology 58, 1941-1952 (2013).
-
(2013)
Hepatology
, vol.58
, pp. 1941-1952
-
-
Staels, B.1
-
145
-
-
84886402812
-
Pharmacokinetics safety, and tolerability of saroglitazar (ZYH1), a predominantly PPARa agonist with moderate PPARy agonist activity in healthy human subjects
-
Jani, R. H., Kansagra, K., Jain, M. R. & Patel, H. Pharmacokinetics, safety, and tolerability of saroglitazar (ZYH1), a predominantly PPARa agonist with moderate PPARy agonist activity in healthy human subjects. Clin. Drug. Investig. 33, 809-816 (2013).
-
(2013)
Clin. Drug. Investig.
, vol.33
, pp. 809-816
-
-
Jani, R.H.1
Kansagra, K.2
Jain, M.R.3
Patel, H.4
-
146
-
-
7844224790
-
N-(2 benzoylphenyl)-L-tyrosine PPARy agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents
-
Henke, B. R. et al. N-(2 benzoylphenyl)-L-tyrosine PPARy agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents. J. Med. Chem. 41, 5020-5036 (1998).
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5020-5036
-
-
Henke, B.R.1
-
147
-
-
0842308111
-
Pioglitazone prevents hepatic steatosis, fibrosis, and enzyme-altered lesions in rat liver cirrhosis induced by a choline-deficient L amino acid-defined diet
-
Kawaguchi, K. et al. Pioglitazone prevents hepatic steatosis, fibrosis, and enzyme-altered lesions in rat liver cirrhosis induced by a choline-deficient L amino acid-defined diet. Biochem. Biophys. Res. Commun. 31 5, 187-195 (2004).
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.315
, pp. 187-195
-
-
Kawaguchi, K.1
-
148
-
-
84890713835
-
HS-173, a novel PI3K inhibitor, attenuates the activation of hepatic stellate cells in liver fibrosis
-
Son, M. K. et al. HS-173, a novel PI3K inhibitor, attenuates the activation of hepatic stellate cells in liver fibrosis. Scientif. Rep. 3, 3470 (2013).
-
(2013)
Scientif. Rep.
, vol.3
, pp. 3470
-
-
Son, M.K.1
-
149
-
-
0031657020
-
Chemical modification of rapamycin: The discovery of SDZ RAD Transplant
-
Sedrani, R., Cottens, S., Kallen, J. & Schuler, W. Chemical modification of rapamycin: the discovery of SDZ RAD Transplant. Proc. 30, 2192-2194 (1998).
-
(1998)
Proc.
, vol.30
, pp. 2192-2194
-
-
Sedrani, R.1
Cottens, S.2
Kallen, J.3
Schuler, W.4
-
150
-
-
84874556145
-
Large FK506 binding proteins shape the pharmacology of rapamycin
-
März, A. M., Fabian, A. K., Kozany, C, Bracher, A. & Hausch, F Large FK506 binding proteins shape the pharmacology of rapamycin. Mol. Cell. Biol. 33, 1357-1367 (2013).
-
(2013)
Mol. Cell. Biol.
, vol.33
, pp. 1357-1367
-
-
März, A.M.1
Fabian, A.K.2
Kozany, C.3
Bracher, A.4
Hausch, F.5
-
151
-
-
67649950978
-
Rapamycin prevents transforming growth factor-a-induced pulmonary fibrosis
-
Korfhagen, T. R. et al. Rapamycin prevents transforming growth factor-a-induced pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol. 41, 562-572 (2009).
-
(2009)
Am. J. Respir. Cell. Mol. Biol.
, vol.41
, pp. 562-572
-
-
Korfhagen, T.R.1
-
152
-
-
33745269545
-
Rapamycin attenuates unilateral ureteral obstruction-induced renal fibrosis
-
Wu, M. J. et al. Rapamycin attenuates unilateral ureteral obstruction-induced renal fibrosis. Kidney Int. 69, 2029-2036 (2006).
-
(2006)
Kidney Int.
, vol.69
, pp. 2029-2036
-
-
Wu, M.J.1
-
153
-
-
84872287557
-
Synthesis and biological evaluation of analogues of the kinase inhibitor nilotinib as Abl and Kit inhibitors
-
Duveau, D. Y. et al. Synthesis and biological evaluation of analogues of the kinase inhibitor nilotinib as Abl and Kit inhibitors. Bioorg. Med. Chem. Lett. 23, 682 (2013).
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 682
-
-
Duveau, D.Y.1
-
154
-
-
13844251975
-
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl
-
Weisberg, E. et al. Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell 7, 129-141 (2005).
-
(2005)
Cancer Cell
, vol.7
, pp. 129-141
-
-
Weisberg, E.1
-
155
-
-
84860390569
-
Inhibition of PDGF TGF-p and Abl signaling and reduction of liver fibrosis by the small molecule Bcr-Abl tyrosine kinase antagonist nilotinib
-
Liu, Y et al. Inhibition of PDGF, TGF-p, and Abl signaling and reduction of liver fibrosis by the small molecule Bcr-Abl tyrosine kinase antagonist nilotinib. J. Hepatol. 55, 612-625 (2011).
-
(2011)
J. Hepatol.
, vol.55
, pp. 612-625
-
-
Liu, Y.1
-
156
-
-
79960952805
-
Nilotinib attenuates renal injury and prolongs survival in chronic kidney disease
-
Iyoda, M., Shibata, T., Hirai, Y, Kuno, Y & Akizawa, T. Nilotinib attenuates renal injury and prolongs survival in chronic kidney disease. J. Am. Soc. Nephrol. 22, 1486-1496 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 1486-1496
-
-
Iyoda, M.1
Shibata, T.2
Hirai, Y.3
Kuno, Y.4
Akizawa, T.5
-
157
-
-
80051786966
-
Effect of nilotinib on bleomycin-induced acute lung injury and pulmonary fibrosis in mice
-
Rhee, C. K. et al. Effect of nilotinib on bleomycin-induced acute lung injury and pulmonary fibrosis in mice. Respiration 82, 273-287 (2011).
-
(2011)
Respiration
, vol.82
, pp. 273-287
-
-
Rhee, C.K.1
-
158
-
-
4944249117
-
BAY 43-9006 exhibits broad spectrum oral anti-tumor activity and targets the Raf/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis
-
Wilhelm, S. M. et al. BAY 43-9006 exhibits broad spectrum oral anti-tumor activity and targets the Raf/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis. Cancer Res. 64, 7099-7109 (2004).
-
(2004)
Cancer Res.
, vol.64
, pp. 7099-7109
-
-
Wilhelm, S.M.1
-
159
-
-
77953552969
-
New insights into the antifibrotic effects of sorafenib on hepatic stellate cells and liver fibrosis
-
Wang, Y. et al. New insights into the antifibrotic effects of sorafenib on hepatic stellate cells and liver fibrosis. J. Hepatol. 53, 132-144 (2010).
-
(2010)
J. Hepatol.
, vol.53
, pp. 132-144
-
-
Wang, Y.1
-
160
-
-
79955087925
-
Sorafenib inhibits transforming growth factor p 1-mediated epithelial-mesenchymal transition and apoptosis in mouse hepatocytes
-
Chen, Y. L. et al. Sorafenib inhibits transforming growth factor p 1-mediated epithelial-mesenchymal transition and apoptosis in mouse hepatocytes. Hepatology 53, 1708-1718 (2011).
-
(2011)
Hepatology
, vol.53
, pp. 1708-1718
-
-
Chen, Y.L.1
-
161
-
-
33750989362
-
2-aminothiazole as a novel kinase inhibitor template.structure-activity relationship studies toward the discovery of n-(2-chloro-6 methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl)]-2-methyl-4 pyrimidinyl]amino)]-1, 3-thiazole-5 carboxamide (dasatinib, BMS 354825) as a potent pan-src kinase inhibitor
-
Das, J. et al. 2-aminothiazole as a novel kinase inhibitor template. structure-activity relationship studies toward the discovery of n-(2-chloro-6 methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl)]-2-methyl-4 pyrimidinyl]amino)]-1, 3-thiazole-5 carboxamide (dasatinib, BMS 354825) as a potent pan-src kinase inhibitor. J. Med. Chem. 49, 6819 (2006).
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6819
-
-
Das, J.1
-
162
-
-
46749154199
-
Dual inhibition of c-abl and PDGF receptor signaling by dasatinib and nilotinib for the treatment of dermal fibrosis
-
Akhmetshina, A. et al. Dual inhibition of c-abl and PDGF receptor signaling by dasatinib and nilotinib for the treatment of dermal fibrosis. FASEB. 22, 2214-2222 (2008).
-
(2008)
FASEB.
, vol.22
, pp. 2214-2222
-
-
Akhmetshina, A.1
-
163
-
-
77954531991
-
Selective inhibition of JAK1 and JAK2 is efficacious in rodent models of arthritis: Preclinical characterization of INCB028050
-
Fridman, J. S. et al. Selective inhibition of JAK1 and JAK2 is efficacious in rodent models of arthritis: preclinical characterization of INCB028050. J. Immunol. 184, 5298-5307 (2010).
-
(2010)
J. Immunol.
, vol.184
, pp. 5298-5307
-
-
Fridman, J.S.1
-
164
-
-
84865637745
-
JAK 2 as a novel mediator of the profibrotic effects of transforming growth factor β in systemic sclerosis
-
Dees, C. et al. JAK 2 as a novel mediator of the profibrotic effects of transforming growth factor β in systemic sclerosis. Arthritis Rheum. 64, 3006-3015 (2012).
-
(2012)
Arthritis Rheum.
, vol.64
, pp. 3006-3015
-
-
Dees, C.1
-
165
-
-
84856509517
-
Ruxolitinib
-
Mesa, R. A., Yasothan, U. & Kirkpatrick, P. Ruxolitinib. Nat. Rev. Drug Discov. 11, 103-104 (2012).
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 103-104
-
-
Mesa, R.A.1
Yasothan, U.2
Kirkpatrick, P.3
-
166
-
-
84862776641
-
Discovery of CC 930, an orally active anti-fibrotic JNK inhibitor
-
Krenitsky, V. P. et al. Discovery of CC 930, an orally active anti-fibrotic JNK inhibitor. Bioorg. Med. Chem. Lett. 22, 1433-1438 (2012).
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 1433-1438
-
-
Krenitsky, V.P.1
-
167
-
-
63349085077
-
C Jun N terminal kinase 1 is required for the development of pulmonary fibrosis
-
Alcorn, J. F. et al. c Jun N terminal kinase 1 is required for the development of pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol. 40, 422-432 (2009).
-
(2009)
Am. J. Respir. Cell. Mol. Biol.
, vol.40
, pp. 422-432
-
-
Alcorn, J.F.1
-
168
-
-
84859500859
-
Jun N terminal kinase as a potential molecular target for prevention and treatment of dermal fibrosis
-
Reich, N. et al. Jun N terminal kinase as a potential molecular target for prevention and treatment of dermal fibrosis. Ann. Rheum. Dis. 71, 737-745 (2012).
-
(2012)
Ann. Rheum. Dis.
, vol.71
, pp. 737-745
-
-
Reich, N.1
-
169
-
-
79958239562
-
Peptide inhibitors of MK2 show promise for inhibition of abdominal adhesions
-
Ward, B. C. et al. Peptide inhibitors of MK2 show promise for inhibition of abdominal adhesions. J. Surg. Res. 169, e27-e36 (2011).
-
(2011)
J. Surg. Res.
, vol.169
, pp. e27-e36
-
-
Ward, B.C.1
-
170
-
-
84908323191
-
MMI 0100 inhibits cardiac fibrosis in myocardial infarction by direct actions on cardiomyocytes and fibroblasts via MK2 inhibition
-
Xu, L. et al. MMI 0100 inhibits cardiac fibrosis in myocardial infarction by direct actions on cardiomyocytes and fibroblasts via MK2 inhibition. J. Mol. Cell. Cardiol. 77, 86-101 (2014).
-
(2014)
J. Mol. Cell. Cardiol.
, vol.77
, pp. 86-101
-
-
Xu, L.1
-
171
-
-
84856245312
-
Inhibition of mitogen activated protein kinase activated protein kinase II with MMI 0100 reduces intimal hyperplasia ex vivo and in vivo
-
Muto, A. et al. Inhibition of mitogen activated protein kinase activated protein kinase II with MMI 0100 reduces intimal hyperplasia ex vivo and in vivo. Vascul. Pharmacol. 56, 47-55 (2012).
-
(2012)
Vascul. Pharmacol.
, vol.56
, pp. 47-55
-
-
Muto, A.1
-
172
-
-
57349133022
-
Pharmacology of macitentan, an orally active tissue-targeting dual endothelin receptor antagonist
-
Iglarz, M. et al. Pharmacology of macitentan, an orally active tissue-targeting dual endothelin receptor antagonist. J. Pharmacol. Exp. Ther. 327, 736-745 (2008).
-
(2008)
J. Pharmacol. Exp. Ther.
, vol.327
, pp. 736-745
-
-
Iglarz, M.1
-
173
-
-
84870740909
-
Optimization of tissue targeting properties of macitentan, a new dual endothelin receptor antagonist, improves its efficacy in a rat model of pulmonary fibrosis associated with pulmonary arterial hypertension
-
Iglarz, M. et al. Optimization of tissue targeting properties of macitentan, a new dual endothelin receptor antagonist, improves its efficacy in a rat model of pulmonary fibrosis associated with pulmonary arterial hypertension. Am. J. Respir. Crit. Care Med. 183, A6445 (2011).
-
(2011)
Am. J. Respir. Crit. Care Med.
, vol.183
, pp. A6445
-
-
Iglarz, M.1
-
174
-
-
84888166435
-
Macitentan for the treatment of idiopathic pulmonary fibrosis: The randomised controlled MUSIC trial
-
Raghu, G. et al. Macitentan for the treatment of idiopathic pulmonary fibrosis: the randomised controlled MUSIC trial. Eur. Respir. J. 42, 1622-1632 (2013).
-
(2013)
Eur. Respir. J.
, vol.42
, pp. 1622-1632
-
-
Raghu, G.1
-
175
-
-
37849034911
-
Discovery of potent and selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis
-
Bunnage, M. E. et al. Discovery of potent and selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis. J. Med. Chem. 50, 6095-6103 (2007).
-
(2007)
J. Med. Chem.
, vol.50
, pp. 6095-6103
-
-
Bunnage, M.E.1
-
176
-
-
84942987239
-
Inhibition of activated thrombin activatable fibrinolysis inhibitor (TAFI) demonstrates therapeutic efficacy in bleomycin-induced pulmonary fibrosis in mice
-
Knoerzer, D. et al. Inhibition of activated thrombin activatable fibrinolysis inhibitor (TAFI) demonstrates therapeutic efficacy in bleomycin-induced pulmonary fibrosis in mice. Am. J. Respir. Crit. Care Med. 181, A2000 (2010).
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.181
, pp. A2000
-
-
Knoerzer, D.1
-
177
-
-
33645451489
-
Thrombin-activatable fibrinolysis inhibitor deficiency attenuates bleomycin-induced lung fibrosis
-
Fujimoto, H. et al. Thrombin-activatable fibrinolysis inhibitor deficiency attenuates bleomycin-induced lung fibrosis. Am. J. Pathol. 168, 1086-1096 (2006).
-
(2006)
Am. J. Pathol.
, vol.168
, pp. 1086-1096
-
-
Fujimoto, H.1
-
178
-
-
79960067831
-
Cation-independent mannose-6-phosphate receptor inhibitor (PXS25) inhibits fibrosis in human proximal tubular cells by inhibiting conversion of latent to active TGF-β1
-
Wong, M. G. et al. Cation-independent mannose-6-phosphate receptor inhibitor (PXS25) inhibits fibrosis in human proximal tubular cells by inhibiting conversion of latent to active TGF-β1. Am. J. Physiol. Renal. Physiol. 301, F84-F93 (2011).
-
(2011)
Am. J. Physiol. Renal. Physiol.
, vol.301
, pp. F84-F93
-
-
Wong, M.G.1
-
179
-
-
84942997902
-
PXS-25, a mannose-6-phosphate derivative, is effective in decreasing the production of extracellular matrix by TGF-β stimulated fibroblasts
-
Maldonado, F., Kottom, T. J. & Limper, A. H. PXS-25, a mannose-6-phosphate derivative, is effective in decreasing the production of extracellular matrix by TGF-β stimulated fibroblasts. Am. J. Respir. Crit. Care. Med. 179, A3471 (2009).
-
(2009)
Am. J. Respir. Crit. Care. Med.
, vol.179
, pp. A3471
-
-
Maldonado, F.1
Kottom, T.J.2
Limper, A.H.3
-
181
-
-
77954321169
-
A novel, orally active LPA(1) receptor antagonist inhibits lung fibrosis in the mouse bleomycin model
-
Swaney, J. S. et al. A novel, orally active LPA(1) receptor antagonist inhibits lung fibrosis in the mouse bleomycin model. Br. J. Pharmacol. 160, 1699-1713 (2010).
-
(2010)
Br. J. Pharmacol.
, vol.160
, pp. 1699-1713
-
-
Swaney, J.S.1
-
182
-
-
38049091636
-
The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak
-
Tager, A. M. et al. The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak. Nat. Med. 14, 45-54 (2008).
-
(2008)
Nat. Med.
, vol.14
, pp. 45-54
-
-
Tager, A.M.1
-
184
-
-
84942982442
-
Protective effect of LPA1 and 3 receptor antagonism in experimental skin fibrosis is linked to LPA activity in dermal fibroblasts of SSc patients
-
Illiano, S. et al. Protective effect of LPA1 and 3 receptor antagonism in experimental skin fibrosis is linked to LPA activity in dermal fibroblasts of SSc patients. Ann. Rheum. Dis. 72, 129 (2013).
-
(2013)
Ann. Rheum. Dis.
, vol.72
, pp. 129
-
-
Illiano, S.1
-
185
-
-
0026080801
-
Thalidomide selectively inhibits tumor necrosis factor α production by stimulated human monocytes
-
Sampaio, E. P. et al. Thalidomide selectively inhibits tumor necrosis factor α production by stimulated human monocytes. J. Exp. Med. 173, 699-703 (1991).
-
(1991)
J. Exp. Med.
, vol.173
, pp. 699-703
-
-
Sampaio, E.P.1
-
186
-
-
34250872717
-
Thalidomide prevents bleomycin-induced pulmonary fibrosis in mice
-
Tabata, C. et al. Thalidomide prevents bleomycin-induced pulmonary fibrosis in mice. J. Immunol. 179, 708-714 (2007).
-
(2007)
J. Immunol.
, vol.179
, pp. 708-714
-
-
Tabata, C.1
-
187
-
-
77749340411
-
Anti-fibrotic effect of thalidomide through inhibiting TGF-β-induced ERK1/2 pathways in bleomycin-induced lung fibrosis in mice
-
Choe, J. Y. et al. Anti-fibrotic effect of thalidomide through inhibiting TGF-β-induced ERK1/2 pathways in bleomycin-induced lung fibrosis in mice. Inflamm. Res. 59, 177-188 (2010).
-
(2010)
Inflamm. Res.
, vol.59
, pp. 177-188
-
-
Choe, J.Y.1
-
188
-
-
84871009309
-
Isosteric analogs of lenalidomide and pomalidomide: Synthesis and biological activity
-
Ruchelman, A. L. et al. Isosteric analogs of lenalidomide and pomalidomide: synthesis and biological activity. Bioorg. Med. Chem. Lett. 23, 360-365 (2013).
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 360-365
-
-
Ruchelman, A.L.1
-
189
-
-
84867404501
-
Pomalidomide is effective for prevention and treatment of experimental skin fibrosis
-
Weingärtner, S. et al. Pomalidomide is effective for prevention and treatment of experimental skin fibrosis. Ann. Rheum. Dis. 71, 1895-1899 (2012).
-
(2012)
Ann. Rheum. Dis.
, vol.71
, pp. 1895-1899
-
-
Weingärtner, S.1
-
190
-
-
84942997903
-
Efficacy of a reversible cathepsin B inhibitor in a rodent model of liver fibrosis and human pharmacokinetic profile (Poster)
-
Holsinger, L. J. et al. Efficacy of a reversible cathepsin B inhibitor in a rodent model of liver fibrosis and human pharmacokinetic profile (Poster). AASLD Annual Meeting [online] http://www.virobayinc.com/docs/AASLD-Poster-2010.pdf (2010).
-
(2010)
AASLD Annual Meeting [Online]
-
-
Holsinger, L.J.1
-
192
-
-
27444447723
-
First in class pan caspase inhibitor developed for the treatment of liver disease
-
Linton, S. D. et al. First in class pan caspase inhibitor developed for the treatment of liver disease. J. Med. Chem. 48, 6779-6782 (2005).
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6779-6782
-
-
Linton, S.D.1
-
193
-
-
1342329725
-
The caspase inhibitor IDN 6556 attenuates hepatic injury and fibrosis in the bile duct ligated mouse
-
Canbay, A. et al. The caspase inhibitor IDN 6556 attenuates hepatic injury and fibrosis in the bile duct ligated mouse. J. Pharmacol. Exp. Ther. 308, 1191-1196 (2004).
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.308
, pp. 1191-1196
-
-
Canbay, A.1
-
194
-
-
33847071146
-
Targeting antioxidants to mitochondria by conjugation to lipophilic cations
-
Murphy, M. P. & Smith, R. A. J. Targeting antioxidants to mitochondria by conjugation to lipophilic cations. Annu. Rev. Pharmacol. Toxicol. 47, 629-656 (2007).
-
(2007)
Annu. Rev. Pharmacol. Toxicol.
, vol.47
, pp. 629-656
-
-
Murphy, M.P.1
Smith, R.A.J.2
-
195
-
-
78649755150
-
+/-AkitaJ mice by the mitochondria-targeted therapy MitoQ
-
+/-AkitaJ mice by the mitochondria-targeted therapy MitoQ. Biochem. J. 432, 9-19 (2010).
-
(2010)
Biochem. J.
, vol.432
, pp. 9-19
-
-
Chacko, B.K.1
-
196
-
-
0030871070
-
Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells
-
Kiriyama, M. et al. Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells. Br. J. Pharmacol. 122, 217-224 (1997).
-
(1997)
Br. J. Pharmacol.
, vol.122
, pp. 217-224
-
-
Kiriyama, M.1
-
197
-
-
68649086860
-
Effect of beraprost sodium (BPS) in a new rat partial unilateral ureteral obstruction model
-
Takenaka, M. et al. Effect of beraprost sodium (BPS) in a new rat partial unilateral ureteral obstruction model. Prostaglandins Leukot. Essent. Fatty Acids 80, 263-267 (2009).
-
(2009)
Prostaglandins Leukot. Essent. Fatty Acids
, vol.80
, pp. 263-267
-
-
Takenaka, M.1
-
198
-
-
84860659739
-
Binding and activity of the prostacyclin receptor (IP) agonists, treprostinil and iloprost, at human prostanoid receptors: Treprostinil is a potent DP1 and EP2 agonist
-
Whittle, B. J., Silverstein, A. M., Mottola, D. M. & Clapp, L. H. Binding and activity of the prostacyclin receptor (IP) agonists, treprostinil and iloprost, at human prostanoid receptors: Treprostinil is a potent DP1 and EP2 agonist. Biochem. Pharmacol. 84, 68-75 (2012).
-
(2012)
Biochem. Pharmacol.
, vol.84
, pp. 68-75
-
-
Whittle, B.J.1
Silverstein, A.M.2
Mottola, D.M.3
Clapp, L.H.4
-
199
-
-
0034953832
-
Iloprost suppresses connective tissue growth factor production in fibroblasts and in the skin of scleroderma patients
-
Stratton, R. et al. Iloprost suppresses connective tissue growth factor production in fibroblasts and in the skin of scleroderma patients. J. Clin. Invest. 10 8, 241-250 (2001).
-
(2001)
J. Clin. Invest.
, vol.108
, pp. 241-250
-
-
Stratton, R.1
-
200
-
-
77954573839
-
A prostacyclin analogue, iloprost, protects from bleomycin-induced pulmonary fibrosis in mice
-
Zhu, Y. et al. A prostacyclin analogue, iloprost, protects from bleomycin-induced pulmonary fibrosis in mice. Respir. Res. 11, 34 (2010).
-
(2010)
Respir. Res.
, vol.11
, pp. 34
-
-
Zhu, Y.1
-
201
-
-
33646099173
-
A pilot trial of treprostinil for the treatment and prevention of digital ulcers in patients with systemic sclerosis
-
Chung, L. & Fiorentino, D. A pilot trial of treprostinil for the treatment and prevention of digital ulcers in patients with systemic sclerosis. J. Am. Acad. Dermatol. 54, 880-882 (2006).
-
(2006)
J. Am. Acad. Dermatol.
, vol.54
, pp. 880-882
-
-
Chung, L.1
Fiorentino, D.2
-
202
-
-
10744230462
-
A synthetic peptide from transforming growth factor β type III receptor inhibits liver fibrogenesis in rats with carbon tetrachloride liver injury
-
Ezquerro, I. J. et al. A synthetic peptide from transforming growth factor β type III receptor inhibits liver fibrogenesis in rats with carbon tetrachloride liver injury. Cytokine 22, 12-20 (2003).
-
(2003)
Cytokine
, vol.22
, pp. 12-20
-
-
Ezquerro, I.J.1
-
203
-
-
59449111178
-
A synthetic peptide from transforming growth factor-β1 type III receptor prevents myocardial fibrosis in spontaneously hypertensive rats
-
Hermida, N. et al. A synthetic peptide from transforming growth factor-β1 type III receptor prevents myocardial fibrosis in spontaneously hypertensive rats. Cardiovasc. Res. 81, 601-609 (2009).
-
(2009)
Cardiovasc. Res.
, vol.81
, pp. 601-609
-
-
Hermida, N.1
-
204
-
-
27144458232
-
Topical application of a peptide inhibitor of transforming growth factor-β1 ameliorates bleomycin-induced skin fibrosis
-
Santiago, B. et al. Topical application of a peptide inhibitor of transforming growth factor-β1 ameliorates bleomycin-induced skin fibrosis. J. Invest. Dermatol. 125, 450-455 (2005).
-
(2005)
J. Invest. Dermatol.
, vol.125
, pp. 450-455
-
-
Santiago, B.1
-
205
-
-
65949111512
-
Identification of human S100A9 as a novel target for treatment of autoimmune disease via binding to quinoline 3-carboxamides
-
Björk, P. et al. Identification of human S100A9 as a novel target for treatment of autoimmune disease via binding to quinoline 3-carboxamides. PLoS Biol. 7, e97 (2009).
-
(2009)
PLoS Biol.
, vol.7
, pp. e97
-
-
Björk, P.1
-
206
-
-
84942985479
-
An open-label study to evaluate biomarkers and safety in systemic sclerosis (SSc) patients treated with paquinimod (ABR 215757)
-
Hesselstrand, R. et al. An open-label study to evaluate biomarkers and safety in systemic sclerosis (SSc) patients treated with paquinimod (ABR 215757). Ann. Rheum. Dis. 73 (Suppl. 2), 566-567 (2014).
-
(2014)
Ann. Rheum. Dis.
, vol.73
, pp. 566-567
-
-
Hesselstrand, R.1
-
207
-
-
84942983555
-
Paquinimod (ABR 215757), an immunomodulatory compound, reduces fibrosis in the tight skin 1 (TSK 1) model for systemic sclerosis
-
Stenström, M. et al. Paquinimod (ABR 215757), an immunomodulatory compound, reduces fibrosis in the tight skin 1 (TSK 1) model for systemic sclerosis. Ann. Rheum. Dis. 73 (Suppl. 2), 574 (2014).
-
(2014)
Ann. Rheum. Dis.
, vol.73
, pp. 574
-
-
Stenström, M.1
-
208
-
-
0037101810
-
6α-ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity
-
Pellicciari, R. et al. 6α-ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity. J. Med. Chem. 45, 3569-3572 (2002).
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3569-3572
-
-
Pellicciari, R.1
-
209
-
-
84880664792
-
Efficacy and safety of the farnesoid X receptor agonist obeticholic acid in patients with type 2 diabetes and nonalcoholic fatty liver disease
-
Mudaliar, S. et al. Efficacy and safety of the farnesoid X receptor agonist obeticholic acid in patients with type 2 diabetes and nonalcoholic fatty liver disease. Gastroenterology 145, 574-582 (2013).
-
(2013)
Gastroenterology
, vol.145
, pp. 574-582
-
-
Mudaliar, S.1
-
210
-
-
71449109826
-
The farnesoid X receptor modulates renal lipid metabolism and diet-induced renal inflammation, fibrosis, and proteinuria
-
Wang, X. X. et al. The farnesoid X receptor modulates renal lipid metabolism and diet-induced renal inflammation, fibrosis, and proteinuria. Am. J. Physiol. Renal Physiol. 297, 1587-1596 (2009).
-
(2009)
Am. J. Physiol. Renal Physiol.
, vol.297
, pp. 1587-1596
-
-
Wang, X.X.1
-
211
-
-
84869205703
-
Synthetic farnesoid X receptor agonists induce high-density lipoprotein-mediated transhepatic cholesterol efflux in mice and monkeys and prevent atherosclerosis in cholesteryl ester transfer protein transgenic low-density lipoprotein receptor (-/-) mice
-
Hambruch, E. et al. Synthetic farnesoid X receptor agonists induce high-density lipoprotein-mediated transhepatic cholesterol efflux in mice and monkeys and prevent atherosclerosis in cholesteryl ester transfer protein transgenic low-density lipoprotein receptor (-/-) mice. J. Pharmacol. Exp. Ther. 343, 556-567 (2012).
-
(2012)
J. Pharmacol. Exp. Ther.
, vol.343
, pp. 556-567
-
-
Hambruch, E.1
-
213
-
-
0026697982
-
S-adenosylmethionine treatment prevents carbon tetrachloride-induced S-adenosyl-methionine synthetase inactivation and attenuates liver injury
-
Corrales, F. et al. S-adenosylmethionine treatment prevents carbon tetrachloride-induced S-adenosyl-methionine synthetase inactivation and attenuates liver injury. Hepatology 16, 1022-1027 (1992).
-
(1992)
Hepatology
, vol.16
, pp. 1022-1027
-
-
Corrales, F.1
-
214
-
-
24744448896
-
S-adenosylmethionine blocks collagen 1 production by preventing transforming growth factor β induction of the COL1A2 promoter
-
Nieto, N. & Cederbaum, A. I. S-adenosylmethionine blocks collagen 1 production by preventing transforming growth factor β induction of the COL1A2 promoter. J. Biol. Chem. 280, 30963-30974 (2005).
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 30963-30974
-
-
Nieto, N.1
Cederbaum, A.I.2
-
215
-
-
84880994816
-
Heavy drugs draw heavy interest from pharma backers
-
Katsnelson, A. Heavy drugs draw heavy interest from pharma backers. Nat. Med. 19, 656 (2013).
-
(2013)
Nat. Med.
, vol.19
, pp. 656
-
-
Katsnelson, A.1
-
216
-
-
84942997905
-
CTP-499, a novel drug for the treatment of chronic kidney disease, ameliorates renal fibrosis and inflammation in vivo (Poster)
-
Aslanian, A., Hogan, K., West, K., Bridson, G. W. & Wu, L. CTP-499, a novel drug for the treatment of chronic kidney disease, ameliorates renal fibrosis and inflammation in vivo (Poster). J. Am. Soc. Nephrol. 23 (Suppl. 1) (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
-
-
Aslanian, A.1
Hogan, K.2
West, K.3
Bridson, G.W.4
Wu, L.5
-
217
-
-
0034647739
-
Pyridoxamine an inhibitor of advanced glycation reactions, also inhibits advanced lipoxidation reactions
-
Onorato, J. M., Jenkins, A. J., Thorpe, S. R. & Baynes, J. W. Pyridoxamine, an inhibitor of advanced glycation reactions, also inhibits advanced lipoxidation reactions. J. Biol. Chem. 275, 21177-21184 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 21177-21184
-
-
Onorato, J.M.1
Jenkins, A.J.2
Thorpe, S.R.3
Baynes, J.W.4
-
218
-
-
0036479252
-
A post-amadori inhibitor pyridoxamine also inhibits chemical modification of proteins by scavenging carbonyl intermediates of carbohydrate and lipid degradation
-
Voziyan, P. A., Metz, T. O., Baynes, J. W. & Hudson, B. G. A post-amadori inhibitor pyridoxamine also inhibits chemical modification of proteins by scavenging carbonyl intermediates of carbohydrate and lipid degradation. J. Biol. Chem. 277, 3397-3403 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 3397-3403
-
-
Voziyan, P.A.1
Metz, T.O.2
Baynes, J.W.3
Hudson, B.G.4
-
219
-
-
35548975242
-
Effects of pyridoxamine in combined phase 2 studies of patients with type 1 and type 2 diabetes and overt nephropathy
-
Williams, M. E. et al. Effects of pyridoxamine in combined phase 2 studies of patients with type 1 and type 2 diabetes and overt nephropathy. Am. J. Nephrol. 27, 605-614 (2007).
-
(2007)
Am. J. Nephrol.
, vol.27
, pp. 605-614
-
-
Williams, M.E.1
-
220
-
-
0036183727
-
Pyridoxamine inhibits early renal disease and dyslipidemia in the streptozotocin-diabetic rat
-
Degenhardt, T. P. et al. Pyridoxamine inhibits early renal disease and dyslipidemia in the streptozotocin-diabetic rat. Kidney Int. 61, 939-950 (2002).
-
(2002)
Kidney Int.
, vol.61
, pp. 939-950
-
-
Degenhardt, T.P.1
-
221
-
-
84878245048
-
Tocopherol activity correlates with its location in a membrane: A new perspective on the antioxidant Vitamin E
-
Marquardt, D. et al. Tocopherol activity correlates with its location in a membrane: a new perspective on the antioxidant vitamin E. J. Am. Chem. Soc. 135, 7523-7533 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 7523-7533
-
-
Marquardt, D.1
-
222
-
-
77951874018
-
Pioglitazone, Vitamin E, or placebo for nonalcoholic steatohepatitis
-
Sanyal, A. J. et al. Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N. Engl. J. Med. 362, 1675-1685 (2010).
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 1675-1685
-
-
Sanyal, A.J.1
-
223
-
-
58149390072
-
Impact of the anti-inflammatory agent bindarit on the chemokinome: Selective inhibition of the monocyte chemotactic proteins
-
Mirolo, M. et al. Impact of the anti-inflammatory agent bindarit on the chemokinome: selective inhibition of the monocyte chemotactic proteins. Eur. Cytokine Netw. 19, 119-122 (2008).
-
(2008)
Eur. Cytokine Netw.
, vol.19
, pp. 119-122
-
-
Mirolo, M.1
-
224
-
-
70350448297
-
The chemokine monocyte chemoattractant protein 1 contributes to renal dysfunction in swine renovascular hypertension
-
Zhu, X. Y. et al. The chemokine monocyte chemoattractant protein 1 contributes to renal dysfunction in swine renovascular hypertension. J. Hypertens. 27, 2063-2073 (2009).
-
(2009)
J. Hypertens.
, vol.27
, pp. 2063-2073
-
-
Zhu, X.Y.1
-
225
-
-
27644510382
-
Maraviroc (UK 427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
-
Dorr, P. et al. Maraviroc (UK 427, 857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob. Agents Chemother. 49, 4721-4732 (2005).
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
-
226
-
-
84872245893
-
Maraviroc, a CCR5 antagonist, prevents development of hepatocellular carcinoma in a mouse model
-
Ochoa-Callejero, L. et al. Maraviroc, a CCR5 antagonist, prevents development of hepatocellular carcinoma in a mouse model. PLoS ONE 8, e53992 (2013).
-
(2013)
PLoS ONE
, vol.8
, pp. e53992
-
-
Ochoa-Callejero, L.1
-
227
-
-
84902435362
-
Maraviroc, a CCR5 antagonist, ameliorates the development of hepatic steatosis in a mouse model of non-alcoholic fatty liver disease (NAFLD)
-
Pérez-Martínez, L. et al. Maraviroc, a CCR5 antagonist, ameliorates the development of hepatic steatosis in a mouse model of non-alcoholic fatty liver disease (NAFLD). J. Antimicrob. Chemother. 69, 1903-1910 (2014).
-
(2014)
J. Antimicrob. Chemother.
, vol.69
, pp. 1903-1910
-
-
Pérez-Martínez, L.1
-
228
-
-
0034682767
-
Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists
-
Mirzadegan, T. et al. Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists. J. Biol. Chem. 275, 25562-25571 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 25562-25571
-
-
Mirzadegan, T.1
-
229
-
-
3042692326
-
Blockade of CCR2 ameliorates progressive fibrosis in kidney
-
Kitagawa, K. et al. Blockade of CCR2 ameliorates progressive fibrosis in kidney. Am. J. Path. 165, 237-246 (2004).
-
(2004)
Am. J. Path.
, vol.165
, pp. 237-246
-
-
Kitagawa, K.1
-
230
-
-
0034017744
-
Pharmacological properties of Y-27632, a specific inhibitor of RHO-associated kinases
-
Ishizaki, T. et al. Pharmacological properties of Y-27632, a specific inhibitor of RHO-associated kinases. Am. Soc. Pharmacol. Exp. Ther. 57, 976-983 (2000).
-
(2000)
Am. Soc. Pharmacol. Exp. Ther.
, vol.57
, pp. 976-983
-
-
Ishizaki, T.1
-
231
-
-
0036236193
-
Y-27632 prevents tubulointerstitial fibrosis in mouse kidneys with unilateral ureteral obstruction
-
Nagatoya, K. et al. Y-27632 prevents tubulointerstitial fibrosis in mouse kidneys with unilateral ureteral obstruction. Kidney Int. 61, 1684-1695 (2002).
-
(2002)
Kidney Int.
, vol.61
, pp. 1684-1695
-
-
Nagatoya, K.1
-
232
-
-
0035059634
-
A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats
-
Tada, S. et al. A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats. J. Hepatol. 34, 529-536 (2001).
-
(2001)
J. Hepatol.
, vol.34
, pp. 529-536
-
-
Tada, S.1
-
233
-
-
80051760309
-
Development of focal adhesion kinase inhibitors in cancer therapy
-
Ma, W. W. Development of focal adhesion kinase inhibitors in cancer therapy. Anticancer Agents Med. Chem. 11, 638-642 (2011).
-
(2011)
Anticancer Agents Med. Chem.
, vol.11
, pp. 638-642
-
-
Ma, W.W.1
-
234
-
-
84860487954
-
Inhibition of focal adhesion kinase prevents experimental lung fibrosis and myofibroblast formation
-
Lagares, D. et al. Inhibition of focal adhesion kinase prevents experimental lung fibrosis and myofibroblast formation. Arthritis Rheum. 64 1653-1664 (2012).
-
(2012)
Arthritis Rheum.
, vol.64
, pp. 1653-1664
-
-
Lagares, D.1
-
235
-
-
10444259759
-
Selective inhibition of activin receptorlike kinase 5 signaling blocks profibrotic transforming growth factor p responses in skin fibroblasts
-
Mori, Y. et al. Selective inhibition of activin receptorlike kinase 5 signaling blocks profibrotic transforming growth factor p responses in skin fibroblasts. Arthritis Rheum. 50, 4008-4021 (2004).
-
(2004)
Arthritis Rheum.
, vol.50
, pp. 4008-4021
-
-
Mori, Y.1
-
236
-
-
31044448265
-
Characterization of SIS3, a novel specific inhibitor of Smad3, and its effect on transforming growth factor-p 1 induced extracellular matrix expression
-
Jinnin, M., Ihn, H. & Tamaki, K. Characterization of SIS3, a novel specific inhibitor of Smad3, and its effect on transforming growth factor-p 1 induced extracellular matrix expression. Mol. Pharmacol. 69, 597-607 (2006).
-
(2006)
Mol. Pharmacol.
, vol.69
, pp. 597-607
-
-
Jinnin, M.1
Ihn, H.2
Tamaki, K.3
-
237
-
-
77957573525
-
Blockade of endothelial-mesenchymal transition by a Smad3 inhibitor delays the early development of streptozotocin-induced diabetic nephropathy
-
Li, J. et al. Blockade of endothelial-mesenchymal transition by a Smad3 inhibitor delays the early development of streptozotocin-induced diabetic nephropathy. Diabetes 59, 2612-2624 (2010).
-
(2010)
Diabetes
, vol.59
, pp. 2612-2624
-
-
Li, J.1
-
238
-
-
85060262201
-
The avp1 integrin plays a critical in vivo role in tissue fibrosis
-
Reed, N. I. et al. The avp1 integrin plays a critical in vivo role in tissue fibrosis. Sci. Transl. Med. 7, 288ra79 (2015).
-
(2015)
Sci. Transl. Med.
, vol.7
, pp. 288ra79
-
-
Reed, N.I.1
-
239
-
-
0031670654
-
Interactions between growth factors and integrins: Latent forms of transforming growth factor-p are ligands for the integrin avp 1
-
Munger, J. S., Harpel, J. G., Giancotti, F. G. & Rifkin, D. B. Interactions between growth factors and integrins: Latent forms of transforming growth factor-p are ligands for the integrin avp 1. Mol. Biol. Cell 9, 2627-2638 (1998).
-
(1998)
Mol. Biol. Cell
, vol.9
, pp. 2627-2638
-
-
Munger, J.S.1
Harpel, J.G.2
Giancotti, F.G.3
Rifkin, D.B.4
-
240
-
-
0020078304
-
P-aminopropionitrile prevents bleomycin-induced pulmonary fibrosis in the hamster
-
Riley, D. J. et al. p-aminopropionitrile prevents bleomycin-induced pulmonary fibrosis in the hamster. Am. Rev. Respir. Dis. 125, 67-73 (1982).
-
(1982)
Am. Rev. Respir. Dis.
, vol.125
, pp. 67-73
-
-
Riley, D.J.1
-
241
-
-
36849037032
-
Transglutaminase inhibition reduces fibrosis and preserves function in experimental chronic kidney disease
-
Johnson, T. S. et al. Transglutaminase inhibition reduces fibrosis and preserves function in experimental chronic kidney disease. J. Am. Soc. Nephrol. 18, 3078-3088 (2007).
-
(2007)
J. Am. Soc. Nephrol.
, vol.18
, pp. 3078-3088
-
-
Johnson, T.S.1
-
242
-
-
68249108415
-
Transglutaminase inhibition ameliorates experimental diabetic nephropathy
-
Huang, L. et al. Transglutaminase inhibition ameliorates experimental diabetic nephropathy Kidney Int. 76, 383-394 (2009).
-
(2009)
Kidney Int.
, vol.76
, pp. 383-394
-
-
Huang, L.1
-
243
-
-
0025995424
-
Beneficial effects of inhibitors of prolyl 4 hydroxylase in carbon tetrachloride-induced fibrosis of the liver in rats
-
Bickel, M. et al. Beneficial effects of inhibitors of prolyl 4 hydroxylase in carbon tetrachloride-induced fibrosis of the liver in rats. J. Hepatol. 13, S26-S34 (1991).
-
(1991)
J. Hepatol.
, vol.13
, pp. S26-S34
-
-
Bickel, M.1
-
244
-
-
0029923670
-
The prolyl 4 hydroxylase inhibitor HOE 077 prevents activation of ito cells, reducing procollagen gene expression in rat liver fibrosis induced by choline-deficient L amino acid-defined diet
-
Sakaida, I. et al. The prolyl 4 hydroxylase inhibitor HOE 077 prevents activation of ito cells, reducing procollagen gene expression in rat liver fibrosis induced by choline-deficient L amino acid-defined diet. Hepatology 23, 755-763 (1996).
-
(1996)
Hepatology
, vol.23
, pp. 755-763
-
-
Sakaida, I.1
-
245
-
-
0030806437
-
Prolyl 4-hydroxylase inhibitor (HOE 077) inhibits pig serum-induced rat liver fibrosis by preventing stellate cell activation
-
Matsumura, Y. et al. Prolyl 4-hydroxylase inhibitor (HOE 077) inhibits pig serum-induced rat liver fibrosis by preventing stellate cell activation. J. Hepatol. 27, 185-192 (1997).
-
(1997)
J. Hepatol.
, vol.27
, pp. 185-192
-
-
Matsumura, Y.1
-
246
-
-
34547558291
-
Potent and selective nonpeptidic inhibitors of procollagen C proteinase
-
Fish, P. V. et al. Potent and selective nonpeptidic inhibitors of procollagen C proteinase. J. Med. Chem. 50, 3442-3456 (2007).
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3442-3456
-
-
Fish, P.V.1
-
247
-
-
0034670162
-
Inhibition of cellular action of thrombin by N3-cyclopropyl-7-[[4-(1 methylethyl) phenyl] methyl]-7H-pyrrolo[3, 2 f]quinazoline-1, 3-diamine (SCH 79797), a nonpeptide thrombin receptor antagonist
-
Ahn, H. S. et al. Inhibition of cellular action of thrombin by N3-cyclopropyl-7-[[4-(1 methylethyl) phenyl]methyl]-7H-pyrrolo[3, 2 f]quinazoline-1, 3-diamine (SCH 79797), a nonpeptide thrombin receptor antagonist. Biochem. Pharmacol. 60, 1425-1434 (2000).
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 1425-1434
-
-
Ahn, H.S.1
-
248
-
-
84882278338
-
Protease-activated receptor 1 inhibition by SCH79797 attenuates left ventricular remodeling and profibrotic activities of cardiac fibroblasts
-
Sonin, D. L. et al. Protease-activated receptor 1 inhibition by SCH79797 attenuates left ventricular remodeling and profibrotic activities of cardiac fibroblasts. J. Cardiovasc. Pharmacol. Ther. 18, 460-475 (2013).
-
(2013)
J. Cardiovasc. Pharmacol. Ther.
, vol.18
, pp. 460-475
-
-
Sonin, D.L.1
-
249
-
-
77952011905
-
A novel inhibitor of plasminogen activator inhibitor-1 provides antithrombotic benefits devoid of bleeding effect in nonhuman primates
-
Izuhara, Y. et al. A novel inhibitor of plasminogen activator inhibitor-1 provides antithrombotic benefits devoid of bleeding effect in nonhuman primates. J. Cereb. Blood Flow Metab. 30, 904-912 (2010).
-
(2010)
J. Cereb. Blood Flow Metab.
, vol.30
, pp. 904-912
-
-
Izuhara, Y.1
-
250
-
-
84855397962
-
Therapeutic value of small molecule inhibitor to plasminogen activator inhibitor-1 for lung fibrosis
-
Huang, W. T. et al. Therapeutic value of small molecule inhibitor to plasminogen activator inhibitor-1 for lung fibrosis. Am. J. Respir. Cell. Mol. Biol. 46, 87-95 (2012).
-
(2012)
Am. J. Respir. Cell. Mol. Biol.
, vol.46
, pp. 87-95
-
-
Huang, W.T.1
-
251
-
-
0025767185
-
ONO 5046, a novel inhibitor of human neutrophil elastase
-
Kawabata, K. et al. ONO 5046, a novel inhibitor of human neutrophil elastase. Biochem. Biophys. Res. Commun. 177, 814-820 (1991).
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.177
, pp. 814-820
-
-
Kawabata, K.1
-
252
-
-
0030741005
-
Effects of neutrophil elastase inhibitor on bleomycin-induced pulmonary fibrosis in mice
-
Taooka, Y. et al. Effects of neutrophil elastase inhibitor on bleomycin-induced pulmonary fibrosis in mice. Am. J. Respir. Crit. Care Med. 156, 260-265 (1997).
-
(1997)
Am. J. Respir. Crit. Care Med.
, vol.156
, pp. 260-265
-
-
Taooka, Y.1
-
253
-
-
84871228345
-
A neutrophil elastase inhibitor prevents bleomycin-induced pulmonary fibrosis in mice
-
Takemasa, A., Ishii, Y. & Fukuda, T. A neutrophil elastase inhibitor prevents bleomycin-induced pulmonary fibrosis in mice. Eur. Respir. J. 40, 1475-1482 (2012).
-
(2012)
Eur. Respir. J.
, vol.40
, pp. 1475-1482
-
-
Takemasa, A.1
Ishii, Y.2
Fukuda, T.3
-
254
-
-
0036121027
-
Halofuginone an inhibitor of type 1 collagen synthesis and skin sclerosis, blocks transforming-growth-factor-β-mediated Smad3 activation in fibroblasts
-
McGaha, T. L., Phelps, R. G., Spiera, H. & Bona, C. Halofuginone, an inhibitor of type 1 collagen synthesis and skin sclerosis, blocks transforming-growth-factor-β-mediated Smad3 activation in fibroblasts. J. Invest. Dermatol. 118, 461-470 (2002).
-
(2002)
J. Invest. Dermatol.
, vol.118
, pp. 461-470
-
-
McGaha, T.L.1
Phelps, R.G.2
Spiera, H.3
Bona, C.4
-
255
-
-
84862776804
-
Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase
-
Keller, T. L. et al. Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase. Nat. Chem. Biol. 8, 311-317 (2012).
-
(2012)
Nat. Chem. Biol.
, vol.8
, pp. 311-317
-
-
Keller, T.L.1
-
256
-
-
66749107425
-
Halofuginone inhibits Th17 cell differentiation by activating the amino acid starvation response
-
Sundrud, M. S. et al. Halofuginone inhibits Th17 cell differentiation by activating the amino acid starvation response. Science 324, 1334 (2009).
-
(2009)
Science
, vol.324
, pp. 1334
-
-
Sundrud, M.S.1
-
257
-
-
0035142629
-
Halofuginone to prevent and treat thioacetamide-induced liver fibrosis in rats
-
Bruck, R. et al. Halofuginone to prevent and treat thioacetamide-induced liver fibrosis in rats. Hepatology 33, 379-386 (2001).
-
(2001)
Hepatology
, vol.33
, pp. 379-386
-
-
Bruck, R.1
-
258
-
-
0029858861
-
Reduction in pulmonary fibrosis in vivo by halofuginone
-
Nagler, A. et al. Reduction in pulmonary fibrosis in vivo by halofuginone. Am. J. Respir. Crit. Care. Med. 154, 1082-1086 (1996).
-
(1996)
Am. J. Respir. Crit. Care. Med.
, vol.154
, pp. 1082-1086
-
-
Nagler, A.1
-
259
-
-
0037025357
-
A point mutation that confers constitutive activity to CXCR4 reveals that T140 is an inverse agonist and that AMD3100 and ALX40 4C are weak partial agonists
-
Zhang, W. b. et al. A point mutation that confers constitutive activity to CXCR4 reveals that T140 is an inverse agonist and that AMD3100 and ALX40 4C are weak partial agonists. J. Biol. Chem. 277, 24515-24521 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 24515-24521
-
-
Zhang, W.B.1
-
260
-
-
77954734117
-
Inhibitory effect of CXC chemokine receptor 4 antagonist AMD3100 on bleomycin induced murine pulmonary fibrosis
-
Song, J. S. et al. Inhibitory effect of CXC chemokine receptor 4 antagonist AMD3100 on bleomycin induced murine pulmonary fibrosis. Exp. Mol. Med. 42, 465-476 (2010).
-
(2010)
Exp. Mol. Med.
, vol.42
, pp. 465-476
-
-
Song, J.S.1
-
261
-
-
84876015454
-
Antifibrotic effects of CXCR4 antagonist in bleomycin-induced pulmonary fibrosis in mice
-
Makino, H. et al. Antifibrotic effects of CXCR4 antagonist in bleomycin-induced pulmonary fibrosis in mice. J. Med. Invest. 60, 127-137 (2013).
-
(2013)
J. Med. Invest.
, vol.60
, pp. 127-137
-
-
Makino, H.1
-
262
-
-
0032498303
-
An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway
-
Kliewer, S. A. et al. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway. Cell 92, 73-82 (1998).
-
(1998)
Cell
, vol.92
, pp. 73-82
-
-
Kliewer, S.A.1
-
263
-
-
18844432520
-
Pregnenolone 16α carbonitrile inhibits rodent liver fibrogenesis via PXR (pregnane X receptor)-dependent and PXR-independent mechanisms
-
Marek, C. J. et al. Pregnenolone 16α carbonitrile inhibits rodent liver fibrogenesis via PXR (pregnane X receptor)-dependent and PXR-independent mechanisms. Biochem. J. 387, 601-608 (2005).
-
(2005)
Biochem. J.
, vol.387
, pp. 601-608
-
-
Marek, C.J.1
-
264
-
-
0037077308
-
The immune modulator FTY720 targets sphingosine 1 phosphate receptors
-
Brinkmann, V. et al. The immune modulator FTY720 targets sphingosine 1 phosphate receptors. J. Biol. Chem. 277, 21453-21457 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 21453-21457
-
-
Brinkmann, V.1
-
265
-
-
67650654395
-
The lymphocyte migration inhibitor FTY720 attenuates experimental hypertensive nephropathy
-
Krämer, S. et al. The lymphocyte migration inhibitor FTY720 attenuates experimental hypertensive nephropathy. Am. J. Physiol. Renal Physiol. 297, F218-F227 (2009).
-
(2009)
Am. J. Physiol. Renal Physiol.
, vol.297
, pp. F218-F227
-
-
Krämer, S.1
-
266
-
-
39149123166
-
Cross-talk between PDGF and S1P signalling elucidates the inhibitory effect and potential antifibrotic action of the immunomodulator FTY720 in activated HSC-cultures
-
Brunati, A. M. et al. Cross-talk between PDGF and S1P signalling elucidates the inhibitory effect and potential antifibrotic action of the immunomodulator FTY720 in activated HSC-cultures. Biochim. Biophys. Acta. 1783, 347-359 (2008).
-
(2008)
Biochim. Biophys. Acta.
, vol.1783
, pp. 347-359
-
-
Brunati, A.M.1
-
267
-
-
70349695861
-
Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling
-
Huang, S. M. A. et al. Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling. Nature 461, 614-620 (2009).
-
(2009)
Nature
, vol.461
, pp. 614-620
-
-
Huang, S.M.A.1
-
268
-
-
84881480768
-
Inactivation of tankyrases reduces experimental fibrosis by inhibiting canonical Wnt signalling
-
Distler, A. et al. Inactivation of tankyrases reduces experimental fibrosis by inhibiting canonical Wnt signalling. Ann. Rheum. Dis. 72, 1575-1580 (2013).
-
(2013)
Ann. Rheum. Dis.
, vol.72
, pp. 1575-1580
-
-
Distler, A.1
-
269
-
-
33846036984
-
ICG-001, a novel small molecule regulator of TCF/β-catenin transcription
-
Eguchi, M., Nguyen, C., Lee, S. C. & Kahn, M. ICG-001, a novel small molecule regulator of TCF/β-catenin transcription. Med. Chem. 1, 467-472 (2005).
-
(2005)
Med. Chem.
, vol.1
, pp. 467-472
-
-
Eguchi, M.1
Nguyen, C.2
Lee, S.C.3
Kahn, M.4
-
270
-
-
77956288500
-
Inhibition of Wnt/β catenin/CREB binding protein (CBP) signaling reverses pulmonary fibrosis
-
Henderson, W. R. et al. Inhibition of Wnt/β catenin/CREB binding protein (CBP) signaling reverses pulmonary fibrosis. Proc. Natl Acad. Sci. USA 107, 14309-14314 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 14309-14314
-
-
Henderson, W.R.1
-
271
-
-
84878406860
-
Blockade of canonical Wnt signalling ameliorates experimental dermal fibrosis
-
Beyer, C. et al. Blockade of canonical Wnt signalling ameliorates experimental dermal fibrosis. Ann. Rheum. Dis. 72, 1255-1258 (2013).
-
(2013)
Ann. Rheum. Dis.
, vol.72
, pp. 1255-1258
-
-
Beyer, C.1
-
272
-
-
0033971515
-
The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogs
-
Abramovitz, M. et al. The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogs. Biochim. Biophys. Acta 1483, 285-293 (2000).
-
(2000)
Biochim. Biophys. Acta
, vol.1483
, pp. 285-293
-
-
Abramovitz, M.1
-
273
-
-
33847037980
-
Prostaglandin E2 inhibits collagen expression and proliferation in patient-derived normal lung fibroblasts via e prostanoid 2 receptor and cAMP signalling
-
Huang, S. et al. Prostaglandin E2 inhibits collagen expression and proliferation in patient-derived normal lung fibroblasts via E prostanoid 2 receptor and cAMP signalling. Am. J. Physiol. Lung Cell Mol. Physiol. 292, L405-L413 (2007).
-
(2007)
Am. J. Physiol. Lung Cell Mol. Physiol.
, vol.292
, pp. L405-L413
-
-
Huang, S.1
-
274
-
-
0032774749
-
AAL-8810: A novel prostaglandin F2a analog with selective antagonist effects at the prostaglandin F2a (FP) receptor
-
Griffin, B. W., Klimko, P., Crider, J. Y. & Sharif, N. AAL-8810: a novel prostaglandin F2a analog with selective antagonist effects at the prostaglandin F2a (FP) receptor. J. Pharmacol. Exp. Ther. 290, 1278-1284 (1999).
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 1278-1284
-
-
Griffin, B.W.1
Klimko, P.2
Crider, J.Y.3
Sharif, N.4
-
275
-
-
84860265884
-
Prostaglandin F2a facilitates collagen synthesis in cardiac fibroblasts via an F prostanoid receptor/protein kinase C/Rho kinase pathway independent of transforming growth factor p 1
-
Ding, W. y. et al. Prostaglandin F2a facilitates collagen synthesis in cardiac fibroblasts via an F prostanoid receptor/protein kinase C/Rho kinase pathway independent of transforming growth factor p 1. Int. J. Biochem. Cell Biol. 44, 1031-1039 (2012).
-
(2012)
Int. J. Biochem. Cell Biol.
, vol.44
, pp. 1031-1039
-
-
Ding, W.Y.1
-
276
-
-
33745142545
-
Structure-activity relationship studies on a series of novel, substituted 1 benzyl-5 phenyltetrazole P2X7 antagonists
-
Nelson, D. W. et al. Structure-activity relationship studies on a series of novel, substituted 1 benzyl-5 phenyltetrazole P2X7 antagonists. J. Med. Chem. 49, 3659-3666 (2006).
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3659-3666
-
-
Nelson, D.W.1
-
277
-
-
34347333404
-
F Discovery of P2X7 receptor-selective antagonists offers new insights into P2X7 receptor function and indicates a role in chronic pain states
-
Donnelly-Roberts, D. L. & Jarvis, M. F Discovery of P2X7 receptor-selective antagonists offers new insights into P2X7 receptor function and indicates a role in chronic pain states. Br. J. Pharmacol. 151, 571-579 (2007).
-
(2007)
Br. J. Pharmacol.
, vol.151
, pp. 571-579
-
-
Donnelly-Roberts, D.L.1
Jarvis, M.2
-
278
-
-
84856752602
-
P2X7 receptor antagonism attenuates the hypertension and renal injury in Dahl salt-sensitive rats
-
Ji, X. et al. P2X7 receptor antagonism attenuates the hypertension and renal injury in Dahl salt-sensitive rats. Hypertens. Res. 35, 173-179 (2012).
-
(2012)
Hypertens. Res.
, vol.35
, pp. 173-179
-
-
Ji, X.1
-
279
-
-
0034608869
-
Design of a potent and selective inhibitor of the intermediate-conductance Ca21 activated K1 channel, IKCa1: A potential immunosuppressant
-
Wulff, H. et al. Design of a potent and selective inhibitor of the intermediate-conductance Ca21 activated K1 channel, IKCa1: a potential immunosuppressant. Proc. Natl Acad. Sci. USA 97, 8151-8156 (2000).
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 8151-8156
-
-
Wulff, H.1
-
280
-
-
70149108319
-
Renal fibrosis is attenuated by targeted disruption of KCa3.1 potassium channels
-
Grgic, I. et al. Renal fibrosis is attenuated by targeted disruption of KCa3.1 potassium channels. Proc. Natl Acad. Sci. USA 106, 14518-14523 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 14518-14523
-
-
Grgic, I.1
-
281
-
-
84885407930
-
Blockade of KCa3.1 ameliorates renal fibrosis through the TGF-p 1/Smad pathway in diabetic mice
-
Huang, C. et al. Blockade of KCa3.1 ameliorates renal fibrosis through the TGF-p 1/Smad pathway in diabetic mice. Diabetes 62, 2923-2934 (2013).
-
(2013)
Diabetes
, vol.62
, pp. 2923-2934
-
-
Huang, C.1
-
283
-
-
40849085208
-
T type calcium channel blockade as a therapeutic strategy against renal injury in rats with subtotal nephrectomy
-
Sugano, N. et al. T type calcium channel blockade as a therapeutic strategy against renal injury in rats with subtotal nephrectomy. Kidney Int. 73, 826-834 (2008).
-
(2008)
Kidney Int.
, vol.73
, pp. 826-834
-
-
Sugano, N.1
-
284
-
-
14944349361
-
Identification of small molecule chemical inhibitors of the collagen-specific chaperone Hsp47
-
Thomson, C. A., Atkinson, H. M. & Ananthanarayanan, V. S. Identification of small molecule chemical inhibitors of the collagen-specific chaperone Hsp47. J. Med. Chem. 48, 1680-1684 (2005).
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1680-1684
-
-
Thomson, C.A.1
Atkinson, H.M.2
Ananthanarayanan, V.S.3
-
285
-
-
36249016888
-
Suppression of renal tubulointerstitial fibrosis by small interfering RNA targeting heat shock protein 47
-
Xia, Z. et al. Suppression of renal tubulointerstitial fibrosis by small interfering RNA targeting heat shock protein 47. Am. J. Nephrol. 28, 34-46 (2008).
-
(2008)
Am. J. Nephrol.
, vol.28
, pp. 34-46
-
-
Xia, Z.1
-
286
-
-
84857881755
-
Regulation of transforming growth factor-p 1-driven lung fibrosis by galectin 3
-
MacKinnon, A. C. et al. Regulation of transforming growth factor-p 1-driven lung fibrosis by galectin 3. Am. J. Respir. Crit. Care Med. 185, 537-546 (2012).
-
(2012)
Am. J. Respir. Crit. Care Med.
, vol.185
, pp. 537-546
-
-
MacKinnon, A.C.1
-
287
-
-
0346957401
-
Selective protein kinase C inhibitors and their applications
-
Shen, G. X. Selective protein kinase C inhibitors and their applications. Curr. Drug Targets Cardiovasc. Haematol. Disord. 3, 301-307 (2003).
-
(2003)
Curr. Drug Targets Cardiovasc. Haematol. Disord.
, vol.3
, pp. 301-307
-
-
Shen, G.X.1
-
288
-
-
84874181070
-
PKC5 as a regulator for TGFp1 induced cc-SMA production in a murine nonalcoholic steatohepatitis model
-
Lee, S. J. et al. PKC5 as a regulator for TGFp1 induced cc-SMA production in a murine nonalcoholic steatohepatitis model. PLoS ONE 8, e55979 (2013).
-
(2013)
PLoS ONE
, vol.8
, pp. e55979
-
-
Lee, S.J.1
-
289
-
-
13844288120
-
SB 239063, a p38 MAPK inhibitor, reduces neutrophilia, inflammatory cytokines, MMP-9, and fibrosis in lung
-
Underwood, D. C. et al. SB 239063, a p38 MAPK inhibitor, reduces neutrophilia, inflammatory cytokines, MMP-9, and fibrosis in lung. Am. J. Physiol. Lung Cell Mol. Physiol. 279, L895-L902 (2000).
-
(2000)
Am. J. Physiol. Lung Cell Mol. Physiol.
, vol.279
, pp. L895-L902
-
-
Underwood, D.C.1
-
290
-
-
0019274399
-
A new class of angiotensin-converting enzyme inhibitors
-
Patchett, A. A. et al. A new class of angiotensin-converting enzyme inhibitors. Nature 288, 280-283 (1980).
-
(1980)
Nature
, vol.288
, pp. 280-283
-
-
Patchett, A.A.1
-
291
-
-
0028233556
-
Enalapril reduces collagen type IV synthesis and expansion of the interstitium in the obstructed rat kidney
-
Kaneto, H. et al. Enalapril reduces collagen type IV synthesis and expansion of the interstitium in the obstructed rat kidney. Kidney Int. 45, 1637-1647 (1994).
-
(1994)
Kidney Int.
, vol.45
, pp. 1637-1647
-
-
Kaneto, H.1
-
292
-
-
0038401338
-
2C receptor subtypes by molecular modelling
-
2C receptor subtypes by molecular modelling. Life Sci. 73, 193-207 (2003).
-
(2003)
Life Sci.
, vol.73
, pp. 193-207
-
-
Rashid, M.1
-
293
-
-
84875054830
-
2A receptor antagonists inhibit hepatic stellate cell activation and facilitate apoptosis
-
2A receptor antagonists inhibit hepatic stellate cell activation and facilitate apoptosis. Liver Int. 33, 535-543 (2013).
-
(2013)
Liver Int.
, vol.33
, pp. 535-543
-
-
Kim, D.C.1
-
294
-
-
84890336184
-
A 5-hydroxytryptamine receptor antagonist, sarpogrelate, reduces renal tubulointerstitial fibrosis by suppressing PAI-1
-
Hamasaki, Y. et al. A 5-hydroxytryptamine receptor antagonist, sarpogrelate, reduces renal tubulointerstitial fibrosis by suppressing PAI-1. Am. J. Physiol. Renal Physiol. 305, F1796-F1803 (2013).
-
(2013)
Am. J. Physiol. Renal Physiol.
, vol.305
, pp. F1796-F1803
-
-
Hamasaki, Y.1
-
295
-
-
80051789015
-
Aromatic phosphonates inhibit the lysophospholipase D activity of autotaxin
-
Jiang, G., Madan, D. & Prestwich, G. D. Aromatic phosphonates inhibit the lysophospholipase D activity of autotaxin. Bioorg. Med. Chem. Lett. 21, 5098-5101 (2011).
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 5098-5101
-
-
Jiang, G.1
Madan, D.2
Prestwich, G.D.3
-
296
-
-
84868335823
-
Pulmonary autotaxin expression contributes to the pathogenesis of pulmonary fibrosis
-
Oikonomou, N. et al. Pulmonary autotaxin expression contributes to the pathogenesis of pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol. 47, 566-574 (2012).
-
(2012)
Am. J. Respir. Cell. Mol. Biol.
, vol.47
, pp. 566-574
-
-
Oikonomou, N.1
-
297
-
-
84879636804
-
Identification and optimization of small-molecule agonists of the human relaxin hormone receptor RXFP1
-
Xiao, J. et al. Identification and optimization of small-molecule agonists of the human relaxin hormone receptor RXFP1. Nat. Commun. 4, 1953 (2013).
-
(2013)
Nat. Commun.
, vol.4
, pp. 1953
-
-
Xiao, J.1
-
298
-
-
78649588934
-
Prevention of bleomycin-induced pulmonary fibrosis by a novel antifibrotic peptide with relaxin-like activity
-
Pini, A. et al. Prevention of bleomycin-induced pulmonary fibrosis by a novel antifibrotic peptide with relaxin-like activity. J. Pharmacol. Exp. Ther. 335, 589-599 (2010).
-
(2010)
J. Pharmacol. Exp. Ther.
, vol.335
, pp. 589-599
-
-
Pini, A.1
-
299
-
-
78650847770
-
Selective inhibition of BET bromodomains
-
Filippakopoulos, P. et al. Selective inhibition of BET bromodomains. Nature 468, 1067-1073 (2010).
-
(2010)
Nature
, vol.468
, pp. 1067-1073
-
-
Filippakopoulos, P.1
-
300
-
-
84871599585
-
BET bromodomain proteins mediate downstream signaling events following growth factor stimulation in human lung fibroblasts and are involved in bleomycin-induced pulmonary fibrosis
-
Tang, X. et al. BET bromodomain proteins mediate downstream signaling events following growth factor stimulation in human lung fibroblasts and are involved in bleomycin-induced pulmonary fibrosis. Mol. Pharmacol. 83, 283-293 (2013).
-
(2013)
Mol. Pharmacol.
, vol.83
, pp. 283-293
-
-
Tang, X.1
-
302
-
-
84885190612
-
BML-11, a lipoxin receptor agonist, protected carbon tetrachloride-induced hepatic fibrosis in rats
-
Zhou, X. Y. et al. BML-11, a lipoxin receptor agonist, protected carbon tetrachloride-induced hepatic fibrosis in rats. Inflammation 36, 1101-1106 (2013).
-
(2013)
Inflammation
, vol.36
, pp. 1101-1106
-
-
Zhou, X.Y.1
-
303
-
-
49949089858
-
Cytosporone B is an agonist for nuclear orphan receptor Nur77
-
Zhan, Y. et al. Cytosporone B is an agonist for nuclear orphan receptor Nur77. Nat. Chem. Biol. 4, 548-556 (2008).
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 548-556
-
-
Zhan, Y.1
-
304
-
-
84925537240
-
Orphan nuclear receptor NR4A1 regulates transforming growth factor-ß signaling and fibrosis
-
Palumbo-Zerr, K. et al. Orphan nuclear receptor NR4A1 regulates transforming growth factor-ß signaling and fibrosis. Nat. Med. 21, 150-158 (2015).
-
(2015)
Nat. Med.
, vol.21
, pp. 150-158
-
-
Palumbo-Zerr, K.1
|