-
1
-
-
0026523829
-
Cystic fibrosis: molecular biology and therapeutic implications
-
[1] Collins, F.S., Cystic fibrosis: molecular biology and therapeutic implications. Science 256 (1992), 774–779.
-
(1992)
Science
, vol.256
, pp. 774-779
-
-
Collins, F.S.1
-
2
-
-
50649123290
-
CFTR function and prospects for therapy
-
[2] Riordan, J.R., CFTR function and prospects for therapy. Annu Rev Biochem 77 (2008), 701–726.
-
(2008)
Annu Rev Biochem
, vol.77
, pp. 701-726
-
-
Riordan, J.R.1
-
3
-
-
0027162649
-
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
-
[3] Welsh, M.J., Smith, A.E., Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell 73 (1993), 1251–1254.
-
(1993)
Cell
, vol.73
, pp. 1251-1254
-
-
Welsh, M.J.1
Smith, A.E.2
-
4
-
-
79958746554
-
Cystic fibrosis transmembrane conductance regulator intracellular processing, trafficking, and opportunities for mutation-specific treatment
-
[4] Rogan, M.P., Stoltz, D.A., Hornick, D.B., Cystic fibrosis transmembrane conductance regulator intracellular processing, trafficking, and opportunities for mutation-specific treatment. Chest 139 (2011), 1480–1490.
-
(2011)
Chest
, vol.139
, pp. 1480-1490
-
-
Rogan, M.P.1
Stoltz, D.A.2
Hornick, D.B.3
-
5
-
-
84926249742
-
New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls
-
[5] Bell, S.C., De Boeck, K., Amaral, M.D., New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls. Pharmacol Ther S0163-7258 (2014), 00122–00123.
-
(2014)
Pharmacol Ther
, vol.S0163-7258
, pp. 00122-00123
-
-
Bell, S.C.1
De Boeck, K.2
Amaral, M.D.3
-
6
-
-
84907546443
-
Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability
-
[6] Liu, X., Dawson, D.C., Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability. Biochemistry 53 (2014), 5613–5618.
-
(2014)
Biochemistry
, vol.53
, pp. 5613-5618
-
-
Liu, X.1
Dawson, D.C.2
-
7
-
-
81755163563
-
Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809
-
[7] Van Goor, F. et-al, Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809. Proc Natl Acad Sci U S A 108 (2011), 18843–18848.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 18843-18848
-
-
Van Goor, F.1
-
8
-
-
73249114731
-
Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770
-
[8] Van Goor, F. et-al, Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770. Proc Natl Acad Sci U S A 106 (2009), 18825–18830.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 18825-18830
-
-
Van Goor, F.1
-
9
-
-
84901607989
-
Cystic fibrosis: toward personalized therapies
-
[9] Ikpa, P.T., Bijvelds, M.J.C., de Jonge, H.R., Cystic fibrosis: toward personalized therapies. Int J Biochem Cell Biol 52 (2014), 192–200.
-
(2014)
Int J Biochem Cell Biol
, vol.52
, pp. 192-200
-
-
Ikpa, P.T.1
Bijvelds, M.J.C.2
de Jonge, H.R.3
-
10
-
-
84879000844
-
Cystic fibrosis transmembrane regulator correctors and potentiators
-
[10] Rowe, S.M., Verkman, A.S., Cystic fibrosis transmembrane regulator correctors and potentiators. Cold Spring Harb Perspect Med, 3, 2013.
-
(2013)
Cold Spring Harb Perspect Med
, vol.3
-
-
Rowe, S.M.1
Verkman, A.S.2
-
11
-
-
80455162465
-
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
-
[11] Ramsey, B.W. et-al, A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med 365 (2011), 1663–1672.
-
(2011)
N Engl J Med
, vol.365
, pp. 1663-1672
-
-
Ramsey, B.W.1
-
12
-
-
84911493956
-
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation
-
[12] De Boeck, K. et-al, Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation. J Cyst Fibros 13 (2014), 674–680.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 674-680
-
-
De Boeck, K.1
-
13
-
-
78549279173
-
Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation
-
[13] Accurso, F.J. et-al, Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation. N Engl J Med 363 (2010), 1991–2003.
-
(2010)
N Engl J Med
, vol.363
, pp. 1991-2003
-
-
Accurso, F.J.1
-
14
-
-
84878970875
-
Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation
-
[14] Davies, J.C. et-al, Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation. Am J Respir Crit Care Med 187 (2013), 1219–1225.
-
(2013)
Am J Respir Crit Care Med
, vol.187
, pp. 1219-1225
-
-
Davies, J.C.1
-
15
-
-
84904002908
-
A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial
-
[15] Boyle, M.P. et-al, A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial. Lancet Respir Med 2 (2014), 527–538.
-
(2014)
Lancet Respir Med
, vol.2
, pp. 527-538
-
-
Boyle, M.P.1
-
16
-
-
84990019335
-
Lumacaftor-Ivacaftor in patients with cystic fibrosis homozygous for Phe508del CFTR
-
[16] Wainwright, C.E. et-al, Lumacaftor-Ivacaftor in patients with cystic fibrosis homozygous for Phe508del CFTR. N Engl J Med 365 (2011), 1663–1672.
-
(2011)
N Engl J Med
, vol.365
, pp. 1663-1672
-
-
Wainwright, C.E.1
-
17
-
-
84895543366
-
A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor
-
e88564
-
[17] Char, J.E. et-al, A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor. PLoS One, 9, 2014, e88564.
-
(2014)
PLoS One
, vol.9
-
-
Char, J.E.1
-
18
-
-
0030850643
-
Genistein activates CFTR Cl hsp sp=“0.10”− channels via a tyrosine kinase- and protein phosphatase-independent mechanism
-
[18] French, P.J. et-al, Genistein activates CFTR Cl hsp sp=“0.10”− channels via a tyrosine kinase- and protein phosphatase-independent mechanism. Am J Physiol 273 (1997), C747–C753.
-
(1997)
Am J Physiol
, vol.273
, pp. C747-C753
-
-
French, P.J.1
-
19
-
-
0029202027
-
Genistein and tyrphostin 47 stimulate CFTR-mediated Cl hsp sp=“0.10”− secretion in T84 cell monolayers
-
[19] Sears, C.L. et-al, Genistein and tyrphostin 47 stimulate CFTR-mediated Cl hsp sp=“0.10”− secretion in T84 cell monolayers. Am J Physiol 269 (1995), G874–G882.
-
(1995)
Am J Physiol
, vol.269
, pp. G874-G882
-
-
Sears, C.L.1
-
20
-
-
2442543305
-
The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein
-
[20] Melin, P. et-al, The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein. Biochem Pharmacol 67 (2004), 2187–2196.
-
(2004)
Biochem Pharmacol
, vol.67
, pp. 2187-2196
-
-
Melin, P.1
-
21
-
-
33947543364
-
Curcumin opens cystic fibrosis transmembrane conductance regulator channels by a novel mechanism that requires neither ATP binding nor dimerization of the nucleotide-binding domains
-
[21] Wang, W., Bernard, K., Li, G., Kirk, K.L., Curcumin opens cystic fibrosis transmembrane conductance regulator channels by a novel mechanism that requires neither ATP binding nor dimerization of the nucleotide-binding domains. J Biol Chem 282 (2007), 4533–4544.
-
(2007)
J Biol Chem
, vol.282
, pp. 4533-4544
-
-
Wang, W.1
Bernard, K.2
Li, G.3
Kirk, K.L.4
-
22
-
-
71449094315
-
Curcumin cross-links cystic fibrosis transmembrane conductance regulator (CFTR) polypeptides and potentiates CFTR channel activity by distinct mechanisms
-
[22] Bernard, K., Wang, W., Narlawar, R., Schmidt, B., Kirk, K.L., Curcumin cross-links cystic fibrosis transmembrane conductance regulator (CFTR) polypeptides and potentiates CFTR channel activity by distinct mechanisms. J Biol Chem 284 (2009), 30754–30765.
-
(2009)
J Biol Chem
, vol.284
, pp. 30754-30765
-
-
Bernard, K.1
Wang, W.2
Narlawar, R.3
Schmidt, B.4
Kirk, K.L.5
-
23
-
-
14044277547
-
Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl hsp sp=“0.10”− channel activity
-
[23] Berger, A.L. et-al, Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl hsp sp=“0.10”− channel activity. J Biol Chem 280 (2005), 5221–5226.
-
(2005)
J Biol Chem
, vol.280
, pp. 5221-5226
-
-
Berger, A.L.1
-
24
-
-
84868243529
-
Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner
-
[24] Eckford, P.D.W., Li, C., Ramjeesingh, M., Bear, C.E., Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner. J Biol Chem 287 (2012), 36639–36649.
-
(2012)
J Biol Chem
, vol.287
, pp. 36639-36649
-
-
Eckford, P.D.W.1
Li, C.2
Ramjeesingh, M.3
Bear, C.E.4
-
25
-
-
84875048537
-
Vx-770 potentiates CFTR function by promoting decoupling between the gating cycle and ATP hydrolysis cycle
-
[25] Jih, K.-Y., Hwang, T.-C., Vx-770 potentiates CFTR function by promoting decoupling between the gating cycle and ATP hydrolysis cycle. Proc Natl Acad Sci U S A 110 (2013), 4404–4409.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 4404-4409
-
-
Jih, K.-Y.1
Hwang, T.-C.2
-
26
-
-
15044353957
-
Binding site of activators of the cystic fibrosis transmembrane conductance regulator in the nucleotide binding domains
-
[26] Moran, O., Galietta, L.J.V., Zegarra-Moran, O., Binding site of activators of the cystic fibrosis transmembrane conductance regulator in the nucleotide binding domains. Cell Mol Life Sci 62 (2005), 446–460.
-
(2005)
Cell Mol Life Sci
, vol.62
, pp. 446-460
-
-
Moran, O.1
Galietta, L.J.V.2
Zegarra-Moran, O.3
-
27
-
-
84887394805
-
Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implications
-
[27] Sohma, Y., Yu, Y.-C., Hwang, T.-C., Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implications. Curr Pharm Des 19 (2013), 3521–3528.
-
(2013)
Curr Pharm Des
, vol.19
, pp. 3521-3528
-
-
Sohma, Y.1
Yu, Y.-C.2
Hwang, T.-C.3
-
28
-
-
79958276128
-
Curcumin and genistein additively potentiate G551D-CFTR
-
[28] Yu, Y.-C. et-al, Curcumin and genistein additively potentiate G551D-CFTR. J Cyst Fibros 10 (2011), 243–252.
-
(2011)
J Cyst Fibros
, vol.10
, pp. 243-252
-
-
Yu, Y.-C.1
-
29
-
-
84880292828
-
A functional CFTR assay using primary cystic fibrosis intestinal organoids
-
[29] Dekkers, J.F. et-al, A functional CFTR assay using primary cystic fibrosis intestinal organoids. Nat Med 19 (2013), 939–945.
-
(2013)
Nat Med
, vol.19
, pp. 939-945
-
-
Dekkers, J.F.1
-
30
-
-
84902335825
-
Novel opportunities for CFTR-targeting drug development using organoids
-
e27112
-
[30] Dekkers, J.F., van der Ent, C.K., Beekman, J.M., Novel opportunities for CFTR-targeting drug development using organoids. Rare Dis, 1, 2013, e27112.
-
(2013)
Rare Dis
, vol.1
-
-
Dekkers, J.F.1
van der Ent, C.K.2
Beekman, J.M.3
-
31
-
-
84890033064
-
Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients
-
[31] Schwank, G. et-al, Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients. Cell Stem Cell 13 (2013), 653–658.
-
(2013)
Cell Stem Cell
, vol.13
, pp. 653-658
-
-
Schwank, G.1
-
32
-
-
84912572110
-
Modulation of the maladaptive stress response to manage diseases of protein folding
-
e1001998
-
[32] Roth, D.M. et-al, Modulation of the maladaptive stress response to manage diseases of protein folding. PLoS Biol, 12, 2014, e1001998.
-
(2014)
PLoS Biol
, vol.12
-
-
Roth, D.M.1
-
33
-
-
84879410121
-
Mechanism-based corrector combination restores ΔF508-CFTR folding and function
-
[33] Okiyoneda, T. et-al, Mechanism-based corrector combination restores ΔF508-CFTR folding and function. Nat Chem Biol 9 (2013), 444–454.
-
(2013)
Nat Chem Biol
, vol.9
, pp. 444-454
-
-
Okiyoneda, T.1
-
34
-
-
84901398808
-
VX-809 and related corrector compounds exhibit secondary activity stabilizing active F508del-CFTR after its partial rescue to the cell surface
-
[34] Eckford, P.D.W. et-al, VX-809 and related corrector compounds exhibit secondary activity stabilizing active F508del-CFTR after its partial rescue to the cell surface. Chem Biol 21 (2014), 666–678.
-
(2014)
Chem Biol
, vol.21
, pp. 666-678
-
-
Eckford, P.D.W.1
-
35
-
-
78751644734
-
Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts
-
[35] Sato, T. et-al, Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts. Nature 469 (2011), 415–418.
-
(2011)
Nature
, vol.469
, pp. 415-418
-
-
Sato, T.1
-
36
-
-
80054857419
-
Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium
-
[36] Sato, T. et-al, Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. Gastroenterology 141 (2011), 1762–1772.
-
(2011)
Gastroenterology
, vol.141
, pp. 1762-1772
-
-
Sato, T.1
-
37
-
-
80053978141
-
Isolation and in vitro expansion of human colonic stem cells
-
[37] Jung, P. et-al, Isolation and in vitro expansion of human colonic stem cells. Nat Med 17 (2011), 1225–1227.
-
(2011)
Nat Med
, vol.17
, pp. 1225-1227
-
-
Jung, P.1
-
38
-
-
84878760040
-
Growing self-organizing mini-guts from a single intestinal stem cell: mechanism and applications
-
[38] Sato, T., Clevers, H., Growing self-organizing mini-guts from a single intestinal stem cell: mechanism and applications. Science 340 (2013), 1190–1194.
-
(2013)
Science
, vol.340
, pp. 1190-1194
-
-
Sato, T.1
Clevers, H.2
-
39
-
-
78650509172
-
Identification of synergistic combinations of F508del cystic fibrosis transmembrane conductance regulator (CFTR) modulators
-
[39] Lin, S. et-al, Identification of synergistic combinations of F508del cystic fibrosis transmembrane conductance regulator (CFTR) modulators. Assay Drug Dev Technol 8 (2010), 669–684.
-
(2010)
Assay Drug Dev Technol
, vol.8
, pp. 669-684
-
-
Lin, S.1
-
40
-
-
84901453811
-
Synergy-based small-molecule screen using a human lung epithelial cell line yields ΔF508-CFTR correctors that augment VX-809 maximal efficacy
-
[40] Phuan, P.-W. et-al, Synergy-based small-molecule screen using a human lung epithelial cell line yields ΔF508-CFTR correctors that augment VX-809 maximal efficacy. Mol Pharmacol 86 (2014), 42–51.
-
(2014)
Mol Pharmacol
, vol.86
, pp. 42-51
-
-
Phuan, P.-W.1
-
41
-
-
84988009573
-
Searching for combinations of small-molecule correctors to restore f508del-cystic fibrosis transmembrane conductance regulator function and processing
-
[41] Boinot, C., Jollivet Souchet, M., Ferru-Clément, R., Becq, F., Searching for combinations of small-molecule correctors to restore f508del-cystic fibrosis transmembrane conductance regulator function and processing. J Pharmacol Exp Ther 350 (2014), 624–634.
-
(2014)
J Pharmacol Exp Ther
, vol.350
, pp. 624-634
-
-
Boinot, C.1
Jollivet Souchet, M.2
Ferru-Clément, R.3
Becq, F.4
-
42
-
-
80052328287
-
The K hsp sp=“0.10”+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients
-
e24445
-
[42] Roth, E.K. et-al, The K hsp sp=“0.10”+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients. PLoS One, 6, 2011, e24445.
-
(2011)
PLoS One
, vol.6
-
-
Roth, E.K.1
-
43
-
-
84883799745
-
Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function
-
e73905
-
[43] Clancy, J.P. et-al, Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function. PLoS One, 8, 2013, e73905.
-
(2013)
PLoS One
, vol.8
-
-
Clancy, J.P.1
-
44
-
-
84902343264
-
CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy: report on the pre-conference meeting to the 11th ECFS Basic Science Conference, Malta, 26-29 March 2014
-
[44] Beekman, J.M. et-al, CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy: report on the pre-conference meeting to the 11th ECFS Basic Science Conference, Malta, 26-29 March 2014. J Cyst Fibros 13 (2014), 363–372.
-
(2014)
J Cyst Fibros
, vol.13
, pp. 363-372
-
-
Beekman, J.M.1
-
45
-
-
0031881489
-
Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects
-
[45] Wang, F., Zeltwanger, S., Yang, I.C., Nairn, A.C., Hwang, T.C., Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects. J Gen Physiol 111 (1998), 477–490.
-
(1998)
J Gen Physiol
, vol.111
, pp. 477-490
-
-
Wang, F.1
Zeltwanger, S.2
Yang, I.C.3
Nairn, A.C.4
Hwang, T.C.5
-
46
-
-
0034655847
-
Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl hsp sp=“0.10”− channels expressed in murine cell line
-
[46] Lansdell, K.A., Cai, Z., Kidd, J.F., Sheppard, D.N., Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl hsp sp=“0.10”− channels expressed in murine cell line. J Physiol Lond 524 Pt 2 (2000), 317–330.
-
(2000)
J Physiol Lond
, vol.524 Pt 2
, pp. 317-330
-
-
Lansdell, K.A.1
Cai, Z.2
Kidd, J.F.3
Sheppard, D.N.4
-
47
-
-
0037183975
-
The cystic fibrosis mutation G551D alters the non-Michaelis–Menten behavior of the cystic fibrosis transmembrane conductance regulator (CFTR) channel and abolishes the inhibitory Genistein binding site
-
[47] Derand, R., Bulteau-Pignoux, L., Becq, F., The cystic fibrosis mutation G551D alters the non-Michaelis–Menten behavior of the cystic fibrosis transmembrane conductance regulator (CFTR) channel and abolishes the inhibitory Genistein binding site. J Biol Chem 277 (2002), 35999–36004.
-
(2002)
J Biol Chem
, vol.277
, pp. 35999-36004
-
-
Derand, R.1
Bulteau-Pignoux, L.2
Becq, F.3
-
48
-
-
2442659029
-
Function of the ABC signature sequences in the human multidrug resistance protein 1
-
[48] Ren, X.-Q. et-al, Function of the ABC signature sequences in the human multidrug resistance protein 1. Mol Pharmacol 65 (2004), 1536–1542.
-
(2004)
Mol Pharmacol
, vol.65
, pp. 1536-1542
-
-
Ren, X.-Q.1
-
49
-
-
84908261565
-
A single amino acid substitution in CFTR converts ATP to an inhibitory ligand
-
[49] Lin, W.-Y., Jih, K.-Y., Hwang, T.-C., A single amino acid substitution in CFTR converts ATP to an inhibitory ligand. J Gen Physiol 144 (2014), 311–320.
-
(2014)
J Gen Physiol
, vol.144
, pp. 311-320
-
-
Lin, W.-Y.1
Jih, K.-Y.2
Hwang, T.-C.3
-
50
-
-
84907211027
-
Some gating potentiators, including VX-770, diminish ΔF508-CFTR functional expression
-
[50] Veit, G. et-al, Some gating potentiators, including VX-770, diminish ΔF508-CFTR functional expression. Sci Transl Med, 6, 2014, 246ra97.
-
(2014)
Sci Transl Med
, vol.6
, pp. 246ra97
-
-
Veit, G.1
-
51
-
-
84907223425
-
Potentiator ivacaftor abrogates pharmacological correction of ΔF508 CFTR in cystic fibrosis
-
[51] Cholon, D.M. et-al, Potentiator ivacaftor abrogates pharmacological correction of ΔF508 CFTR in cystic fibrosis. Sci Transl Med, 6, 2014, 246ra96.
-
(2014)
Sci Transl Med
, vol.6
, pp. 246ra96
-
-
Cholon, D.M.1
-
52
-
-
84855202429
-
Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation
-
[52] Clancy, J.P. et-al, Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation. Thorax 67 (2012), 12–18.
-
(2012)
Thorax
, vol.67
, pp. 12-18
-
-
Clancy, J.P.1
-
53
-
-
37549051274
-
Bioavailability of curcumin: problems and promises
-
[53] Anand, P., Kunnumakkara, A.B., Newman, R.A., Aggarwal, B.B., Bioavailability of curcumin: problems and promises. Mol Pharm 4 (2007), 807–818.
-
(2007)
Mol Pharm
, vol.4
, pp. 807-818
-
-
Anand, P.1
Kunnumakkara, A.B.2
Newman, R.A.3
Aggarwal, B.B.4
-
54
-
-
84870212371
-
Bioavailability and pharmacokinetics of genistein: mechanistic studies on its ADME
-
[54] Yang, Z., Kulkarni, K., Zhu, W., Hu, M., Bioavailability and pharmacokinetics of genistein: mechanistic studies on its ADME. Anticancer Agents Med Chem 12 (2012), 1264–1280.
-
(2012)
Anticancer Agents Med Chem
, vol.12
, pp. 1264-1280
-
-
Yang, Z.1
Kulkarni, K.2
Zhu, W.3
Hu, M.4
-
55
-
-
38349011007
-
Curcumin: preventive and therapeutic properties in laboratory studies and clinical trials
-
[55] Strimpakos, A.S., Sharma, R.A., Curcumin: preventive and therapeutic properties in laboratory studies and clinical trials. Antioxid Redox Signal 10 (2008), 511–545.
-
(2008)
Antioxid Redox Signal
, vol.10
, pp. 511-545
-
-
Strimpakos, A.S.1
Sharma, R.A.2
-
56
-
-
79958083917
-
New clinical diagnostic procedures for cystic fibrosis in Europe
-
[56] De Boeck, K. et-al, New clinical diagnostic procedures for cystic fibrosis in Europe. J Cyst Fibros 10:Suppl. 2 (2011), S53–S66.
-
(2011)
J Cyst Fibros
, vol.10
, pp. S53-S66
-
-
De Boeck, K.1
-
57
-
-
11044232030
-
Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating using chambers
-
[57] de Jonge, H.R. et-al, Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating using chambers. J Cyst Fibros 3:Suppl. 2 (2004), 159–163.
-
(2004)
J Cyst Fibros
, vol.3
, pp. 159-163
-
-
de Jonge, H.R.1
|