-
2
-
-
78651023652
-
Characterisation and separation of an inhibitor of viral hemagglutination present in urine
-
Tamm I, Horsfall FL. Characterisation and separation of an inhibitor of viral hemagglutination present in urine. Proc Soc Exp Biol Med 1950; 74: 108-114.
-
(1950)
Proc Soc Exp Biol Med
, vol.74
, pp. 108-114
-
-
Tamm, I.1
Horsfall, F.L.2
-
3
-
-
0034805901
-
Mechanism of release of urinary Tamm-Horsfall glycoprotein from the kidney GPI-anchored counterpart
-
Cavallone D, Malagolini N, Serafini-Cessi F. Mechanism of release of urinary Tamm-Horsfall glycoprotein from the kidney GPI-anchored counterpart. Biochem Biophys Res Commun 2001; 280: 110-114.
-
(2001)
Biochem Biophys Res Commun
, vol.280
, pp. 110-114
-
-
Cavallone, D.1
Malagolini, N.2
Serafini-Cessi, F.3
-
5
-
-
0035930894
-
Analysis of the C-terminal structure of urinary Tamm-Horsfall protein reveals that the release of the glycosyl phosphatidylinositol-anchored counterpart from the kidney occurs by phenylalanine-specific proteolysis
-
Fukuoka S, Kobayashi K. Analysis of the C-terminal structure of urinary Tamm-Horsfall protein reveals that the release of the glycosyl phosphatidylinositol-anchored counterpart from the kidney occurs by phenylalanine-specific proteolysis. Biochem Biophys Res Commun 2001; 289: 1044-1048.
-
(2001)
Biochem Biophys Res Commun
, vol.289
, pp. 1044-1048
-
-
Fukuoka, S.1
Kobayashi, K.2
-
6
-
-
0022406053
-
Ultrastructural localization of Tamm-Horsfall glycoprotein (THP) in rat kidney as revealed by protein A-gold immunocytochemistry
-
Bachmann S, Koeppen-Hagemann I, Kriz W. Ultrastructural localization of Tamm-Horsfall glycoprotein (THP) in rat kidney as revealed by protein A-gold immunocytochemistry. Histochemistry 1985; 83: 531-538.
-
(1985)
Histochemistry
, vol.83
, pp. 531-538
-
-
Bachmann, S.1
Koeppen-Hagemann, I.2
Kriz, W.3
-
7
-
-
0026671080
-
Mechanoelectrical transduction, ion movement and water stasis in uromodulin
-
Mattey M, Naftalin L. Mechanoelectrical transduction, ion movement and water stasis in uromodulin. Experientia 1992; 48: 975-980.
-
(1992)
Experientia
, vol.48
, pp. 975-980
-
-
Mattey, M.1
Naftalin, L.2
-
8
-
-
1342322652
-
Tamm-Horsfall protein knockout mice are more prone to urinary tract infection: Rapid communication
-
Bates JM, Raffi HM, Prasadan K, Mascarenhas R, Laszik Z, Maeda N, Hultgren SJ, Kumar S. Tamm-Horsfall protein knockout mice are more prone to urinary tract infection: Rapid communication. Kidney Int 2004; 65: 791-797.
-
(2004)
Kidney Int
, vol.65
, pp. 791-797
-
-
Bates, J.M.1
Raffi, H.M.2
Prasadan, K.3
Mascarenhas, R.4
Laszik, Z.5
Maeda, N.6
Hultgren, S.J.7
Kumar, S.8
-
9
-
-
1642306406
-
Ablation of the Tamm-Horsfall protein gene increases susceptibility of mice to bladder colonization by type 1-fimbriated Escherichia coli
-
Mo L, Zhu XH, Huang HY, Shapiro E, Hasty DL, Wu XR. Ablation of the Tamm-Horsfall protein gene increases susceptibility of mice to bladder colonization by type 1-fimbriated Escherichia coli. Am J Physiol Renal Physiol 2004; 286: F795-F802.
-
(2004)
Am J Physiol Renal Physiol
, vol.286
-
-
Mo, L.1
Zhu, X.H.2
Huang, H.Y.3
Shapiro, E.4
Hasty, D.L.5
Wu, X.R.6
-
10
-
-
29144443665
-
Tamm-Horsfall protein acts as a general host-defense factor against bacterial cystitis
-
Raffi HS, Bates JM Jr, Laszik Z, Kumar S. Tamm-Horsfall protein acts as a general host-defense factor against bacterial cystitis. Am J Nephrol 2005; 25: 570-578.
-
(2005)
Am J Nephrol
, vol.25
, pp. 570-578
-
-
Raffi, H.S.1
Bates Jr., J.M.2
Laszik, Z.3
Kumar, S.4
-
11
-
-
4344664015
-
Tamm-Horsfall protein is a critical renal defense factor protecting against calcium oxalate crystal formation
-
Mo L, Huang HY, Zhu XH, Shapiro E, Hasty DL, Wu XR. Tamm-Horsfall protein is a critical renal defense factor protecting against calcium oxalate crystal formation. Kidney Int 2004; 66: 1159-1166.
-
(2004)
Kidney Int
, vol.66
, pp. 1159-1166
-
-
Mo, L.1
Huang, H.Y.2
Zhu, X.H.3
Shapiro, E.4
Hasty, D.L.5
Wu, X.R.6
-
12
-
-
20144373629
-
Tamm-Horsfall glycoprotein links innate immune cell activation with adaptive immunity via a Toll-like receptor-4-dependent mechanism
-
Saemann MD, Weichhart T, Zeyda M, Staffler G, Schunn M, Stuhlmeier KM, Sobanov Y, Stulnig TM, Akira S, von Gabain A, von Ahsen U, Horl WH, Zlabinger GJ. Tamm-Horsfall glycoprotein links innate immune cell activation with adaptive immunity via a Toll-like receptor-4-dependent mechanism. J Clin Invest 2005; 115: 468-475.
-
(2005)
J Clin Invest
, vol.115
, pp. 468-475
-
-
Saemann, M.D.1
Weichhart, T.2
Zeyda, M.3
Staffler, G.4
Schunn, M.5
Stuhlmeier, K.M.6
Sobanov, Y.7
Stulnig, T.M.8
Akira, S.9
von Gabain, A.10
von Ahsen, U.11
Horl, W.H.12
Zlabinger, G.J.13
-
13
-
-
17444381195
-
Tamm-Horsfall protein: A multilayered defence molecule against urinary tract infection
-
Saemann MD, Weichhart T, Horl WH, Zlabinger GJ. Tamm-Horsfall protein: A multilayered defence molecule against urinary tract infection. Eur J Clin Invest 2005; 35: 227-235.
-
(2005)
Eur J Clin Invest
, vol.35
, pp. 227-235
-
-
Saemann, M.D.1
Weichhart, T.2
Horl, W.H.3
Zlabinger, G.J.4
-
14
-
-
0036914069
-
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy
-
Hart TC, Gorry MC, Hart PS, Woodard AS, Shihabi Z, Sandhu J, Shirts B, Xu L, Zhu H, Barmada MM, Bleyer AJ. Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy. J Med Genet 2002; 39: 882-892.
-
(2002)
J Med Genet
, vol.39
, pp. 882-892
-
-
Hart, T.C.1
Gorry, M.C.2
Hart, P.S.3
Woodard, A.S.4
Shihabi, Z.5
Sandhu, J.6
Shirts, B.7
Xu, L.8
Zhu, H.9
Barmada, M.M.10
Bleyer, A.J.11
-
15
-
-
0346752171
-
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics
-
Rampoldi L, Caridi G, Santon D, Boaretto F, Bernascone I, Lamorte G, Tardanico R, Dagnino M, Colussi G, Scolari F, Ghiggeri GM, Amoroso A, Casari G. Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. Hum Mol Genet 2003; 12: 3369-3384.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3369-3384
-
-
Rampoldi, L.1
Caridi, G.2
Santon, D.3
Boaretto, F.4
Bernascone, I.5
Lamorte, G.6
Tardanico, R.7
Dagnino, M.8
Colussi, G.9
Scolari, F.10
Ghiggeri, G.M.11
Amoroso, A.12
Casari, G.13
-
16
-
-
20544476406
-
A novel pattern of mutation in uromodulin disorders: Autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease
-
Lens XM, Banet JF, Outeda P, Barrio-Lucia V. A novel pattern of mutation in uromodulin disorders: Autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease. Am J Kidney Dis 2005; 46: 52-57.
-
(2005)
Am J Kidney Dis
, vol.46
, pp. 52-57
-
-
Lens, X.M.1
Banet, J.F.2
Outeda, P.3
Barrio-Lucia, V.4
-
17
-
-
0242639932
-
Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene
-
Bleyer AJ, Trachtman H, Sandhu J, Gorry MC, Hart TC. Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene. Am J Kidney Dis 2003; 42: E20-E26.
-
(2003)
Am J Kidney Dis
, vol.42
-
-
Bleyer, A.J.1
Trachtman, H.2
Sandhu, J.3
Gorry, M.C.4
Hart, T.C.5
-
18
-
-
0037341801
-
Uromodulin mutations cause familial juvenile hyperuricemic nephropathy
-
Turner JJ, Stacey JM, Harding B, Kotanko P, Lhotta K, Puig JG, Roberts I, Torres RJ, Thakker RV. Uromodulin mutations cause familial juvenile hyperuricemic nephropathy. J Clin Endocrinol Metab 2003; 88: 1398-1401.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 1398-1401
-
-
Turner, J.J.1
Stacey, J.M.2
Harding, B.3
Kotanko, P.4
Lhotta, K.5
Puig, J.G.6
Roberts, I.7
Torres, R.J.8
Thakker, R.V.9
-
19
-
-
10744226387
-
A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin
-
Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M, Cochat P, Cosyns JP, Mougenot B, Rider MH, et al. A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin. J Am Soc Nephrol 2003; 14: 2883-2893.
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 2883-2893
-
-
Dahan, K.1
Devuyst, O.2
Smaers, M.3
Vertommen, D.4
Loute, G.5
Poux, J.M.6
Viron, B.7
Jacquot, C.8
Gagnadoux, M.F.9
Chauveau, D.10
Buchler, M.11
Cochat, P.12
Cosyns, J.P.13
Mougenot, B.14
Rider, M.H.15
-
20
-
-
33749535090
-
Familial juvenile hyperuricemic nephropathy (FJHN): Linkage analysis in 17 families, transcriptional characterization of the FJHN critical region on chromosome 16p11.2 and the analyses of uromodulin and other candidate genes
-
Poster 2324
-
Hodanova K, Kalbacova M, Stiburkova B, Majewski J, Marinaki A, Simmonds HA, Matthijs G, Fryns JP, Ott J, Kmoch S. Familial juvenile hyperuricemic nephropathy (FJHN): Linkage analysis in 17 families, transcriptional characterization of the FJHN critical region on chromosome 16p11.2 and the analyses of uromodulin and other candidate genes. Am J Hum Genet 2003; 73: 565 (Poster 2324).
-
(2003)
Am J Hum Genet
, vol.73
, pp. 565
-
-
Hodanova, K.1
Kalbacova, M.2
Stiburkova, B.3
Majewski, J.4
Marinaki, A.5
Simmonds, H.A.6
Matthijs, G.7
Fryns, J.P.8
Ott, J.9
Kmoch, S.10
-
21
-
-
10744224657
-
Mutations of the uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains
-
Wolf MT, Mucha BE, Attanasio M, Zalewski I, Karle SM, Neumann HP, Rahman N, Bader B, Baldamus CA, Otto E, Witzgall R, Fuchshuber A, Hildebrandt F. Mutations of the uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains. Kidney Int 2003; 64: 1580-1587.
-
(2003)
Kidney Int
, vol.64
, pp. 1580-1587
-
-
Wolf, M.T.1
Mucha, B.E.2
Attanasio, M.3
Zalewski, I.4
Karle, S.M.5
Neumann, H.P.6
Rahman, N.7
Bader, B.8
Baldamus, C.A.9
Otto, E.10
Witzgall, R.11
Fuchshuber, A.12
Hildebrandt, F.13
-
22
-
-
2342453842
-
Familial juvenile hyperuricemic nephropathy: Detection of mutations in the uromodulin gene in five Japanese families
-
Kudo E, Kamatani N, Tezuka O, Taniguchi A, Yamanaka H, Yabe S, Osabe D, Shinohara S, Nomura K, Segawa M, Miyamoto T, Moritani M, Kunika K, Itakura M. Familial juvenile hyperuricemic nephropathy: Detection of mutations in the uromodulin gene in five Japanese families. Kidney Int 2004; 65: 1589-1597.
-
(2004)
Kidney Int
, vol.65
, pp. 1589-1597
-
-
Kudo, E.1
Kamatani, N.2
Tezuka, O.3
Taniguchi, A.4
Yamanaka, H.5
Yabe, S.6
Osabe, D.7
Shinohara, S.8
Nomura, K.9
Segawa, M.10
Miyamoto, T.11
Moritani, M.12
Kunika, K.13
Itakura, M.14
-
23
-
-
11244309689
-
Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy
-
Tinschert S, Ruf N, Bernascone I, Sacherer K, Lamorte G, Neumayer HH, Nurnberg P, Luft FC, Rampoldi L. Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy. Nephrol Dial Transplant 2004; 19: 3150-3154.
-
(2004)
Nephrol Dial Transplant
, vol.19
, pp. 3150-3154
-
-
Tinschert, S.1
Ruf, N.2
Bernascone, I.3
Sacherer, K.4
Lamorte, G.5
Neumayer, H.H.6
Nurnberg, P.7
Luft, F.C.8
Rampoldi, L.9
-
24
-
-
18644384361
-
Clinico-pathologic findings in medullary cystic kidney disease type 2
-
Bleyer AJ, Hart TC, Willingham MC, Iskandar SS, Gorry MC, Trachtman H. Clinico-pathologic findings in medullary cystic kidney disease type 2. Pediatr Nephrol 2005; 20: 824-827.
-
(2005)
Pediatr Nephrol
, vol.20
, pp. 824-827
-
-
Bleyer, A.J.1
Hart, T.C.2
Willingham, M.C.3
Iskandar, S.S.4
Gorry, M.C.5
Trachtman, H.6
-
25
-
-
26444591591
-
A novel heterozygous missense mutation in the UMOD gene responsible for familial juvenile hyperuricemic nephropathy
-
Calado J, Gaspar A, Clemente C, Rueff J. A novel heterozygous missense mutation in the UMOD gene responsible for familial juvenile hyperuricemic nephropathy. BMC Med Genet 2005; 6: 5.
-
(2005)
BMC Med Genet
, vol.6
, pp. 5
-
-
Calado, J.1
Gaspar, A.2
Clemente, C.3
Rueff, J.4
-
26
-
-
10044220812
-
Identification and characterization of D8C, a novel domain present in liver-specific LZP, uromodulin and glycoprotein 2, mutated in familial juvenile hyperuricaemic nephropathy
-
Yang H, Wu C, Zhao S, Guo J. Identification and characterization of D8C, a novel domain present in liver-specific LZP, uromodulin and glycoprotein 2, mutated in familial juvenile hyperuricaemic nephropathy. FEBS Lett 2004; 578: 236-238.
-
(2004)
FEBS Lett
, vol.578
, pp. 236-238
-
-
Yang, H.1
Wu, C.2
Zhao, S.3
Guo, J.4
-
28
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
Ng PC, Henikoff S. SIFT: Predicting amino acid changes that affect protein function. Nucleic Acids Res 2003; 31: 3812-3814.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
29
-
-
25144496606
-
PMUT: A web-based tool for the annotation of pathological mutations on proteins
-
Ferrer-Costa C, Gelpi JL, Zamakola L, Parraga I, de la Cruz X, Orozco M. PMUT: A web-based tool for the annotation of pathological mutations on proteins. Bioinformatics 2005; 21: 3176-3178.
-
(2005)
Bioinformatics
, vol.21
, pp. 3176-3178
-
-
Ferrer-Costa, C.1
Gelpi, J.L.2
Zamakola, L.3
Parraga, I.4
de la Cruz, X.5
Orozco, M.6
-
30
-
-
33644847172
-
Prediction of protein stability changes for single-site mutations using support vector machines
-
Cheng J, Randall A, Baldi P. Prediction of protein stability changes for single-site mutations using support vector machines. Proteins 2006; 62: 1125-1132.
-
(2006)
Proteins
, vol.62
, pp. 1125-1132
-
-
Cheng, J.1
Randall, A.2
Baldi, P.3
-
31
-
-
0014870016
-
Tamm-Horsfall urinary glycoprotein. The chemical composition
-
Fletcher AP, Neuberger A, Ratcliffe WA. Tamm-Horsfall urinary glycoprotein. The chemical composition. Biochem J 1970; 120: 417-424.
-
(1970)
Biochem J
, vol.120
, pp. 417-424
-
-
Fletcher, A.P.1
Neuberger, A.2
Ratcliffe, W.A.3
-
32
-
-
0030000090
-
Solution structure of a pair of calcium-binding epidermal growth factor-like domains: Implications for the Marfan syndrome and other genetic disorders
-
Downing AK, Knott V, Werner JM, Cardy CM, Campbell ID, Handford PA. Solution structure of a pair of calcium-binding epidermal growth factor-like domains: Implications for the Marfan syndrome and other genetic disorders. Cell 1996; 85: 597-605.
-
(1996)
Cell
, vol.85
, pp. 597-605
-
-
Downing, A.K.1
Knott, V.2
Werner, J.M.3
Cardy, C.M.4
Campbell, I.D.5
Handford, P.A.6
-
33
-
-
0742289582
-
Plasma membrane targeting of podocin through the classical exocytic pathway: Effect of NPHS2 mutations
-
Roselli S, Moutkine I, Gribouval O, Benmerah A, Antignac C. Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. Traffic 2004; 5: 37-44.
-
(2004)
Traffic
, vol.5
, pp. 37-44
-
-
Roselli, S.1
Moutkine, I.2
Gribouval, O.3
Benmerah, A.4
Antignac, C.5
-
34
-
-
0030724926
-
Intracellular transport, cell-surface exposure and release of recombinant Tamm-Horsfall glycoprotein
-
Malagolini N, Cavallone D, Serafini-Cessi F. Intracellular transport, cell-surface exposure and release of recombinant Tamm-Horsfall glycoprotein. Kidney Int 1997; 52: 1340-1350.
-
(1997)
Kidney Int
, vol.52
, pp. 1340-1350
-
-
Malagolini, N.1
Cavallone, D.2
Serafini-Cessi, F.3
-
35
-
-
4344575076
-
Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein
-
Bleyer AJ, Hart TC, Shihabi Z, Robins V, Hoyer JR. Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein. Kidney Int 2004; 66: 974-977.
-
(2004)
Kidney Int
, vol.66
, pp. 974-977
-
-
Bleyer, A.J.1
Hart, T.C.2
Shihabi, Z.3
Robins, V.4
Hoyer, J.R.5
-
36
-
-
33645258309
-
Mutant Tamm-Horsfall glycoprotein accumulation in endoplasmic reticulum induces apoptosis reversed by colchicine and sodium 4-phenylbutyrate
-
Choi SW, Ryu OH, Choi SJ, Song IS, Bleyer AJ, Hart TC. Mutant Tamm-Horsfall glycoprotein accumulation in endoplasmic reticulum induces apoptosis reversed by colchicine and sodium 4-phenylbutyrate. J Am Soc Nephrol 2005; 16: 3006-3014.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 3006-3014
-
-
Choi, S.W.1
Ryu, O.H.2
Choi, S.J.3
Song, I.S.4
Bleyer, A.J.5
Hart, T.C.6
-
37
-
-
0036843129
-
Traffic jams II: An update of diseases of intracellular transport
-
Aridor M, Hannan LA. Traffic jams II: An update of diseases of intracellular transport. Traffic 2002; 3: 781-790.
-
(2002)
Traffic
, vol.3
, pp. 781-790
-
-
Aridor, M.1
Hannan, L.A.2
-
38
-
-
0034330457
-
Traffic jam: A compendium of human diseases that affect intracellular transport processes
-
Aridor M, Hannan LA. Traffic jam: A compendium of human diseases that affect intracellular transport processes. Traffic 2000; 1: 836-851.
-
(2000)
Traffic
, vol.1
, pp. 836-851
-
-
Aridor, M.1
Hannan, L.A.2
-
39
-
-
0031067089
-
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels
-
Mulders SM, Knoers NV, Van Lieburg AF, Monnens LA, Leumann E, Wuhl E, Schober E, Rijss JP, Van Os CH, Deen PM. New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels. J Am Soc Nephrol 1997; 8: 242-248.
-
(1997)
J Am Soc Nephrol
, vol.8
, pp. 242-248
-
-
Mulders, S.M.1
Knoers, N.V.2
Van Lieburg, A.F.3
Monnens, L.A.4
Leumann, E.5
Wuhl, E.6
Schober, E.7
Rijss, J.P.8
Van Os, C.H.9
Deen, P.M.10
-
40
-
-
0034278759
-
Aggresomes and Russell bodies. Symptoms of cellular indigestion?
-
Kopito RR, Sitia R. Aggresomes and Russell bodies. Symptoms of cellular indigestion? EMBO Rep 2000; 1: 225-231.
-
(2000)
EMBO Rep
, vol.1
, pp. 225-231
-
-
Kopito, R.R.1
Sitia, R.2
-
41
-
-
10444226462
-
ER stress and the unfolded protein response
-
Schroder M, Kaufman RJ. ER stress and the unfolded protein response. Mutat Res 2005; 569: 29-63.
-
(2005)
Mutat Res
, vol.569
, pp. 29-63
-
-
Schroder, M.1
Kaufman, R.J.2
-
42
-
-
2142768895
-
Activation of endoplasmic reticulum-specific stress responses associated with the conformational disease Z alpha 1-antitrypsin deficiency
-
Lawless MW, Greene CM, Mulgrew A, Taggart CC, O'Neill SJ, McElvaney NG. Activation of endoplasmic reticulum-specific stress responses associated with the conformational disease Z alpha 1-antitrypsin deficiency. J Immunol 2004; 172: 5722-5726.
-
(2004)
J Immunol
, vol.172
, pp. 5722-5726
-
-
Lawless, M.W.1
Greene, C.M.2
Mulgrew, A.3
Taggart, C.C.4
O'Neill, S.J.5
McElvaney, N.G.6
-
43
-
-
0032779694
-
Signal transduction from the endoplasmic reticulum to the cell nucleus
-
Pahl HL. Signal transduction from the endoplasmic reticulum to the cell nucleus. Physiol Rev 1999; 79: 683-701.
-
(1999)
Physiol Rev
, vol.79
, pp. 683-701
-
-
Pahl, H.L.1
-
44
-
-
0034610743
-
Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta
-
Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA, Yuan J. Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta. Nature 2000; 403: 98-103.
-
(2000)
Nature
, vol.403
, pp. 98-103
-
-
Nakagawa, T.1
Zhu, H.2
Morishima, N.3
Li, E.4
Xu, J.5
Yankner, B.A.6
Yuan, J.7
-
45
-
-
21644448744
-
ER Ca2+ depletion triggers apoptotic signals for endoplasmic reticulum (ER) overload response induced by overexpressed reticulon 3 (RTN3/HAP)
-
Kuang E, Wan Q, Li X, Xu H, Liu Q, Qi Y. ER Ca2+ depletion triggers apoptotic signals for endoplasmic reticulum (ER) overload response induced by overexpressed reticulon 3 (RTN3/HAP). J Cell Physiol 2005; 204: 549-559.
-
(2005)
J Cell Physiol
, vol.204
, pp. 549-559
-
-
Kuang, E.1
Wan, Q.2
Li, X.3
Xu, H.4
Liu, Q.5
Qi, Y.6
-
46
-
-
0345687308
-
Mechanism of constitutive export from the golgi: Bulk flow via the formation, protrusion, and en bloc cleavage of large trans-golgi network tubular domains
-
Polishchuk EV, Di Pentima A, Luini A, Polishchuk RS. Mechanism of constitutive export from the golgi: Bulk flow via the formation, protrusion, and en bloc cleavage of large trans-golgi network tubular domains. Mol Biol Cell 2003; 14: 4470-4485.
-
(2003)
Mol Biol Cell
, vol.14
, pp. 4470-4485
-
-
Polishchuk, E.V.1
Di Pentima, A.2
Luini, A.3
Polishchuk, R.S.4
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