-
1
-
-
7644234109
-
Bile formation: Do not ignore the role of plasma membrane-cytoskeleton linking proteins
-
K.N. Lazaridis, N.F. La Russo Bile formation do not ignore the role of plasma membrane-cytoskeleton linking proteins Hepatology 37 2003 218 220
-
(2003)
Hepatology
, vol.37
, pp. 218-220
-
-
Lazaridis, K.N.1
La Russo, N.F.2
-
3
-
-
0037994064
-
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
-
V.E.H. Carlton, B.Z. Harris, E.G. Puffenberger, A.K. Batta, A.S. Knisely, D.L. Robinson, K.A. Strauss, B.L. Shneider, W.A. Lim, G. Salen, D.H. Morton, L.N. Bull Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT Nat Genet 34 2003 91 96
-
(2003)
Nat Genet
, vol.34
, pp. 91-96
-
-
Carlton, V.E.H.1
Harris, B.Z.2
Puffenberger, E.G.3
Batta, A.K.4
Knisely, A.S.5
Robinson, D.L.6
Strauss, K.A.7
Shneider, B.L.8
Lim, W.A.9
Salen, G.10
Morton, D.H.11
Bull, L.N.12
-
4
-
-
0036773738
-
Claudin-based barrier in simple and stratified cellular sheets
-
S. Tsukita, M. Furuse Claudin-based barrier in simple and stratified cellular sheets Curr Opin Cell Biol 14 2002 531 536
-
(2002)
Curr Opin Cell Biol
, vol.14
, pp. 531-536
-
-
Tsukita, S.1
Furuse, M.2
-
6
-
-
18644377817
-
Homozygosity mapping for a novel syndromic ichthyosis to chromosome 3q27-q28
-
L. Baala, S. Hadj-Rabia, D. Hamel-Teillac, M. Hadchouel, C. Prost, S.M. Leal, E. Jacquemin, A. Sefiani, Y. de Prost, G. Courtois, A. Munnich, S. Lyonnet, P. Vabres Homozygosity mapping for a novel syndromic ichthyosis to chromosome 3q27-q28 J Invest Dermatol 119 2002 70 76
-
(2002)
J Invest Dermatol
, vol.119
, pp. 70-76
-
-
Baala, L.1
Hadj-Rabia, S.2
Hamel-Teillac, D.3
Hadchouel, M.4
Prost, C.5
Leal, S.M.6
Jacquemin, E.7
Sefiani, A.8
De Prost, Y.9
Courtois, G.10
Munnich, A.11
Lyonnet, S.12
Vabres, P.13
-
7
-
-
0037128938
-
Claudin-based tight junctions are crucial for the mammalian epidermal barrier: A lesson from claudin-1-deficient mice
-
M. Furuse, M. Hata, K. Furuse, Y. Yoshida, A. Haratake, Y. Sugitani, T. Noda, A. Kobo, S. Tsukita Claudin-based tight junctions are crucial for the mammalian epidermal barrier a lesson from claudin-1-deficient mice J Cell Biol 156 2002 1099 1111
-
(2002)
J Cell Biol
, vol.156
, pp. 1099-1111
-
-
Furuse, M.1
Hata, M.2
Furuse, K.3
Yoshida, Y.4
Haratake, A.5
Sugitani, Y.6
Noda, T.7
Kobo, A.8
Tsukita, S.9
-
8
-
-
0028085138
-
Sclerosing cholangitis in children
-
D. Debray, D. Pariente, E. Urvoas, M. Hadchouel, O. Bernard Sclerosing cholangitis in children J Pediatr 124 1994 49 56
-
(1994)
J Pediatr
, vol.124
, pp. 49-56
-
-
Debray, D.1
Pariente, D.2
Urvoas, E.3
Hadchouel, M.4
Bernard, O.5
-
9
-
-
0033780963
-
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer
-
F. Kramer, K. White, M. Kubbies, K. Swisshelm, B.H. Weber, F. Kramer, K. White, M. Kubbies, K. Swisshelm, B.H. Weber Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer Hum Genet 107 2000 249 256
-
(2000)
Hum Genet
, vol.107
, pp. 249-256
-
-
Kramer, F.1
White, K.2
Kubbies, M.3
Swisshelm, K.4
Weber, B.H.5
Kramer, F.6
White, K.7
Kubbies, M.8
Swisshelm, K.9
Weber, B.H.10
-
10
-
-
0032577975
-
Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin
-
M. Furuse, K. Fujita, T. Hiiragi, K. Fujimoto, S. Tsukita Claudin-1 and -2 novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin J Cell Biol 141 1998 1539 1548
-
(1998)
J Cell Biol
, vol.141
, pp. 1539-1548
-
-
Furuse, M.1
Fujita, K.2
Hiiragi, T.3
Fujimoto, K.4
Tsukita, S.5
-
11
-
-
0033851771
-
Molecular physiology and pathophysiology of tight junctions. Tight junction structure and function: Lessons from mutant animal and proteins
-
L.L. Mitic, C.M. van Itallie, J.M. Anderson Molecular physiology and pathophysiology of tight junctions. Tight junction structure and function: lessons from mutant animal and proteins Am J Physiol 279 2000 250 254
-
(2000)
Am J Physiol
, vol.279
, pp. 250-254
-
-
Mitic, L.L.1
Van Itallie, C.M.2
Anderson, J.M.3
-
12
-
-
0034988157
-
Alterations in tight junctions differ between primary biliary cirrhosis and primary sclerosing cholangitis
-
S. Sakisata, T. Kawaguchi, E. Taniguchi, S. Hanada, K. Sasatomi, H. Koga, M. Harada, R. Kimura, M. Sata, N. Sawada, M. Mori, S. Todo, T. Kurohiji Alterations in tight junctions differ between primary biliary cirrhosis and primary sclerosing cholangitis Hepatology 33 2001 1460 1468
-
(2001)
Hepatology
, vol.33
, pp. 1460-1468
-
-
Sakisata, S.1
Kawaguchi, T.2
Taniguchi, E.3
Hanada, S.4
Sasatomi, K.5
Koga, H.6
Harada, M.7
Kimura, R.8
Sata, M.9
Sawada, N.10
Mori, M.11
Todo, S.12
Kurohiji, T.13
-
13
-
-
0035129369
-
Heterogeneity in expression and subcellular localization of claudins 2, 3, 4 and 5 in rat liver, pancreas, and gut
-
C. Rahner, L.L. Mitic, J.M. Anderson Heterogeneity in expression and subcellular localization of claudins 2, 3, 4 and 5 in rat liver, pancreas, and gut Gastroenterology 120 2001 411 422
-
(2001)
Gastroenterology
, vol.120
, pp. 411-422
-
-
Rahner, C.1
Mitic, L.L.2
Anderson, J.M.3
-
14
-
-
0036085515
-
Claudins create charge-selective channels in the paracellular pathway between epithelial cells
-
O.R. Colegio, C.M. van Itallie, H.J. McCrea, C. Rahner, J.M. Anderson Claudins create charge-selective channels in the paracellular pathway between epithelial cells Am J Physiol 282 2002 142 147
-
(2002)
Am J Physiol
, vol.282
, pp. 142-147
-
-
Colegio, O.R.1
Van Itallie, C.M.2
McCrea, H.J.3
Rahner, C.4
Anderson, J.M.5
-
15
-
-
17744380785
-
Mutations in the gene encoding tight junction claudin-14 cause recessive deafness DFNB29
-
E.R. Wilcox, Q.L. Burton, S. Naz, S. Riazuddin, T.N. Smith, B. Ploplis, I. Belyatseva, T. Ben-Yosef, N.A. Liburd, R.J. Morell, B. Kachar, D.K. Wu, A.J. Griffith, S. Riazuddin, T.B. Friedman Mutations in the gene encoding tight junction claudin-14 cause recessive deafness DFNB29 Cell 104 2001 165 172
-
(2001)
Cell
, vol.104
, pp. 165-172
-
-
Wilcox, E.R.1
Burton, Q.L.2
Naz, S.3
Riazuddin, S.4
Smith, T.N.5
Ploplis, B.6
Belyatseva, I.7
Ben-Yosef, T.8
Liburd, N.A.9
Morell, R.J.10
Kachar, B.11
Wu, D.K.12
Griffith, A.J.13
Riazuddin, S.14
Friedman, T.B.15
-
16
-
-
0033516683
-
Paracellin-1, a renal tight junction protein required for paracellular Mg(2+) resorption
-
D.B. Simon, Y. Lu, K.A. Choate, H. Velazquez, E. Al-Sabban, M. Praga, G. Casari, A. Bettinelli, G. Colussi, J. Rodriguez-Soriano, D. McCredle, D. Milford, S. Sanjad, R.P. Lifton Paracellin-1, a renal tight junction protein required for paracellular Mg(2+) resorption Science 285 1999 103 106
-
(1999)
Science
, vol.285
, pp. 103-106
-
-
Simon, D.B.1
Lu, Y.2
Choate, K.A.3
Velazquez, H.4
Al-Sabban, E.5
Praga, M.6
Casari, G.7
Bettinelli, A.8
Colussi, G.9
Rodriguez-Soriano, J.10
McCredle, D.11
Milford, D.12
Sanjad, S.13
Lifton, R.P.14
-
17
-
-
0028109285
-
Localization of the 7H6 antigen at tight junctions correlates with the paracellular barrier function of MDCK cells
-
Y. Zhong, K. Enomoto, H. Isomura, N. Sawada, T. Minase, M. Oyamada, Y. Konishi, M. Mori Localization of the 7H6 antigen at tight junctions correlates with the paracellular barrier function of MDCK cells Exp Cell Res 214 1994 614 620
-
(1994)
Exp Cell Res
, vol.214
, pp. 614-620
-
-
Zhong, Y.1
Enomoto, K.2
Isomura, H.3
Sawada, N.4
Minase, T.5
Oyamada, M.6
Konishi, Y.7
Mori, M.8
-
18
-
-
0036247733
-
Connexin mutations in hearing loss, dermatological and neurological disorders
-
R. Rabionet, N. Lopez-Bigas, M.L. Arbones, X. Estivill Connexin mutations in hearing loss, dermatological and neurological disorders Trends Mol Med 8 2002 205 212
-
(2002)
Trends Mol Med
, vol.8
, pp. 205-212
-
-
Rabionet, R.1
Lopez-Bigas, N.2
Arbones, M.L.3
Estivill, X.4
|