-
1
-
-
2442519456
-
Genetic variation in DLG5 is associated with inflammatory bowel disease
-
Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S. Genetic variation in DLG5 is associated with inflammatory bowel disease. Nat Genet 2004; 36: 476-480
-
(2004)
Nat Genet
, vol.36
, pp. 476-480
-
-
Stoll, M.1
Corneliussen, B.2
Costello, C.M.3
Waetzig, G.H.4
Mellgard, B.5
Koch, W.A.6
Rosenstiel, P.7
Albrecht, M.8
Croucher, P.J.9
Seegert, D.10
Nikolaus, S.11
Hampe, J.12
Lengauer, T.13
Pierrou, S.14
Foelsch, U.R.15
Mathew, C.G.16
Lagerstrom-Fermer, M.17
Schreiber, S.18
-
2
-
-
0038795589
-
Dlg, Scribble and Lgl in cell polarity, cell proliferation and cancer
-
Humbert P, Russell S, Richardson H. Dlg, Scribble and Lgl in cell polarity, cell proliferation and cancer. Bioessays 2003; 25: 542-553
-
(2003)
Bioessays
, vol.25
, pp. 542-553
-
-
Humbert, P.1
Russell, S.2
Richardson, H.3
-
3
-
-
0037821783
-
Interaction of lp-dlg/KIAA0583, a membrane-associated guanylate kinase family protein, with vinexin and beta-catenin at sites of cell-cell contact
-
Wakabayashi M, Ito T, Mitsushima M, Aizawa S, Ueda K, Amachi T, Kioka N. Interaction of lp-dlg/KIAA0583, a membrane-associated guanylate kinase family protein, with vinexin and beta-catenin at sites of cell-cell contact. J Biol Chem 2003; 278: 21709-21714
-
(2003)
J Biol Chem
, vol.278
, pp. 21709-21714
-
-
Wakabayashi, M.1
Ito, T.2
Mitsushima, M.3
Aizawa, S.4
Ueda, K.5
Amachi, T.6
Kioka, N.7
-
4
-
-
12744274602
-
Association analysis of SL-C22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
-
Yamazaki K, Takazoe M, Tanaka T, Ichimori T, Saito S, Iida A, Onouchi Y, Hata A, Nakamura Y. Association analysis of SL-C22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease. J Hum Genet 2004; 49: 664-668
-
(2004)
J Hum Genet
, vol.49
, pp. 664-668
-
-
Yamazaki, K.1
Takazoe, M.2
Tanaka, T.3
Ichimori, T.4
Saito, S.5
Iida, A.6
Onouchi, Y.7
Hata, A.8
Nakamura, Y.9
-
5
-
-
0037265610
-
Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations
-
Croucher PJ, Mascheretti S, Hampe J, Huse K, Frenzel H, Stoll M, Lu T, Nikolaus S, Yang SK, Krawczak M, Kim WH, Schreiber S. Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations. Eur J Hum Genet 2003; 11: 6-16
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 6-16
-
-
Croucher, P.J.1
Mascheretti, S.2
Hampe, J.3
Huse, K.4
Frenzel, H.5
Stoll, M.6
Lu, T.7
Nikolaus, S.8
Yang, S.K.9
Krawczak, M.10
Kim, W.H.11
Schreiber, S.12
-
6
-
-
0036373539
-
Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
-
Yamazaki K, Takazoe M, Tanaka T, Kazumori T, Nakamura Y. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease. J Hum Genet 2002; 47: 469-472
-
(2002)
J Hum Genet
, vol.47
, pp. 469-472
-
-
Yamazaki, K.1
Takazoe, M.2
Tanaka, T.3
Kazumori, T.4
Nakamura, Y.5
-
7
-
-
21744442434
-
Association of DLG5 R30Q variant with inflammatory bowel disease
-
Daly MJ, Pearce AV, Farwell L, Fisher SA, Latiano A, Prescott NJ, Forbes A, Mansfield J, Sanderson J, Langelier D, Cohen A, Bitton A, Wild G, Lewis CM, Annese V, Mathew CG, Rioux JD. Association of DLG5 R30Q variant with inflammatory bowel disease. Eur J Hum Genet 2005; 13: 835-839
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 835-839
-
-
Daly, M.J.1
Pearce, A.V.2
Farwell, L.3
Fisher, S.A.4
Latiano, A.5
Prescott, N.J.6
Forbes, A.7
Mansfield, J.8
Sanderson, J.9
Langelier, D.10
Cohen, A.11
Bitton, A.12
Wild, G.13
Lewis, C.M.14
Annese, V.15
Mathew, C.G.16
Rioux, J.D.17
-
8
-
-
21344435414
-
DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population
-
Noble CL, Nimmo ER, Drummond H, Smith L, Arnott ID, Satsangi J. DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population. Gut 2005; 54: 1416-1420
-
(2005)
Gut
, vol.54
, pp. 1416-1420
-
-
Noble, C.L.1
Nimmo, E.R.2
Drummond, H.3
Smith, L.4
Arnott, I.D.5
Satsangi, J.6
-
9
-
-
4344671141
-
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: Evidence for genetic heterogeneity within Europe?
-
Arnott ID, Nimmo ER, Drummond HE, Fennell J, Smith BR, MacKinlay E, Morecroft J, Anderson N, Kelleher D, O'Sullivan M, McManus R, Satsangi J. NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe? Genes Immun 2004; 5: 417-425
-
(2004)
Genes Immun
, vol.5
, pp. 417-425
-
-
Arnott, I.D.1
Nimmo, E.R.2
Drummond, H.E.3
Fennell, J.4
Smith, B.R.5
MacKinlay, E.6
Morecroft, J.7
Anderson, N.8
Kelleher, D.9
O'Sullivan, M.10
McManus, R.11
Satsangi, J.12
-
10
-
-
33646201287
-
Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations
-
Medici V, Mascheretti S, Croucher PJ, Stoll M, Hampe J, Grebe J, Sturniolo GC, Solberg C, Jahnsen J, Moum B, Schreiber S, Vatn MH. Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations. Eur J Hum Genet 2006; 14: 459-468
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 459-468
-
-
Medici, V.1
Mascheretti, S.2
Croucher, P.J.3
Stoll, M.4
Hampe, J.5
Grebe, J.6
Sturniolo, G.C.7
Solberg, C.8
Jahnsen, J.9
Moum, B.10
Schreiber, S.11
Vatn, M.H.12
-
11
-
-
31144473386
-
Single nucleoticle polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease
-
Gazouli M, Mantzaris G, Archimandritis AJ, Nasioulas G, Anagnou NP. Single nucleoticle polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease. World J Gastroenterol 2005; 11: 7525-7530
-
(2005)
World J Gastroenterol
, vol.11
, pp. 7525-7530
-
-
Gazouli, M.1
Mantzaris, G.2
Archimandritis, A.J.3
Nasioulas, G.4
Anagnou, N.P.5
-
12
-
-
33645144075
-
Association of DLG5 and inflammatory bowel disease across populations
-
author reply 260-261
-
Tenesa A, Noble C, Satsangi J, Dunlop M. Association of DLG5 and inflammatory bowel disease across populations. Eur J Hum Genet 2006; 14: 259-60; author reply 260-261
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 259-260
-
-
Tenesa, A.1
Noble, C.2
Satsangi, J.3
Dunlop, M.4
-
13
-
-
0033358425
-
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
-
Hampe J, Schreiber S, Shaw SH, Lau KF, Bridger S, Macpherson AJ, Cardon LR, Sakul H, Harris TJ, Buckler A, Hall J, Stokkers P, van Deventer SJ, Nurnberg P, Mirza M, Lee JC, Lennard-Jones JE, Mathew CG, Curran ME. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. Am J Hum Genet 1999; 64: 808-816
-
(1999)
Am J Hum Genet
, vol.64
, pp. 808-816
-
-
Hampe, J.1
Schreiber, S.2
Shaw, S.H.3
Lau, K.F.4
Bridger, S.5
Macpherson, A.J.6
Cardon, L.R.7
Sakul, H.8
Harris, T.J.9
Buckler, A.10
Hall, J.11
Stokkers, P.12
van Deventer, S.J.13
Nurnberg, P.14
Mirza, M.15
Lee, J.C.16
Lennard-Jones, J.E.17
Mathew, C.G.18
Curran, M.E.19
-
14
-
-
85047697768
-
Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6
-
Fisher SA, Hampe J, Macpherson AJ, Forbes A, Lennard-Jones JE, Schreiber S, Curran ME, Mathew CG, Lewis CM. Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6. Eur J Hum Genet 2002; 10: 259-265
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 259-265
-
-
Fisher, S.A.1
Hampe, J.2
Macpherson, A.J.3
Forbes, A.4
Lennard-Jones, J.E.5
Schreiber, S.6
Curran, M.E.7
Mathew, C.G.8
Lewis, C.M.9
-
15
-
-
33645012263
-
Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men
-
Friedrichs F, Brescianini S, Annese V, Latiano A, Berger K, Kugathasan S, Broeckel U, Nikolaus S, Daly MJ, Schreiber S, Rioux JD, Stoll M. Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men. Hum Genet 2006; 119: 305-311
-
(2006)
Hum Genet
, vol.119
, pp. 305-311
-
-
Friedrichs, F.1
Brescianini, S.2
Annese, V.3
Latiano, A.4
Berger, K.5
Kugathasan, S.6
Broeckel, U.7
Nikolaus, S.8
Daly, M.J.9
Schreiber, S.10
Rioux, J.D.11
Stoll, M.12
-
16
-
-
0037622913
-
Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31
-
Armuzzi A, Ahmad T, Ling KL, de Silva A, Cullen S, van Heel D, Orchard TR, Welsh KI, Marshall SE, Jewell DP. Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31. Gut 2003; 52: 1133-1139
-
(2003)
Gut
, vol.52
, pp. 1133-1139
-
-
Armuzzi, A.1
Ahmad, T.2
Ling, K.L.3
de Silva, A.4
Cullen, S.5
van Heel, D.6
Orchard, T.R.7
Welsh, K.I.8
Marshall, S.E.9
Jewell, D.P.10
-
17
-
-
0038389762
-
IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitis
-
Giallourakis C, Stoll M, Miller K, Hampe J, Lander ES, Daly MJ, Schreiber S, Rioux JD. IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis. Am J Hum Genet 2003; 73: 205-211
-
(2003)
Am J Hum Genet
, vol.73
, pp. 205-211
-
-
Giallourakis, C.1
Stoll, M.2
Miller, K.3
Hampe, J.4
Lander, E.S.5
Daly, M.J.6
Schreiber, S.7
Rioux, J.D.8
-
18
-
-
0035897904
-
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
-
Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001; 357: 1925-1928
-
(2001)
Lancet
, vol.357
, pp. 1925-1928
-
-
Hampe, J.1
Cuthbert, A.2
Croucher, P.J.3
Mirza, M.M.4
Mascheretti, S.5
Fisher, S.6
Frenzel, H.7
King, K.8
Hasselmeyer, A.9
MacPherson, A.J.10
Bridger, S.11
van Deventer, S.12
Forbes, A.13
Nikolaus, S.14
Lennard-Jones, J.E.15
Foelsch, U.R.16
Krawczak, M.17
Lewis, C.18
Schreiber, S.19
Mathew, C.G.20
more..
-
19
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001; 411: 599-603
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
Macry, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
20
-
-
0347362514
-
Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis
-
McGovern DP, Van Heel DA, Negoro K, Ahmad T, Jewell DP. Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis. Am J Hum Genet 2003; 73: 1465-1466
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1465-1466
-
-
McGovern, D.P.1
Van Heel, D.A.2
Negoro, K.3
Ahmad, T.4
Jewell, D.P.5
-
21
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nunez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001; 411: 603-606
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
22
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, Kulbokas EJ, O'Leary S, Winchester E, Dewar K, Green T, Stone V, Chow C, Cohen A, Langelier D, Lapointe G, Gaudet D, Faith J, Branco N, Bull SB, McLeod RS, Griffiths AM, Bitton A, Greenberg GR, Lander ES, Siminovitch KA, Hudson TJ. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 2001; 29: 223-228
-
(2001)
Nat Genet
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
Kocher, K.8
Miller, K.9
Guschwan, S.10
Kulbokas, E.J.11
O'Leary, S.12
Winchester, E.13
Dewar, K.14
Green, T.15
Stone, V.16
Chow, C.17
Cohen, A.18
Langelier, D.19
Lapointe, G.20
Gaudet, D.21
Faith, J.22
Branco, N.23
Bull, S.B.24
McLeod, R.S.25
Griffiths, A.M.26
Bitton, A.27
Greenberg, G.R.28
Lander, E.S.29
Siminovitch, K.A.30
Hudson, T.J.31
more..
-
23
-
-
18444381172
-
CARD15 genetic variation in a Quebec population: Prevalence, genotype-phenotype relationship, and haplotype structure
-
Vermeire S, Wild G, Kocher K, Cousineau J, Dufresne L, Bitton A, Langelier D, Pare P, Lapointe G, Cohen A, Daly MJ, Rioux JD. CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure. Am J Hum Genet 2002; 71: 74-83
-
(2002)
Am J Hum Genet
, vol.71
, pp. 74-83
-
-
Vermeire, S.1
Wild, G.2
Kocher, K.3
Cousineau, J.4
Dufresne, L.5
Bitton, A.6
Langelier, D.7
Pare, P.8
Lapointe, G.9
Cohen, A.10
Daly, M.J.11
Rioux, J.D.12
-
24
-
-
28844459843
-
Association of organic cation transporter risk haplotype with perianal penetrating Crohn's disease but not with susceptibility to IBD
-
Vermeire S, Pierik M, Hlavaty T, Claessens G, van Schuerbeeck N, Joossens S, Ferrante M, Henckaerts L, Bueno de Mesquita M, Vlietinck R, Rutgeerts P. Association of organic cation transporter risk haplotype with perianal penetrating Crohn's disease but not with susceptibility to IBD. Gastroenterology 2005; 129: 1845-1853
-
(2005)
Gastroenterology
, vol.129
, pp. 1845-1853
-
-
Vermeire, S.1
Pierik, M.2
Hlavaty, T.3
Claessens, G.4
van Schuerbeeck, N.5
Joossens, S.6
Ferrante, M.7
Henckaerts, L.8
Bueno de Mesquita, M.9
Vlietinck, R.10
Rutgeerts, P.11
-
25
-
-
33645789855
-
DLG5 variants contribute to Crohn disease risk in a Canadian population
-
Newman WG, Gu X, Wintle RF, Liu X, van Oene M, Amos CI, Siminovitch KA. DLG5 variants contribute to Crohn disease risk in a Canadian population. Hum Mutat 2006; 27: 353-358
-
(2006)
Hum Mutat
, vol.27
, pp. 353-358
-
-
Newman, W.G.1
Gu, X.2
Wintle, R.F.3
Liu, X.4
van Oene, M.5
Amos, C.I.6
Siminovitch, K.A.7
-
26
-
-
21344449654
-
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease
-
Torok HP, Glas J, Tonenchi L, Lohse P, Muller-Myhsok B, Limbersky O, Neugebauer C, Schnitzler F, Seiderer J, Tillack C, Brand S, Brunnler G, Jagiello P, Epplen JT, Griga T, Klein W, Schiemann U, Folwaczny M, Ochsenkuhn T, Folwaczny C. Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. Gut 2005; 54: 1421-1427
-
(2005)
Gut
, vol.54
, pp. 1421-1427
-
-
Torok, H.P.1
Glas, J.2
Tonenchi, L.3
Lohse, P.4
Muller-Myhsok, B.5
Limbersky, O.6
Neugebauer, C.7
Schnitzler, F.8
Seiderer, J.9
Tillack, C.10
Brand, S.11
Brunnler, G.12
Jagiello, P.13
Epplen, J.T.14
Griga, T.15
Klein, W.16
Schiemann, U.17
Folwaczny, M.18
Ochsenkuhn, T.19
Folwaczny, C.20
more..
|