-
1
-
-
1542435317
-
Genetic and pathogenetic insights into inflammatory bowel disease
-
Pallone F, Blanco Gdel V, Vavassori P, Monteleone I, Fina D, Monteleone G: Genetic and pathogenetic insights into inflammatory bowel disease. Curr Gastroenterol Rep 2003, 5:487-92.
-
(2003)
Curr. Gastroenterol. Rep.
, vol.5
, pp. 487-492
-
-
Pallone, F.1
Blanco Gdel, V.2
Vavassori, P.3
Monteleone, I.4
Fina, D.5
Monteleone, G.6
-
2
-
-
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, Karalluskas 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
Karalluskas, 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
-
3
-
-
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'Moraln CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbalou 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'Moraln, 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
Sahbalou, M.19
Thomas, G.20
more..
-
4
-
-
0037458665
-
Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease
-
Inohara N, Ogura Y, Fontalba A, Guttierrez O, Pons F, Crespo J, Fukase K, Inamura S, Kusumoto S, Hashimoto M, Foster SJ, Moran AP, Fernandez-Luna JL, Nunez G: Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease. J Biol Chem 2003, 278:5509-12.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 5509-5512
-
-
Inohara, N.1
Ogura, Y.2
Fontalba, A.3
Guttierrez, O.4
Pons, F.5
Crespo, J.6
Fukase, K.7
Inamura, S.8
Kusumoto, S.9
Hashimoto, M.10
Foster, S.J.11
Moran, A.P.12
Fernandez-Luna, J.L.13
Nunez, G.14
-
5
-
-
10744222688
-
Expression of NOD2 in Paneth cells: A possible link to Crohn's ileitis
-
Ogura Y, Lala S, Xin W, Smith E, Dowds TA, Chen FF, Zimmermann E, Tretiakova M, Cho JH, Hart J, Greenson JK, Keshav S, Nunez G: Expression of NOD2 in Paneth cells: a possible link to Crohn's ileitis. Gut 2003, 52:591-7.
-
(2003)
Gut
, vol.52
, pp. 591-597
-
-
Ogura, Y.1
Lala, S.2
Xin, W.3
Smith, E.4
Dowds, T.A.5
Chen, F.F.6
Zimmermann, E.7
Tretiakova, M.8
Cho, J.H.9
Hart, J.10
Greenson, J.K.11
Keshav, S.12
Nunez, G.13
-
6
-
-
9144224852
-
MDR1 Ala893 polymorphism is associated with inflammatory bowel disease
-
Brant SR, Panhuysen CI, Nicolae D, Reddy DM, Bonen DK, Karaliukas R, Zhang L, Swanson E, Datta LW, Moran T, Ravenhill G, Duerr RH, Achkar JP, Karban AS, Cho JH: MDR1 Ala893 polymorphism is associated with inflammatory bowel disease. Am J Hum Genet 2003, 73:1282-92.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1282-1292
-
-
Brant, S.R.1
Panhuysen, C.I.2
Nicolae, D.3
Reddy, D.M.4
Bonen, D.K.5
Karaliukas, R.6
Zhang, L.7
Swanson, E.8
Datta, L.W.9
Moran, T.10
Ravenhill, G.11
Duerr, R.H.12
Achkar, J.P.13
Karban, A.S.14
Cho, J.H.15
-
7
-
-
0037223561
-
Association between the C3435T MDR1 gene polymorphism and susceptibility for ulcerative colitis
-
Schwab M, Schaeffeler E, Marx C, Fromm MF, Kaskas B, Metzler J, Stange E, Herfarth H, Schoelmerich J, Gregor M, Walker S, Cascorbi I, Roots I, Brinkmann U, Zanger UM, Eichelbaum M: Association between the C3435T MDR1 gene polymorphism and susceptibility for ulcerative colitis. Gastroenterology 2003, 124:26-33.
-
(2003)
Gastroenterology
, vol.124
, pp. 26-33
-
-
Schwab, M.1
Schaeffeler, E.2
Marx, C.3
Fromm, M.F.4
Kaskas, B.5
Metzler, J.6
Stange, E.7
Herfarth, H.8
Schoelmerich, J.9
Gregor, M.10
Walker, S.11
Cascorbi, I.12
Roots, I.13
Brinkmann, U.14
Zanger, U.M.15
Eichelbaum, M.16
-
8
-
-
0032534043
-
A novel model of inflammatory bowel disease: Mice deficient fro the multiple drug resistance gene, mdr1a, spontaneously develop colitis
-
Panwala CM, Jones JC, Viney JL: A novel model of inflammatory bowel disease: mice deficient fro the multiple drug resistance gene, mdr1a, spontaneously develop colitis. J Immunol 1998, 161:5733-5744.
-
(1998)
J. Immunol.
, vol.161
, pp. 5733-5744
-
-
Panwala, C.M.1
Jones, J.C.2
Viney, J.L.3
-
9
-
-
0033910870
-
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci
-
Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, McLeod RS, Griffiths AM, Green T, Brettin TS, Stone V, Bull SB, Bitton A, Williams CN, Greenberg GR, Cohen Z, Lander ES, Hudson TJ, Siminovitch KA: Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci. Am J Hum Genet 2000, 66:1863-70.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1863-1870
-
-
Rioux, J.D.1
Silverberg, M.S.2
Daly, M.J.3
Steinhart, A.H.4
McLeod, R.S.5
Griffiths, A.M.6
Green, T.7
Brettin, T.S.8
Stone, V.9
Bull, S.B.10
Bitton, A.11
Williams, C.N.12
Greenberg, G.R.13
Cohen, Z.14
Lander, E.S.15
Hudson, T.J.16
Siminovitch, K.A.17
-
10
-
-
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, Longelier 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, 29:223-8.
-
(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
Longelier, 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..
-
11
-
-
2442585704
-
Functional variants of OCTN cation transporter genes are associated with Crohn disease
-
Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA: Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet 2004, 36:471-5.
-
(2004)
Nat. Genet.
, vol.36
, pp. 471-475
-
-
Peltekova, V.D.1
Wintle, R.F.2
Rubin, L.A.3
Amos, C.I.4
Huang, Q.5
Gu, X.6
Newman, B.7
Van Oene, M.8
Cescon, D.9
Greenberg, G.10
Griffiths, A.M.11
St George-Hyslop, P.H.12
Siminovitch, K.A.13
-
12
-
-
0344364566
-
An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis
-
Tokuhiro S, Yamada R, Chang X, Suzuki A, Kochi Y, Sawada T, Suzuki M, Nagasaki M, Ohtsuki M, Ono M, Furukawa H, Nagashima M, Yoshino S, Mabuchi A, Sekine A, Saito S, Takahashi A, Tsunoda T, Nakamura Y, Yamamoto K: An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis. Nat Genet 2003, 35:341-8.
-
(2003)
Nat. Genet.
, vol.35
, pp. 341-348
-
-
Tokuhiro, S.1
Yamada, R.2
Chang, X.3
Suzuki, A.4
Kochi, Y.5
Sawada, T.6
Suzuki, M.7
Nagasaki, M.8
Ohtsuki, M.9
Ono, M.10
Furukawa, H.11
Nagashima, M.12
Yoshino, S.13
Mabuchi, A.14
Sekine, A.15
Saito, S.16
Takahashi, A.17
Tsunoda, T.18
Nakamura, Y.19
Yamamoto, K.20
more..
-
13
-
-
18244370045
-
A polymorphism in the CD14 gene is associated with Crohn disease
-
Klein W, Tromm A, Griga T, Fricke H, Folwaczny C, Hocke M, Eitner K, Marx M, Duerig N, Epplen JT: A polymorphism in the CD14 gene is associated with Crohn disease. Scand J Gastroenterol 2002, 37:189-91.
-
(2002)
Scand. J. Gastroenterol.
, vol.37
, pp. 189-191
-
-
Klein, W.1
Tromm, A.2
Griga, T.3
Fricke, H.4
Folwaczny, C.5
Hocke, M.6
Eitner, K.7
Marx, M.8
Duerig, N.9
Epplen, J.T.10
-
14
-
-
0037269186
-
C-fms expression correlates with monocytic differentiation in PML-RAR alpha+ acute promyelocytic leukemia
-
Riccioni R, Saulle E, Militi S, Sposi NM, Gualtiero M, Mauro N, Mancini M, Diverio D, Lo Coco F, Peschle C, Testa U: C-fms expression correlates with monocytic differentiation in PML-RAR alpha+ acute promyelocytic leukemia. Leukemia 2003, 17:98-113.
-
(2003)
Leukemia
, vol.17
, pp. 98-113
-
-
Riccioni, R.1
Saulle, E.2
Militi, S.3
Sposi, N.M.4
Gualtiero, M.5
Mauro, N.6
Mancini, M.7
Diverio, D.8
Lo Coco, F.9
Peschle, C.10
Testa, U.11
-
15
-
-
0032008524
-
Expression of CSF-1 and CSF-1 receptor by normal lactating mammary epithelial cells
-
Sapi E, Flick MB, Rodov S, Carter D, Kacinski BM: Expression of CSF-1 and CSF-1 receptor by normal lactating mammary epithelial cells. J Soc Gynecol Investig 1998, 5:94-101.
-
(1998)
J. Soc. Gynecol. Investig.
, vol.5
, pp. 94-101
-
-
Sapi, E.1
Flick, M.B.2
Rodov, S.3
Carter, D.4
Kacinski, B.M.5
-
16
-
-
0028105274
-
Expression of transcripts for CSF-1 and for the "macrophage" and "epithelial" Isoforms of the CSF-1R transcripts in human ovarian carcinomas
-
Buaknecht T, Kiechle-Schwarz M, du Bois A, Wolfle J, Kacinski B: Expression of transcripts for CSF-1 and for the "macrophage" and "epithelial" isoforms of the CSF-1R transcripts in human ovarian carcinomas. Cancer Detect Prev 1994, 18:231-9.
-
(1994)
Cancer Detect. Prev.
, vol.18
, pp. 231-239
-
-
Buaknecht, T.1
Kiechle-Schwarz, M.2
du Bois, A.3
Wolfle, J.4
Kacinski, B.5
-
17
-
-
20244365170
-
The role of colony-stimulating factor 1 and its receptor in the etiopathogenesis of endometrial adenocarcinoma
-
Smith HO, Anderson PS, Kuo DY, Goldberg GL, DeVictoria CL, Boocock CA, Jones JG, Runowicz CD, Stanley ER, Pollard JW: The role of colony-stimulating factor 1 and its receptor in the etiopathogenesis of endometrial adenocarcinoma. Clin Cancer Res 1995, 1:313-25.
-
(1995)
Clin. Cancer Res.
, vol.1
, pp. 313-325
-
-
Smith, H.O.1
Anderson, P.S.2
Kuo, D.Y.3
Goldberg, G.L.4
DeVictoria, C.L.5
Boocock, C.A.6
Jones, J.G.7
Runowicz, C.D.8
Stanley, E.R.9
Pollard, J.W.10
-
18
-
-
0037195106
-
Expression of colonystimulating factor 1 receptor during prostate development and prostate cancer progression
-
Ide H, Seligson DB, Memarzadeh S, Xin L, Horvath S, Dubey P, Flick MB, Kacinski BM, Palotie A, Witte ON: Expression of colonystimulating factor 1 receptor during prostate development and prostate cancer progression. Proc Natl Acad Sci U S A 2002, 99:14404-9.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 14404-14409
-
-
Ide, H.1
Seligson, D.B.2
Memarzadeh, S.3
Xin, L.4
Horvath, S.5
Dubey, P.6
Flick, M.B.7
Kacinski, B.M.8
Palotie, A.9
Witte, O.N.10
-
19
-
-
0027283586
-
Long-term followup of patients with invasive fungal disease who received adjunctive therapy with recombinant human macrophage colony-stimulating factor
-
Nemunaitis J, Shannon-Dorcy K, Appelbaum FR, Meyers J, Owens A, Day R, Ando D, O'Neill C, Buckner D, Singer J: Long-term followup of patients with invasive fungal disease who received adjunctive therapy with recombinant human macrophage colony-stimulating factor. Blood 1993, 82:1422-7.
-
(1993)
Blood
, vol.82
, pp. 1422-1427
-
-
Nemunaitis, J.1
Shannon-Dorcy, K.2
Appelbaum, F.R.3
Meyers, J.4
Owens, A.5
Day, R.6
Ando, D.7
O'Neill, C.8
Buckner, D.9
Singer, J.10
-
20
-
-
0036077317
-
Colony-stimulating factor 1-dependent cells protect against systemic infection with Listeria monocytogenes but facilitate neuroinvasion
-
Jin Y, Dons L, Kristensson K, Rottenberg ME: Colony-stimulating factor 1-dependent cells protect against systemic infection with Listeria monocytogenes but facilitate neuroinvasion. Infect Immun 2002, 70:4682-6.
-
(2002)
Infect. Immun.
, vol.70
, pp. 4682-4686
-
-
Jin, Y.1
Dons, L.2
Kristensson, K.3
Rottenberg, M.E.4
-
21
-
-
0033523803
-
i2 proteins of v-fms-induced proliferation and transformation via Srckinase and STAT3
-
i2 proteins of v-fms-induced proliferation and transformation via Srckinase and STAT3. Oncogene 1999, 18:6335-6342.
-
(1999)
Oncogene
, vol.18
, pp. 6335-6342
-
-
Corre, I.1
Baumann, H.2
Hermouet, S.3
-
22
-
-
0029061801
-
Ulcerative colitis and adenocarcinoma of the colon in G alpha i2-deficient mice
-
Rudolph U, Finegold MJ, Rich SS, Harriman GR, Srinivasan Y, Brabet P, Boulay G, Bradley A, Birnbaumer L: Ulcerative colitis and adenocarcinoma of the colon in G alpha i2-deficient mice. Nat Genet 1995, 10:143-50.
-
(1995)
Nat. Genet.
, vol.10
, pp. 143-150
-
-
Rudolph, U.1
Finegold, M.J.2
Rich, S.S.3
Harriman, G.R.4
Srinivasan, Y.5
Brabet, P.6
Boulay, G.7
Bradley, A.8
Birnbaumer, L.9
-
23
-
-
0037452789
-
STAT3 deletion during hematopoiesis causes Crohn's disease-like pathogenesis and lethality: A critical role of STAT3 in innate immunity
-
Welte T, Zhang SS, Wang T, Zhang Z, Hesslein DG, Yin Z, Kano A, Iwamoto Y, Li E, Craft JE, Bothwell AL, Fikrig E, Koni PA, Flavell RA, Fu XY: STAT3 deletion during hematopoiesis causes Crohn's disease-like pathogenesis and lethality: a critical role of STAT3 in innate immunity. Proc Natl Acad Sci U S A 2003, 100:1879-84.
-
(2003)
Proc. Natl. Acad. Sci. U. S A.
, vol.100
, pp. 1879-1884
-
-
Welte, T.1
Zhang, S.S.2
Wang, T.3
Zhang, Z.4
Hesslein, D.G.5
Yin, Z.6
Kano, A.7
Iwamoto, Y.8
Li, E.9
Craft, J.E.10
Bothwell, A.L.11
Fikrig, E.12
Koni, P.A.13
Flavell, R.A.14
Fu, X.Y.15
-
24
-
-
0033034365
-
Enhanced Th1 activity and development of chronic enterocolitis in mice devoid of Stat3 in macrophages and neutrophils
-
Takeda K, Clausen BE, Kaisho T, Tsujimura T, Terada N, Forster I, Akira S: Enhanced Th1 activity and development of chronic enterocolitis in mice devoid of Stat3 in macrophages and neutrophils. Immunity 1999, 10:39-49.
-
(1999)
Immunity
, vol.10
, pp. 39-49
-
-
Takeda, K.1
Clausen, B.E.2
Kaisho, T.3
Tsujimura, T.4
Terada, N.5
Forster, I.6
Akira, S.7
-
25
-
-
0025190309
-
FMS mutations in myelodysplastic, leukemic, and normal subjects
-
Ridge SA, Worwood M, Oscier D, Jacobs A, Padua RA: FMS mutations in myelodysplastic, leukemic, and normal subjects. Proc Natl Acad Sci U S A 1990, 87:1377-1380.
-
(1990)
Proc. Natl. Acad. Sci. U. S. A.
, vol.87
, pp. 1377-1380
-
-
Ridge, S.A.1
Worwood, M.2
Oscier, D.3
Jacobs, A.4
Padua, R.A.5
-
26
-
-
0029152855
-
De novo acute myeloid leukemia in patients with Crohn's disease
-
Dombret H, Marolleau JP: De novo acute myeloid leukemia in patients with Crohn's disease. Nouv Rev Fr Hematol 1995, 37:193-6.
-
(1995)
Nouv. Rev. Fr. Hematol.
, vol.37
, pp. 193-196
-
-
Dombret, H.1
Marolleau, J.P.2
-
27
-
-
0033127860
-
Concurrent inflammatory bowel disease and myelodysplastic syndromes
-
Harewood GC, Loftus EV Jr, Tefferi A, Tremaine WJ, Sandborn WJ: Concurrent inflammatory bowel disease and myelodysplastic syndromes. Inflamm Bowel Dis 1999, 5:98-103.
-
(1999)
Inflamm. Bowel Dis.
, vol.5
, pp. 98-103
-
-
Harewood, G.C.1
Loftus Jr., E.V.2
Tefferi, A.3
Tremaine, W.J.4
Sandborn, W.J.5
-
28
-
-
0020540636
-
Isolation of v-fms and its human cellular homolog
-
Heisterkamp N, Groffen J, Stephenson JR: Isolation of v-fms and its human cellular homolog. Virology 1983, 126:248-58.
-
(1983)
Virology
, vol.126
, pp. 248-258
-
-
Heisterkamp, N.1
Groffen, J.2
Stephenson, J.R.3
-
29
-
-
0035136875
-
Protein tyrosine phosphatase φ regulates paxillin tyrosine phosphorylation and mediates colony stimulating factor 1-induced morphological changes in macrophages
-
Pixley FJ, Lee PSW, Condeelis JS, Stanley ER: Protein tyrosine phosphatase φ regulates paxillin tyrosine phosphorylation and mediates colony stimulating factor 1-induced morphological changes in macrophages. Mol Cell Biol 2001, 21:1795-1809.
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 1795-1809
-
-
Pixley, F.J.1
Lee, P.S.W.2
Condeelis, J.S.3
Stanley, E.R.4
-
30
-
-
0036201577
-
EPWG-IBD Group, EPIMAD Group, GETAID Group: CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
-
Lesage S, Zouali H, Cezard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, Chamaillard M, Jannot AS, Thomas G, Hugot JP, EPWG-IBD Group, EPIMAD Group, GETAID Group: CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. Am J Hum Genet 2002, 70:845-57.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 845-857
-
-
Lesage, S.1
Zouali, H.2
Cezard, J.P.3
Colombel, J.F.4
Belaiche, J.5
Almer, S.6
Tysk, C.7
O'Morain, C.8
Gassull, M.9
Binder, V.10
Finkel, Y.11
Modigliani, R.12
Gower-Rousseau, C.13
Macry, J.14
Merlin, F.15
Chamaillard, M.16
Jannot, A.S.17
Thomas, G.18
Hugot, J.P.19
-
31
-
-
0037373316
-
A novel NOD2/ CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews
-
Sugimura K, Taylor KD, Lin YC, Hang T, Wang D, Tang YM, Fischel- Ghodsian N, Targan SR, Rotter JI, Yang H: A novel NOD2/ CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews. Am J Human Genet 2003, 72:509-18.
-
(2003)
Am. J. Human Genet.
, vol.72
, pp. 509-518
-
-
Sugimura, K.1
Taylor, K.D.2
Lin, Y.C.3
Hang, T.4
Wang, D.5
Tang, Y.M.6
Fischel-Ghodsian, N.7
Targan, S.R.8
Rotter, J.I.9
Yang, H.10
-
32
-
-
0037265610
-
Haplotype structure and association to Crohn's diseas 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 diseas 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
-
33
-
-
0344099132
-
Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes
-
Nielsen C, Hansen D, Husby S, Jacobsen BB, Lellevang ST: Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes. Tissue Antigens 2003, 62:492-7.
-
(2003)
Tissue Antigens
, vol.62
, pp. 492-497
-
-
Nielsen, C.1
Hansen, D.2
Husby, S.3
Jacobsen, B.B.4
Lellevang, S.T.5
-
34
-
-
0345659216
-
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
-
Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM: A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nat Genet 2003, 35:349-56.
-
(2003)
Nat. Genet.
, vol.35
, pp. 349-356
-
-
Helms, C.1
Cao, L.2
Krueger, J.G.3
Wijsman, E.M.4
Chamian, F.5
Gordon, D.6
Heffernan, M.7
Daw, J.A.8
Robarge, J.9
Ott, J.10
Kwok, P.Y.11
Menter, A.12
Bowcock, A.M.13
-
35
-
-
13244277850
-
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
-
Prokunina L, Castillejo-Lopez C, Oberg F, Gunnarsson I, Berg L, Magnusson V, Broookes AJ, Tentler D, Kristiansdottir H, Grondal G, Bolstad AI, Svenungsson E, Lundberg I, Sturfelt G, Jonssen A, Truedsson L, Lima G, Alcocer-Varela J, Johsson R, Gyllensten UB, Harley JB, Alarcon-Segovia D, Steinsson K, Alarcon-Riquelme ME: A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet 2002, 32:666-9.
-
(2002)
Nat. Genet.
, vol.32
, pp. 666-669
-
-
Prokunina, L.1
Castillejo-Lopez, C.2
Oberg, F.3
Gunnarsson, I.4
Berg, L.5
Magnusson, V.6
Broookes, A.J.7
Tentler, D.8
Kristiansdottir, H.9
Grondal, G.10
Bolstad, A.I.11
Svenungsson, E.12
Lundberg, I.13
Sturfelt, G.14
Jonssen, A.15
Truedsson, L.16
Lima, G.17
Alcocer-Varela, J.18
Johsson, R.19
Gyllensten, U.B.20
Harley, J.B.21
Alarcon-Segovia, D.22
Steinsson, K.23
Alarcon-Riquelme, M.E.24
more..
-
36
-
-
0031043018
-
Functional characterization of ETV6 and ETV6/CBFA2 in the regulation of the MCSFR proximal promoter
-
Fears S, Gavin M, Zhang DE, Hetherington C, Ben-David Y, Rowley JD, Nucifora G: Functional characterization of ETV6 and ETV6/CBFA2 in the regulation of the MCSFR proximal promoter. Proc Natl Acad Sci USA 1997, 94:1949-1954.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 1949-1954
-
-
Fears, S.1
Gavin, M.2
Zhang, D.E.3
Hetherington, C.4
Ben-David, Y.5
Rowley, J.D.6
Nucifora, G.7
|