Found: 19
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Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs.
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- Human Genetics, 2000, v. 106, n. 3, p. 345, doi. 10.1007/s004390051048
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- Article
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer.
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- PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0188911
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- Article
Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 24, p. 4930, doi. 10.1093/hmg/ddq411
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- Article
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1828, doi. 10.1093/hmg/ddq041
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- Article
Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.
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- International Journal of Colorectal Disease, 2007, v. 22, n. 4, p. 419, doi. 10.1007/s00384-006-0151-4
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- Article
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
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- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 619, doi. 10.1038/sj.ejhg.5201996
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- Article
Association of DLG5 R30Q variant with inflammatory bowel disease.
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- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 835, doi. 10.1038/sj.ejhg.5201403
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- Article
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
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- Nature Genetics, 2009, v. 41, n. 12, p. 1330, doi. 10.1038/ng.483
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- Article
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.
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- Nature Genetics, 2008, v. 40, n. 6, p. 710, doi. 10.1038/ng.145
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- Article
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
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- Nature Genetics, 2007, v. 39, n. 7, p. 830, doi. 10.1038/ng2061
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- Article
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
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- Nature Genetics, 2007, v. 39, n. 2, p. 207, doi. 10.1038/ng1954
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- Article
Pooled Sequencing of 531 Genes in Inflammatory Bowel Disease Identifies an Associated Rare Variant in BTNL2 and Implicates Other Immune Related Genes.
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- PLoS Genetics, 2015, v. 11, n. 2, p. 1, doi. 10.1371/journal.pgen.1004955
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- Article
Association of a Deletion of GSTT2B with an Altered Risk of Oesophageal Squamous Cell Carcinoma in a South African Population: A Case-Control Study.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029366
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- Article
Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.
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- Carcinogenesis, 2019, v. 40, n. 4, p. 513, doi. 10.1093/carcin/bgz026
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- Article
Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.
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- Carcinogenesis, 2012, v. 33, n. 11, p. 2155, doi. 10.1093/carcin/bgs262
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- Article
Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa.
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- Carcinogenesis, 2011, v. 32, n. 12, p. 1855, doi. 10.1093/carcin/bgr211
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- Article
Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.
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- Journal of Crohn's & Colitis, 2018, v. 12, n. 3, p. 321, doi. 10.1093/ecco-jcc/jjx157
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- Article
Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease.
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- BMC Gastroenterology, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12876-015-0305-3
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- Article
Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn’s disease.
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- BMC Gastroenterology, 2015, v. 15, n. 1, p. 75, doi. 10.1186/s12876-015-0305-3
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- Article