✦ LIBER ✦

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

✍ Scribed by Frackelton, Edward C; Annaiah, Kiran; Kugathasan, Subra; Baldassano, Robert N; Bradfield, Jonathan P; Sleiman, Patrick M A; Imielinski, Marcin; Guthery, Stephen L; Cucchiara, Salvatore; Kim, Cecilia E

Book ID: 109914297
Publisher: Nature Publishing Group
Year: 2008
Tongue: English
Weight: 421 KB
Volume: 40
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.203

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Investigation of Reported Associations B

Investigation of Reported Associations Between the 20q13 and 21q22 Loci and Pediatric-Onset Crohn's Disease in Canadian Children

✍ Amre, Devendra K; Mack, David R; Morgan, Kenneth; Fujiwara, Mary; Israel, David; 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 116 KB

Prenatal and Perinatal Characteristics A

Prenatal and Perinatal Characteristics Associated with Pediatric-Onset Inflammatory Bowel Disease

✍ Susan Hutfless, De-Kun Li, Melvin B. Heyman, Theodore M. Bayless, Oren Abramson, 📂 Article 📅 2012 🏛 Springer US 🌐 English ⚖ 185 KB

Common variants at five new loci associa

Common variants at five new loci associated with early-onset inflammatory bowel disease

✍ Imielinski, Marcin; Baldassano, Robert N; Griffiths, Anne; Russell, Richard K; A 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 476 KB

Filaggrin loss-of-function variants are

Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease

✍ J. Van Limbergen; R.K. Russell; E.R. Nimmo; Y. Zhao; H. Liao; H.E. Drummond; G. 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 100 KB

Background: Pediatric inflammatory bowel disease (IBD) has a high prevalence of coexistent atopy. Filaggrin (FLG) loss-of-function variants (null-alleles) are associated with eczema and asthma in association with eczema. The aim was to assess the contribution of FLG null-alleles to pediatric IBD sus

NCF1 (p47phox) and NCF1 pseudogenes are

NCF1 (p47phox) and NCF1 pseudogenes are not associated with inflammatory bowel disease

✍ Nirosha Suraweera; Evi Zampeli; Pauline Rogers; Wendy Atkin; Alistair Forbes; Ma 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB

Keratin 8 Y54H and G62C mutations are no

Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel disease

✍ C. Büning; J. Halangk; A. Dignass; J. Ockenga; P. Deindl; R. Nickel; J. Genschel 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 52 KB