Evolution of Crohn’s disease-associated Nod2 mutations

By Gasche Christoph   Nemeth Manuela   Grundtner Paul   Willheim-Polli Claudia   Ferenci Peter   Schwarzenbacher Robert  

Immunogenetics, Vol. 60, Iss. 2, 2008-02 ,pp. : 115-120

Springer Publishing Company

Access to resources Recommend Favorite

The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants

By van Heel David A.  

Human Molecular Genetics, Vol. 12, Iss. 20, 2003-10 ,pp. : 2569-2575

Oxford University Press

Access to resources Recommend Favorite

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

By Piton Amlie   Michaud Jacques L.   Peng Huashan   Aradhya Swaroop   Gauthier Julie   Mottron Laurent   Champagne Nathalie   Lafrenire Ronald G.   Hamdan Fadi F.   Joober Ridha   Fombonne Eric   Marineau Claude   Cossette Patrick   Dub Marie-Pierre   Haghighi Pejmun   Drapeau Pierre   Barker Philip A.   Carbonetto Salvatore   Rouleau Guy A.  

Human Molecular Genetics, Vol. 17, Iss. 24, 2008-12 ,pp. : 3965-3974

Oxford University Press

Access to resources Recommend Favorite

An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6

By Fairfax Benjamin P.   Vannberg Fredrik O.   Radhakrishnan Jayachandran   Hakonarson Hakon   Keating Brendan J.   Hill Adrian V.S.   Knight Julian C.  

Human Molecular Genetics, Vol. 19, Iss. 4, 2010-02 ,pp. : 720-730

Oxford University Press

Access to resources Recommend Favorite

Association between a complex insertion/deletion polymorphism in NOD1 ( CARD4 ) and susceptibility to inflammatory bowel disease

By McGovern Dermot P.B.  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1245-1250

Oxford University Press

Access to resources Recommend Favorite