(Q58054028)

Valérie Senée

4

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Claude Chelala

Claude Chelala

2

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Sophie Caillat-Zucman

Sophie Caillat-Zucman

5

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Ingrid Kockum

Ingrid Kockum

6

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Flemming Pociot

Flemming Pociot

9

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Danièle Dubois-Laforgue

3

Danièle Dubois-Laforgue

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Cécile Julier

11

Cécile Julier

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author name string

Holgar Luthman

7

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Jorn Nerup

8

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José Timsit

Molecular Genetics and Metabolism

10

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publication date

November 2005

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published in

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volume

86

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issue

3

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page(s)

379-383

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cites work

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Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

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The genetics of complex autoimmune diseases: non-MHC susceptibility genes

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International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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Molecular genetics of Crohn's disease

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CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis

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Association between polymorphisms in caspase recruitment domain containing protein 15 and allergy in two German populations

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NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses

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Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing

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Mycobacteria and other environmental organisms as immunomodulators for immunoregulatory disorders.

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Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15.

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CARD15/NOD2 analyses in spondylarthropathy

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Crohn's associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis.

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