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Remmers, Elaine F; Plenge, Robert M; Lee, Hye-Soon; Lee, Annette T; Graham, Robert R; Hom, Geoffrey; Behrens, Timothy W; de Bakker, Paul I.W; Le, Julie M; Batliwalla, Franak; Li, Wentian; Masters, Seth L; Booty, Matthew G; Carulli, John P; Padyukov, Leonid; Alfredsson, Lars; Klareskog, Lars; Chen, Wei V; Amos, Christopher I; Criswell, Lindsey A; Seldin, Michael F; Kastner, Daniel L; Gregersen, Peter K
The New England journal of medicine, 09/2007, Letnik: 357, Številka: 10Journal Article
Susceptibility to rheumatoid arthritis and systemic lupus erythematosus has been linked to a region on chromosome 2q. Fine-mapping of this locus, in patients with rheumatoid arthritis and in patients with lupus, traces the association to a single variant of the gene STAT4, which encodes a transcription factor activated by cytokines. Fine mapping of a region on chromosome 2q, in patients with rheumatoid arthiritis and in patients with lupus, traces an association to a single variant of the gene STAT4, which encodes a transcription factor activated by cytokines. Rheumatoid arthritis is the most common cause of adult inflammatory arthritis and is associated with considerable disability and early mortality. 1 Studies of twins clearly show a genetic contribution to disease susceptibility, 2 and the siblings of patients with seropositive, erosive rheumatoid arthritis have an estimated risk of developing the disease of between 5 and 10 times that of the general population. 3 The highly polymorphic HLA region is a major contributor to genetic risk of rheumatoid arthritis. 4 Several other genes associated with more modest risks have recently been identified, including the Arg620→Trp variant of the intracellular phosphatase gene PTPN22 . 5 , 6 However, . . .
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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