The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study.

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The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study.

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http://www.wikidata.org/entity/Q36127496

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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name

The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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P1476

The common NOD2/CARD15 variant ...... tious uveitis: a cohort study.

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P2860

The Nod-like receptor (NLR) family: a tale of similarities and differences

Nucleotide oligomerization domain-2 (NOD2)-induced uveitis: dependence on IFN-gamma.

NOD2 deficiency results in increased susceptibility to peptidoglycan-induced uveitis in mice

International Uveitis Study Group (IUSG): clinical classification of uveitis.

Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease.

Analysis of Crohn's disease-related CARD15 polymorphisms in Spanish patients with idiopathic uveitis.

Pediatric uveitis: new and future treatments.

The roles of genetic factors in uveitis and their clinical significance.

Clinical and transcriptional response to the long-acting interleukin-1 blocker canakinumab in Blau syndrome-related uveitis.

Blau syndrome-related CARD15/NOD2 mutations are not linked to idiopathic uveitis in Spanish patients.

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s12969-015-0037-5

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scholarly article

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10.1186/S12969-015-0037-5

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