Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Syndrome and CARD15[original query] |
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NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis. The Journal of rheumatology 2003 Feb 30 (2): 305-7. Newman Bill, Rubin Laurence A, Siminovitch Katherine |
Analysis of CARD15 polymorphisms in Korean patients with ankylosing spondylitis reveals absence of common variants seen in western populations. The Journal of rheumatology 2004 Oct 31 (10): 1959-61. Kim Tae-Hwan, Rahman Proton, Jun Jae-Bum, Lee Hye-Soon, Park Yong-Wook, Im Ho Joon, Snelgrove Tara, Peddle Lynette, Hallett David, Inman Robert |
Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene. Genomics 2007 Oct 90 (4): 493-501. King Kathy, Bagnall Richard, Fisher Sheila A, Sheikh Faisal, Cuthbert Andrew, Tan Sipin, Mundy Nicholas I, Rosenstiel Philip, Schreiber Stefan, Mathew Christopher G, Roberts Roland |
Analysis of the NOD2/CARD15 gene in patients affected with the aseptic abscesses syndrome with or without inflammatory bowel disease. Digestive diseases and sciences 2008 Feb 53 (2): 490-9. André Marc François Jean, Aumaître Olivier, Piette Jean-Charles, Grateau Gilles, Cardoso Marie-Céleste, Ouchchane Lemlih, Kémény Jean-Louis, Dastugue Bernard, Delpech Marc, Creveaux Isabel |
Blau syndrome-associated mutations in exon 4 of the caspase activating recruitment domain 15 (CARD 15) gene are not found in ethnic Danes with sarcoidosis. The clinical respiratory journal 2007 Dec 1 (2): 74-9. Milman Nils, Nielsen Finn Cilius, Hviid Thomas Vauvert F, Hansen Thomas van Overe |
Mutation screening of the CARD15 gene in sarcoidosis. Tissue antigens 2008 Jun 71 (6): 564-7. Akahoshi M, Ishihara M, Namba K, Kitaichi N, Ando Y, Takenaka S, Ishida T, Ohno S, Mizuki N, Nakashima H, Shirakawa |
MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA. Rheumatology international 2010 Mar 30 (5): 633-6. Dagan Efrat, Gershoni-Baruch Ruth, Khatib Ihab, Mori Adi, Brik Ri |
NOD2/CARD15 genotype and common gastrointestinal diseases in 43,600 individuals. Journal of internal medicine 2010 Feb 267 (2): 228-36. Yazdanyar S, Nordestgaard B |
Genetic susceptibility factors in a cohort of 38 patients with SAPHO syndrome: a study of PSTPIP2, NOD2, and LPIN2 genes. The Journal of rheumatology 2010 Feb 37 (2): 401-9. Hurtado-Nedelec Margarita, Chollet-Martin Sylvie, Chapeton Diana, Hugot Jean-Pierre, Hayem Gilles, Gérard Bénédic |
Blau syndrome-related CARD15/NOD2 mutations are not linked to idiopathic uveitis in Spanish patients. Disease markers 2009 27 (1): 1-5. Rodríguez-Pérez Noelia, Aguinaga-Barrilero Ana, Gorroño-Echebarría Marina B, Pérez-Blas Mercedes, Martín-Villa José |
Association between NOD2/CARD15 polymorphisms and coronary artery disease: a case-control study. Human immunology 2011 Aug 72 (8): 636-40. Galluzzo Sara, Patti Giuseppe, Dicuonzo Giordano, Di Sciascio Germano, Tonini Giuseppe, Ferraro Elisabetta, Spoto Chiara, Campanale Roberto, Zoccoli Alice, Angeletti Silv |
MEFV, TNFRSF1A and CARD15 mutation analysis in Behçet's disease. Clinical and experimental rheumatology 0 29 (4 Suppl 67): S24-7. Baruch Yoav, Dagan Efrat, Rosner Itzhak, Fiorilli Massimo, Gershoni-Baruch Ruth, Rozenbaum Micha |
Detection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B). Medical microbiology and immunology 2014 Jun 203 (3): 195-205. Dalton James P, Desmond Alan, Shanahan Fergus, Hill Col |
Clinical and Genetic Features of Korean Patients with Recurrent Fever and Multi-System Inflammation without Infectious or Autoimmune Evidence. Journal of Korean medical science 2016 Feb 31 (2): 196-201. Yang Ji Ae, Choi Ji Yong, Kang Eun Ha, Ha You-Jung, Lee Yun Jong, Song Yeong Wo |
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- Page last updated:May 06, 2024
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