Literature DB >> 15744042

Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study.

H Qu, M-C Tessier, T J Hudson, C Polychronakos.   

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Year:  2005        PMID: 15744042      PMCID: PMC1736025          DOI: 10.1136/jmg.2004.026971

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  20 in total

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Review 3.  Genetic epidemiology of type 1 diabetes.

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6.  Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?

Authors:  M-C Tessier; H-Q Qu; R Fréchette; F Bacot; R Grabs; S P Taback; M L Lawson; S E Kirsch; T J Hudson; C Polychronakos
Journal:  J Med Genet       Date:  2005-07-13       Impact factor: 6.318

7.  PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

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8.  rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.

Authors:  A K Steck; E E Baschal; J M Jasinski; B O Boehm; N Bottini; P Concannon; C Julier; G Morahan; J A Noble; C Polychronakos; J X She; G S Eisenbarth
Journal:  Genes Immun       Date:  2009-12       Impact factor: 2.676

9.  Genetic evidence that the differential expression of the ligand-independent isoform of CTLA-4 is the molecular basis of the Idd5.1 type 1 diabetes region in nonobese diabetic mice.

Authors:  Manabu Araki; Denise Chung; Sue Liu; Daniel B Rainbow; Giselle Chamberlain; Valerie Garner; Kara M D Hunter; Lalitha Vijayakrishnan; Laurence B Peterson; Mohamed Oukka; Arlene H Sharpe; Raymond Sobel; Vijay K Kuchroo; Linda S Wicker
Journal:  J Immunol       Date:  2009-09-25       Impact factor: 5.422

10.  Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population.

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Journal:  BMC Med Genet       Date:  2010-01-20       Impact factor: 2.103

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