๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Role of an intronic polymorphism in thePDCD1gene with the risk of sporadic systemic lupus erythematosus and the occurrence of antiphospholipid antibodies

โœ Scribed by Dharambir K. Sanghera; Susan Manzi; Franklin Bontempo; Cara Nestlerode; M. Ilyas Kamboh

Publisher
Springer
Year
2004
Tongue
English
Weight
101 KB
Volume
115
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Evaluation of the genetic association of
Evaluation of the genetic association of the PTPN22 R620W polymorphism in familial and sporadic systemic lupus erythematosus
โœ Kenneth M. Kaufman; Jennifer A. Kelly; Billy J. Herring; Adam J. Adler; Stuart B ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 81 KB ๐Ÿ‘ 1 views

## Abstract ## Objective The R620W (1858Cโ†’T) polymorphism in __PTPN2__2 has been implicated in type 1 diabetes mellitus, rheumatoid arthritis, Graves' disease, Hashimoto thyroiditis, autoimmune thyroid disease, and systemic lupus erythematosus (SLE). The aim of this study was to evaluate this poly

Different manifestations of the antiphos
Different manifestations of the antiphospholipid antibody syndrome in a family with systemic lupus erythematosus
โœ Kimberly P. May; Sterling G. West; Joann Moulds; Brian L. Kotzin ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 524 KB

Familial associations of the antiphospholipid antibody syndrome (APS) offer the opportunity to study genetic mechanisms of autoantibody production and disease, but are unusual. We identified a family, including identical twins and their mother, in which all members had systemic lupus erythematosus (