✦ LIBER ✦

Protein tyrosine phosphatase-22 (PTPN-22) polymorphism in the pathogenesis of chronic urticaria

✍ Scribed by Zenon Brzoza; Władysław Grzeszczak; Wanda Trautsolt; Dariusz Moczulski

Book ID: 110887414
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 207 KB
Volume: 66
Category: Article
ISSN: 0105-4538
DOI: 10.1111/j.1398-9995.2011.02651.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Protein tyrosine phosphatase gene (PTPN2

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis

✍ F. Matesanz; B. Rueda; G. Orozco; O. Fernandez; L. Leyva; A. Alcina; J. Martín 📂 Article 📅 2005 🏛 Springer 🌐 English ⚖ 169 KB

Protein Tyrosine Phosphatase Gene PTPN22

Protein Tyrosine Phosphatase Gene PTPN22 Polymorphism in Psoriasis: Lack of Evidence for Association

✍ Nistor, Ioana ;Nair, Rajan P. ;Stuart, Philip ;Hiremagalore, Ravi ;Thompson, Rac 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 56 KB

A single-nucleotide polymorphism in the

A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo

✍ Cantón, I; Akhtar, S; Gavalas, N G; Gawkrodger, D J; Blomhoff, A; Watson, P F; W 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 89 KB

The Role of Polymorphic Protein Tyrosine

The Role of Polymorphic Protein Tyrosine Phosphatase Non-Receptor Type 22 in Leprosy

✍ Rani, Rajni; Singh, Anamika; Israni, Neetu; Singh, Archana; Sharma, Pankaj; Kar, 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 75 KB

Association of a functional polymorphism

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

✍ Jose A. Lopez-Escamez; Pablo Saenz-Lopez; Lourdes Acosta; Antonia Moreno; Irene 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 83 KB

## Abstract ## Objectives/Hypothesis: Bilateral Meniere's disease (BMD) is a severe disease that usually results in bilateral severe or profound sensorineural hearing loss and chronic disequilibrium with loss of vestibular function. We examined single nucleotide polymorphisms (SNPs) in the __PTPN2

Evaluating the role of the 620W allele o

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis

✍ De Jager, Philip L; Sawcer, Stephen; Waliszewska, Alicja; Farwell, Lisa; Wild, G 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 81 KB