Protein tyrosine phosphatase receptor-type C exon 4 gene mutation distribution in an Italian multiple sclerosis population

Neuroscience Letters

Volumn 328, Issue 3, 2002, Pages 325-327

  Ballerini, Clara ^a   Rosati, Eleonora ^a   Salvetti, Marco ^b   Ristori, Giovanni ^b   Cannoni, Stefania ^b   Biagioli, Tiziana ^a   Massacesi, Luca ^a   Sorbi, Sandro ^a   Vergelli, Marco ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Genetic susceptibility; Multiple sclerosis; Protein tyrosine phosphatase receptor type C

Indexed keywords

PHOSPHOTYROSINE;

ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; EXON; FISHER EXACT TEST; GENE MUTATION; GENETIC STRAIN; GENETIC SUSCEPTIBILITY; HUMAN; ITALY; MULTIPLE SCLEROSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SWEDEN; UNITED STATES;

ANTIGENS, CD45; BASE SEQUENCE; CASE-CONTROL STUDIES; EXONS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ITALY; MULTIPLE SCLEROSIS; MUTATION; REFERENCE VALUES;

EID: 0037119252     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(02)00565-7     Document Type: Article

References (11)

1. PTPRC (CD45) is not associated with development of multiple sclerosis in U.S. patients
2. Genetics of multiple sclerosis
3. A point mutation in PTPRC is associated with development of multiple sclerosis
4. T cell development in mice expressing splice variants of the protein tyrosine phosphatase CD45
5. A CD45 polymorphism associated with multiple sclerosis disrupts an exonic splicing silencer
6. New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
7. Inheritance of susceptibility to multiple sclerosis
8. Regulation of integrin-mediated T cell adhesion by the transmembrane protein tyrosine phosphatase CD45
9. Thymic selection generates T cells expressing self-reactive TCRs in the absence of CD45
10. Does 77C→G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?
11. A point mutation within CD45 exon A is the cause of variant CD45RA splicing in humans