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Inflammatory Bowel Disease: Are There Gender Differences in the Genetics of Signal Transduction? A Preliminary Study of Cytosolic Low Molecular Weight Protein Tyrosine Phosphatase
Author(s) -
Nunzio Bottini,
F. GloriaBottini,
N. Lucarini,
P Ronchetti,
Luigi Fontana
Publication year - 2000
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2000/101739
Subject(s) - protein tyrosine phosphatase , signal transduction , gene isoform , phenotype , ulcerative colitis , biology , cytosol , endocrinology , tyrosine , receptor tyrosine kinase , inflammatory bowel disease , enzyme , medicine , phosphatase , receptor , kinase , tyrosine kinase , immunology , disease , genetics , biochemistry , gene
The phenotype of cytosolic Low Molecular Weight Protein Tyrosine Phosphatase (cLMWPTP or ACP1), an enzyme involved in signal transduction of insulin, PDGF and T-cell receptors, has been determined in 71 patients with Crohn's Disease (CD: 37 males and 34 females), 49 patients with Ulcerative Colitis (UC: 27 males and 22 females) and 358 consecutive newborns (194 males and 164 females). cLMWPTP phenotypes showing a high concentration of F isoforms are associated with CD in females and with UC in males. Since PTPases counteract the effects of protein tyrosines kinases, a high concentration of F isoform of cLMWPTP may influence the mucosal response to pathogenic factors, increasing susceptibility to CD in females and to UC in males.

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