30 results match your criteria: "University of California San Diego Medical School[Affiliation]"
Cancer Res
October 1999
Ludwig Institute for Cancer Research, Department of Medicine and Cancer Center, University of California San Diego Medical School, La Jolla 92093-0660, USA.
Hereditary nonpolyposis colorectal carcinoma (HNPCC) is due primarily to inherited mutations in two mismatch repair genes, MSH2 and MLH1, whereas germ-line mutations in other mismatch repair genes are rare. We examined the frequency of germ-line msh6 mutations in a population-based series of 140 colorectal cancer patients, including 45 sporadic cases, 91 familial non-HNPCC cases, and 4 HNPCC cases. Among the 91 population-based familial non-HNPCC cases, germ-line msh6 mutations were found in 6 patients (7.
View Article and Find Full Text PDFJ Mol Med (Berl)
January 1999
The Islet Research Laboratory, Department of Pediatrics, University of California San Diego Medical School, La Jolla 92037, USA.
The paucity of human adult islets available for transplantation in IDDM makes the use of human fetal pancreas a potential alternative. Fetal pancreatic endocrine cells grow and differentiate over time when fresh explants or cultured islet-like cell clusters (ICCs) are transplanted under the kidney capsule in athymic nude mice. We have recently developed a procedure to isolate fetal islets, which differ from ICCs in their beta-cell content.
View Article and Find Full Text PDFAm J Physiol
February 1993
Department of Medicine, University of California San Diego Medical School, La Jolla 92093-0671.
The central nervous system effects of thyrotropin-releasing hormone (TRH) and calcitonin gene-related peptide (CGRP) on exocrine pancreatic secretion were studied in freely moving rats. TRH (0.05-0.
View Article and Find Full Text PDFJ Allergy Clin Immunol
December 1991
University of California-San Diego Medical School, La Jolla.
Eur Arch Otorhinolaryngol
September 1990
Division of Otolaryngology, University of California San Diego Medical School.
The distribution of immunoglobulin-bearing cells and the pattern of histopathological changes in the middle ear (ME) mucosa, round window membrane (RWM), and inner ear were compared during acute and chronic immune-mediated otitis media with effusion (OME) in the guinea pig as an animal model. In both acute and chronic immune responses (IRs), mucosal hyperplasia, edema, neovascularization, and cellular infiltration were observed. IgG+ cells were predominant in both the acute and chronic IRs.
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