Analysis of the human pancreatic secretory trypsin inhibitor ( PSTI ) gene mutations in Japanese patients with chronic pancreatitis (original) (raw)

Mutations of the pancreatic secretory trypsin inhibitor (PSTI) gene in idiopathic chronic pancreatitis

Gastroenterology, 2001

Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis

Maria Fotoulaki

Clinical Genetics, 2007

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Mutations in the pancreatic secretory trypsin inhibitor (SPINKI1/PSTI) gene in Japanese patients with pancreatitis

Muhammad Bashir Idris

Gastroenterology, 2003

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Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis

Muhammad Idris

Journal of Medical Genetics, 2002

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Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis

Johann Ockenga

The American journal …, 2000

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Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis

David Whitcomb

Gastroenterology, 1997

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Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial and/or hereditary pancreatitis

Nadia Chuzhanova

Human Mutation, 2004

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Absence of PRSS1 mutations and association of SPINK1 trypsin inhibitor mutations in hereditary and non-hereditary chronic pancreatitis

Mani Venkat

Gut, 2004

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Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis

Cinzia Battaggia

Human Mutation, 2007

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Identification of CFTR, PRSS1, and SPINK1 mutations in 381 patients with pancreatitis

Steven Keiles

Pancreas, 2006

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Pancreatitis in fibrocalculous pancreatic diabetes mellitus is not associated with common mutations in the trypsinogen gene

WILLIAM Ogunkolade

Diabetes/metabolism …, 2000

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Comprehensive screening for PRSS1, SPINK1, CFTR, CTRC and CLDN2 gene mutations in Chinese paediatric patients with idiopathic chronic pancreatitis: a cohort study

xiao weng

BMJ open, 2013

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Identification of a Novel Frame-Shift Mutation in PRSS1 Gene in Han Patients with Autoimmune Pancreatitis

ben salah mohamed

Current Molecular Medicine, 2014

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Evidence that hereditary pancreatitis is genetically heterogeneous disorder

Michael Dean

Pfl?gers Archiv European Journal of Physiology, 2000

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Interaction between trypsinogen isoforms in genetically determined pancreatitis: Mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2)

Karel Caca, Claude Férec

Human Mutation, 2004

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CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in Brazilian patients

Martha Pedroso

JOP : Journal of the pancreas, 2003

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The course of genetically determined chronic pancreatitis

Hans Bödeker

JOP : Journal of the pancreas, 2003

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Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations

Eugene Dimagno

Gastroenterology, 2001

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Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis

Cecilia Surace

Molecular medicine (Cambridge, Mass.), 2016

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Gene Conversion Between Cationic Trypsinogen (PRSS1 ) and the Pseudogene Trypsinogen 6 (PRSS3P2 ) in Patients with Chronic Pancreatitis

Andrzej Tysarowski

Human Mutation, 2015

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Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis

C. Férec

Journal of Medical Genetics, 1999

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R116C Mutation of Cationic Trypsinogen in a Turkish Family with Recurrent Pancreatitis Illustrates Genetic Microheterogeneity of Hereditary Pancreatitis

Susanne Dertinger

Digestion, 2001

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Trypsinogen copy number mutations in patients with idiopathic chronic pancreatitis

Swapna Mahurkar

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2008

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Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis

Johann Ockenga

Nature Genetics, 2008

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Complete Analysis of the Human Mesotrypsinogen Gene (PRSS3) in Patients with Chronic Pancreatitis

Johann Ockenga

Pancreatology, 2010

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Hereditary pancreatitis: clinical features and inheritance characteristics of the R122C mutation in the cationic trypsinogen gene (PRSS1) in six Spanish families

Ana Fontalba

JOP : Journal of the pancreas, 2009

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Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation

Johann Ockenga

Gastroenterology, 2000

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Analysis of the human pancreatic secretory trypsin inhibitor ( PSTI ) gene mutations in Japanese patients with chronic pancreatitis (original) (raw)

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