Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
about
Hereditary pancreatitis caused by mutation-induced misfolding of human cationic trypsinogen: a novel disease mechanismMutations of human cationic trypsinogen (PRSS1) and chronic pancreatitisHereditary pancreatitis: current perspectivesCharacterisation of a transgenic mouse expressing R122H human cationic trypsinogen.The effect of renin angiotensin system genetic variants in acute pancreatitis.The prevalence of cationic trypsinogen (PRSS1) and serine protease inhibitor, Kazal type 1 (SPINK1) gene mutations in Polish patients with alcoholic and idiopathic chronic pancreatitisEvaluating Adults With Idiopathic Pancreatitis for Genetic Predisposition: Higher Prevalence of Abnormal Results With Use of Complete Gene Sequencing.A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 geneChronic pancreatitis and cystic fibrosis.Hereditary Pancreatitis Associated With the N29T Mutation of the PRSS1 Gene in a Brazilian Family: A Case-Control Study.Pathogenic cellular role of the p.L104P human cationic trypsinogen variant in chronic pancreatitisFunctional effects of 13 rare PRSS1 variants presumed to cause chronic pancreatitis.Role of genetic disorders in acute recurrent pancreatitis.Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girlHuman cationic trypsinogen (PRSS1) variants and chronic pancreatitis.Chymotrypsin C (caldecrin) stimulates autoactivation of human cationic trypsinogen.Expression of human cationic trypsinogen with an authentic N terminus using intein-mediated splicing in aminopeptidase P deficient Escherichia coli.Genetic risk in chronic pancreatitis: the misfolding-dependent pathwayExpression of recombinant proteins with uniform N-terminiThe Differential Role of Human Cationic Trypsinogen (PRSS1) p.R122H Mutation in Hereditary and Nonhereditary Chronic Pancreatitis: A Systematic Review and Meta-Analysis.Rare hereditary cause of chronic pancreatitis in a young male: SPINK1 mutation.
P2860
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P2860
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Mutational screening of patien ...... further trypsinogen variants.
@en
Mutational screening of patien ...... further trypsinogen variants.
@nl
type
label
Mutational screening of patien ...... further trypsinogen variants.
@en
Mutational screening of patien ...... further trypsinogen variants.
@nl
prefLabel
Mutational screening of patien ...... further trypsinogen variants.
@en
Mutational screening of patien ...... further trypsinogen variants.
@nl
P2093
P2860
P1476
Mutational screening of patien ...... further trypsinogen variants.
@en
P2093
Joachim Mössner
Nadine Bauer
Niels Teich
Volker Keim
P2860
P304
P356
10.1111/J.1572-0241.2002.05467.X
P407
P577
2002-02-01T00:00:00Z