Trypsinogen copy number mutations in patients with idiopathic chronic pancreatitis

scientific article published on 11 December 2007

Trypsinogen copy number mutations in patients with idiopathic chronic pancreatitis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.CGH.2007.10.004
P698PubMed publication ID18063422
P5875ResearchGate publication ID5785687

P2093author name stringGiriraj R Chandak
Jian-Min Chen
D Nageshwar Reddy
Claude Férec
Cédric Le Maréchal
Seema Bhaskar
Emmanuelle Masson
Swapna Mahurkar
Jérôme Lamoril
Stephane Bezieau
P2860cites workGlobal variation in copy number in the human genomeQ24658083
Common deletion polymorphisms in the human genome.Q54618648
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)82-88
P577publication date2007-12-11
P1433published inClinical Gastroenterology and HepatologyQ5133759
P1476titleTrypsinogen copy number mutations in patients with idiopathic chronic pancreatitis
P478volume6

Reverse relations

cites work (P2860)
Q30000783A conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patients
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Q86874923Characterization of two deletions of the CTRC locus
Q27693296Chymotrypsin C mutations in chronic pancreatitis
Q50921436Clinical and morphological characteristics of sporadic genetically determined pancreatitis as compared to idiopathic pancreatitis: higher risk of pancreatic cancer in CFTR variants.
Q30528817Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
Q33792938Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci
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Q46039825Elucidation of the complex structure and origin of the human trypsinogen locus triplication.
Q39708458Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis.
Q26801332Framework for interpretation of trypsin-antitrypsin imbalance and genetic heterogeneity in pancreatitis
Q36927073Functional effects of 13 rare PRSS1 variants presumed to cause chronic pancreatitis.
Q33843764Genetic Risk in Chronic Pancreatitis: The Trypsin-Dependent Pathway
Q34667122Genetic and phenotypic heterogeneity in tropical calcific pancreatitis
Q37208470Genetic aspects of tropical calcific pancreatitis
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Q34508844Genetics of acute and chronic pancreatitis: An update
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Q30479569Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.
Q27315852In vivo imaging with fluorescent smart probes to assess treatment strategies for acute pancreatitis
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Q52687572PRSS1 (R122H) mutation in an Indian family with low penetrance is associated with pancreatitis phenotype.
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Q37225060Proteases: multifunctional enzymes in life and disease
Q42145402Robust autoactivation, chymotrypsin C independence and diminished secretion define a subset of hereditary pancreatitis-associated cationic trypsinogen mutants.
Q33970780Sequence analysis of the human tyrosylprotein sulfotransferase-2 gene in subjects with chronic pancreatitis
Q45202693Strong purifying selection against gene conversions in the trypsin genes of primates
Q35013336The c.1275A>G putative chronic pancreatitis-associated synonymous polymorphism in the glycoprotein 2 (GP2) gene decreases exon 9 inclusion

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