Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis

H Witt, W Luck, HC Hennies, M Claßen, A Kage… - Nature …, 2000 - nature.com
Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas.
In approximately one-third of all cases, no aetiological factor can be found, and these …

Functional roles of SPINK1 in cancers

TC Lin - International Journal of Molecular Sciences, 2021 - mdpi.com
Serine Peptidase Inhibitor Kazal Type 1 (SPINK1) is a secreted protein known as a protease
inhibitor of trypsin in the pancreas. However, emerging evidence shows its function in …

[HTML][HTML] Genetics of acute and chronic pancreatitis: an update

VVR Kanth, DN Reddy - World journal of gastrointestinal …, 2014 - ncbi.nlm.nih.gov
Progress made in identifying the genetic susceptibility underlying acute and chronic
pancreatitis has benefitted the clinicians in understanding the pathogenesis of the disease …

[HTML][HTML] Complete nucleotide sequence of human reg gene and its expression in normal and tumoral tissues. The reg protein, pancreatic stone protein, and pancreatic …

T Watanabe, H Yonekura, K Terazono… - Journal of Biological …, 1990 - Elsevier
We previously identified a novel gene, reg (ie regenerating gene), in the screening of a rat
regenerating islet-derived cDNA library, and isolated its human cDNA homologue which …

Primary structure of a putative serine protease specific for IGF-binding proteins

J Zumbrunn, B Trueb - FEBS letters, 1996 - Elsevier
From a subtracted cDNA library we have isolated a cDNA clone coding for a novel
transformation-sensitive protein which is expressed by human fibroblasts, but not by their …

The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease

J Threadgold, W Greenhalf, I Ellis, N Howes, MM Lerch… - Gut, 2002 - gut.bmj.com
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary
pancreatitis (HP) but many HP families have no PRSS1 mutation. Recently, an association …

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

GR Chandak, MM Idris, DN Reddy, S Bhaskar… - Journal of Medical …, 2002 - jmg.bmj.com
Pancreatitis is a global health care problem with varied aetiologies. Alcoholism is
responsible in the majority of patients while other causes, such as heredity, gallstones …

Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the …

MP Audrézet, JM Chen, C Le Maréchal… - European Journal of …, 2002 - nature.com
In the last 5 years, mutations in three genes, the cystic fibrosis transmembrane conductance
regulator (CFTR) gene, the cationic trypsinogen (PRSS1) gene, and the pancreatic secretory …

Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis

JM Chen, B Mercier, MP Audrezet… - Journal of medical genetics, 2000 - jmg.bmj.com
EDITOR—Ocular angioma (haemangioblastoma) is the most common presenting feature of
the multisystem familial cancer syndrome von Hippel-Lindau disease (VHL). 1 Recognition …

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

GR Chandak, MM Idris, DN Reddy, KR Mani… - Gut, 2004 - gut.bmj.com
Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1);
PRSS1) gene are causally associated with recurrent acute and chronic pancreatitis. We …