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Volumn 18, Issue 5, 2002, Pages 545-551

Genetics and pancreatic disease

Author keywords

[No Author keywords available]

Indexed keywords

APROTININ; TRANSMEMBRANE CONDUCTANCE REGULATOR; TRYPSINOGEN;

EID: 0036720002     PISSN: 02671379     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001574-200209000-00004     Document Type: Review
Times cited : (5)

References (59)
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    • Witt, H.1
  • 3
    • 0035553388 scopus 로고    scopus 로고
    • Hereditary pancreatitis: A model for understanding the genetic basis of acute and chronic pancreatitis
    • (2001) Pancreatology , vol.1 , pp. 565-570
    • Whitcomb, D.C.1
  • 16
    • 0034809120 scopus 로고    scopus 로고
    • Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations
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    • Chen, J.M.1    Montier, T.2    Ferec, C.3
  • 19
    • 18544365392 scopus 로고    scopus 로고
    • Hereditary pancreatitis caused by a novel PRSS1 mutation (Arg-122 ->Cys) that alters autoactivation and autodegradation of cationic trypsinogen
    • (2002) J Biol Chem , vol.277 , pp. 5404-5410
    • Simon, P.1    Weiss, F.U.2    Sahin-Toth, M.3
  • 21
    • 0034322389 scopus 로고    scopus 로고
    • A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis
    • (2000) J Med Genet , vol.37
    • Chen, J.M.1    Raguenes, O.2    Ferec, C.3
  • 22
    • 0034725697 scopus 로고    scopus 로고
    • Human cationic trypsinogen: Role of Asn-21 in zymogen activation and implications in hereditary pancreatitis
    • (2000) J Biol Chem , vol.275 , pp. 22750-22755
    • Sahin-Toth, M.1
  • 23
    • 2942615503 scopus 로고    scopus 로고
    • Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography
    • (2001) BMC Genet , vol.2 , pp. 19
    • Le Marechal, C.1    Chen, J.M.2    Quere, I.I.3
  • 25
    • 0035714189 scopus 로고    scopus 로고
    • R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis
    • (2001) Digestion , vol.64 , pp. 226-232
    • Tautermann, G.1    Ruebsamen, H.2    Beck, M.3
  • 27
    • 0035702382 scopus 로고    scopus 로고
    • Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene
    • (2001) Am J Med , vol.111 , pp. 622-626
    • Keim, V.1    Bauer, N.2    Teich, N.3
  • 30
    • 0034039578 scopus 로고    scopus 로고
    • Mutations in the gene encoding the serine protease inhibitor, kazal type 1 are associated with chronic pancreatitis
    • (2000) Nat Genet , vol.25 , pp. 213-216
    • Witt, H.1    Luck, W.2    Hennies, H.C.3
  • 40
    • 0036102601 scopus 로고    scopus 로고
    • The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease
    • (2002) Gut , vol.50 , pp. 675-681
    • Threadgold, J.1    Greenhalf, W.2    Ellis, I.3
  • 41
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    • Mutation in the SPINK1 trypsin inhibitor gene, alcohol use, and chronic pancreatitis
    • (2001) JAMA , vol.285 , pp. 2716-2717
    • Witt, H.1    Luck, W.2    Becker, M.3
  • 48
    • 0036143702 scopus 로고    scopus 로고
    • Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: The familial atypical mole melanoma-pancreatic carcinoma syndrome
    • (2002) Cancer , vol.94 , pp. 84-96
    • Lynch, H.T.1    Brand, R.E.2    Hogg, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.