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Volumn 47, Issue 8, 2004, Pages 1437-1441

Large-scale studies of the functional K variant of the butyrylcholinesterase gene in relation to Type 2 diabetes and insulin secretion

Author keywords

Butyrylcholinesterase; Genetic epidemiology; K variant; Mutation; Type 2 diabetes mellitus

Indexed keywords

C PEPTIDE; CHOLINESTERASE; GLUCOSE; INSULIN; ORAL ANTIDIABETIC AGENT;

EID: 4544290582     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00125-004-1459-7     Document Type: Article
Times cited : (26)

References (23)
  • 1
    • 0035969513 scopus 로고    scopus 로고
    • Islet amyloid and Type 2 diabetes: From molecular misfolding to islet pathophysiology
    • Jaikaran ETAS, Clark A (2001) Islet amyloid and Type 2 diabetes: from molecular misfolding to islet pathophysiology. Biochim Biophys Acta 1537:179-203
    • (2001) Biochim. Biophys. Acta , vol.1537 , pp. 179-203
    • Jaikaran, E.T.A.S.1    Clark, A.2
  • 2
    • 0038798523 scopus 로고    scopus 로고
    • Studies of variability in the islet amyloid polypeptide gene in relation to Type 2 diabetes
    • Pildal J, Lajer M, Hansen SK et al. (2003) Studies of variability in the islet amyloid polypeptide gene in relation to Type 2 diabetes. Diabet Med 20:491-494
    • (2003) Diabet. Med. , vol.20 , pp. 491-494
    • Pildal, J.1    Lajer, M.2    Hansen, S.K.3
  • 4
    • 0027973241 scopus 로고
    • Butyrylcholinesterase reactivity differentiates the amyloid plaques of aging from those of dementia
    • Mesulam MM, Geula C (1994) Butyrylcholinesterase reactivity differentiates the amyloid plaques of aging from those of dementia. Ann Neurol 36:722-727
    • (1994) Ann. Neurol. , vol.36 , pp. 722-727
    • Mesulam, M.M.1    Geula, C.2
  • 5
    • 0032513557 scopus 로고    scopus 로고
    • Distribution of butyrylcholinesterase in the human amygdala and hippocampal formation
    • Darvesh S, Graham DL, Hopkins DA (1998) Distribution of butyrylcholinesterase in the human amygdala and hippocampal formation. J Comp Neurol 393:374-390
    • (1998) J. Comp. Neurol. , vol.393 , pp. 374-390
    • Darvesh, S.1    Graham, D.L.2    Hopkins, D.A.3
  • 6
    • 0242600761 scopus 로고    scopus 로고
    • Glycosylation of acetylcholinesterase and butyrylcholinesterase changes as a function of the duration of Alzheimer's disease
    • Sáez-Valero J, Fodero LR, Sjögren M et al. (2003) Glycosylation of acetylcholinesterase and butyrylcholinesterase changes as a function of the duration of Alzheimer's disease. J Neurol Res 72:520-526
    • (2003) J. Neurol. Res. , vol.72 , pp. 520-526
    • Sáez-Valero, J.1    Fodero, L.R.2    Sjögren, M.3
  • 7
    • 0036498992 scopus 로고    scopus 로고
    • Age-dependent association between butyrylcholinesterase K-variant and Alzheimer disease-related neuropathology in human brains
    • Ghebremedhin E, Thal DR, Schultz C, Braak H (2002) Age-dependent association between butyrylcholinesterase K-variant and Alzheimer disease-related neuropathology in human brains. Neurosci Lett 320:25-28
    • (2002) Neurosci. Lett. , vol.320 , pp. 25-28
    • Ghebremedhin, E.1    Thal, D.R.2    Schultz, C.3    Braak, H.4
  • 8
    • 0026695539 scopus 로고
    • DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage the atypical variant mutation and other polymorphic sites
    • Bartels CF, Jensen FS, Lockridge O et al. (1992) DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage the atypical variant mutation and other polymorphic sites. Am J Hum Genet 50:1086-1103
    • (1992) Am. J. Hum. Genet. , vol.50 , pp. 1086-1103
    • Bartels, C.F.1    Jensen, F.S.2    Lockridge, O.3
  • 9
    • 0041866793 scopus 로고    scopus 로고
    • Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in an Australian population
    • Yen T, Nightingale BN, Burns JC, Sullivan DR, Stewart PM (2003) Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in an Australian population. Clin Chem 49:1297-1308
    • (2003) Clin. Chem. , vol.49 , pp. 1297-1308
    • Yen, T.1    Nightingale, B.N.2    Burns, J.C.3    Sullivan, D.R.4    Stewart, P.M.5
  • 10
    • 0028176595 scopus 로고
    • Measurement of the β-sheet-forming propensities of amino acids
    • Minor DL, Kim PS (1994) Measurement of the β-sheet-forming propensities of amino acids. Nature 367:660-663
    • (1994) Nature , vol.367 , pp. 660-663
    • Minor, D.L.1    Kim, P.S.2
  • 11
    • 0027506498 scopus 로고
    • Human lysozyme gene mutations cause hereditary systemic amyloidosis
    • Pepys MB, Hawkins PN, Booth DR et al. (1993) Human lysozyme gene mutations cause hereditary systemic amyloidosis. Nature 362:553-557
    • (1993) Nature , vol.362 , pp. 553-557
    • Pepys, M.B.1    Hawkins, P.N.2    Booth, D.R.3
  • 12
    • 0033020325 scopus 로고    scopus 로고
    • Further evidence for a synergistic association between APOE E4 and BCHE-K in confirmed Alzheimer's disease
    • Wiebusch H, Poirier J, Sevigny P, Schappert K (1999) Further evidence for a synergistic association between APOE E4 and BCHE-K in confirmed Alzheimer's disease. Hum Genet 104:158-163
    • (1999) Hum. Genet. , vol.104 , pp. 158-163
    • Wiebusch, H.1    Poirier, J.2    Sevigny, P.3    Schappert, K.4
  • 13
    • 0034096612 scopus 로고    scopus 로고
    • Butyrylcholinesterase K variant is genetically associated with late onset Alzheimer's disease in Northern Ireland
    • McIlroy SP, Crawford VL, Dynan KB et al. (2000) Butyrylcholinesterase K variant is genetically associated with late onset Alzheimer's disease in Northern Ireland. J Med Genet 37:182-185
    • (2000) J. Med. Genet. , vol.37 , pp. 182-185
    • McIlroy, S.P.1    Crawford, V.L.2    Dynan, K.B.3
  • 14
    • 0035237706 scopus 로고    scopus 로고
    • Using meta-analysis to explain the diversity of results in genetic studies of late-onset Alzheimer's disease and to identify high-risk subgroups
    • Lehmann DJ, Williams J, Mcbroom J, Smith AD (2001) Using meta-analysis to explain the diversity of results in genetic studies of late-onset Alzheimer's disease and to identify high-risk subgroups. Neuroscience 108:541-554
    • (2001) Neuroscience , vol.108 , pp. 541-554
    • Lehmann, D.J.1    Williams, J.2    Mcbroom, J.3    Smith, A.D.4
  • 15
    • 0033652271 scopus 로고    scopus 로고
    • Genomewide search for Type 2 diabetes susceptibility genes in French Whites: Evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a Type 2 diabetes locus on chromosome 1q21-q24
    • Vionnet N, Hani EH, Dupont S et al. (2000) Genomewide search for Type 2 diabetes susceptibility genes in French Whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a Type 2 diabetes locus on chromosome 1q21-q24. Am J Hum Genet 67:1470-1480
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 1470-1480
    • Vionnet, N.1    Hani, E.H.2    Dupont, S.3
  • 16
    • 0035085146 scopus 로고    scopus 로고
    • Increasing prevalence of diabetes mellitus and impaired glucose tolerance among 60-year-old Danes
    • Drivsholm T, Ibsen H, Schroll M, Davidsen M, Borch-Johnsen K (2001) Increasing prevalence of diabetes mellitus and impaired glucose tolerance among 60-year-old Danes. Diabet Med 18:126-132
    • (2001) Diabet. Med. , vol.18 , pp. 126-132
    • Drivsholm, T.1    Ibsen, H.2    Schroll, M.3    Davidsen, M.4    Borch-Johnsen, K.5
  • 17
    • 17644434640 scopus 로고    scopus 로고
    • Prevalences of diabetes and impaired glucose regulation in a Danish population: The Inter99 study
    • Glümer C, Jørgensen T, Borch-Johnsen K (2003) Prevalences of diabetes and impaired glucose regulation in a Danish population: the Inter99 study. Diabetes Care 26:2335-2340
    • (2003) Diabetes Care , vol.26 , pp. 2335-2340
    • Glümer, C.1    Jørgensen, T.2    Borch-Johnsen, K.3
  • 18
    • 0003725205 scopus 로고    scopus 로고
    • Report of a WHO consultation: Part 1: Diagnosis and classification of diabetes mellitus
    • WHO Study Group World Health Organization, Geneva
    • WHO Study Group (1999) Report of a WHO consultation: part 1: diagnosis and classification of diabetes mellitus. World Health Organization, Geneva
    • (1999)
  • 19
    • 0035676129 scopus 로고    scopus 로고
    • Mutation analysis of peroxisome proliferator-activated receptor-γ coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus
    • Ek J, Andersen G, Urhammer SA et al. (2001) Mutation analysis of peroxisome proliferator-activated receptor-γ coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus. Diabetologia 44:2220-2226
    • (2001) Diabetologia , vol.44 , pp. 2220-2226
    • Ek, J.1    Andersen, G.2    Urhammer, S.A.3
  • 20
    • 0035895258 scopus 로고    scopus 로고
    • High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
    • Buetow KH, Edmonson M, MacDonald R et al. (2001) High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci USA 98:581-584
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , pp. 581-584
    • Buetow, K.H.1    Edmonson, M.2    MacDonald, R.3
  • 21
    • 0035672219 scopus 로고    scopus 로고
    • Butyrylcholinesterase K variant on chromosome 3 q is associated with Type II diabetes in white Caucasian subjects
    • Hashim Y, Sheperd D, Wiltshire S et al. (2001) Butyrylcholinesterase K variant on chromosome 3 q is associated with Type II diabetes in white Caucasian subjects. Diabetologia 44:2227-2230
    • (2001) Diabetologia , vol.44 , pp. 2227-2230
    • Hashim, Y.1    Sheperd, D.2    Wiltshire, S.3
  • 22
    • 85086813645 scopus 로고    scopus 로고
    • Butyrylcholinesterase K variant on chromosome 3 q is associated with Type II diabetes in white Caucasian subjects
    • (Errata)
    • Hashim Y, Sheperd D, Wiltshire S et al. (2002) Butyrylcholinesterase K variant on chromosome 3 q is associated with Type II diabetes in white Caucasian subjects. Diabetologia 45:459 (Errata)
    • (2002) Diabetologia , vol.45 , pp. 459
    • Hashim, Y.1    Sheperd, D.2    Wiltshire, S.3
  • 23
    • 0037442235 scopus 로고    scopus 로고
    • Genetic associations in large versus small studies: An empirical assessment
    • Ioannidis JPA, Trikalinos TA, Ntzani EE et al. (2003) Genetic associations in large versus small studies: an empirical assessment. Lancet 361:567-571
    • (2003) Lancet , vol.361 , pp. 567-571
    • Ioannidis, J.P.A.1    Trikalinos, T.A.2    Ntzani, E.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.