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Volumn 41, Issue 4, 1997, Pages 493-495

Lack of association of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia

Author keywords

Catechol O methyltransferase; Dopamine; Polymorphism; Schizophrenia

Indexed keywords

CATECHOL METHYLTRANSFERASE;

EID: 0031568907     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3223(96)00474-X     Document Type: Article
Times cited : (71)

References (35)
  • 1
    • 0027469794 scopus 로고
    • Catechol-O-methyltransferase pharmacogenetics: Photoaffinity labelling and western blot analysis of human liver samples
    • Aksoy S, Klener J, Weinshilboum RM (1993): Catechol-O-methyltransferase pharmacogenetics: Photoaffinity labelling and Western blot analysis of human liver samples. Pharmacogenetics 3:116-122.
    • (1993) Pharmacogenetics , vol.3 , pp. 116-122
    • Aksoy, S.1    Klener, J.2    Weinshilboum, R.M.3
  • 2
    • 70449228544 scopus 로고
    • Enzymatic O-methylation of epinephrine and other catechols
    • Axelrod J, Tomchick R (1958): Enzymatic O-methylation of epinephrine and other catechols. J Biol Chem 233:702-705.
    • (1958) J Biol Chem , vol.233 , pp. 702-705
    • Axelrod, J.1    Tomchick, R.2
  • 4
    • 0028205578 scopus 로고
    • Genetic studyof dopamine D1, D2 and D4 receptors in schizophrenia
    • Campion D, d'Amato T, Bastard C, et al (1994): Genetic studyof dopamine D1, D2 and D4 receptors in schizophrenia. Psychiatry Res 51:215-230.
    • (1994) Psychiatry Res , vol.51 , pp. 215-230
    • Campion, D.1    D'Amato, T.2    Bastard, C.3
  • 5
    • 0024247522 scopus 로고
    • The current status of the dopamine hypothesis of schizophrenia
    • Carlsson A (1988): The current status of the dopamine hypothesis of schizophrenia. Neuropsychopharmacology 1:179-186.
    • (1988) Neuropsychopharmacology , vol.1 , pp. 179-186
    • Carlsson, A.1
  • 6
    • 0028290441 scopus 로고
    • Velo-cardio-facial syndrome and psychotic disorders: Implications for psychiatric genetics
    • Chow EWC, Bassett AS, Weksberg R (1994): Velo-cardio-facial syndrome and psychotic disorders: Implications for psychiatric genetics. Am J Med Genet 54:107-112.
    • (1994) Am J Med Genet , vol.54 , pp. 107-112
    • Chow, E.W.C.1    Bassett, A.S.2    Weksberg, R.3
  • 7
    • 0027471250 scopus 로고
    • Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees
    • Coon H, Bylerley W, Holik J, et al (1993): Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees. Am J Hum Genet 52:327-334.
    • (1993) Am J Hum Genet , vol.52 , pp. 327-334
    • Coon, H.1    Bylerley, W.2    Holik, J.3
  • 8
    • 13344284664 scopus 로고    scopus 로고
    • No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity
    • Daniels JK, Williams NM, Williams J, et al (1996): No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. Am J Psychiatry 153:268-270.
    • (1996) Am J Psychiatry , vol.153 , pp. 268-270
    • Daniels, J.K.1    Williams, N.M.2    Williams, J.3
  • 9
    • 0027370619 scopus 로고
    • Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndrome: Implications for genetic counselling and prenatal diagnosis
    • Driscoll DA, Salvin J, Sellinger B, et al (1993): Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndrome: Implications for genetic counselling and prenatal diagnosis. J Med Genet 30:813-817.
    • (1993) J Med Genet , vol.30 , pp. 813-817
    • Driscoll, D.A.1    Salvin, J.2    Sellinger, B.3
  • 10
    • 0017579456 scopus 로고
    • Erythrocyte catechol-O-methyltransferase activity in primary affective disorder
    • Dunner DL, Levitt M, Kumbaraci T, Fieve RR (1977): Erythrocyte catechol-O-methyltransferase activity in primary affective disorder. Biol Psychiatry 12:237-244.
    • (1977) Biol Psychiatry , vol.12 , pp. 237-244
    • Dunner, D.L.1    Levitt, M.2    Kumbaraci, T.3    Fieve, R.R.4
  • 11
    • 13344275183 scopus 로고    scopus 로고
    • Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking
    • Ebstein EP, Novick O, Umansky R, et al (1996): Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking. Nat Genet 12:78-80.
    • (1996) Nat Genet , vol.12 , pp. 78-80
    • Ebstein, E.P.1    Novick, O.2    Umansky, R.3
  • 12
    • 0026518652 scopus 로고
    • Chromosomal mapping of the human catechol-O-methyl transferase gene to 22q11.1-q11.2
    • Grossman MH, Emanual BS, Budarf ML (1992): Chromosomal mapping of the human catechol-O-methyl transferase gene to 22q11.1-q11.2. Genomics 12:822-825.
    • (1992) Genomics , vol.12 , pp. 822-825
    • Grossman, M.H.1    Emanual, B.S.2    Budarf, M.L.3
  • 13
    • 0023412469 scopus 로고
    • The decrease of erythrocyte catechol-O-methyltransferase activity in depressed patients and its diagnostic significance
    • Karege F, Bovier J-M, Tissot R (1987): The decrease of erythrocyte catechol-O-methyltransferase activity in depressed patients and its diagnostic significance. Acta Psychiatr Scand 76:303-308.
    • (1987) Acta Psychiatr Scand , vol.76 , pp. 303-308
    • Karege, F.1    Bovier, J.-M.2    Tissot, R.3
  • 14
    • 0030004521 scopus 로고    scopus 로고
    • Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
    • Lachman HL, Papolos DF, Saito T, Yu YM, Szumlanski CL, Weinshilboum RM (1996a): Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics 6:243-250.
    • (1996) Pharmacogenetics , vol.6 , pp. 243-250
    • Lachman, H.L.1    Papolos, D.F.2    Saito, T.3    Yu, Y.M.4    Szumlanski, C.L.5    Weinshilboum, R.M.6
  • 15
    • 0029745410 scopus 로고    scopus 로고
    • Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial-syndrome
    • Lachman HL, Morrow B, Shprintzen R, et al (1996b): Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial-syndrome. Am J Med Genet 67:468-472.
    • (1996) Am J Med Genet , vol.67 , pp. 468-472
    • Lachman, H.L.1    Morrow, B.2    Shprintzen, R.3
  • 16
    • 0029634412 scopus 로고
    • Velo-cardio-facial syndrome: Frequency and extent of 22q11 deletions
    • Lindsay EA, Goldberg R, Jurecic V (1995): Velo-cardio-facial syndrome: Frequency and extent of 22q11 deletions. Am J Med Genet 57:514-522.
    • (1995) Am J Med Genet , vol.57 , pp. 514-522
    • Lindsay, E.A.1    Goldberg, R.2    Jurecic, V.3
  • 17
    • 0028918413 scopus 로고
    • Kinetics of human soluble and membrane bound catechol-O-methyltransferase: A revised mechanism and description of the thermolabile variant of the enzyme
    • Lotta T, Vidgren J, Tilgmann C, et al (1995): Kinetics of human soluble and membrane bound catechol-O-methyltransferase: A revised mechanism and description of the thermolabile variant of the enzyme. Biochemistry 34:4202-4210.
    • (1995) Biochemistry , vol.34 , pp. 4202-4210
    • Lotta, T.1    Vidgren, J.2    Tilgmann, C.3
  • 18
    • 0025801604 scopus 로고
    • Cloning and characterization of human placental catechol-O-methyltransferase cDNA
    • Lundstrom K, Salminen M, Jalanko A, Savolainen R, Ulmanen I (1991): Cloning and characterization of human placental catechol-O-methyltransferase cDNA. DNA Cell Biol 10:181-189.
    • (1991) DNA Cell Biol , vol.10 , pp. 181-189
    • Lundstrom, K.1    Salminen, M.2    Jalanko, A.3    Savolainen, R.4    Ulmanen, I.5
  • 19
    • 0028019708 scopus 로고
    • An association study between schizophrenia and the dopamine receptor genes DRD3 and DRD4 using haplotype relative risk
    • Macciardi F, Verga M, Kennedy JL, et al (1995): An association study between schizophrenia and the dopamine receptor genes DRD3 and DRD4 using haplotype relative risk. Hum Hered 44:328-336.
    • (1995) Hum Hered , vol.44 , pp. 328-336
    • Macciardi, F.1    Verga, M.2    Kennedy, J.L.3
  • 20
    • 0029033626 scopus 로고
    • Molecular definition of the 22q11 deletions in velo-cardio facial syndrome
    • Morrow B, Goldberg R, Carlson C, et al (1995): Molecular definition of the 22q11 deletions in velo-cardio facial syndrome. Am J Hum Genet 56:1391-1403.
    • (1995) Am J Hum Genet , vol.56 , pp. 1391-1403
    • Morrow, B.1    Goldberg, R.2    Carlson, C.3
  • 21
    • 0011290394 scopus 로고
    • Bipolar spectrum in patients diagnosed with velo-cardio-facial-syndrome: Does hemizygous deletion of chromosome 22q 11 result in bipolar affective disorder
    • in press
    • Papolos DF, Faedda G, Veit S, et al (1995): Bipolar spectrum in patients diagnosed with velo-cardio-facial-syndrome: Does hemizygous deletion of chromosome 22q 11 result in bipolar affective disorder. Am J Psychiatry (in press).
    • (1995) Am J Psychiatry
    • Papolos, D.F.1    Faedda, G.2    Veit, S.3
  • 22
    • 0028837510 scopus 로고
    • Exclusion of close linkage of the dopamine transporter gene with schizophrenia spectrum disorders
    • Persico AM, Wang ZW, Black DW, Andreasen NC, Uhl GR, Crowe RR (1995): Exclusion of close linkage of the dopamine transporter gene with schizophrenia spectrum disorders. Am J Psychiatry 152:134-136.
    • (1995) Am J Psychiatry , vol.152 , pp. 134-136
    • Persico, A.M.1    Wang, Z.W.2    Black, D.W.3    Andreasen, N.C.4    Uhl, G.R.5    Crowe, R.R.6
  • 24
    • 0027989917 scopus 로고
    • Psychotic illness in patients diagnosed with velo-cardio facial syndrome and their relatives
    • Pulver AE, Nestadt G, Goldberg R, et al (1994): Psychotic illness in patients diagnosed with velo-cardio facial syndrome and their relatives. J Nerv Ment Dis 182:476-478.
    • (1994) J Nerv Ment Dis , vol.182 , pp. 476-478
    • Pulver, A.E.1    Nestadt, G.2    Goldberg, R.3
  • 25
    • 0020676590 scopus 로고
    • Studies on biogenic amine metabolizing enzymes (DBH, COMT, MAO) and pathogenesis of affective illness: II. Erythrocyte catechol-O-methyltransferase activity in endogenous depression
    • Puzynski S, Bidzinsky A, Mrozek S, Zaluska M (1983): Studies on biogenic amine metabolizing enzymes (DBH, COMT, MAO) and pathogenesis of affective illness: II. Erythrocyte catechol-O-methyltransferase activity in endogenous depression. Acta Psychiatr Scand 67:96-100.
    • (1983) Acta Psychiatr Scand , vol.67 , pp. 96-100
    • Puzynski, S.1    Bidzinsky, A.2    Mrozek, S.3    Zaluska, M.4
  • 26
    • 0028128976 scopus 로고
    • Linkage analysis between schizophrenia and a microsatellite polymorphism for the D5 receptor gene
    • Ravindranathan A, Coon H, DeLisi L, et al (1994): Linkage analysis between schizophrenia and a microsatellite polymorphism for the D5 receptor gene. Psychiatr Genet 4:77-80.
    • (1994) Psychiatr Genet , vol.4 , pp. 77-80
    • Ravindranathan, A.1    Coon, H.2    DeLisi, L.3
  • 27
    • 0027953283 scopus 로고
    • Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophrenia
    • Sabate O, Campion D, d'Amato T, et al (1994): Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophrenia. Am J Psychiatry 151:107-111.
    • (1994) Am J Psychiatry , vol.151 , pp. 107-111
    • Sabate, O.1    Campion, D.2    D'Amato, T.3
  • 28
    • 0026511084 scopus 로고
    • Velo cardio facial syndrome associated with chromosome 22q11 deletions encompassing the DiGeorge locus
    • Scambler P, Kelly D, Lindsay E, et al (1992): Velo cardio facial syndrome associated with chromosome 22q11 deletions encompassing the DiGeorge locus. Lancet 339:1138-1139.
    • (1992) Lancet , vol.339 , pp. 1138-1139
    • Scambler, P.1    Kelly, D.2    Lindsay, E.3
  • 29
    • 0018378334 scopus 로고
    • Catechol-O-methyltransferase; thermolahile enzyme in erythrocytes of subjects homozygous for the allele for low activity
    • Scanlon PD, Raymond FA, Weinshilboum RA, (1979): catechol-O-methyltransferase; thermolahile enzyme in erythrocytes of subjects homozygous for the allele for low activity. Science 203:63-65.
    • (1979) Science , vol.203 , pp. 63-65
    • Scanlon, P.D.1    Raymond, F.A.2    Weinshilboum, R.A.3
  • 30
    • 0017821181 scopus 로고
    • A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: Velo-cardio-facial syndrome
    • Shprintzen RJ, Goldberg RB, Lewin ML, et al (1978): A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: Velo-cardio-facial syndrome. Cleft Palate J 15:56-62.
    • (1978) Cleft Palate J , vol.15 , pp. 56-62
    • Shprintzen, R.J.1    Goldberg, R.B.2    Lewin, M.L.3
  • 32
    • 0028960869 scopus 로고
    • The D5 dopamine receptor gene in schizophrenia: Identification of a nonsense change and multiple missense changes but lack of association with disease
    • Sobell JL, Lind TJ, Sigurdson C, et al (1995): The D5 dopamine receptor gene in schizophrenia: Identification of a nonsense change and multiple missense changes but lack of association with disease. Hum Mol Genet 4:507-514.
    • (1995) Hum Mol Genet , vol.4 , pp. 507-514
    • Sobell, J.L.1    Lind, T.J.2    Sigurdson, C.3
  • 33
    • 0019775115 scopus 로고
    • Genetics of red cell COMT activity: Analysis of thermal stability and family data
    • Spielman RS, Weinshilboum RM (1981): Genetics of red cell COMT activity: Analysis of thermal stability and family data. Am J Med Genet 10:279-290.
    • (1981) Am J Med Genet , vol.10 , pp. 279-290
    • Spielman, R.S.1    Weinshilboum, R.M.2
  • 34
    • 0027964721 scopus 로고
    • Genomic organization of the human catechol-O-methyltransferase gene and its expression from two distinct promoters
    • Tenhunen J, Salminen M, Lundstrom K, Kiviluoto T, Savolainen R, Ulmanen I (1994): Genomic organization of the human catechol-O-methyltransferase gene and its expression from two distinct promoters. Eur J Biochem 223:1049-1054.
    • (1994) Eur J Biochem , vol.223 , pp. 1049-1054
    • Tenhunen, J.1    Salminen, M.2    Lundstrom, K.3    Kiviluoto, T.4    Savolainen, R.5    Ulmanen, I.6
  • 35
    • 0017335027 scopus 로고
    • Inheritance of low erythrocyte catechol-O-methyl transferase activity in man
    • Weinshilboum RM, Raymond FA (1977): Inheritance of low erythrocyte catechol-O-methyl transferase activity in man. Am J Hum Genet 29:125-135.
    • (1977) Am J Hum Genet , vol.29 , pp. 125-135
    • Weinshilboum, R.M.1    Raymond, F.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.