-
1
-
-
0027469794
-
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
-
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
-
3
-
-
0026034792
-
Human catechol-O-methyltransferase: Cloning and expression of the membrance associated form
-
Bertocci B, Miggiano V, Da Prada M, Dembric Z, Lahm H-W, Malherbe P (1991): Human catechol-O-methyltransferase: Cloning and expression of the membrance associated form. Proc Natl Acad Sci USA 88:1416-1420.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 1416-1420
-
-
Bertocci, B.1
Miggiano, V.2
Da Prada, M.3
Dembric, Z.4
Lahm, H.-W.5
Malherbe, P.6
-
4
-
-
0028205578
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
23
-
-
0019430374
-
Catechol-O-methyltransferase activity of erythrocytes in patients with endogenous psychosis
-
Philippu C, Hoo JJ, Milech U, Argarwall DP, Schrappe O, Goedde HW (1981): Catechol-O-methyltransferase activity of erythrocytes in patients with endogenous psychosis. Psychiatry Res 4:139-146.
-
(1981)
Psychiatry Res
, vol.4
, pp. 139-146
-
-
Philippu, C.1
Hoo, J.J.2
Milech, U.3
Argarwall, D.P.4
Schrappe, O.5
Goedde, H.W.6
-
24
-
-
0027989917
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|