-
1
-
-
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
-
2
-
-
0027483404
-
Structure of the rat catechol-O-methyltransferase gene: Separate promoters are used to produce mRNAs for soluble and membrane-bound forms of the enzyme
-
Tenhunen J, Salminen M, Jalanko A, Ukkonen S, Ulmanen I (1993) Structure of the rat catechol-O-methyltransferase gene: separate promoters are used to produce mRNAs for soluble and membrane-bound forms of the enzyme. DNA Cell Biol 12: 253-263.
-
(1993)
DNA Cell Biol
, vol.12
, pp. 253-263
-
-
Tenhunen, J.1
Salminen, M.2
Jalanko, A.3
Ukkonen, S.4
Ulmanen, I.5
-
3
-
-
33745703902
-
Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond
-
Tunbridge EM, Harrison PJ, Weinberger DR (2006) Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond. Biol Psychiatry 60: 141-151.
-
(2006)
Biol Psychiatry
, vol.60
, pp. 141-151
-
-
Tunbridge, E.M.1
Harrison, P.J.2
Weinberger, D.R.3
-
6
-
-
70350199597
-
Association between the COMT locus and obsessive-compulsive disorder in females but not males
-
Alsobrook JP 2nd, Zohar AH, Leboyer M, Chabane N, Ebstein RP, et al. (2002) Association between the COMT locus and obsessive-compulsive disorder in females but not males. Am J Med Genet 114: 116-120.
-
(2002)
Am J Med Genet
, vol.114
, pp. 116-120
-
-
Alsobrook 2nd, J.P.1
Zohar, A.H.2
Leboyer, M.3
Chabane, N.4
Ebstein, R.P.5
-
7
-
-
0030895285
-
Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder
-
Karayiorgou M, Altemus M, Galke BL, Goldman D, Murphy DL, et al. (1997) Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proc Natl Acad Sci U S A 94: 4572-4575.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 4572-4575
-
-
Karayiorgou, M.1
Altemus, M.2
Galke, B.L.3
Goldman, D.4
Murphy, D.L.5
-
8
-
-
3042678514
-
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women
-
Domschke K, Freitag CM, Kuhlenbaumer G, Schirmacher A, Sand P, et al. (2004) Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women. Int J Neuropsychopharmacol 7: 183-188.
-
(2004)
Int J Neuropsychopharmacol
, vol.7
, pp. 183-188
-
-
Domschke, K.1
Freitag, C.M.2
Kuhlenbaumer, G.3
Schirmacher, A.4
Sand, P.5
-
9
-
-
4444269807
-
Association between catechol-O-methyltransferase and phobic anxiety
-
McGrath M, Kawachi I, Ascherio A, Colditz GA, Hunter DJ, et al. (2004) Association between catechol-O-methyltransferase and phobic anxiety. Am J Psychiatry 161: 1703-1705.
-
(2004)
Am J Psychiatry
, vol.161
, pp. 1703-1705
-
-
McGrath, M.1
Kawachi, I.2
Ascherio, A.3
Colditz, G.A.4
Hunter, D.J.5
-
10
-
-
2942534594
-
The association between panic disorder and the L/L genotype of catechol-O-methyltransferase
-
Woo JM, Yoon KS, Choi YH, Oh KS, Lee YS, et al. (2004) The association between panic disorder and the L/L genotype of catechol-O-methyltransferase. J Psychiatr Res 38: 365-370.
-
(2004)
J Psychiatr Res
, vol.38
, pp. 365-370
-
-
Woo, J.M.1
Yoon, K.S.2
Choi, Y.H.3
Oh, K.S.4
Lee, Y.S.5
-
11
-
-
0038755196
-
-
Qian Q, Wang Y, Zhou R, Li J, Wang B, et al. (2003) Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism. Am J Med Genet B Neuropsychiatr Genet 118B: 103-109.
-
Qian Q, Wang Y, Zhou R, Li J, Wang B, et al. (2003) Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism. Am J Med Genet B Neuropsychiatr Genet 118B: 103-109.
-
-
-
-
12
-
-
57349088822
-
-
Neuropsychopharmacology
-
Sengupta S, Grizenko N, Schmitz N, Schwartz G, Bellingham J, et al. (2008) COMT Val(108/158)Met Polymorphism and the Modulation of Task-Oriented Behavior in Children with ADHD. Neuropsychopharmacology.
-
(2008)
COMT Val(108/158)Met Polymorphism and the Modulation of Task-Oriented Behavior in Children with ADHD
-
-
Sengupta, S.1
Grizenko, N.2
Schmitz, N.3
Schwartz, G.4
Bellingham, J.5
-
13
-
-
11044219969
-
Alcoholism: Genes and mechanisms
-
Oroszi G, Goldman D (2004) Alcoholism: genes and mechanisms. Pharmacogenomics 5: 1037-1048.
-
(2004)
Pharmacogenomics
, vol.5
, pp. 1037-1048
-
-
Oroszi, G.1
Goldman, D.2
-
14
-
-
17744363444
-
Association of anorexia nervosa with the high activity allele of the COMT gene: A family-based study in Israeli patients
-
Frisch A, Laufer N, Danziger Y, Michaelovsky E, Leor S, et al. (2001) Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patients. Mol Psychiatry 6: 243-245.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 243-245
-
-
Frisch, A.1
Laufer, N.2
Danziger, Y.3
Michaelovsky, E.4
Leor, S.5
-
15
-
-
41649100270
-
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS
-
Michaelovsky E, Gothelf D, Korostishevsky M, Frisch A, Burg M, et al. (2008) Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. Int J Neuropsychopharmacol 11: 351-363.
-
(2008)
Int J Neuropsychopharmacol
, vol.11
, pp. 351-363
-
-
Michaelovsky, E.1
Gothelf, D.2
Korostishevsky, M.3
Frisch, A.4
Burg, M.5
-
16
-
-
0031015324
-
High and low activity alleles of catechol-O-methyltransferase gene: Ethnic difference and possible association with Parkinson's disease
-
Kunugi H, Nanko S, Ueki A, Otsuka E, Hattori M, et al. (1997) High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease. Neurosci Lett 221: 202-204.
-
(1997)
Neurosci Lett
, vol.221
, pp. 202-204
-
-
Kunugi, H.1
Nanko, S.2
Ueki, A.3
Otsuka, E.4
Hattori, M.5
-
17
-
-
0031436062
-
Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication
-
Yoritaka A, Hattori N, Yoshino H, Mizuno Y (1997) Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication. J Neural Transm 104: 1313-1317.
-
(1997)
J Neural Transm
, vol.104
, pp. 1313-1317
-
-
Yoritaka, A.1
Hattori, N.2
Yoshino, H.3
Mizuno, Y.4
-
18
-
-
58949086592
-
Val/Met Polymorphism of the COMT Gene Moderates the Association Between Job Strain and Early Atherosclerosis in Young Men
-
Hintsanen M, Elovainio M, Puttonen S, Kivimaki M, Lehtimaki T, et al. (2008) Val/Met Polymorphism of the COMT Gene Moderates the Association Between Job Strain and Early Atherosclerosis in Young Men. J Occup Environ Med 50: 649-657.
-
(2008)
J Occup Environ Med
, vol.50
, pp. 649-657
-
-
Hintsanen, M.1
Elovainio, M.2
Puttonen, S.3
Kivimaki, M.4
Lehtimaki, T.5
-
19
-
-
33845370070
-
Association of genetic polymorphisms of ACADSB and COMT with human hypertension
-
Kamide K, Kokubo Y, Yang J, Matayoshi T, Inamoto N, et al. (2007) Association of genetic polymorphisms of ACADSB and COMT with human hypertension. J Hypertens 25: 103-110.
-
(2007)
J Hypertens
, vol.25
, pp. 103-110
-
-
Kamide, K.1
Kokubo, Y.2
Yang, J.3
Matayoshi, T.4
Inamoto, N.5
-
20
-
-
15144339383
-
An association between the allele coding for a low activity variant of catechol-Omethyltransferase and the risk for breast cancer
-
Lavigne JA, Helzlsouer KJ, Huang HY, Strickland PT, Bell DA, et al. (1997) An association between the allele coding for a low activity variant of catechol-Omethyltransferase and the risk for breast cancer. Cancer Res 57: 5493-5497.
-
(1997)
Cancer Res
, vol.57
, pp. 5493-5497
-
-
Lavigne, J.A.1
Helzlsouer, K.J.2
Huang, H.Y.3
Strickland, P.T.4
Bell, D.A.5
-
21
-
-
14444276295
-
Genetic polymorphisms in catechol-O-methyltransferase, menopausal status, and breast cancer risk
-
Thompson PA, Shields PG, Freudenheim JL, Stone A, Vena JE, et al. (1998) Genetic polymorphisms in catechol-O-methyltransferase, menopausal status, and breast cancer risk. Cancer Res 58: 2107-2110.
-
(1998)
Cancer Res
, vol.58
, pp. 2107-2110
-
-
Thompson, P.A.1
Shields, P.G.2
Freudenheim, J.L.3
Stone, A.4
Vena, J.E.5
-
22
-
-
33847616664
-
Catechol-O-methyltransferase inhibition increases pain sensitivity through activation of both beta2- and beta3-adrenergic receptors
-
Nackley AG, Tan KS, Fecho K, Flood P, Diatchenko L, et al. (2007) Catechol-O-methyltransferase inhibition increases pain sensitivity through activation of both beta2- and beta3-adrenergic receptors. Pain 128: 199-208.
-
(2007)
Pain
, vol.128
, pp. 199-208
-
-
Nackley, A.G.1
Tan, K.S.2
Fecho, K.3
Flood, P.4
Diatchenko, L.5
-
23
-
-
33847619467
-
-
Washington, DC
-
Nackley AG, Tan KS, Fecho K, Flood P, Maixner W, et al. COMT modulates pain sensitivity and cytokine production through both β2 and β3 adrenergic receptors; 2005; Washington, DC.
-
(2005)
COMT modulates pain sensitivity and cytokine production through both β2 and β3 adrenergic receptors
-
-
Nackley, A.G.1
Tan, K.S.2
Fecho, K.3
Flood, P.4
Maixner, W.5
-
24
-
-
0017178435
-
Erythrocyte catechol-O-methyltransferase activity in facial pain patients
-
Marbach JJ, Levitt M (1976) Erythrocyte catechol-O-methyltransferase activity in facial pain patients. J Dent Res 55: 711.
-
(1976)
J Dent Res
, vol.55
, pp. 711
-
-
Marbach, J.J.1
Levitt, M.2
-
25
-
-
0038512578
-
Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome
-
Gursoy S, Erdal E, Herken H, Madenci E, Alasehirli B, et al. (2003) Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome. Rheumatol Int 23: 104-107.
-
(2003)
Rheumatol Int
, vol.23
, pp. 104-107
-
-
Gursoy, S.1
Erdal, E.2
Herken, H.3
Madenci, E.4
Alasehirli, B.5
-
26
-
-
36849018585
-
Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia
-
Vargas-Alarcon G, Fragoso JM, Cruz-Robles D, Vargas A, Vargas A, et al. (2007) Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia. Arthritis Res Ther 9: R110.
-
(2007)
Arthritis Res Ther
, vol.9
-
-
Vargas-Alarcon, G.1
Fragoso, J.M.2
Cruz-Robles, D.3
Vargas, A.4
Vargas, A.5
-
27
-
-
19944427292
-
Genetic basis for individual variations in pain perception and the development of a chronic pain condition
-
Diatchenko L, Slade GD, Nackley AG, Bhalang K, Sigurdsson A, et al. (2005) Genetic basis for individual variations in pain perception and the development of a chronic pain condition. Hum Mol Genet 14: 135-143.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 135-143
-
-
Diatchenko, L.1
Slade, G.D.2
Nackley, A.G.3
Bhalang, K.4
Sigurdsson, A.5
-
28
-
-
0037458277
-
COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor
-
Zubieta JK, Heitzeg MM, Smith YR, Bueller JA, Xu K, et al. (2003) COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor. Science 299: 1240-1243.
-
(2003)
Science
, vol.299
, pp. 1240-1243
-
-
Zubieta, J.K.1
Heitzeg, M.M.2
Smith, Y.R.3
Bueller, J.A.4
Xu, K.5
-
29
-
-
20444451123
-
The Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients
-
Rakvag TT, Klepstad P, Baar C, Kvam TM, Dale O, et al. (2005) The Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients. Pain 116: 73-78.
-
(2005)
Pain
, vol.116
, pp. 73-78
-
-
Rakvag, T.T.1
Klepstad, P.2
Baar, C.3
Kvam, T.M.4
Dale, O.5
-
30
-
-
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, Ulmanen I, Melen K, 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
Ulmanen, I.4
Melen, K.5
-
31
-
-
0030020650
-
Second-site suppression of regulatory phosphorylation in Escherichia coli isocitrate dehydrogenase
-
Chen R, Grobler JA, Hurley JH, Dean AM (1996) Second-site suppression of regulatory phosphorylation in Escherichia coli isocitrate dehydrogenase. Protein Sci 5: 287-295.
-
(1996)
Protein Sci
, vol.5
, pp. 287-295
-
-
Chen, R.1
Grobler, J.A.2
Hurley, J.H.3
Dean, A.M.4
-
32
-
-
84878748906
-
-
Hong JP, Lee JS, Chung S, Jung J, Yoo HK, et al. (2008) New functional single nucleotide polymorphism (Ala72Ser) in the COMT gene is associated with aggressive behavior in male schizophrenia. Am J Med Genet B Neuropsychiatr Genet 147B: 658-660.
-
Hong JP, Lee JS, Chung S, Jung J, Yoo HK, et al. (2008) New functional single nucleotide polymorphism (Ala72Ser) in the COMT gene is associated with aggressive behavior in male schizophrenia. Am J Med Genet B Neuropsychiatr Genet 147B: 658-660.
-
-
-
-
33
-
-
14044255978
-
Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans
-
Lee SG, Joo Y, Kim B, Chung S, Kim HL, et al. (2005) Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans. Hum Genet 116: 319-328.
-
(2005)
Hum Genet
, vol.116
, pp. 319-328
-
-
Lee, S.G.1
Joo, Y.2
Kim, B.3
Chung, S.4
Kim, H.L.5
-
34
-
-
4644248763
-
COMT haplotypes suggest P2 promoter region relevance for schizophrenia
-
Palmatier MA, Pakstis AJ, Speed W, Paschou P, Goldman D, et al. (2004) COMT haplotypes suggest P2 promoter region relevance for schizophrenia. Mol Psychiatry 9: 859-870.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 859-870
-
-
Palmatier, M.A.1
Pakstis, A.J.2
Speed, W.3
Paschou, P.4
Goldman, D.5
-
35
-
-
0036913209
-
A highly significant association between a COMT haplotype and schizophrenia
-
Shifman S, Bronstein M, Sternfeld M, Pisante-Shalom A, Lev-Lehman E, et al. (2002) A highly significant association between a COMT haplotype and schizophrenia. Am J Hum Genet 71: 1296-1302.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisante-Shalom, A.4
Lev-Lehman, E.5
-
36
-
-
33750697663
-
Catechol-O-methyltransferase gene polymorphisms are associated with multiple pain-evoking stimuli
-
Diatchenko L, Nackley AG, Slade GD, Bhalang K, Belfer I, et al. (2006) Catechol-O-methyltransferase gene polymorphisms are associated with multiple pain-evoking stimuli. Pain 125: 216-224.
-
(2006)
Pain
, vol.125
, pp. 216-224
-
-
Diatchenko, L.1
Nackley, A.G.2
Slade, G.D.3
Bhalang, K.4
Belfer, I.5
-
37
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
Nackley AG, Shabalina SA, Tchivileva IE, Satterfield K, Korchynskyi O, et al. (2006) Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 314: 1930-1933.
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
Satterfield, K.4
Korchynskyi, O.5
-
38
-
-
52449148668
-
The role of compensatory neutral mutations in molecular evolution
-
Kimura M (1985) The role of compensatory neutral mutations in molecular evolution. J Genet 64: 7-19.
-
(1985)
J Genet
, vol.64
, pp. 7-19
-
-
Kimura, M.1
-
39
-
-
0025970149
-
Inferring the evolutionary histories of the Adh and Adh-dup loci in Drosophila melanogaster from patterns of polymorphism and divergence
-
Kreitman M, Hudson RR (1991) Inferring the evolutionary histories of the Adh and Adh-dup loci in Drosophila melanogaster from patterns of polymorphism and divergence. Genetics 127: 565-582.
-
(1991)
Genetics
, vol.127
, pp. 565-582
-
-
Kreitman, M.1
Hudson, R.R.2
-
41
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, et al. (1999) Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet 22: 231-238.
-
(1999)
Nat Genet
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
-
42
-
-
0035029051
-
Issues concerning association studies for fine mapping a susceptibility gene for a complex disease
-
Kaplan N, Morris R (2001) Issues concerning association studies for fine mapping a susceptibility gene for a complex disease. Genet Epidemiol 20: 432-457.
-
(2001)
Genet Epidemiol
, vol.20
, pp. 432-457
-
-
Kaplan, N.1
Morris, R.2
-
44
-
-
0028321985
-
Polymorphism and divergence at the prune locus in Drosophila melanogaster and D. simulans
-
Simmons GM, Kwok W, Matulonis P, Venkatesh T (1994) Polymorphism and divergence at the prune locus in Drosophila melanogaster and D. simulans. Mol Biol Evol 11: 666-671.
-
(1994)
Mol Biol Evol
, vol.11
, pp. 666-671
-
-
Simmons, G.M.1
Kwok, W.2
Matulonis, P.3
Venkatesh, T.4
-
45
-
-
0029026878
-
Maintenance of pre-mRNA secondary structure by epistatic selection
-
Kirby DA, Muse SV, Stephan W (1995) Maintenance of pre-mRNA secondary structure by epistatic selection. Proc Natl Acad Sci U S A 92: 9047-9051.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 9047-9051
-
-
Kirby, D.A.1
Muse, S.V.2
Stephan, W.3
-
46
-
-
0042121256
-
Mfold web server for nucleic acid folding and hybridization prediction
-
Zuker M (2003) Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res 31: 3406-3415.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3406-3415
-
-
Zuker, M.1
-
48
-
-
0033583089
-
Intragenic suppression of an active site mutation in the human apurinic/ apyrimidinic endonuclease
-
Izumi T, Malecki J, Chaudhry MA, Weinfeld M, Hill JH, et al. (1999) Intragenic suppression of an active site mutation in the human apurinic/ apyrimidinic endonuclease. J Mol Biol 287: 47-57.
-
(1999)
J Mol Biol
, vol.287
, pp. 47-57
-
-
Izumi, T.1
Malecki, J.2
Chaudhry, M.A.3
Weinfeld, M.4
Hill, J.H.5
-
49
-
-
0035896639
-
Functional rescue of the nephrogenic diabetes insipidus-causing vasopressin V2 receptor mutants G185C and R202C by a second site suppressor mutation
-
Schulein R, Zuhlke K, Krause G, Rosenthal W (2001) Functional rescue of the nephrogenic diabetes insipidus-causing vasopressin V2 receptor mutants G185C and R202C by a second site suppressor mutation. J Biol Chem 276: 8384-8392.
-
(2001)
J Biol Chem
, vol.276
, pp. 8384-8392
-
-
Schulein, R.1
Zuhlke, K.2
Krause, G.3
Rosenthal, W.4
-
50
-
-
0037320652
-
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
-
Duan J, Wainwright MS, Comeron JM, Saitou N, Sanders AR, et al. (2003) Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum Mol Genet 12: 205-216.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 205-216
-
-
Duan, J.1
Wainwright, M.S.2
Comeron, J.M.3
Saitou, N.4
Sanders, A.R.5
-
51
-
-
16544384596
-
Mechanisms and convergence of compensatory evolution in mammalian mitochondrial tRNAs
-
Kern AD, Kondrashov FA (2004) Mechanisms and convergence of compensatory evolution in mammalian mitochondrial tRNAs. Nat Genet 36: 1207-1212.
-
(2004)
Nat Genet
, vol.36
, pp. 1207-1212
-
-
Kern, A.D.1
Kondrashov, F.A.2
-
52
-
-
35348988170
-
Recent and ongoing selection in the human genome
-
Nielsen R, Hellmann I, Hubisz M, Bustamante C, Clark AG (2007) Recent and ongoing selection in the human genome. Nat Rev Genet 8: 857-868.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 857-868
-
-
Nielsen, R.1
Hellmann, I.2
Hubisz, M.3
Bustamante, C.4
Clark, A.G.5
-
53
-
-
12144261893
-
Differential expression of human COMT alleles in brain and lymphoblasts detected by RT-coupled 5′ nuclease assay
-
Zhu G, Lipsky RH, Xu K, Ali S, Hyde T, et al. (2004) Differential expression of human COMT alleles in brain and lymphoblasts detected by RT-coupled 5′ nuclease assay. Psychopharmacology (Berl) 177: 178-184.
-
(2004)
Psychopharmacology (Berl)
, vol.177
, pp. 178-184
-
-
Zhu, G.1
Lipsky, R.H.2
Xu, K.3
Ali, S.4
Hyde, T.5
-
54
-
-
33747857635
-
Scan of human genome reveals no new Loci under ancient balancing selection
-
Bubb KL, Bovee D, Buckley D, Haugen E, Kibukawa M, et al. (2006) Scan of human genome reveals no new Loci under ancient balancing selection. Genetics 173: 2165-2177.
-
(2006)
Genetics
, vol.173
, pp. 2165-2177
-
-
Bubb, K.L.1
Bovee, D.2
Buckley, D.3
Haugen, E.4
Kibukawa, M.5
-
55
-
-
0035919696
-
Haplotype diversity and linkage disequilibrium at human G6PD: Recent origin of alleles that confer malarial resistance
-
Tishkoff SA, Varkonyi R, Cahinhinan N, Abbes S, Argyropoulos G, et al. (2001) Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science 293: 455-462.
-
(2001)
Science
, vol.293
, pp. 455-462
-
-
Tishkoff, S.A.1
Varkonyi, R.2
Cahinhinan, N.3
Abbes, S.4
Argyropoulos, G.5
-
56
-
-
6344265879
-
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): Effects on mRNA, protein, and enzyme activity in postmortem human brain
-
Chen J, Lipska BK, Halim N, Ma QD, Matsumoto M, et al. (2004) Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain. Am J Hum Genet 75: 807-821.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 807-821
-
-
Chen, J.1
Lipska, B.K.2
Halim, N.3
Ma, Q.D.4
Matsumoto, M.5
-
57
-
-
0038389841
-
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain
-
Bray NJ, Buckland PR, Williams NM, Williams HJ, Norton N, et al. (2003) A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. Am J Hum Genet 73: 152-161.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 152-161
-
-
Bray, N.J.1
Buckland, P.R.2
Williams, N.M.3
Williams, H.J.4
Norton, N.5
-
58
-
-
0036791893
-
On the mechanism of homocysteine pathophysiology and pathogenesis: A unifying hypothesis
-
Zhu BT (2002) On the mechanism of homocysteine pathophysiology and pathogenesis: a unifying hypothesis. Histol Histopathol 17: 1283-1291.
-
(2002)
Histol Histopathol
, vol.17
, pp. 1283-1291
-
-
Zhu, B.T.1
-
59
-
-
0034703861
-
Glutamate carboxypeptidase II: A polymorphism associated with lower levels of serum folate and hyperhomocysteinemia
-
Devlin AM, Ling EH, Peerson JM, Fernando S, Clarke R, et al. (2000) Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia. Hum Mol Genet 9: 2837-2844.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2837-2844
-
-
Devlin, A.M.1
Ling, E.H.2
Peerson, J.M.3
Fernando, S.4
Clarke, R.5
-
60
-
-
0028890671
-
Thermolabile 5, 10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen AM, Franken DG, Boers GH, Stevens EM, Trijbels FJ, et al. (1995) Thermolabile 5, 10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 56: 142-150.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 142-150
-
-
Engbersen, A.M.1
Franken, D.G.2
Boers, G.H.3
Stevens, E.M.4
Trijbels, F.J.5
-
61
-
-
0036801570
-
Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C→T) on plasma homocysteine, folate and vitamin B(12) levels and its relationship to cardiovascular disease risk
-
Lievers KJ, Kluijtmans LA, Boers GH, Verhoef P, den Heijer M, et al. (2002) Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C→T) on plasma homocysteine, folate and vitamin B(12) levels and its relationship to cardiovascular disease risk. Atherosclerosis 164: 269-273.
-
(2002)
Atherosclerosis
, vol.164
, pp. 269-273
-
-
Lievers, K.J.1
Kluijtmans, L.A.2
Boers, G.H.3
Verhoef, P.4
den Heijer, M.5
-
62
-
-
37349122511
-
Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia
-
Muntjewerff JW, Gellekink H, den Heijer M, Hoogendoorn ML, Kahn RS, et al. (2008) Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia. Eur Neuropsychopharmacol 18: 99-106.
-
(2008)
Eur Neuropsychopharmacol
, vol.18
, pp. 99-106
-
-
Muntjewerff, J.W.1
Gellekink, H.2
den Heijer, M.3
Hoogendoorn, M.L.4
Kahn, R.S.5
-
63
-
-
0242457281
-
Catecholamines and stress
-
Goldstein DS (2003) Catecholamines and stress. Endocr Regul 37: 69-80.
-
(2003)
Endocr Regul
, vol.37
, pp. 69-80
-
-
Goldstein, D.S.1
-
64
-
-
6444225797
-
Increased systemic catecholamines in complex regional pain syndrome and relationship to psychological factors: A pilot study
-
table of contents
-
Harden RN, Rudin NJ, Bruehl S, Kee W, Parikh DK, et al. (2004) Increased systemic catecholamines in complex regional pain syndrome and relationship to psychological factors: a pilot study. Anesth Analg 99: 1478-1485. table of contents.
-
(2004)
Anesth Analg
, vol.99
, pp. 1478-1485
-
-
Harden, R.N.1
Rudin, N.J.2
Bruehl, S.3
Kee, W.4
Parikh, D.K.5
-
65
-
-
0029019264
-
Role of the sympathetic nervous system in acute pain and inflammation
-
Raja SN (1995) Role of the sympathetic nervous system in acute pain and inflammation. Ann Med 27: 241-246.
-
(1995)
Ann Med
, vol.27
, pp. 241-246
-
-
Raja, S.N.1
-
66
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, et al. (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10: 111-113.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
-
67
-
-
2642676850
-
Major lifestyle determinants of plasma total homocysteine distribution: The Hordaland Homocysteine Study
-
Nygard O, Refsum H, Ueland PM, Vollset SE (1998) Major lifestyle determinants of plasma total homocysteine distribution: the Hordaland Homocysteine Study. Am J Clin Nutr 67: 263-270.
-
(1998)
Am J Clin Nutr
, vol.67
, pp. 263-270
-
-
Nygard, O.1
Refsum, H.2
Ueland, P.M.3
Vollset, S.E.4
-
68
-
-
43649088361
-
Orthodontic Treatment, Genetic Factors and Risk of Temporomandibular Disorder
-
Slade GD, Diatchenko L, Ohrbach R, Maixner W (2008) Orthodontic Treatment, Genetic Factors and Risk of Temporomandibular Disorder. Semin Orthod 14: 146-156.
-
(2008)
Semin Orthod
, vol.14
, pp. 146-156
-
-
Slade, G.D.1
Diatchenko, L.2
Ohrbach, R.3
Maixner, W.4
-
69
-
-
33745779714
-
-
Diatchenko L, Anderson AD, Slade GD, Fillingim RB, Shabalina SA, et al. (2006) Three major haplotypes of the beta2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder. Am J Med Genet B Neuropsychiatr Genet 141B: 449-462.
-
Diatchenko L, Anderson AD, Slade GD, Fillingim RB, Shabalina SA, et al. (2006) Three major haplotypes of the beta2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder. Am J Med Genet B Neuropsychiatr Genet 141B: 449-462.
-
-
-
-
70
-
-
33646838978
-
A periodic pattern of mRNA secondary structure created by the genetic code
-
Shabalina SA, Ogurtsov AY, Spiridonov NA (2006) A periodic pattern of mRNA secondary structure created by the genetic code. Nucleic Acids Res 34: 2428-2437.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 2428-2437
-
-
Shabalina, S.A.1
Ogurtsov, A.Y.2
Spiridonov, N.A.3
-
71
-
-
0033591465
-
Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure
-
Mathews DH, Sabina J, Zuker M, Turner DH (1999) Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. J Mol Biol 288: 911-940.
-
(1999)
J Mol Biol
, vol.288
, pp. 911-940
-
-
Mathews, D.H.1
Sabina, J.2
Zuker, M.3
Turner, D.H.4
-
72
-
-
0029144780
-
SAMSON: A software package for the biopolymer primary structure analysis
-
Nazipova NN, Shabalina SA, Ogurtsov A, Kondrashov AS, Roytberg MA, et al. (1995) SAMSON: a software package for the biopolymer primary structure analysis. Comput Appl Biosci 11: 423-426.
-
(1995)
Comput Appl Biosci
, vol.11
, pp. 423-426
-
-
Nazipova, N.N.1
Shabalina, S.A.2
Ogurtsov, A.3
Kondrashov, A.S.4
Roytberg, M.A.5
-
73
-
-
0027200335
-
Intermolecular mRNA-rRNA hybridization and the distribution of potential interaction regions in murine 18S rRNA
-
Matveeva OV, Shabalina SA (1993) Intermolecular mRNA-rRNA hybridization and the distribution of potential interaction regions in murine 18S rRNA. Nucleic Acids Res 21: 1007-1011.
-
(1993)
Nucleic Acids Res
, vol.21
, pp. 1007-1011
-
-
Matveeva, O.V.1
Shabalina, S.A.2
-
74
-
-
0036845342
-
Assay of catechol-Omethyltransferase activity in human erythrocytes using norepinephrine as a natural substrate
-
Masuda M, Tsunoda M, Yusa Y, Yamada S, Imai K (2002) Assay of catechol-Omethyltransferase activity in human erythrocytes using norepinephrine as a natural substrate. Ann Clin Biochem 39: 589-594.
-
(2002)
Ann Clin Biochem
, vol.39
, pp. 589-594
-
-
Masuda, M.1
Tsunoda, M.2
Yusa, Y.3
Yamada, S.4
Imai, K.5
|