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Results: 1-9 |
Results: 9
Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1)
Authors: Blaveri, E Kalsi, G Lawrence, J Quested, D Moorey, H Lamb, G Kohen, D Shiwach, R Chowdhury, U Curtis, D McQuillin, A Gramoustianou, ES Gurling, HMD
Citation: E. Blaveri et al., Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1), EUR J HUM G, 9(6), 2001, pp. 469-472
Enhanced cationic liposome-mediated transfection using the DNA-binding peptide mu (mu) from the adenovirus core
Authors: Murray, KD Etheridge, CJ Shah, SI Matthews, DA Russell, W Gurling, HMD Miller, AD
Citation: Kd. Murray et al., Enhanced cationic liposome-mediated transfection using the DNA-binding peptide mu (mu) from the adenovirus core, GENE THER, 8(6), 2001, pp. 453-460
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23
Authors: Gurling, HMD Kalsi, G Brynjolfson, J Sigmundsson, T Sherrington, R Mankoo, BS Read, T Murphy, P Blaveri, E McQuillin, A Petursson, H Curtis, D
Citation: Hmd. Gurling et al., Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23, AM J HU GEN, 68(3), 2001, pp. 661-673
Identification of a novel gene on chromosome 7q31 that is interrupted by atranslocation breakpoint in an autistic individual
Authors: Vincent, JB Herbrick, JA Gurling, HMD Bolton, PF Roberts, W Scherer, SW
Citation: Jb. Vincent et al., Identification of a novel gene on chromosome 7q31 that is interrupted by atranslocation breakpoint in an autistic individual, AM J HU GEN, 67(2), 2000, pp. 510-514
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: A common expansion lotus
Authors: Vincent, JB Neves-Pereira, ML Paterson, AD Yamamoto, E Parikh, SV Macciardi, F Gurling, HMD Potkin, SG Pato, CN Macedo, A Kovacs, M Davies, M Lieberman, JA Meltzer, HY Petronis, A Kennedy, JL
Citation: Jb. Vincent et al., An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: A common expansion lotus, AM J HU GEN, 66(3), 2000, pp. 819-829
Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon
Authors: Murray, KD McQuillin, A Stewart, L Etheridge, CJ Cooper, RG Miller, AD Gurling, HMD
Citation: Kd. Murray et al., Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon, GENE THER, 6(2), 1999, pp. 190-197
The genetic predisposition to alcohol dependence
Authors: Gurling, HMD Cook, CCH
Citation: Hmd. Gurling et Cch. Cook, The genetic predisposition to alcohol dependence, CUR OPIN P, 12(3), 1999, pp. 269-275
D-2 dopamine receptor but not AMPA and kainate glutamate receptor genes show altered expression in response to long term treatment with trans- and cis-flupenthixol in the rat brain
Authors: Chen, ACH Gurling, HMD
Citation: Ach. Chen et Hmd. Gurling, D-2 dopamine receptor but not AMPA and kainate glutamate receptor genes show altered expression in response to long term treatment with trans- and cis-flupenthixol in the rat brain, MOL BRAIN R, 68(1-2), 1999, pp. 14-21
Genetic association analysis of serotonin system genes in bipolar affective disorder
Authors: Vincent, JB Masellis, M Lawrence, J Choi, V Gurling, HMD Parikh, SV Kennedy, JL
Citation: Jb. Vincent et al., Genetic association analysis of serotonin system genes in bipolar affective disorder, AM J PSYCHI, 156(1), 1999, pp. 136-138
Risultati: 1-9 |