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A W Charney, D M Ruderfer, E A Stahl, J L Moran, K Chambert, R A Belliveau, L Forty, K Gordon-Smith, A Di Florio, P H Lee, E J Bromet, P F Buckley, M A Escamilla, A H Fanous, L J Fochtmann, D S Lehrer, D Malaspina, S R Marder, C P Morley, H Nicolini, D O Perkins, J J Rakofsky, M H Rapaport, H Medeiros, J L Sobell, E K Green, L Backlund, S E Bergen, A Juréus, M Schalling, P Lichtenstein, P Roussos, J A Knowles, I Jones, L A Jones, C M Hultman, R H Perlis, S M Purcell, S A McCarroll, C N Pato, M T Pato, N Craddock, M Landén, J W Smoller, P Sklar

Translational psychiatry 2017;7(1):e993

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Disorders of glutamate metabolism.

A Kelly, C A Stanley

Mental retardation and developmental disabilities research reviews 2002;7(4):287-95

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Replication pattern of the pericentromeric region of chromosome 10q and expression of the RET protooncogene.

R Cinti, F Schena, M Passalacqua, I Ceccherini, R Ravazzolo

Experimental cell research 2004;298(2):602-10

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Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics.

Y Ji, J M Biernacka, S Hebbring, Y Chai, G D Jenkins, A Batzler, K A Snyder, M S Drews, Z Desta, D Flockhart, T Mushiroda, M Kubo, Y Nakamura, N Kamatani, D Schaid, R M Weinshilboum, D A Mrazek

The pharmacogenomics journal 2014;13(5):456-63

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Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Ann B Goodman, Arthur B Pardee

Proceedings of the National Academy of Sciences of the United States of America 2003;100(5):2901-5

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Results for ""Chromosomes, Human, Pair 10""[mesh_terms]

Is GAD2 on chromosome 10p12 a potential candidate gene for morbid obesity?

PECULIARITIES OF THE STRUCTURE AND EXPRESSION OF HUMAN SPHINGOMYELIN SYNTHASE 1 GENE (SGMS1).

Accelerated Skeletal Maturation in Disorders of Retinoic Acid Metabolism: A Case Report and Focused Review of the Literature.

Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease.

Genetics of age-related macular degeneration.

Urokinase gene 3'-UTR T/C polymorphism is associated with urolithiasis.

Alterations in molecular pathways of diffusely infiltrating glial neoplasms: application to tumor classification and anti-tumor therapy (Review).

Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development.

Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects.

ANXA7-GTPase as Tumor Suppressor: Mechanisms and Therapeutic Opportunities.

Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.

Disorders of glutamate metabolism.

Replication pattern of the pericentromeric region of chromosome 10q and expression of the RET protooncogene.

Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics.

Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Results for
""Chromosomes, Human, Pair 10""[mesh_terms]