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Desmond Smith, M.D., Ph.D.

Work Email Address:
dsmith@mednet.ucla.edu

Work Address:
Office
CHS
Los Angeles, CA 90095
UNITED STATES

23-120 CHS
Campus - 173517
CA
UNITED STATES

Laboratory
CHS
Los Angeles, CA 90095
UNITED STATES

Lab Number:
310-794-5711
Office Phone Number:
310-206-0086



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Department / Division Affiliations
Professor, Molecular & Medical Pharmacology
Member, ACCESS Program: Dept. of Molecular & Medical Pharmacology, Access Genetics and Genomics Home Area, Access Molecular Pharmacology: Therapeutics, Diagnostics, and Biology of Disease Home Area, Access Neuroscience Home Area, Brain Research Institute, Neuroscience IDP
Faculty, Biomedical Engineering IDP

Bio:

Desmond Smith's first degree was in Physics from Oxford University, England. He went on to obtain a PhD from Cambridge University in Molecular Biology and a medical degree from Oxford University. After postgraduate medical training in the UK, Dr Smith went to Harvard University to do a postdoctoral fellowship in Drosophila genetics and another postdoc at Lawrence Berkeley National Laboratory in mouse genetics. Dr Smith is currently a Professor at the Department of Molecular and Medical Pharmacology at UCLA.

Publications:

Zacharaki EI, Skoura A, An L, Smith DJ, Megalooikonomou V. Combining gene expression and function in a spatially localized approach. Artificial Intelligence Applications and Innovations, IFIP Advances in Information and Communication Technology 2012; 382: 566-575.
Khan AH, Lin A, Smith DJ. Discovery and characterization of human exonic transcriptional regulatory elements. PLoS ONE 2012; 7: e46098.
An L, Ling H, Obradovic Z, Smith DJ, Megalooikonomou V. Learning pair-wise gene functional similarity by multiplex gene expression maps. BMC Bioinformatics 2012; 13(Suppl 3): S1.
Chin MH, Geng AB, Khan AH, Qian WJ, Petyuk VA, Boline J, Levy S, Toga AW, Smith RD, Leahy RM, Smith DJ. A genome-scale map of expression for a mouse brain section obtained using voxelation. Physiol Genomics 2007; 30: 313-321.
Petyuk VA, Qian WJ, Chin MH, Wang H, Livesay EA, Monroe ME, Adkins JN, Jaitly N, Anderson DJ, Camp DG 2nd, Smith DJ, Smith RD. Spatial mapping of protein abundances in the mouse brain by voxelation integrated with high-throughput liquid chromatography-mass spectrometry. Genome Res 2007; 17: 328-336.
Leil TA, Ossadtchi A, Nichols TE, Leahy RM, Smith DJ. Genes regulated by learning in the hippocampus. J Neurosci Res. 2003; 71: 763-768.
Sforza DM, Smith DJ. Genetic and genomic strategies in learning and memory. Curr Genomics 2003; 4:: 475-485.
Liu D, Singh RP, Khan AH, Lusis AJ, Davis RC, Smith DJ Mapping behavioral traits by use of genome-tagged mice. The American Journal of Geriatric Psychiatry 2003; 12(2): 158-65.
Shai S-Y, Harpf AE, Babbitt CJ, Jordan MC, Fishbein MC, Chen J, Omura M, Leil TA, Becker, KD, Jiang M, Smith DJ, Cherry SR, Loftus JC, Ross RS. Cardiac-specific Cre-lox excision of the beta 1 integrin gene results in progressive fibrosis, defective mechanotransduction and cardiac failure. Circ Res 2002; 90: 458-464.
Smith DJ. Chips for brains. Curr Genomics 2002; 3: 1-5.
Leil TA, Ossadtchi A, Cortes J, Leahy RM, Smith DJ. Finding new candidate genes for learning and memory. J Neurosci Res 2002; 68: 127-137.
Brown VM, Ossadtchi A, Khan AH, Gambhir SS, Cherry SR, Leahy RM, Smith DJ. Gene expression tomography. Physiol Genomics. 2002; 8: 159-167.
Brown VM, Ossadtchi A, Khan AH, Cherry SR, Leahy RM, Smith DJ. High-throughput imaging of brain gene expression. Genome Res. 2002; 12: 244-254.
Smith DJ, Lusis AJ. The allelic structure of common disease. Hum Mol Genetics. 2002; 11: 2455-2461.
Smith, DJ In vivo libraries of large insert transgenic mice for genetic mapping. Methods in Molecular Biology 2001; 158: 335-349.
Smith, DJ RAGE and PRAY. The Pharmacogenomics Journal 2001; 1(2): 90-91.
Xie CW, Sayah D, Chen QS, Wei WZ, Smith DJ, Liu, X. Deficient long-term memory and long-term potentiation in mice with a targeted deletion of neurotrophin-4 gene. Proc Natl Acad Sci USA. 2000; 97: 8116-8121.
Wang Richard T, Ahn Sangtae, Park Christopher C, Khan Arshad H, Lange Kenneth, Smith Desmond J Effects of genome-wide copy number variation on expression in mammalian cells. BMC genomics. 2011; 12(1): 562.
Ghazalpour Anatole, Bennett Brian, Petyuk Vladislav A, Orozco Luz, Hagopian Raffi, Mungrue Imran N, Farber Charles R, Sinsheimer Janet, Kang Hyun M, Furlotte Nicholas, Park Christopher C, Wen Ping-Zi, Brewer Heather, Weitz Karl, Camp David G, Pan Calvin, Yordanova Roumyana, Neuhaus Isaac, Tilford Charles, Siemers Nathan, Gargalovic Peter, Eskin Eleazar, Kirchgessner Todd, Smith Desmond J, Smith Richard D, Lusis Aldons J Comparative analysis of proteome and transcriptome variation in mouse. PLoS genetics. 2011; 7(6): e1001393.
Park Christopher C, Gale Greg D, de Jong Simone, Ghazalpour Anatole, Bennett Brian J, Farber Charles R, Langfelder Peter, Lin Andy, Khan Arshad H, Eskin Eleazar, Horvath Steve, Lusis Aldons J, Ophoff Roel A, Smith Desmond J Gene networks associated with conditional fear in mice identified using a systems genetics approach. BMC systems biology. 2011; 5(6): 43.
Ranola John M O, Ahn Sangtae, Sehl Mary, Smith Desmond J, Lange Kenneth A Poisson model for random multigraphs. Bioinformatics (Oxford, England). 2010; 26(16): 2004-11.
Lin Andy, Wang Richard T, Ahn Sangtae, Park Christopher C, Smith Desmond J A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes. Genome research. 2010; 20(8): 1122-32.
Zhang Xu, Monroe Matthew E, Chen Baowei, Chin Mark H, Heibeck Tyler H, Schepmoes Athena A, Yang Feng, Petritis Brianne O, Camp David G, Pounds Joel G, Jacobs Jon M, Smith Desmond J, Bigelow Diana J, Smith Richard D, Qian Wei-Jun Endogenous 3,4-dihydroxyphenylalanine and dopaquinone modifications on protein tyrosine: links to mitochondrially derived oxidative stress via hydroxyl radical. Molecular & cellular proteomics : MCP. 2010; 9(6): 1199-208.
Zhang Xu, Zhou Jian-Ying, Chin Mark H, Schepmoes Athena A, Petyuk Vladislav A, Weitz Karl K, Petritis Brianne O, Monroe Matthew E, Camp David G, Wood Stephen A, Melega William P, Bigelow Diana J, Smith Desmond J, Qian Wei-Jun, Smith Richard D Region-specific protein abundance changes in the brain of MPTP-induced Parkinson's disease mouse model. Journal of proteome research. 2010; 9(3): 1496-509.
Petyuk Vladislav A, Qian Wei-Jun, Smith Richard D, Smith Desmond J Mapping protein abundance patterns in the brain using voxelation combined with liquid chromatography and mass spectrometry. Methods (San Diego, Calif.). 2010; 50(2): 77-84.
Bojanic Dragana D, Tarr Paul T, Gale Greg D, Smith Desmond J, Bok Dean, Chen Bryan, Nusinowitz Steven, L├vgren-Sandblom Anita, Bj├rkhem Ingemar, Edwards Peter A Differential expression and function of ABCG1 and ABCG4 during development and aging. Journal of lipid research. 2010; 51(1): 169-81.
Smith Desmond J Mitochondrial dysfunction in mouse models of Parkinson's disease revealed by transcriptomics and proteomics. Journal of bioenergetics and biomembranes. 2009; 41(6): 487-91.
An Li, Xie Hongbo, Chin Mark H, Obradovic Zoran, Smith Desmond J, Megalooikonomou Vasileios Analysis of multiplex gene expression maps obtained by voxelation. BMC bioinformatics. 2009; 10 Suppl 4(6): S10.
Ahn Sangtae, Wang Richard T, Park Christopher C, Lin Andy, Leahy Richard M, Lange Kenneth, Smith Desmond J Directed mammalian gene regulatory networks using expression and comparative genomic hybridization microarray data from radiation hybrids. PLoS computational biology. 2009; 5(6): e1000407.
Park Christopher C, Petyuk Vladislav A, Qian Wei-Jun, Smith Richard D, Smith Desmond J Dual spatial maps of transcript and protein abundance in the mouse brain. Expert review of proteomics. 2009; 6(3): 243-9.
Farber Charles R, van Nas Atila, Ghazalpour Anatole, Aten Jason E, Doss Sudheer, Sos Brandon, Schadt Eric E, Ingram-Drake Leslie, Davis Richard C, Horvath Steve, Smith Desmond J, Drake Thomas A, Lusis Aldons J An integrative genetics approach to identify candidate genes regulating BMD: combining linkage, gene expression, and association. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2009; 24(1): 105-16.
Guedj Fay├al, S├bri├ Catherine, Rivals Isabelle, Ledru Aurelie, Paly Evelyne, Bizot Jean C, Smith Desmond, Rubin Edward, Gillet Brigitte, Arbones Mariona, Delabar Jean M Green tea polyphenols rescue of brain defects induced by overexpression of DYRK1A. PloS one. 2009; 4(2): e4606.
Ghazalpour Anatole, Doss Sudheer, Kang Hyun, Farber Charles, Wen Ping-Zi, Brozell Alec, Castellanos Ruth, Eskin Eleazar, Smith Desmond J, Drake Thomas A, Lusis Aldons J High-resolution mapping of gene expression using association in an outbred mouse stock. PLoS genetics. 2008; 4(8): e1000149.
Chen Hsuan Pu, Lin Andy, Bloom Joshua S, Khan Arshad H, Park Christopher C, Smith Desmond J Screening reveals conserved and nonconserved transcriptional regulatory elements including an E3/E4 allele-dependent APOE coding region enhancer. Genomics. 2008; 92(5): 292-300.
Park Christopher C, Ahn Sangtae, Bloom Joshua S, Lin Andy, Wang Richard T, Wu Tongtong, Sekar Aswin, Khan Arshad H, Farr Christine J, Lusis Aldons J, Leahy Richard M, Lange Kenneth, Smith Desmond J Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids. Nature genetics. 2008; 40(4): 421-9.
Sebri├ Catherine, Chabert Caroline, Ledru Aur├lie, Guedj Fay├al, Po Chrystelle, Smith Desmond J, Rubin Edward, Rivals Isabelle, Beloeil Jean-Claude, Gillet Brigitte, Delabar Jean-Maurice Increased dosage of DYRK1A and brain volumetric alterations in a YAC model of partial trisomy 21. Anatomical record (Hoboken, N.J. : 2007). 2008; 291(3): 254-62.
Chin Mark H, Qian Wei-Jun, Wang Haixing, Petyuk Vladislav A, Bloom Joshua S, Sforza Daniel M, La─çan Goran, Liu Dahai, Khan Arshad H, Cantor Rita M, Bigelow Diana J, Melega William P, Camp David G, Smith Richard D, Smith Desmond J Mitochondrial dysfunction, oxidative stress, and apoptosis revealed by proteomic and transcriptomic analyses of the striata in two mouse models of Parkinson's disease. Journal of proteome research. 2008; 7(2): 666-77.
Rachidi Mohammed, Lopes Carmela, Vayssettes Catherine, Smith Desmond J, Rubin Edward M, Delabar Jean-Maurice New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1. Biochemical and biophysical research communications. 2007; 364(3): 488-94.
Davis RC, Schadt EE, Smith DJ, Hsieh EW, Cervino AC, van Nas A, Rosales M, Doss S, Meng H, Allayee H, Lusis AJ. A genome-wide set of congenic mouse strains derived from DBA/2J on a C57BL/6J background. Genomics 2005; 86: 259-270.
Sforza DM, Annese J, Liu D, Levy S, Toga AW, Smith DJ Anatomical methods for voxelation of the mammalian brain. Neurochemical Research 2004; 29(6): 1299-306.
Singh RP, Liu D, Chaudhari A, Cherry SR, Leahy RM, Smith DJ Investigation of different transcript quantitation tools for high-throughput mapping of brain gene expression using voxelation. Journal of Molecular Histology 2004; 35(4): 397-402.
Branchi I, Bichler Z, Minghetti L, Delabar JM, Malchiodi-Albedi F, Gonzalez MC, Chettouh Z, Nicolini A, Chabert C, Smith DJ, Rubin EM, Migliore-Samour D, Alleva E Transgenic mouse in vivo library of human Down syndrome critical region 1: association between DYRK1A overexpression, brain development abnormalities, and cell cycle protein alteration. Journal of Neuropathology and Experimental Neurology 2004; 63(5): 429-440.
Sforza DM, Smith DJ Voxelation methods for genome scale imaging of brain gene expression. Methods in enzymology. . 2004; 386: 314-23.
Liu D, Smith DJ Voxelation and gene expression tomography for the acquisition of 3-D gene expression maps in the brain. Methods (San Diego, Calif.) . 2003; 31(4): 317-25.
Liu D, Singh RP, Khan AH, Bhavsar K, Lusis AJ, Davis RC, Smith DJ Identifying loci for behavioral traits using genome-tagged mice. Journal of neuroscience research. . 2003; 74(4): 562-9.
Singh RP, Smith DJ Genome scale mapping of brain gene expression. Biological psychiatry. . 2003; 53(12): 1069-74.
Singh RP, Brown VM, Chaudhari A, Khan AH, Ossadtchi A, Sforza DM, Meadors AK, Cherry SR, Leahy RM, Smith DJ High-resolution voxelation mapping of human and rodent brain gene expression. Journal of Neuroscience Methods. 2003; 125(1-2): 93-101.
Smith DJ, Leil TA, Liu X Neurotrophin-4 is required for tolerance to morphine in the mouse. Neuroscience Letters 2003; 340(2): 103-6.
Khan AH, Ossadtchi A, Leahy RM, Smith DJ Error-correcting microarray design. Genomics. . 2003; 81(2): 157-65.
Ossadtchi A, Brown VM, Khan AH, Cherry SR, Nichols TE, Leahy RM, Smith DJ Statistical analysis of multiplex brain gene expression images. Neurochemical research. . 2002; 27(10): 1113-21.
Brown VM, Ossadtchi A, Khan AH, Yee S, Lacan G, Melega WP, Cherry SR, Leahy RM, Smith DJ, Multiplex three-dimensional brain gene expression mapping in a mouse model of Parkinson's disease. Genome research. . 2002; 12(6): 868-84.
Sayah DM, Khan AH, Gasperoni TL, Smith DJ A genetic screen for novel behavioral mutations in mice. Molecular psychiatry. . 2000; 5(4): 369-77.
Hodgson JG, Agopyan N, Gutekunst CA, Leavitt BR, LePiane F, Singaraja R, Smith DJ, Bissada N, McCutcheon K, Nasir J, Jamot L, Li XJ, Stevens ME, Rosemond E, Roder JC, Phillips AG, Rubin EM, Hersch SM, Hayden MR A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration. Neuron. . 1999; 23(1): 181-92.
Sago H, Carlson EJ, Smith DJ, Kilbridge J, Rubin EM, Mobley WC, Epstein CJ, Huang TT Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities. Proceedings of the National Academy of Sciences of the United States of America. . 1998; 95(11): 6256-61.
Rubin EM, Smith DJ Optimizing the mouse to sift sequence for function. Trends in genetics : TIG. . 1997; 13(11): 423-6.
Smith DJ, Stevens ME, Sudanagunta SP, Bronson RT, Makhinson M, Watabe AM, O'Dell TJ, Fung J, Weier HU, Cheng JF, Rubin EM Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome. Nature genetics. . 1997; 16(1): 28-36.
Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, Daly MJ, Kruglyak L, Reeve MP, Nemhauser JL, Hawkins TL, Rubin EM, Lander ES The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron. . 1997; 18(5): 711-22.