This application is for continued support of the administrative and research cores of the UCLA Mental Retardation Research Center. This MRRC was first established in 1969 and housed with Child Psychiatry in a four floors addition to the Neuropsychiatric Institute. This MRRC provides a comprehensive multi-disciplinary in the field of mental retardation and developmental disabilities (MRDD). The research investigations carried out by the Center Investigators address most of the MRDD research priorities listed in the current RFA issued by National Institute of Child Health and Human Development (NICHD) for MRDD Research Centers. The long-term goals of the Center are to discover ways to prevent mental retardation and improve the quality of life for mentally retarded and other developmentally disabled individuals. To accomplish this, five multi- disciplinary research groups have been organized: Clinical Research, Molecular and Developmental Neuroscience Neurobiochemistry and Molecular Genetics, Systems Neuroscience and Socio-behavioral Research. To foster research excellence and innovation through inter- disciplinary interactions among investigators. An Administrative Core and eight research cores have been organized: (1) Molecular Biology, (2) Cell Biology, (3) Neurocytology and Cellular Imaging, (4) Animal Maintenance and Assessment, (5) Field Work Training and Outcome, (6) Data Management and Analysis, (7) Microcomputers and/Media Graphics and (8) Technical Services. The essential scope and mission of the Center are to elucidate the molecular, cellular and behavioral mechanisms underlying the pathogenesis of MRDD and to translate this fundamental knowledge into novel diagnostic, preventive and therapeutic approach which ultimately an be applied to clinical care. The function of the Center is to provide an environment promoting the highest level of research in mental retardation at UCLA by fostering interaction among investigators and providing free access to cutting edge and efficient core services. The Center assigns high priority to the support of talented young investigators and the training of pre- and post-doctoral fellows in a variety of disciplines related to its goals.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
3P30HD004612-31S2
Application #
6361693
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Hanson, James W
Project Start
2001-08-28
Project End
2005-06-30
Budget Start
2001-08-28
Budget End
2002-06-30
Support Year
31
Fiscal Year
2001
Total Cost
$122,027
Indirect Cost
Name
University of California Los Angeles
Department
Pediatrics
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Van, Christina; Condro, Michael C; Lov, Kenny et al. (2018) PACAP/PAC1 Regulation of Inflammation via Catecholaminergic Neurons in a Model of Multiple Sclerosis. J Mol Neurosci :
Ago, Yukio; Hayata-Takano, Atsuko; Kawanai, Takuya et al. (2017) Impaired extinction of cued fear memory and abnormal dendritic morphology in the prelimbic and infralimbic cortices in VPAC2 receptor (VIPR2)-deficient mice. Neurobiol Learn Mem 145:222-231
Yvone, Griselda M; Zhao-Fleming, Hannah H; Udeochu, Joe C et al. (2017) Disabled-1 dorsal horn spinal cord neurons co-express Lmx1b and function in nociceptive circuits. Eur J Neurosci 45:733-747
Espinosa-Jeffrey, Araceli; Blanchi, Bruno; Biancotti, Juan Carlos et al. (2016) Efficient Generation of Viral and Integration-Free Human Induced Pluripotent Stem Cell-Derived Oligodendrocytes. Curr Protoc Stem Cell Biol 38:2D.18.1-2D.18.27
Condro, Michael C; Matynia, Anna; Foster, Nicholas N et al. (2016) High-resolution characterization of a PACAP-EGFP transgenic mouse model for mapping PACAP-expressing neurons. J Comp Neurol 524:3827-3848
Espinosa-Jeffrey, Araceli; Nguyen, Kevin; Kumar, Shalini et al. (2016) Simulated microgravity enhances oligodendrocyte mitochondrial function and lipid metabolism. J Neurosci Res 94:1434-1450
Krityakiarana, Warin; Zhao, Paul M; Nguyen, Kevin et al. (2016) Erratum to: Proof-of Concept that an Acute Trophic Factors Intervention After Spinal Cord Injury Provides an Adequate Niche for Neuroprotection, Recruitment of Nestin-Expressing Progenitors and Regeneration. Neurochem Res 41:1844
Abad, Catalina; Jayaram, Bhavaani; Becquet, Laurine et al. (2016) VPAC1 receptor (Vipr1)-deficient mice exhibit ameliorated experimental autoimmune encephalomyelitis, with specific deficits in the effector stage. J Neuroinflammation 13:169
Khankan, Rana R; Griffis, Khris G; Haggerty-Skeans, James R et al. (2016) Olfactory Ensheathing Cell Transplantation after a Complete Spinal Cord Transection Mediates Neuroprotective and Immunomodulatory Mechanisms to Facilitate Regeneration. J Neurosci 36:6269-86
Krityakiarana, Warin; Zhao, Paul M; Nguyen, Kevin et al. (2016) Proof-of Concept that an Acute Trophic Factors Intervention After Spinal Cord Injury Provides an Adequate Niche for Neuroprotection, Recruitment of Nestin-Expressing Progenitors and Regeneration. Neurochem Res 41:431-49

Showing the most recent 10 out of 82 publications