This application is for continued support of the administrative and research cores of the UCLA Mental Retardation Research Center (MRRC). This MRRC was first established in 1969 and housed with the Department of Child Psychiatry in a four-floor addition to the Neuropsychiatric Institute. It will move next March to a new five-story neuroscience research building. This MRRC provides a comprehensive multidisciplinary research program in the field of mental retardation and developmental disabilities (MRDD). The investigations carried out by the Center investigators address 26 of the 31 MRRD research priorities listed in the current RFA issued by NICHD for MRDD Research Centers. The long-term goals of the Center are to discover ways to prevent mental retardation, and to improve the quality of life for mentally retarded and other developmentally disabled individuals. To accomplish this, four multidisciplinary research groups have been organized: Clinical Research, Cellular and Molecular Neuroscience and Neurogenetics, Systems Neuroscience, and Socio-Behavioral Research. To foster research innovation through interdisciplinary interactions among investigators, five cores have been organized: (A) Administration and Communications, (B) Neuroscience and Imaging, (C) Animal Models, (D) Functional Neurogenomics and Bioinformatics, and (E) Fieldwork Training and Qualitative Data. In addition, this application proposes support for a New Program Development project. Each of the cores is designed to offer investigators an integrated approach to support their multidisciplinary research projects from experimental design to data management and publication. This is achieved by the direct involvement in each core of several faculty and staff with expertise in the relevant scientific disciplines and techniques, working as a team rather than as a single provider of a technique. The mission of the Center is to provide an environment promoting the highest level of research in MRDD by fostering interaction among investigators and providing open 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. The Center's mission is facilitated by strong tie with faculty in more than ten departments and institutes at UCLA, excelling in neuroscience, genetics, imaging, molecular biology, psychology, psychiatry, neurology, neurosurgery, pharmacology, pediatrics, education, anthropology, and others. While the focus needs to be still on the molecular, cellular, and behavioral mechanisms of MRDD, the aim is to collaborate with MRDD scientists worldwide to translate this fundamental knowledge into novel diagnostic, preventive, and therapeutic approaches which can be ultimately applied to clinical care. ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
2P30HD004612-35
Application #
7003431
Study Section
Special Emphasis Panel (ZHD1-MRG-C (24))
Program Officer
Vitkovic, Ljubisa
Project Start
1997-08-15
Project End
2010-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
35
Fiscal Year
2005
Total Cost
$1,408,263
Indirect Cost
Name
University of California Los Angeles
Department
Pediatrics
Type
Schools of Medicine
DUNS #
092530369
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
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
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

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