Abstract

STRATEGY I. OBJECTIVES OF THE ADMINISTRATIVE CORE The mission of the IDDRC is to enhance IDD research activities at BCM by supporting research on etiology, diagnosis, prevention, pathogenesis, and the development of therapies to treat IDD. Our objectives are to: 1. Support faculty research into IDD through strategic core facilities and develop new core services as fields advance. 2. Strengthen our multidisciplinary approach to IDD research by fostering interactions between Center investigators and recruiting investigators from other fields into the field of IDD research. 3. Facilitate scientific and collaborative interactions with investigators outside Baylor who have demonstrated a major commitment to study and treat IDD. The Administrative Core will continue to meet these objectives by wisely administering funds awarded to the IDDRC, maintaining a high-quality infrastructure to support the research projects, and spurring collaborations amongst investigators at BCM as well with investigators at other institutions. The Administrative Core will also actively seek additional funding for IDD research and will help new investigators find funding opportunities with the most appropriate agencies and foundations for their research projects.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54HD083092-01
Application #
8924329
Study Section
Special Emphasis Panel (ZHD1-DSR-H (ID))
Program Officer
Parisi, Melissa
Project Start
Project End
Budget Start
2014-09-23
Budget End
2015-06-30
Support Year
1
Fiscal Year
2014
Total Cost
$131,044
Indirect Cost
$47,310

  Institution

Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030

  Publications

Huang, Jui-Yen; Lu, Hui-Chen (2018) mGluR5 Tunes NGF/TrkA Signaling to Orient Spiny Stellate Neuron Dendrites Toward Thalamocortical Axons During Whisker-Barrel Map Formation. Cereb Cortex 28:1991-2006
Marcogliese, Paul C; Shashi, Vandana; Spillmann, Rebecca C et al. (2018) IRF2BPL Is Associated with Neurological Phenotypes. Am J Hum Genet 103:245-260
Xiao, Yang; Hill, Matthew C; Zhang, Min et al. (2018) Hippo Signaling Plays an Essential Role in Cell State Transitions during Cardiac Fibroblast Development. Dev Cell 45:153-169.e6
Gulinello, Maria; Mitchell, Heather A; Chang, Qiang et al. (2018) Rigor and reproducibility in rodent behavioral research. Neurobiol Learn Mem :
De Maio, Antonia; Yalamanchili, Hari Krishna; Adamski, Carolyn J et al. (2018) RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing Proteins. Cell Rep 25:726-736.e7
Gillentine, Madelyn A; Lozoya, Ricardo; Yin, Jiani et al. (2018) CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders. J Affect Disord 239:247-252
Scavuzzo, Marissa A; Teaw, Jessica; Yang, Diane et al. (2018) Generation of Scaffold-free, Three-dimensional Insulin Expressing Pancreatoids from Mouse Pancreatic Progenitors In Vitro. J Vis Exp :
Liu, Gary; Patel, Jay M; Tepe, Burak et al. (2018) An Objective and Reproducible Test of Olfactory Learning and Discrimination in Mice. J Vis Exp :
Nguyen, Lena H; Anderson, Anne E (2018) mTOR-dependent alterations of Kv1.1 subunit expression in the neuronal subset-specific Pten knockout mouse model of cortical dysplasia with epilepsy. Sci Rep 8:3568
Cosmanescu, Filip; Katsamba, Phinikoula S; Sergeeva, Alina P et al. (2018) Neuron-Subtype-Specific Expression, Interaction Affinities, and Specificity Determinants of DIP/Dpr Cell Recognition Proteins. Neuron 100:1385-1400.e6

Showing the most recent 10 out of 311 publications