We are in the midst of a revolution regarding our evolving understanding of the molecular mechanisms underlying normal embryogenesis and neural development, gene-environmental interactions, associated genetic and epigenetic processes and the pathogenesis, classification and treatment of intellectual and developmental disorders (IDDs). The Tissue Engineering and Cellular Reprogramming Core (TECR) has evolved from a traditional Tissue Culture Core in our previous Kennedy Center grant to now providing an extensive, innovative, interdisciplinary, state-of-the-art array of user services to further accelerate the explosive growth in basic, translational and clinical neuroscience knowledge and scientific applications undertaken by Center investigators as a key component of the new Einstein IDDRC application. The broad scientific and technical expertise of our faculty, staff and specialized consultants and the availability of support services (Table F1) ensure that particularly novel and cross-disciplinary investigations can be fostered and adapted to the increasingly sophisticated needs of IDDRC investigators. These services are designed to facilitate research projects employing a wide variety of experimental approaches ranging from the utilization of cellular and molecular biology techniques, genomic, epigenomic and systems biological analyses and neurophysiological approaches to the study of distinct animal and human cellular and tissue preparations. The Core supplies these services in conjunction with other IDDRC Core Facilities and specialized support services by providing extensive training, oversight, facilities and novel and unique resources to expedite these interdisciplinary 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 #
5P30HD071593-03
Application #
8507790
Study Section
Special Emphasis Panel (ZHD1-DSR-Y)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
3
Fiscal Year
2013
Total Cost
$122,484
Indirect Cost
$49,140
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Celestrin, Kevin; Díaz-Balzac, Carlos A; Tang, Leo T H et al. (2018) Four specific immunoglobulin domains in UNC-52/Perlecan function with NID-1/Nidogen during dendrite morphogenesis in Caenorhabditis elegans. Development 145:
Thomsen, Anna M; Gulinello, Maria E; Wen, Jing et al. (2018) Liposomal Cytarabine Induces Less Neurocognitive Dysfunction Than Intrathecal Methotrexate in an Animal Model. J Pediatr Hematol Oncol 40:e91-e96
Saied-Santiago, Kristian; Bülow, Hannes E (2018) Diverse roles for glycosaminoglycans in neural patterning. Dev Dyn 247:54-74
Wang, Ping; Zhao, Dejian; Lachman, Herbert M et al. (2018) Enriched expression of genes associated with autism spectrum disorders in human inhibitory neurons. Transl Psychiatry 8:13
Zhao, Yingjie; Guo, Tingwei; Fiksinski, Ania et al. (2018) Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. Am J Med Genet A 176:2172-2181
Boudewyn, Lauren C; Walkley, Steven U (2018) Current concepts in the neuropathogenesis of mucolipidosis type IV. J Neurochem :
Wilson, Tommy J; Gray, Michael J; Van Klinken, Jan-Willem et al. (2018) Macronutrient composition of a morning meal and the maintenance of attention throughout the morning. Nutr Neurosci 21:729-743
Barnes, Jesse; Salas, Franklin; Mokhtari, Ryan et al. (2018) Modeling the neuropsychiatric manifestations of Lowe syndrome using induced pluripotent stem cells: defective F-actin polymerization and WAVE-1 expression in neuronal cells. Mol Autism 9:44
Pera, Marta; Larrea, Delfina; Guardia-Laguarta, Cristina et al. (2017) Increased localization of APP-C99 in mitochondria-associated ER membranes causes mitochondrial dysfunction in Alzheimer disease. EMBO J 36:3356-3371
Boudewyn, Lauren C; Sikora, Jakub; Kuchar, Ladislav et al. (2017) N-butyldeoxynojirimycin delays motor deficits, cerebellar microgliosis, and Purkinje cell loss in a mouse model of mucolipidosis type IV. Neurobiol Dis 105:257-270

Showing the most recent 10 out of 128 publications