Projects per year
Search results
-
Active
Cell fate choices by Tbx1 in forming the mammalian heart
National Heart, Lung, and Blood Institute
8/20/20 → 4/30/24
Project: Research project
-
Cancer Center Support Grant
Almo, S. C., Hogue-Angeletti, R., Augenlicht, L. H., Condeelis, J. S., Desai, K. K., Edelmann, W., Goldman, I. D., Greally, J. M., Herbst, L. H., Keller, S. M., Kim, M., Mahmood, R., Montagna, C., Morrow, B. E., Pollard, J. W., Porcelli, S. A., Rohan, T. E., Scharff, M. D., Seither, R., Skoultchi, A. I., Sparano, J. A., Stanley, P. M., Chu, E. E., Bresnick, A. R., Skoultchi, A. A. I., Adedimeji, A. A., Beck, A. A. P., Blanchard, J. S., Halmos, B. B., Morrow, B. B., Diamond, B. B., Rapkin, B. D., Chu, E., Montagna, C. C., Stein, D. T., Gaertner, D. D. J., Chu, E. E., Ho, G. G. Y., Goel, S., Hosgood, H. D. H., Strickler, H. H. D., Goldman, I. I. D., Pollard, J. J. W., Condeelis, J. J. S., Dutcher, J. J. P., Greally, J. M., Backer, J. M., Sparano, J., Aguirre-ghiso, J. J. A., Desai, K. K., Gritsman, K., Herbst, L. H., Augenlicht, L. H., Cannizzaro, L. A., Hackett, L. L. E., Scharff, M. M. D., Brenowitz, M. D., Kim, M. M. Y., Ohri, N. N., Stanley, P., Mahmood, R. R., Gupta, R. R. K., Seither, R. R. L., Depinho, R. R. A., Angeletti, R. R. H., Kucherlapati, R. R. S., Schramm, V. L., Keller, S. M., Almo, S. E., Porcelli, S. A., Rohan, T. E., Steidl, U. U. G., Rapkin, B. B. D., Xue, X. N., Alderman, M. H., Atkinson, P. H., Bases, R. E., Birshstein, B. K., Bloom, B. R., Blumenfeld, O. O., Brenowitz, M. D., Brewer, F. C., Buhl, S., Cannizzaro, L. A., Chance, M. R., Chase, J. W., Childs, G. J., Depinho, R., Depinho, R. A., Diamond, B. A., Diamond, B., Duran-reynals, M. L., Dutcher, J. P., Eagle, H., Fant, J., Gaertner, D. J., Grills, G., Gupta, R. K., Ho, G. Y., Band Horwitz, S., Horwitz, M. S., Hurwitz, J., Kadish, A. S., Klinger, H. P., Krauter, K. S., Kucherlapati, R. S., Levine, W. G., Lilly, F., Maio, J. J., Maitra, U., Makman, M. H., Marians, K. J., Nathenson, S. G., Orr, G. A., Peisach, J., Pickering, K., Rajan, T. V., Reid, L. M., Rubin, C. S., Russel, R., Satir, B. H., Schildkraut, C. L., Schulman, L. H., Serrano, L. J., Shapiro, L., Shin, S., Wadler, S. H., Warner, J. R., West, M. & Wiernik, P. H.
6/1/85 → 6/30/24
Project: Research project
-
Finished
Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells
5/12/22 → 4/30/23
Project: Research project
-
Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome
2/1/22 → 1/31/23
Project: Research project
-
Molecular and cellular mechanisms in cardiac outflow tract formation and defects
National Heart, Lung, and Blood Institute
9/1/21 → 8/31/22
Project: Research project
-
-
Genomics & Computational Analysis
Morrow, B. B. E. & Morrow, B. E.
7/1/19 → 6/30/22
Project: Research project
-
-
Project: Genetic basis of intellectual disability in 22q11.2 deletion syndrome
National Institute of Child Health and Human Development
9/22/16 → 5/31/21
Project: Research project
-
Support for the Rose F. Kennedy IDDRC
Walkley, S. U., Dobrenis, K., Greally, J. M., Molholm, S., Morrow, B. E. & Schwartz, G. J.
National Institute of Child Health and Human Development
9/22/16 → 5/31/21
Project: Research project
-
Molecular aspects of CRKL in heart development and human disease
National Heart, Lung, and Blood Institute
7/15/16 → 6/30/21
Project: Research project
-
Genetic modifiers of congenital heart disease
National Institute of Child Health and Human Development
7/1/16 → 6/30/21
Project: Research project
-
Bio-analytics and Administration Core
National Institute of Child Health and Human Development
7/1/16 → 6/30/21
Project: Research project
-
Mouse functional analysis of genes for congenital heart disease
National Institute of Child Health and Human Development
7/1/16 → 6/30/21
Project: Research project
-
Tbx1 and canonical Wnt signaling in the second heart field
Morrow, B. E. & Cai, C.
National Heart, Lung, and Blood Institute
5/1/16 → 8/31/17
Project: Research project
-
Tbx1 and canonical Wnt signaling in the second heart field
Morrow, B. E. & Chenleng, C.
9/15/15 → 8/31/16
Project: Research project
-
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects
Morrow, B. E., Emanuel, B. & Goldmuntz, E.
9/24/11 → 6/30/21
Project: Research project
-
Clinical and Administrative Core
National Institute of Child Health and Human Development
9/24/11 → 6/30/16
Project: Research project
-
Mouse Models of Human Conotruncal Defects
National Institute of Child Health and Human Development
9/24/11 → 6/30/16
Project: Research project
-
Developmental mechanisms of human congenital heart disease
Morrow, B. E., Emanuel, B. S. & Goldmuntz, E.
National Institute of Child Health and Human Development
9/24/11 → 6/30/21
Project: Research project
-
Developmental Genetics of the Pharyngeal Apparatus
Morrow, B. E. & Rose, S. A.
7/1/09 → 6/30/12
Project: Research project
-
Developmental Genetics of the Pharyngeal Apparatus
National Heart, Lung, and Blood Institute
7/1/09 → 6/30/10
Project: Research project
-
Sequence Variations in Low Copy Repeats on 22q11.2
Morrow, B. E. & Rose, S. A.
5/1/09 → 4/30/11
Project: Research project
-
Genetic Basis of Birth Defects in 22q11 Deletion Syndrome
Morrow, B. E. & Rose, S. A.
5/1/09 → 4/30/12
Project: Research project
-
Sequence Variations in Low Copy Repeats on 22q11.2
NATIONAL INSTITUTE OF MENTAL HEALTH
5/1/09 → 4/30/10
Project: Research project
-
Genetic Basis of Birth Defects in 22q11 Deletion Syndrome
National Institute of Neurological Disorders and Stroke
5/1/09 → 4/30/10
Project: Research project
-
-
Role of Genes in Exceptional Longevity in Humans
Barzilai, N., Bergman, A., Crandall, J. P., Kim, M., Lipton, R. B., Morrow, B. E., Schechter, C. B., Morrow, B. B. E., Crandall, J. P., Kim, M. M. Y. & Lipton, R. R. B.
9/1/07 → 7/31/13
Project: Research project
-
-
Genetic Modifiers for 22q 11.2 Deletion Syndrome
Morrow, B. E. & Rose, S. A.
2/1/07 → 1/31/12
Project: Research project
-
Genetic Modifiers for 22q 11.2 Deletion Syndrome
National Heart, Lung, and Blood Institute
2/1/07 → 1/31/12
Project: Research project
-
Molecular Basis of Monosomy 1p36
Morrow, B. E. & Rose, S. A.
8/3/05 → 5/31/08
Project: Research project
-
Molecular Basis of Monosomy 1p36
National Institute of Neurological Disorders and Stroke
8/3/05 → 5/31/06
Project: Research project
-
Genetic Analysis of Tbx1 in Ear Disorders
Morrow, B. E. & Rose, S. A.
12/1/02 → 11/30/14
Project: Research project
-
Genetic Analysis of Tbx1 in Ear Disorders
National Institute on Deafness and Other Communication Disorders
12/1/02 → 11/30/14
Project: Research project
-
Chromosome Rearrangements and Mental Retardation
Lupski, J. R., Morrow, B. E., Nelson, D. L. & Shaffer, L.
6/11/01 → 5/31/07
Project: Research project
-
Molecular mechanism of recurrent rearrangements
National Institute of Child Health and Human Development
10/1/00 → 9/30/02
Project: Research project
-
MOLECULAR ASPECTS OF VELO-CARDIO-FACIAL SYNDROME
Skoultchi, A. I., Kucherlapati, R. S., Morrow, B. E. & Skoultchi, A. I.
12/5/96 → 11/30/04
Project: Research project
-
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS
National Institute of Child Health and Human Development
10/1/96 → 9/30/02
Project: Research project
-
Molecular mechanism of recurrent rearrangements
Morrow, B. E., Shaffer, L., Lupski, J. R., Nelson, D. & Lupski, J. R.
1/1/01 → 5/31/07
Project: Research project
-
MOLECULAR MECHANISMS AND GENOTYPE-PHENOTYPE IN VCFS/DGS
Skoultchi, A. I., Kucherlapati, R. & Morrow, B. E.
1/1/01 → 11/30/04
Project: Research project