Carmen L Cadilla, Ph.D., M.S.
Affiliations: | University of Puerto Rico School of Medicine, San Juan, San Juan, Puerto Rico |
Area:
Genetics, genomics, regulation of gene expressionGoogle:
"Carmen Cadilla"Parents
Sign in to add mentorWaldemar Adam | grad student | 1978-1980 | University of Puerto Rico - Río Piedras Campus (Chemistry Tree) |
Donald E. Olins | grad student | 1983-1986 | University of Tennessee - Knoxville/Oak Ridge National Laboratory |
Francis Thomas Kenney | post-doc | 1986-1989 | University of Tennessee - Knoxville/Oak Ridge National Laboratory (Chemistry Tree) |
Children
Sign in to add trainee
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Casasnovas-Nieves JJ, Rodríguez Y, Franco HL, et al. (2023) Mechanisms of Regulation of the Gene by the TWIST2 and ADD1/SREBP1c Transcription Factors. Genes. 14 |
Crespo NE, Torres-Bracero A, Renta JY, et al. (2021) Expression Profiling Identifies TWIST2 Target Genes in Setleis Syndrome Patient Fibroblast and Lymphoblast Cells. International Journal of Environmental Research and Public Health. 18 |
Montes-Rodríguez IM, Rivera LE, López-Garriga J, et al. (2016) Characterization and Expression of the Lucina pectinata Oxygen and Sulfide Binding Hemoglobin Genes. Plos One. 11: e0147977 |
Montes-Rodríguez IM, Rivera LE, López-Garriga J, et al. (2016) Characterization and expression of the Lucina pectinata oxygen and sulfide binding hemoglobin genes Plos One. 11 |
Rosti RO, Uyguner ZO, Nazarenko I, et al. (2014) Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation. Clinical Genetics |
Carmona-Rivera C, Simeonov DR, Cardillo ND, et al. (2013) A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3). Biochimica Et Biophysica Acta. 1833: 468-78 |
Franco HL, Casasnovas JJ, Leon RG, et al. (2011) Nonsense mutations of the bHLH transcription factor TWIST2 found in Setleis Syndrome patients cause dysregulation of periostin. The International Journal of Biochemistry & Cell Biology. 43: 1523-31 |
Franco HL, Casasnovas J, Rodríguez-Medina JR, et al. (2011) Redundant or separate entities?--roles of Twist1 and Twist2 as molecular switches during gene transcription. Nucleic Acids Research. 39: 1177-86 |
Tukel T, Šošić D, Al-Gazali LI, et al. (2010) Homozygous nonsense mutations in TWIST2 cause setleis syndrome American Journal of Human Genetics. 87: 289-296 |
García-Fragoso L, García-García I, Leavitt G, et al. (2010) MTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers. International Journal of Genetics and Molecular Biology. 2: 43-47 |