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 expression
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"Carmen Cadilla"
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Publications

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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
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