Member Bibliography/Bibliografía de Miembros
This page collects all the personal publications that CienciaPR members have uploaded to their profiles. You can also see all of the authors collected in these publications or all the keywords contained in these publications.
“Restricted HIV-1 replication in placental macrophages is caused by inefficient viral transcription.”, J Leukoc Biol, vol. 87, no. 4, pp. 633-6, 2010.
“Asymptomatic child heterozygous for hemoglobin S and hemoglobin Pôrto Alegre.”, Pediatr Blood Cancer, vol. 56, no. 3, pp. 458-9, 2011.
“Nonsense mutations of the bHLH transcription factor TWIST2 found in Setleis Syndrome patients cause dysregulation of periostin.”, Int J Biochem Cell Biol, vol. 43, no. 10, pp. 1523-31, 2011.
“Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico.”, J Pediatr, vol. 159, no. 4, pp. 623-7.e1, 2011.
“Redundant or separate entities?--roles of Twist1 and Twist2 as molecular switches during gene transcription.”, Nucleic Acids Res, vol. 39, no. 4, pp. 1177-86, 2011.
“Development of a pharmacogenetic-guided warfarin dosing algorithm for Puerto Rican patients.”, Pharmacogenomics, vol. 13, no. 16, pp. 1937-50, 2012.
“Dysregulation of macrophage-secreted cathepsin B contributes to HIV-1-linked neuronal apoptosis.”, PLoS One, vol. 7, no. 5, p. e36571, 2012.
“Prediction of warfarin dose reductions in Puerto Rican patients, based on combinatorial CYP2C9 and VKORC1 genotypes.”, Ann Pharmacother, vol. 46, no. 2, pp. 208-18, 2012.
“CYP2D6's functional status associated with the length of hospitalization stay in psychiatric patients: a twist in the tale or evidence that matters?”, Biomark Med, vol. 7, no. 6, pp. 913-4, 2013.
“A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).”, Biochim Biophys Acta, vol. 1833, no. 3, pp. 468-78, 2013.
“Frequencies of Functional Polymorphisms in Three Pharmacokinetic Genes of Clinical Interest within the Admixed Puerto Rican Population.”, J Pharmacogenomics Pharmacoproteomics, vol. 4, no. 113, 2013.
“Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report.”, Bol Asoc Med P R, vol. 105, no. 2, pp. 62-4, 2013.
“Ocular Findings in Patients with the Hermansky-Pudlak Syndrome (Types 1 and 3).”, Ophthalmic Genet, 2014.
“Pharmacogenetic association study of warfarin safety endpoints in Puerto Ricans.”, P R Health Sci J, vol. 33, no. 3, pp. 97-104, 2014.
“Pharmacogenetics of drug-metabolizing enzymes in US Hispanics.”, Drug Metabol Drug Interact, 2014.
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“Bioinformatic Characterization and Molecular Evolution of the Hemoglobins.”, Genes (Basel), vol. 13, no. 11, 2022.
, “Incidence and Mortality Rates for Childhood Acute Lymphoblastic Leukemia in Puerto Rican Hispanics, 2012-2016.”, Cancer Epidemiol Biomarkers Prev, p. OF1, 2023.
, “Incidence and mortality rates for childhood acute lymphoblastic leukemia in Puerto Rican Hispanics, 2012-2016.”, Cancer Epidemiol Biomarkers Prev, 2023.
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