Carmen Lydia Cadilla

TipoTítuloAutorRespuestasÚltima actualización
BibliographiesPresence of the 5,10-methylenetetrahydrofolate reductase C677T mutation in Puerto Rican patients with neural tube defects. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesErythrocyte volume, folate levels, and the presence of methylenetetrahydrofolate reductase polymorphism. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesThe cDNA-derived amino acid sequence of hemoglobin II from Lucina pectinata. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesFunctional characterization of the purified holo form of hemoglobin I from Lucina pectinata overexpressed in Escherichia coli. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesPoor response to desmopressin acetate (DDAVP) in children with Hermansky-Pudlak syndrome. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesHigh-level production of recombinant sulfide-reactive hemoglobin I from Lucina pectinata in Escherichia coli. High yields of fully functional holoprotein synthesis in the BLi5 E. coli strain. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesTyrosine B10 and heme-ligand interactions of Lucina pectinata hemoglobin II: control of heme reactivity. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesHemoglobin I from Lucina pectinata: a model for distal heme-ligand control. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesGenetic testing for oculocutaneous albinism type 1 and 2 and Hermansky-Pudlak syndrome type 1 and 3 mutations in Puerto Rico. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesHydrogen-bonding conformations of tyrosine B10 tailor the hemeprotein reactivity of ferryl species. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesFoveal thickness and macular volume in patients with oculocutaneous albinism. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesStructure and ligand selection of hemoglobin II from Lucina pectinata. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesPrevalence of CYP2C19 gene polymorphisms in the Puerto Rican population: a preliminary report. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesFactors controlling the reactivity of hydrogen sulfide with hemeproteins. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesPhysiogenomic analysis of the Puerto Rican population. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesPrevalence of combinatorial CYP2C9 and VKORC1 genotypes in Puerto Ricans: implications for warfarin management in Hispanics. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesFor the patient. DNA makeup of Hispanic persons should be determined before warfarin prescription. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesRecombinant hemoglobin II from Lucina pectinata: a large-scale method for hemeprotein expression in E. coli. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesCYP2C9 and VKORC1 genotypes in Puerto Ricans: A case for admixture-matching in clinical pharmacogenetic studies. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesNewborn screening for hermansky-pudlak syndrome type 3 in Puerto Rico. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesMTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesHomozygous nonsense mutations in TWIST2 cause Setleis syndrome. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesAsymptomatic child heterozygous for hemoglobin S and hemoglobin Pôrto Alegre. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesPrevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico. Carmen Lydia Cadilla0Hace 4 años 9 meses
BibliographiesNonsense mutations of the bHLH transcription factor TWIST2 found in Setleis Syndrome patients cause dysregulation of periostin. Carmen Lydia Cadilla0Hace 4 años 9 meses

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