about
Identification and analysis of conserved cis-regulatory regions of the MEIS1 geneMethylation alterations are not a major cause of PTTG1 misregulation.A method for detecting epistasis in genome-wide studies using case-control multi-locus association analysis.Genetic structure of the Spanish population.Dissecting the transcriptional regulatory properties of human chromosome 16 highly conserved non-coding regionsTransphyletic conservation of developmental regulatory state in animal evolution.Genotyping of common SIRPB1 copy number variant using Paralogue Ratio Test coupled to MALDI-MS quantification.Comparative genomics of the Hedgehog loci in chordates and the origins of Shh regulatory novelties.Exploitation of prokaryotic expression systems based on the salicylate-dependent control circuit encompassing nahR/P(sal)::xylS2 for biotechnological applications.Absence of substantial copy number differences in a pair of monozygotic twins discordant for features of autism spectrum disorder.Improvement of recombinant protein yield by a combination of transcriptional amplification and stabilization of gene expression.Differential metabolic profiles associated to movement behaviour of stream-resident brown trout (Salmo trutta).Pyrosequencing for SNP genotyping.Analysis of CXCL12 3'UTR G>A polymorphism in colorectal cancer.SIRPB1 copy-number polymorphism as candidate quantitative trait locus for impulsive-disinhibited personality.Spectrofluorimetric analysis of CCR5-delta 32 allele using real-time polymerase chain reaction: prevalence in southern Spanish HIV(+) patients and noninfected population.The rs2108622 polymorphism is related to the early risk of ischemic stroke in non-valvular atrial fibrillation subjects under oral anticoagulation.Genetic Association Studies in Host-Pathogen Interaction Analysis.Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage.Engineered Salmonella allows real-time heterologous gene expression monitoring within infected zebrafish embryos.Estrogen receptor alpha gene variants are associated with Alzheimer's disease.A common copy-number variant within SIRPB1 correlates with human Out-of-Africa migration after genetic drift correction.Discordance in TLR2 (-196 to -174) polymorphism effect on HIV infection riskIdentification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novelSHOXenhancerDysmorphic contribution of neurotransmitter and neuroendocrine system polymorphisms to subtherapeutic mood statesFluorescence resonance energy transfer analysis of CCR-V64I and SDF1-3'a polymorphisms: prevalence in southern Spain hiv type 1+ cohort and noninfected populationBone morphogenetic protein 15 (BMP15) alleles predict over-response to recombinant follicle stimulation hormone and iatrogenic ovarian hyperstimulation syndrome (OHSS)Lack of association between NOS3 Glu298Asp and breast cancer risk: a case-control studyGenetic analysis of caveolin-1 and eNOS genes in colorectal cancerCAPN10 alleles modify laryngeal cancer risk in the Spanish populationAssociation of genetic markers within the KIT and KITLG genes with human male infertilityExploring allelic imbalance within paraffin-embedded tumor biopsies using pyrosequencing technologyIdentification of a protective haplogenotype within CAPN10 gene influencing colorectal cancer susceptibilityPyrosequencing protocol using a universal biotinylated primer for mutation detection and SNP genotypingAnalysis of the ERalpha germline PvuII marker in breast cancer riskIdentification of a 2244 base pair interstitial deletion within the human ESR1 gene in the Spanish populationAbsence of allelic imbalance involving EMSY, CAPN5, and PAK1 genes in papillary thyroid carcinomaPyrosequencing protocol requiring a unique biotinylated primerGenetic analysis of CAV1 gene in hypertension and metabolic syndromeVariations in the promoter region of the glutaminase gene and the development of hepatic encephalopathy in patients with cirrhosis: a cohort study
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jose Luis Royo
@ast
Jose Luis Royo
@en
Jose Luis Royo
@es
Jose Luis Royo
@nl
type
label
Jose Luis Royo
@ast
Jose Luis Royo
@en
Jose Luis Royo
@es
Jose Luis Royo
@nl
altLabel
José Luis Royo
@en
prefLabel
Jose Luis Royo
@ast
Jose Luis Royo
@en
Jose Luis Royo
@es
Jose Luis Royo
@nl
P1053
H-6935-2012
P106
P21
P31
P4012
P496
0000-0003-2024-4363