Yolanda Espinosa-Parrilla
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MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function
E Miñones-Moyano, S Porta, G Escaramís, R Rabionet, S Iraola, ...
Human molecular genetics 20 (15), 3067-3078, 2011
Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 are associated with panic disorder and regulate several anxiety candidate genes and related pathways
M Muiños-Gimeno, Y Espinosa-Parrilla, M Guidi, B Kagerbauer, T Sipilä, ...
Biological psychiatry 69 (6), 526-533, 2011
Protein S deficiency: a database of mutations--summary of the first update.
S Gandrille, D Borgel, N Sala, Y Espinosa-Parrilla, R Simmonds, ...
Thrombosis and haemostasis 84 (5), 918, 2000
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures
J Amiel, Y Espinosa-Parrilla, J Steffann, P Gosset, A Pelet, M Prieur, ...
The American Journal of Human Genetics 69 (6), 1370-1377, 2001
Allele variants in functional MicroRNA target sites of the neurotrophin‐3 receptor gene (NTRK3) as susceptibility factors for anxiety disorders
M Muiños‐Gimeno, M Guidi, B Kagerbauer, R Martín‐Santos, R Navinés, ...
Human mutation 30 (7), 1062-1071, 2009
Overexpression of miR-128 specifically inhibits the truncated isoform of NTRK3 and upregulates BCL2 in SH-SY5Y neuroblastoma cells
M Guidi, M Muiños-Gimeno, B Kagerbauer, E Martí, X Estivill, ...
BMC molecular biology 11 (1), 95, 2010
Mutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locus
LÏ de Pontual, A Pelet, D Trochet, F Jaubert, Y Espinosa-Parrilla, ...
Journal of medical genetics 43 (5), 419-423, 2006
Genetic association of gastric cancer with miRNA clusters including the cancer‐related genes MIR29, MIR25, MIR93 and MIR106: Results from the EPIC …
Y Espinosa‐Parrilla, X Muñoz, C Bonet, N Garcia, A Venceslá, ...
International journal of cancer 135 (9), 2065-2076, 2014
Expression of the SMADIP1 gene during early human development
Y Espinosa-Parrilla, J Amiel, J Augé, F Encha-Razavi, A Munnich, ...
Mechanisms of development 114 (1-2), 187-191, 2002
Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease
M Muiños-Gimeno, M Montfort, M Bayés, X Estivill, Y Espinosa-Parrilla
European Journal of Human Genetics 18 (2), 218, 2010
Protein S secretion differences of missense mutants account for phenotypic heterogeneity
Y Espinosa-Parrilla, T Yamazaki, N Sala, B Dahlbäck, PG de Frutos
Blood 95 (1), 173-179, 2000
Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency
Y Espinosa‐Parrilla, M Morell, JC Souto, I Tirado, J Fontcuberta, X Estivill, ...
Human mutation 14 (1), 30-39, 1999
Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen allele
Y Espinosa-Parrilla, M Morell, JC Souto, M Borrell, D Heine-Suñer, ...
Blood 89 (8), 2799-2806, 1997
An ancestral miR-1304 allele present in Neanderthals regulates genes involved in enamel formation and could explain dental differences with modern humans
M Lopez-Valenzuela, O Ramírez, A Rosas, S García-Vargas, ...
Molecular biology and evolution 29 (7), 1797-1806, 2012
Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Protein S deficiency: a …
S Gandrille, D Borgel, N Sala, Y Espinosa-Parrilla, R Simmonds, ...
Thromb Haemost 84 (5), 918, 2000
Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors
Y Espinosa-Parrilla, G Navarro, M Morell, E Abella, X Estivill, N Sala
Thrombosis and haemostasis 83 (01), 102-106, 2000
Optimization of a simple and rapid single‐strand conformation analysis for detection of mutations in the PROS1 gene: Identification of seven novel mutations and …
Y Espinosa‐Parrilla, M Morell, M Borrell, JC Souto, J Fontcuberta, ...
Human mutation 15 (5), 463-473, 2000
Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome)
L Sztriha, Y Espinosa-Parrilla, A Gururaj, J Amiel, S Lyonnet, S Gerami, ...
Neuropediatrics 34 (06), 322-325, 2003
Molecular screening of the ZFHX1B gene in prenatally diagnosed isolated agenesis of the corpus callosum
Y Espinosa‐Parrilla, F Encha‐Razavi, T Attié‐Bitach, J Martinovic, ...
Prenatal diagnosis 24 (4), 298-301, 2004
Differences in molecular evolutionary rates among microRNAs in the human and chimpanzee genomes
G Santpere, M Lopez-Valenzuela, N Petit-Marty, A Navarro, ...
BMC genomics 17 (1), 528, 2016
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