C. Méndez-Vidal

发表

267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation

Josephine T. Daub, J. P. Florido, Javier Santoyo-Lopez, 2016, Molecular biology and evolution.

Transcription Factors

Wirth, Ogihara, Maurel, 2004, Handbook of Experimental Pharmacology.

Identification of functional p53‐binding motifs in the mouse wig‐1 promoter

C. Méndez-Vidal, K. Wiman, M. Wilhelm, 2002, FEBS letters.

Human wig-1, a p53 target gene that encodes a growth inhibitory zinc finger protein

C. Méndez-Vidal, K. Wiman, M. Kost-Alimova, 2001, Oncogene.

Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2020, Journal of Translational Medicine.

A Multi-Strategy Sequencing Workflow in Inherited Retinal Dystrophies: Routine Diagnosis, Addressing Unsolved Cases and Candidate Genes Identification

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2020, International journal of molecular sciences.

Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies

J. Dopazo, Alicia Vela-Boza, C. Méndez-Vidal, 2014, PloS one.

Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panel

J. Dopazo, C. Méndez-Vidal, S. Borrego, 2016, Scientific Reports.

Novel RP1 mutations and a recurrent BBS1 variant explain the co-existence of two distinct retinal phenotypes in the same pedigree

J. Dopazo, Alicia Vela-Boza, C. Méndez-Vidal, 2014, BMC Genetics.

Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet–Biedl family

Javier Santoyo-Lopez, J. Dopazo, Alicia Vela-Boza, 2013, Molecular genetics & genomic medicine.

PTTG2 silencing results in induction of epithelial-to-mesenchymal transition and apoptosis

C. Méndez-Vidal, M. Moreno-Mateos, José Antonio Pintor-Toro, 2013, Cell Death and Disease.

Re‐evaluation casts doubt on the pathogenicity of homozygous USH2A p.C759F

J. Dopazo, J. Millán, C. Méndez-Vidal, 2015, American journal of medical genetics. Part A.

Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2020, Journal of Translational Medicine.

Reversal of P-glycoprotein-mediated multidrug resistance in vitro by AV200, a new ardeemin derivative.

C. Méndez-Vidal, A. R. Quesada, 1998, Cancer letters.

A map of human microRNA variation uncovers unexpectedly high levels of variability

Joaquín Dopazo, Ignacio Medina, Eva Alloza, 2012, Genome Medicine.

Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2018, Scientific Reports.

The p53 Transcription Factor as Therapeutic Target in Cancer

C. Méndez-Vidal, K. Wiman, G. Selivanova, 2004 .

Wrap53, a Natural p53 Antisense Transcript Required for p53 Induction upon DNA Damage.

C. Méndez-Vidal, K. Wiman, S. Mahmoudi, 2016, Molecular cell.

Wrap53, a natural p53 antisense transcript required for p53 induction upon DNA damage.

C. Méndez-Vidal, K. Wiman, S. Mahmoudi, 2009, Molecular cell.

Novel small RNA expression libraries uncover hsa-miR-30b and hsa-miR-30c as important factors in anoikis resistance

H. Allgayer, Eugene Berezikov, C. Méndez-Vidal, 2013, RNA.

A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2022, npj Genomic Medicine.

A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2022, NPJ genomic medicine.

Unravelling the genetic basis of simplex Retinitis Pigmentosa cases

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2017, Scientific Reports.

Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa

Francisco J. López-Domingo, Joaquin Dopazo, Salud Borrego, 2013, Molecular vision.

A map of human microRNA variation uncovers unexpectedly high levels of variability

J. Dopazo, I. Medina, J. Jimenez-Almazan, 2012, Genome Medicine.

Induction of Dlk1 by PTTG1 inhibits adipocyte differentiation and correlates with malignant transformation.

C. Méndez-Vidal, M. Moreno-Mateos, José Antonio Pintor-Toro, 2009, Molecular biology of the cell.

Proliferative potential after DNA damage and non-homologous end joining are affected by loss of securin

C. Méndez-Vidal, J. A. Bernal, José Antonio Pintor-Toro, 2007, Cell Death and Differentiation.

The p53-induced mouse zinc finger protein wig-1 binds double-stranded RNA with high affinity.

C. Méndez-Vidal, K. Wiman, M. Wilhelm, 2002, Nucleic acids research.

Wig-1, a p53-Induced Zinc Finger Protein that Binds Double Stranded RNA

C. Méndez-Vidal, K. Wiman, M. Wilhelm, 2005 .

MDR Reversal by Deprenylated Tetracyclic and Hexacyclic Analogues of N-Acetylardeemin: Confirmation of the Ardeemin Pharmacophore

C. Méndez-Vidal, C. Avendaño, J. Menéndez, 2006 .

Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2013, PloS one.

Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2023, Frontiers in cell and developmental biology.

Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2018, Scientific Reports.

Long-read sequencing improves the genetic diagnosis of retinitis pigmentosa by identifying an Alu retrotransposon insertion in the EYS gene

C. Méndez-Vidal, S. Borrego, G. Antiñolo, 2024, Mobile DNA.