J. Vidal-Taboada

发表

Down syndrome critical region gene 2: expression during mouse development and in human cell lines indicates a function related to cell proliferation.

G. Pons, R. Oliva, R Oliva, 2000, Biochemical and biophysical research communications.

Human Proteinpedia enables sharing of human protein data

Y. L. Ramachandra, Christine A. Miller, J. Bader, 2008, Nature Biotechnology.

Polymorphisms, haplotypes and mutations in the protamine 1 and 2 genes.

A. Giwercman, M. Jodar, J. Castillo, 2011, International journal of andrology.

Marked correlations in protein expression identified by proteomic analysis of human spermatozoa

S. de Mateo, J. Ballescà, R. Oliva, 2007, Proteomics.

RNA-Seq transcriptomic profiling of primary murine microglia treated with LPS or LPS + IFNγ

J. Saura, C. Solà, Marta Pulido-Salgado, 2018, Scientific Reports.

C/EBPβ and C/EBPδ transcription factors: Basic biology and roles in the CNS

J. Saura, Marta Pulido-Salgado, J. Vidal-Taboada, 2015, Progress in neurobiology.

Detection of a new variant of the mitochondrial glycerol-3-phosphate dehydrogenase gene in Spanish type 2 DM patients.

R. Gomis, P. Cristóbal, R. Oliva, 1999, Biochemical and biophysical research communications.

HLA-DQB1*05:02, *05:03, and *03:01 alleles as risk factors for myasthenia gravis in a Spanish cohort

J. Gámez, J. Vidal-Taboada, F. Rudilla, 2022, Neurological Sciences.

Comparisons of CCAAT / enhancer binding proteins β and δ : basic biology and roles in the CNS

J. Saura, J. Vidal-Taboada, M. Pulido-Salgado, 2015 .

5′-upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration

Carlos Cruchaga, P. Pástor, M. Ezquerra, 2009, Neurobiology of Disease.

13 Microglia , Calcification and Neurodegenerative Diseases

N. Mahy, J. Vidal-Taboada, M. J. Rodríguez, 2012 .

SPG11 compound mutations in spastic paraparesis with thin corpus callosum

J. Masdeu, M. Riverol, P. Pástor, 2008, Neurology.

Simultaneous genotyping of CYP2C9*2, *3, and 5′ flanking region (C-1189T) polymorphisms in a Spanish population through a new minisequencing multiplex single-base extension analysis

R. Molina, S. Mas, A. Lafuente, 2005, European Journal of Clinical Pharmacology.

Molecular Mechanisms of Acute Brain Injury and Ensuing Neurodegeneration

N. Mahy, J. Vidal-Taboada, F. Ortega, 2012 .

Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammals.

R. Oliva, J. Vidal-Taboada, C. Rebordosa, 1998, Biochemical and biophysical research communications.

Identification of proteomic differences in asthenozoospermic sperm samples.

S. de Mateo, J. Ballescà, R. Oliva, 2008, Human reproduction.

Identification and characterization of a new gene from human chromosome 21 between markers D21S343 and D21S268 encoding a leucine-rich protein.

P. Scartezzini, R. Oliva, J. Vidal-Taboada, 1998, Biochemical and biophysical research communications.

Evolution of the vertebrate H1 histone class: evidence for the functional differentiation of the subtypes.

J. Vidal-Taboada, I. Ponte, P. Suau, 1998, Molecular biology and evolution.

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy

E. Tolosa, F. Valldeoriola, C. Cruchaga, 2011, Neurobiology of Aging.

Genetic variation in APOE cluster region and Alzheimer's disease risk

O. Combarros, M. Bullido, J. Clarimón, 2011, Neurobiology of Aging.

DNA cards: determinants of DNA yield and quality in collecting genetic samples for pharmacogenetic studies.

S. Mas, A. Lafuente, P. Gassó, 2007, Basic & clinical pharmacology & toxicology.

Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer’s Disease

E. Gelpí, À. López-López, J. Vidal-Taboada, 2018, Molecular Neurobiology.

Two novel ligand-independent variants of the VEGFR-1 receptor are expressed in human testis and spermatozoa, one of them with the ability to activate SRC proto-oncogene tyrosine kinases

J. Ballescà, R. Oliva, M. Edel, 2019, Oncotarget.

Astroglia-Microglia Cross Talk during Neurodegeneration in the Rat Hippocampus

M. Pugliese, N. Mahy, J. Vidal-Taboada, 2015, BioMed research international.

Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.

P. Arrigo, S. Giglio, P. Scartezzini, 1998, Biochemical and biophysical research communications.

High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2.

E. Fisher, D. Nižetić, N. Katsanis, 1998, Biochemical and biophysical research communications.

CX3CR1 Is a Modifying Gene of Survival and Progression in Amyotrophic Lateral Sclerosis

À. López-López, N. Mahy, J. Gámez, 2014, PloS one.

CX 3 CR 1 Is a Modifying Gene of Survival and Progression in Amyotrophic Lateral Sclerosis

À. López-López, N. Mahy, J. Gámez, 2014 .

Satisfaction survey with DNA cards method to collect genetic samples for pharmacogenetics studies

A. Lafuente, J. Vidal-Taboada, A. Cobos, 2006, BMC Medical Genetics.

Myeloid C/EBPβ deficiency reshapes microglial gene expression and is protective in experimental autoimmune encephalomyelitis

A. Valledor, J. Serratosa, J. Saura, 2017, Journal of Neuroinflammation.

RNA-Seq transcriptomic profiling of primary murine microglia treated with LPS or LPS + IFNγ

J. Saura, C. Solà, J. Vidal-Taboada, 2018, Scientific Reports.

KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis

M. Pugliese, N. Mahy, J. Gámez, 2018, Molecular Neurobiology.

CHANNEL EXPRESSION AND GENETIC POLYMORPHISMS ASSOCIATED WITH PROGRESSION AND SURVIVAL IN AMYOTROPHIC LATERAL SCLEROSIS

M. Pugliese, J. Gámez, J. Vidal-Taboada, 2018 .

UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort

À. López-López, N. Mahy, J. Gámez, 2015, Journal of Neurology.

Haplotype Analysis of the First A4V-SOD1 Spanish Family: Two Separate Founders or a Single Common Founder?

J. Gámez, J. Vidal-Taboada, M. Morales, 2019, Front. Genet..

Marked correlations in protein expression identified by proteomic analysis of human spermatozoa

S. de Mateo, J. Ballescà, R. Oliva, 2022 .

KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis

M. Pugliese, N. Mahy, J. Gámez, 2018, Molecular Neurobiology.

Microglia, Calcification and Neurodegenerative Diseases

N. Mahy, J. Vidal-Taboada, M. J. Rodríguez, 2011 .

A common protamine 1 promoter polymorphism (-190 C->A) correlates with abnormal sperm morphology and increased protamine P1/P2 ratio in infertile patients.

S. de Mateo, J. Ballescà, R. Oliva, 2008, Journal of andrology.

HLA-DQB1*05:02, *05:03, and *03:01 alleles as risk factors for myasthenia gravis in a Spanish cohort

J. Gámez, J. Vidal-Taboada, F. Rudilla, 2022, Neurological Sciences.

High-resolution physical map and identification of potentially regulatory sequences of the human SH3BGR located in the Down syndrome chromosomal region.

D. Nižetić, P. Scartezzini, R. Oliva, 1997, Biochemical and biophysical research communications.