Marta Díaz

发表

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.

V. Álvarez, E. Coto, María Martín, 2012, The Journal of molecular diagnostics : JMD.

Influence of endothelial nitric oxide synthase polymorphisms in psoriasis risk

V. Álvarez, E. Coto, P. Coto-Segura, 2011, Archives of Dermatological Research.

SNP rs11652075 in the CARD14 gene as a risk factor for psoriasis (PSORS2) in a Spanish cohort.

E. Coto, P. Coto-Segura, J. Santos-Juanes, 2013, DNA and cell biology.

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia

V. Álvarez, E. Coto, J. Rosell, 2010, BMC neurology.

Mutational spectrum of the SPG 4 ( SPAST ) and SPG 3 A ( ATL 1 ) genes in Spanish patients with hereditary spastic paraplegia

V. Álvarez, E. Coto, J. Rosell, 2010 .

FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients

V. Álvarez, E. Coto, B. Alonso, 2010, Neuroscience Letters.

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer’s Disease

V. Álvarez, E. Coto, C. Martínez, 2011, Journal of Molecular Neuroscience.

Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease

V. Álvarez, E. Coto, P. Pástor, 2013, Journal of Molecular Neuroscience.

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease

V. Álvarez, E. Coto, P. Pástor, 2012, Journal of Molecular Neuroscience.

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease

V. Álvarez, E. Coto, C. Martínez, 2011, Brain Research.

Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy.

V. Álvarez, E. Coto, A. Ortiz, 2010, Biochemical and biophysical research communications.

Functional polymorphisms in the CYP 3 A 4 , CYP 3 A 5 , and CYP 21 A 2 genes in the risk for hypertension in pregnancy

V. Álvarez, E. Coto, A. Ortiz, 2010 .

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia

V. Álvarez, E. Coto, J. Infante, 2012, Journal of Neurology.

Mutation analysis of the LCE3B/LCE3C genes in Psoriasis

V. Álvarez, E. Coto, P. Coto-Segura, 2010, BMC Medical Genetics.

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

V. Álvarez, E. Coto, C. Martínez, 2011, neurogenetics.