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Cytokine|June 29, 2012
Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypesNoemí Eiris, Jorge Santos-Juanes, Pablo Coto-Segura, et al.
Neuroscience Letters|May 18, 2010
FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patientsLorena de Mena, Lucía F Cardo, Eliecer Coto, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's diseaseLorena de Mena, Eliecer Coto, Lucía F Cardo, et al.
Neuroscience Letters|February 6, 2008
Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's diseaseVictoria Alvarez, Ana I Corao, Elena Sánchez-Ferrero, et al.
Journal of Molecular Neuroscience : MN|November 15, 2011
A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's diseaseLucía F Cardo, Eliecer Coto, Lorena de Mena, et al.
Journal of Translational Medicine|July 3, 2010
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifierEliecer Coto, María Palacín, María Martín, et al.
The Journal of Molecular Diagnostics : JMD|July 7, 2012
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathyEliecer Coto, Julián R Reguero, María Palacín, et al.
Journal of Neurology|July 5, 2011
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegiaElena Sánchez-Ferrero, Eliecer Coto, Ana I Corao, et al.
Journal of Molecular Neuroscience : MN|January 1, 2013
Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's diseaseLorena de Mena, L Luís Samaranch, Eliecer Coto, et al.
Mitochondrion|September 25, 2010
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup HMaría Palacín, Victoria Alvarez, María Martín, et al.
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