Archivos de Categoría: Publicaciones
RNA Sequencing Analysis and Atrial Natriuretic Peptide Production in Patients with Dilated and Ischemic Cardiomyopathy
RNA Sequencing Analysis and Atrial Natriuretic Peptide Production in Patients with Dilated and Ischemic Cardiomyopathy [...]
Mar
Correlation between aneuploidy, apoptotic markers and DNA fragmentation in spermatozoa from normozoospermic patients
Correlation between aneuploidy, apoptotic markers and DNA fragmentation in spermatozoa from normozoospermic patients Descargar PDF
Feb
Next Generation Diagnostics in Inherited Arrhythmia Syndromes. A Comparison of Two Approaches
Next Generation Diagnostics in Inherited Arrhythmia Syndromes. A Comparison of Two Approaches Descargar PDF
Sep
Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics. Published online 4 April 2013 in Wiley Online Library (www.wiley.com/humanmutation). DOI: 10.1002/humu.22332
Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics. Published online 4 April 2013 [...]
Jul
Study of the Cytoskeleton of the Cardiomyocyte in Patients With Heart Failure Using RNA-Seq
Study of the Cytoskeleton of the Cardiomyocyte in Patients With Heart Failure Using RNA-Seq Descargar [...]
May
Differential Gene Expression of Cardiac Ion Channels in Human Dilated Cardiomyopathy
Differential Gene Expression of Cardiac Ion Channels in Human Dilated Cardiomyopathy Descargar PDF
May
Estudio de los cambios en el citoesqueleto del cardiomiocito de los pacientes con insuficiencia cardiaca mediante la utilización de RNA-Seq. Sociedad Española de Cardilogía
Estudio de los cambios en el citoesqueleto del cardiomiocito de los pacientes con insuficiencia cardiaca [...]
May
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32 Descargar [...]
Abr
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia. The American Journal of Human Genetics, 25 April 2013, doi:10.1016/j.ajhg.2013.04.002.
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia. The American Journal of [...]
Abr
Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients. Hum Mol Genet. 2013 Feb 15;22(4):704-16.
Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type [...]
Feb