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Ana Vega

Showing results (61-70 of 214) with videos related to

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Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|August 7, 2008
Effects of air pollution on cup a 3 allergen in Cupressus arizonica pollen grainsMaria Suárez-Cervera, Teresa Castells, Ana Vega-Maray, et al.
Cancer Management and Research|February 20, 2016
EGFR testing and clinical management of advanced NSCLC: a Galician Lung Cancer Group study (GGCP 048-10)Sergio Vázquez, Joaquín Casal, Francisco Javier Afonso Afonso, et al.
Plos One|February 19, 2020
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutationUxia Esperón-Moldes, Manuel Ginarte-Val, Laura Rodríguez-Pazos, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2014
No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish populationLaura Fachal, Ana Mosquera-Miguel, Pau Pastor, et al.
British Journal of Haematology|June 18, 2010
Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia riskDalemari Crowther-Swanepoel, Mahmoud Mansouri, Anna Enjuanes, et al.
European Journal of Human Genetics : EJHG|December 6, 2012
Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer familiesGorka Ruiz de Garibay, Avellaneda Díaz, Belén Gaviña, et al.
Molecular Genetics & Genomic Medicine|March 28, 2019
A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlationsMartha Montalván-Suárez, Uxia Saraiva Esperón-Moldes, Laura Rodríguez-Pazos, et al.
Clinical Epigenetics|March 6, 2025
Epigenome-wide analysis reveals potential biomarkers for radiation-induced toxicity risk in prostate cancerCarlos Lopez-Pleguezuelos, Miguel E Aguado-Barrera, Ana Carballo-Castro, et al.
Journal of Medical Genetics|April 12, 2012
Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic casesBeatriz Martinez-Delgado, Kira Yanowsky, Lucia Inglada-Perez, et al.
Human Mutation|July 30, 2013
Evaluation of a 5-tier scheme proposed for classification of sequence variants using bioinformatic and splicing assay data: inter-reviewer variability and promotion of minimum reporting guidelinesLogan C Walker, Phillip J Whiley, Claude Houdayer, et al.
Pageof 22

Showing results (61-70 of 214) with videos related to

Sort By:
Pageof 22
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|August 7, 2008
Effects of air pollution on cup a 3 allergen in Cupressus arizonica pollen grainsMaria Suárez-Cervera, Teresa Castells, Ana Vega-Maray, et al.
Cancer Management and Research|February 20, 2016
EGFR testing and clinical management of advanced NSCLC: a Galician Lung Cancer Group study (GGCP 048-10)Sergio Vázquez, Joaquín Casal, Francisco Javier Afonso Afonso, et al.
Plos One|February 19, 2020
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutationUxia Esperón-Moldes, Manuel Ginarte-Val, Laura Rodríguez-Pazos, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2014
No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish populationLaura Fachal, Ana Mosquera-Miguel, Pau Pastor, et al.
British Journal of Haematology|June 18, 2010
Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia riskDalemari Crowther-Swanepoel, Mahmoud Mansouri, Anna Enjuanes, et al.
European Journal of Human Genetics : EJHG|December 6, 2012
Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer familiesGorka Ruiz de Garibay, Avellaneda Díaz, Belén Gaviña, et al.
Molecular Genetics & Genomic Medicine|March 28, 2019
A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlationsMartha Montalván-Suárez, Uxia Saraiva Esperón-Moldes, Laura Rodríguez-Pazos, et al.
Clinical Epigenetics|March 6, 2025
Epigenome-wide analysis reveals potential biomarkers for radiation-induced toxicity risk in prostate cancerCarlos Lopez-Pleguezuelos, Miguel E Aguado-Barrera, Ana Carballo-Castro, et al.
Journal of Medical Genetics|April 12, 2012
Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic casesBeatriz Martinez-Delgado, Kira Yanowsky, Lucia Inglada-Perez, et al.
Human Mutation|July 30, 2013
Evaluation of a 5-tier scheme proposed for classification of sequence variants using bioinformatic and splicing assay data: inter-reviewer variability and promotion of minimum reporting guidelinesLogan C Walker, Phillip J Whiley, Claude Houdayer, et al.
Pageof 22