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Jorge Amigo

Showing results (21-30 of 42) with videos related to

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BMC Genetics|September 1, 2011
The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genomeMaría Laura Catelli, Vanesa Alvarez-Iglesias, Alberto Gómez-Carballa, et al.
Journal of Psychiatric Research|May 7, 2015
Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibilityJosé Javier Suárez-Rama, Manuel Arrojo, Beatriz Sobrino, et al.
European Journal of Human Genetics : EJHG|March 24, 2022
Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disabilityAlejandro J Brea-Fernández, Miriam Álvarez-Barona, Jorge Amigo, et al.
Journal of Medical Genetics|April 19, 2014
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like diseaseEmilia Balboa-Beltran, María J Fernández-Seara, Alejandro Pérez-Muñuzuri, et al.
SLAS Discovery : Advancing Life Sciences R & D|January 25, 2018
tagFinder: A Novel Tag Analysis Methodology That Enables Detection of Molecules from DNA-Encoded Chemical LibrariesJorge Amigo, Ramón Rama-Garda, Xabier Bello, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 24, 2015
An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disordersJulio Rodriguez-Lopez, Noa Carrera, Manuel Arrojo, et al.
Molecular Diagnosis & Therapy|December 1, 2022
Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel SequencingAlejandro Blanco-Verea, Brais Piñeiro, Rocio Gil, et al.
International Journal of Legal Medicine|April 10, 2017
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissectionMarina Gago-Díaz, Eva Ramos-Luis, Silvia Zoppis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 22, 2014
Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic diseaseMarina Gago-Díaz, Alejandro Blanco-Verea, Gisela Teixidó-Turà, et al.
Scientific Reports|November 23, 2017
Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus DiseaseAntonio Salas, Jacobo Pardo-Seco, Miriam Cebey-López, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
BMC Genetics|September 1, 2011
The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genomeMaría Laura Catelli, Vanesa Alvarez-Iglesias, Alberto Gómez-Carballa, et al.
Journal of Psychiatric Research|May 7, 2015
Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibilityJosé Javier Suárez-Rama, Manuel Arrojo, Beatriz Sobrino, et al.
European Journal of Human Genetics : EJHG|March 24, 2022
Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disabilityAlejandro J Brea-Fernández, Miriam Álvarez-Barona, Jorge Amigo, et al.
Journal of Medical Genetics|April 19, 2014
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like diseaseEmilia Balboa-Beltran, María J Fernández-Seara, Alejandro Pérez-Muñuzuri, et al.
SLAS Discovery : Advancing Life Sciences R & D|January 25, 2018
tagFinder: A Novel Tag Analysis Methodology That Enables Detection of Molecules from DNA-Encoded Chemical LibrariesJorge Amigo, Ramón Rama-Garda, Xabier Bello, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 24, 2015
An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disordersJulio Rodriguez-Lopez, Noa Carrera, Manuel Arrojo, et al.
Molecular Diagnosis & Therapy|December 1, 2022
Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel SequencingAlejandro Blanco-Verea, Brais Piñeiro, Rocio Gil, et al.
International Journal of Legal Medicine|April 10, 2017
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissectionMarina Gago-Díaz, Eva Ramos-Luis, Silvia Zoppis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 22, 2014
Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic diseaseMarina Gago-Díaz, Alejandro Blanco-Verea, Gisela Teixidó-Turà, et al.
Scientific Reports|November 23, 2017
Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus DiseaseAntonio Salas, Jacobo Pardo-Seco, Miriam Cebey-López, et al.
Pageof 5