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The Journal of Gene Medicine
|
April 5, 2002
Intratumoral activation of cyclophosphamide by retroviral transfer of the cytochrome P450 2B1 in a pancreatic tumor model. Combination with the HSVtk/GCV system
Meritxell Carrió, Joana Visa, Anna Cascante, et al.
Molecular Biology and Evolution
|
August 5, 2009
Positive selection and gene conversion drive the evolution of a brain-expressed snoRNAs cluster
Miroslava Ogorelkova, Arcadi Navarro, Francesca Vivarelli, et al.
Gene
|
July 8, 2008
Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds
Nina Bosch, Geòrgia Escaramís, Josep M Mercader, et al.
European Journal of Human Genetics : EJHG
|
October 8, 2009
Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease
Margarita Muiños-Gimeno, Magda Montfort, Mònica Bayés, et al.
Briefings in Bioinformatics
|
September 9, 2021
Genome sequencing data analysis for rare disease gene discovery
Umm-Kulthum Ismail Umlai, Dhinoth Kumar Bangarusamy, Xavier Estivill, et al.
Journal of Human Genetics
|
October 21, 2003
Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome
Nuria Andreu, Carmen Carreras, Félix Prieto, et al.
Human Molecular Genetics
|
August 14, 2003
Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements
Lluis Armengol, Miguel Angel Pujana, Joseph Cheung, et al.
British Journal of Sports Medicine
|
March 4, 2018
Geolocalisation of athletes for out-of-competition drug testing: ethical considerations. Position statement by the WADA Ethics Panel
Pascal Borry, Timothy Caulfield, Xavier Estivill, et al.
Human Genetics
|
August 22, 2002
Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression
Eva Thönnissen, Raquel Rabionet, Maria Lourdes Arbonès, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2002
Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons
Miguel Angel Pujana, Marga Nadal, Miriam Guitart, et al.
Page
of 24
Search research articles
Search
Showing results (21-30 of 239) with videos related to
Sort By:
Page
of 24
The Journal of Gene Medicine
|
April 5, 2002
Intratumoral activation of cyclophosphamide by retroviral transfer of the cytochrome P450 2B1 in a pancreatic tumor model. Combination with the HSVtk/GCV system
Meritxell Carrió, Joana Visa, Anna Cascante, et al.
Molecular Biology and Evolution
|
August 5, 2009
Positive selection and gene conversion drive the evolution of a brain-expressed snoRNAs cluster
Miroslava Ogorelkova, Arcadi Navarro, Francesca Vivarelli, et al.
Gene
|
July 8, 2008
Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds
Nina Bosch, Geòrgia Escaramís, Josep M Mercader, et al.
European Journal of Human Genetics : EJHG
|
October 8, 2009
Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease
Margarita Muiños-Gimeno, Magda Montfort, Mònica Bayés, et al.
Briefings in Bioinformatics
|
September 9, 2021
Genome sequencing data analysis for rare disease gene discovery
Umm-Kulthum Ismail Umlai, Dhinoth Kumar Bangarusamy, Xavier Estivill, et al.
Journal of Human Genetics
|
October 21, 2003
Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome
Nuria Andreu, Carmen Carreras, Félix Prieto, et al.
Human Molecular Genetics
|
August 14, 2003
Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements
Lluis Armengol, Miguel Angel Pujana, Joseph Cheung, et al.
British Journal of Sports Medicine
|
March 4, 2018
Geolocalisation of athletes for out-of-competition drug testing: ethical considerations. Position statement by the WADA Ethics Panel
Pascal Borry, Timothy Caulfield, Xavier Estivill, et al.
Human Genetics
|
August 22, 2002
Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression
Eva Thönnissen, Raquel Rabionet, Maria Lourdes Arbonès, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2002
Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons
Miguel Angel Pujana, Marga Nadal, Miriam Guitart, et al.
Page
of 24