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Stacey Gabriel

Showing results (91-100 of 195) with videos related to

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Plos One|January 27, 2012
Genetic mapping and exome sequencing identify variants associated with five novel diseasesErik G Puffenberger, Robert N Jinks, Carrie Sougnez, et al.
Journal of the American College of Cardiology|April 8, 2017
ANGPTL3 Deficiency and Protection Against Coronary Artery DiseaseNathan O Stitziel, Amit V Khera, Xiao Wang, et al.
Cell|August 6, 2013
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorderNaiara Akizu, Vincent Cantagrel, Jana Schroth, et al.
Nature|October 16, 2015
Mutations driving CLL and their evolution in progression and relapseDan A Landau, Eugen Tausch, Amaro N Taylor-Weiner, et al.
Nature Genetics|July 15, 2009
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of FallotSteven C Greenway, Alexandre C Pereira, Jennifer C Lin, et al.
Cancer Cell|April 20, 2005
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosisRoss L Levine, Martha Wadleigh, Jan Cools, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Cancer Discovery|May 19, 2017
Exome Sequencing of African-American Prostate Cancer Reveals Loss-of-Function <i>ERF</i> MutationsFranklin W Huang, Juan Miguel Mosquera, Andrea Garofalo, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Cell|June 19, 2018
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome SequencingSrinivas R Viswanathan, Gavin Ha, Andreas M Hoff, et al.
Pageof 20

Showing results (91-100 of 195) with videos related to

Sort By:
Pageof 20
Plos One|January 27, 2012
Genetic mapping and exome sequencing identify variants associated with five novel diseasesErik G Puffenberger, Robert N Jinks, Carrie Sougnez, et al.
Journal of the American College of Cardiology|April 8, 2017
ANGPTL3 Deficiency and Protection Against Coronary Artery DiseaseNathan O Stitziel, Amit V Khera, Xiao Wang, et al.
Cell|August 6, 2013
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorderNaiara Akizu, Vincent Cantagrel, Jana Schroth, et al.
Nature|October 16, 2015
Mutations driving CLL and their evolution in progression and relapseDan A Landau, Eugen Tausch, Amaro N Taylor-Weiner, et al.
Nature Genetics|July 15, 2009
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of FallotSteven C Greenway, Alexandre C Pereira, Jennifer C Lin, et al.
Cancer Cell|April 20, 2005
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosisRoss L Levine, Martha Wadleigh, Jan Cools, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Cancer Discovery|May 19, 2017
Exome Sequencing of African-American Prostate Cancer Reveals Loss-of-Function <i>ERF</i> MutationsFranklin W Huang, Juan Miguel Mosquera, Andrea Garofalo, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Cell|June 19, 2018
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome SequencingSrinivas R Viswanathan, Gavin Ha, Andreas M Hoff, et al.
Pageof 20