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Jay Shendure

Showing results (321-330 of 437) with videos related to

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Blood|December 4, 2023
Transcriptional control of leukemogenesis by the chromatin reader SGF29Karina Barbosa, Anagha Deshpande, Marlenne Perales, et al.
Human Mutation|August 13, 2015
Expanding the Molecular and Clinical Phenotype of SSR4-CDGBobby G Ng, Kimiyo Raymond, Martin Kircher, et al.
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
Science Advances|October 7, 2022
Oncogenic role of a developmentally regulated <i>NTRK2</i> splice variantSiobhan S Pattwell, Sonali Arora, Nicholas Nuechterlein, et al.
Nature Reviews. Methods Primers|May 22, 2023
High-content CRISPR screeningChristoph Bock, Paul Datlinger, Florence Chardon, et al.
American Journal of Human Genetics|April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylationBobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.
Genome Research|June 27, 2013
The million mutation project: a new approach to genetics in Caenorhabditis elegansOwen Thompson, Mark Edgley, Pnina Strasbourger, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
Science (New York, N.Y.)|April 2, 2016
Long-read sequence assembly of the gorilla genomeDavid Gordon, John Huddleston, Mark J P Chaisson, et al.
Molecular Systems Biology|May 8, 2023
Predicting cellular responses to complex perturbations in high-throughput screensMohammad Lotfollahi, Anna Klimovskaia Susmelj, Carlo De Donno, et al.
Pageof 44

Showing results (321-330 of 437) with videos related to

Sort By:
Pageof 44
Blood|December 4, 2023
Transcriptional control of leukemogenesis by the chromatin reader SGF29Karina Barbosa, Anagha Deshpande, Marlenne Perales, et al.
Human Mutation|August 13, 2015
Expanding the Molecular and Clinical Phenotype of SSR4-CDGBobby G Ng, Kimiyo Raymond, Martin Kircher, et al.
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
Science Advances|October 7, 2022
Oncogenic role of a developmentally regulated <i>NTRK2</i> splice variantSiobhan S Pattwell, Sonali Arora, Nicholas Nuechterlein, et al.
Nature Reviews. Methods Primers|May 22, 2023
High-content CRISPR screeningChristoph Bock, Paul Datlinger, Florence Chardon, et al.
American Journal of Human Genetics|April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylationBobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.
Genome Research|June 27, 2013
The million mutation project: a new approach to genetics in Caenorhabditis elegansOwen Thompson, Mark Edgley, Pnina Strasbourger, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
Science (New York, N.Y.)|April 2, 2016
Long-read sequence assembly of the gorilla genomeDavid Gordon, John Huddleston, Mark J P Chaisson, et al.
Molecular Systems Biology|May 8, 2023
Predicting cellular responses to complex perturbations in high-throughput screensMohammad Lotfollahi, Anna Klimovskaia Susmelj, Carlo De Donno, et al.
Pageof 44