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Michael E Talkowski

Showing results (51-60 of 184) with videos related to

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Human Molecular Genetics|January 14, 2016
Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis†Kusumika Mukherjee, Kana Ishii, Vamsee Pillalamarri, et al.
Molecular Psychiatry|May 26, 2025
Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative deliriumOccam Kelly Graves, Jiayi Kang, Haobo Li, et al.
American Journal of Human Genetics|June 7, 2014
Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism familiesIan Blumenthal, Ashok Ragavendran, Serkan Erdin, et al.
Nature Neuroscience|February 2, 2016
Engineering microdeletions and microduplications by targeting segmental duplications with CRISPRDerek J C Tai, Ashok Ragavendran, Poornima Manavalan, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
Medicine|February 1, 2018
Pain correlates with germline mutation in schwannomatosisJustin T Jordan, Miriam J Smith, James A Walker, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
American Journal of Human Genetics|June 23, 2015
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationHarrison Brand, Ryan L Collins, Carrie Hanscom, et al.
Elife|September 29, 2020
Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease miceMarina Kovalenko, Serkan Erdin, Marissa A Andrew, et al.
The New England Journal of Medicine|December 11, 2012
Clinical diagnosis by whole-genome sequencing of a prenatal sampleMichael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, et al.
Pageof 19

Showing results (51-60 of 184) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|January 14, 2016
Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis†Kusumika Mukherjee, Kana Ishii, Vamsee Pillalamarri, et al.
Molecular Psychiatry|May 26, 2025
Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative deliriumOccam Kelly Graves, Jiayi Kang, Haobo Li, et al.
American Journal of Human Genetics|June 7, 2014
Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism familiesIan Blumenthal, Ashok Ragavendran, Serkan Erdin, et al.
Nature Neuroscience|February 2, 2016
Engineering microdeletions and microduplications by targeting segmental duplications with CRISPRDerek J C Tai, Ashok Ragavendran, Poornima Manavalan, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
Medicine|February 1, 2018
Pain correlates with germline mutation in schwannomatosisJustin T Jordan, Miriam J Smith, James A Walker, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
American Journal of Human Genetics|June 23, 2015
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationHarrison Brand, Ryan L Collins, Carrie Hanscom, et al.
Elife|September 29, 2020
Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease miceMarina Kovalenko, Serkan Erdin, Marissa A Andrew, et al.
The New England Journal of Medicine|December 11, 2012
Clinical diagnosis by whole-genome sequencing of a prenatal sampleMichael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, et al.
Pageof 19