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Showing results (351-360 of 379) with videos related to

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JAMA Neurology|March 7, 2022
Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSarah U Morton, John Christodoulou, Gregory Costain, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
American Journal of Human Genetics|December 22, 2015
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited DisordersDaria Wojtal, Dwi U Kemaladewi, Zeenat Malam, et al.
Human Molecular Genetics|April 19, 2017
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eyeYaqun Zou, Sandra Donkervoort, Antti M Salo, et al.
American Journal of Public Health|May 20, 2016
From Design to Dissemination: Implementing Community-Based Participatory Research in Postdisaster CommunitiesMaureen Lichtveld, Suzanne Kennedy, Rebecca Z Krouse, et al.
Gynecologic Oncology|September 13, 2005
The efficacy of adjuvant platinum-based chemotherapy in Stage I uterine papillary serous carcinoma (UPSC)C S Dietrich, S C Modesitt, P D DePriest, et al.
CMAJ Open|October 13, 2021
SARS-CoV-2 antibodies in Ontario health care workers during and after the first wave of the pandemic: a cohort studyMichelle Science, Shelly Bolotin, Michael Silverman, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Arthritis and Rheumatism|January 13, 2012
Prevalence and sociodemographic correlates of antinuclear antibodies in the United StatesMinoru Satoh, Edward K L Chan, Lindsey A Ho, et al.
Science (New York, N.Y.)|April 8, 2006
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndromeJennifer P Habashi, Daniel P Judge, Tammy M Holm, et al.
Pageof 38

Showing results (351-360 of 379) with videos related to

Sort By:
Pageof 38
JAMA Neurology|March 7, 2022
Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSarah U Morton, John Christodoulou, Gregory Costain, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
American Journal of Human Genetics|December 22, 2015
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited DisordersDaria Wojtal, Dwi U Kemaladewi, Zeenat Malam, et al.
Human Molecular Genetics|April 19, 2017
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eyeYaqun Zou, Sandra Donkervoort, Antti M Salo, et al.
American Journal of Public Health|May 20, 2016
From Design to Dissemination: Implementing Community-Based Participatory Research in Postdisaster CommunitiesMaureen Lichtveld, Suzanne Kennedy, Rebecca Z Krouse, et al.
Gynecologic Oncology|September 13, 2005
The efficacy of adjuvant platinum-based chemotherapy in Stage I uterine papillary serous carcinoma (UPSC)C S Dietrich, S C Modesitt, P D DePriest, et al.
CMAJ Open|October 13, 2021
SARS-CoV-2 antibodies in Ontario health care workers during and after the first wave of the pandemic: a cohort studyMichelle Science, Shelly Bolotin, Michael Silverman, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Arthritis and Rheumatism|January 13, 2012
Prevalence and sociodemographic correlates of antinuclear antibodies in the United StatesMinoru Satoh, Edward K L Chan, Lindsey A Ho, et al.
Science (New York, N.Y.)|April 8, 2006
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndromeJennifer P Habashi, Daniel P Judge, Tammy M Holm, et al.
Pageof 38