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Donna M Martin

Showing results (11-20 of 104) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 25, 2017
New insights and advances in CHARGE syndrome: Diagnosis, etiologies, treatments, and research discoveriesConny van Ravenswaaij-Arts, Donna M Martin
Development (Cambridge, England)|July 14, 2011
Regulation of spinal interneuron development by the Olig-related protein Bhlhb5 and Notch signalingKaia Skaggs, Donna M Martin, Bennett G Novitch
Hearing Research|January 22, 2022
Epigenetic mechanisms of inner ear developmentVinodh Balendran, K Elaine Ritter, Donna M Martin
Human Molecular Genetics|May 21, 2011
Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndromeWanda S Layman, Elizabeth A Hurd, Donna M Martin
Investigative Ophthalmology & Visual Science|December 17, 2015
Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE SyndromePhilip J Gage, Elizabeth A Hurd, Donna M Martin
Stem Cells and Development|January 9, 2015
Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseasesJoseph A Micucci, Ethan D Sperry, Donna M Martin
Experimental Neurology|March 10, 2005
Genetics of subthalamic nucleus in development and diseaseSteven T Philips, Roger L Albin, Donna M Martin
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 31, 2017
Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structuresDaniel I Choo, Kareem O Tawfik, Donna M Martin, et al.
Human Mutation|May 20, 2021
Incorporation of exome-based CNV analysis makes trio-WES a more powerful tool for clinical diagnosis in neurodevelopmental disorders: A retrospective studyYiwen Zhai, Zhanhui Zhang, Panlai Shi, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndromeGabriel E Zentner, Wanda S Layman, Donna M Martin, et al.
Pageof 11

Showing results (11-20 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 25, 2017
New insights and advances in CHARGE syndrome: Diagnosis, etiologies, treatments, and research discoveriesConny van Ravenswaaij-Arts, Donna M Martin
Development (Cambridge, England)|July 14, 2011
Regulation of spinal interneuron development by the Olig-related protein Bhlhb5 and Notch signalingKaia Skaggs, Donna M Martin, Bennett G Novitch
Hearing Research|January 22, 2022
Epigenetic mechanisms of inner ear developmentVinodh Balendran, K Elaine Ritter, Donna M Martin
Human Molecular Genetics|May 21, 2011
Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndromeWanda S Layman, Elizabeth A Hurd, Donna M Martin
Investigative Ophthalmology & Visual Science|December 17, 2015
Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE SyndromePhilip J Gage, Elizabeth A Hurd, Donna M Martin
Stem Cells and Development|January 9, 2015
Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseasesJoseph A Micucci, Ethan D Sperry, Donna M Martin
Experimental Neurology|March 10, 2005
Genetics of subthalamic nucleus in development and diseaseSteven T Philips, Roger L Albin, Donna M Martin
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 31, 2017
Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structuresDaniel I Choo, Kareem O Tawfik, Donna M Martin, et al.
Human Mutation|May 20, 2021
Incorporation of exome-based CNV analysis makes trio-WES a more powerful tool for clinical diagnosis in neurodevelopmental disorders: A retrospective studyYiwen Zhai, Zhanhui Zhang, Panlai Shi, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndromeGabriel E Zentner, Wanda S Layman, Donna M Martin, et al.
Pageof 11