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Showing results (311-320 of 369) with videos related to

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Cell Reports|December 8, 2021
FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instabilityAmit Laxmikant Deshmukh, Marie-Christine Caron, Mohiuddin Mohiuddin, et al.
The International Journal of Social Psychiatry|January 15, 2005
Demographic and social variables associated with psychiatric and school-related indicators for Asian/Pacific-Islander adolescentsEarl S Hishinuma, Ronald C Johnson, Barry S Carlton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 10, 2021
A Phase Ib Study of Atezolizumab with Radium-223 Dichloride in Men with Metastatic Castration-Resistant Prostate CancerLawrence Fong, Michael J Morris, Oliver Sartor, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 17, 2013
Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single centerT K Lau, S W Cheung, P S S Lo, et al.
Eclinicalmedicine|October 27, 2025
Antiseizure medications consumption in 73 countries and regions from 2012 to 2022: a longitudinal trend studyAdrienne Y L Chan, Andrew S C Yuen, Yingfen Hsia, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Plos One|June 27, 2015
Characterization of Endothelial Progenitor Cell Interactions with Human TropoelastinYoung Yu, Steven G Wise, Praveesuda L Michael, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
Science (New York, N.Y.)|December 20, 2014
RNA splicing. The human splicing code reveals new insights into the genetic determinants of diseaseHui Y Xiong, Babak Alipanahi, Leo J Lee, et al.
Neurology. Genetics|December 22, 2017
Germline and somatic mutations in <i>STXBP1</i> with diverse neurodevelopmental phenotypesMohammed Uddin, Marc Woodbury-Smith, Ada Chan, et al.
Pageof 37

Showing results (311-320 of 369) with videos related to

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Pageof 37
Cell Reports|December 8, 2021
FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instabilityAmit Laxmikant Deshmukh, Marie-Christine Caron, Mohiuddin Mohiuddin, et al.
The International Journal of Social Psychiatry|January 15, 2005
Demographic and social variables associated with psychiatric and school-related indicators for Asian/Pacific-Islander adolescentsEarl S Hishinuma, Ronald C Johnson, Barry S Carlton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 10, 2021
A Phase Ib Study of Atezolizumab with Radium-223 Dichloride in Men with Metastatic Castration-Resistant Prostate CancerLawrence Fong, Michael J Morris, Oliver Sartor, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 17, 2013
Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single centerT K Lau, S W Cheung, P S S Lo, et al.
Eclinicalmedicine|October 27, 2025
Antiseizure medications consumption in 73 countries and regions from 2012 to 2022: a longitudinal trend studyAdrienne Y L Chan, Andrew S C Yuen, Yingfen Hsia, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Plos One|June 27, 2015
Characterization of Endothelial Progenitor Cell Interactions with Human TropoelastinYoung Yu, Steven G Wise, Praveesuda L Michael, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
Science (New York, N.Y.)|December 20, 2014
RNA splicing. The human splicing code reveals new insights into the genetic determinants of diseaseHui Y Xiong, Babak Alipanahi, Leo J Lee, et al.
Neurology. Genetics|December 22, 2017
Germline and somatic mutations in <i>STXBP1</i> with diverse neurodevelopmental phenotypesMohammed Uddin, Marc Woodbury-Smith, Ada Chan, et al.
Pageof 37