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Michael Watson

Showing results (121-130 of 146) with videos related to

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JHEP Reports : Innovation in Hepatology|September 30, 2020
Systemic iron reduction by venesection alters the gut microbiome in patients with haemochromatosisBhavika Parmanand, Michael Watson, Karen J Boland, et al.
In Silico Biology|June 30, 2005
Collection of soluble variants of membrane proteins for transcriptomics and proteomicsSteffen Möller, Eilhard Mix, Martin Blüggel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2018
Including ELSI research questions in newborn screening pilot studiesAaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
Ebiomedicine|January 15, 2019
PYY plays a key role in the resolution of diabetes following bariatric surgery in humansClaudia Guida, Sam D Stephen, Michael Watson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and GenomicsSarah S Kalia, Kathy Adelman, Sherri J Bale, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Carrier testing for spinal muscular atrophyJonathan M Gitlin, Kenneth Fischbeck, Thomas O Crawford, et al.
Molecular Genetics and Metabolism|June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolismKathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
Frontiers in Genetics|August 8, 2022
Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)Amy Brower, Kee Chan, Marc Williams, et al.
Genetics, Selection, Evolution : GSE|December 7, 2007
Analysis of a simulated microarray dataset: comparison of methods for data normalisation and detection of differential expression (open access publication)Michael Watson, Mónica Pérez-Alegre, Michael Denis Baron, et al.
Molecular Genetics and Metabolism|October 31, 2023
Variant Classification for Pompe disease; ACMG/AMP specifications from the ClinGen Lysosomal Diseases Variant Curation Expert PanelJennifer L Goldstein, Jennifer McGlaughon, Dona Kanavy, et al.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
JHEP Reports : Innovation in Hepatology|September 30, 2020
Systemic iron reduction by venesection alters the gut microbiome in patients with haemochromatosisBhavika Parmanand, Michael Watson, Karen J Boland, et al.
In Silico Biology|June 30, 2005
Collection of soluble variants of membrane proteins for transcriptomics and proteomicsSteffen Möller, Eilhard Mix, Martin Blüggel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2018
Including ELSI research questions in newborn screening pilot studiesAaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
Ebiomedicine|January 15, 2019
PYY plays a key role in the resolution of diabetes following bariatric surgery in humansClaudia Guida, Sam D Stephen, Michael Watson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and GenomicsSarah S Kalia, Kathy Adelman, Sherri J Bale, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Carrier testing for spinal muscular atrophyJonathan M Gitlin, Kenneth Fischbeck, Thomas O Crawford, et al.
Molecular Genetics and Metabolism|June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolismKathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
Frontiers in Genetics|August 8, 2022
Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)Amy Brower, Kee Chan, Marc Williams, et al.
Genetics, Selection, Evolution : GSE|December 7, 2007
Analysis of a simulated microarray dataset: comparison of methods for data normalisation and detection of differential expression (open access publication)Michael Watson, Mónica Pérez-Alegre, Michael Denis Baron, et al.
Molecular Genetics and Metabolism|October 31, 2023
Variant Classification for Pompe disease; ACMG/AMP specifications from the ClinGen Lysosomal Diseases Variant Curation Expert PanelJennifer L Goldstein, Jennifer McGlaughon, Dona Kanavy, et al.
Pageof 15