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P Barnett

Showing results (471-480 of 501) with videos related to

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Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
Journal of Racial and Ethnic Health Disparities|November 17, 2022
Mapping Implementation Science with Expert Recommendations for Implementing Change (MIS-ERIC): Strategies to Improve PrEP Use among Black Cisgender Women Living in MississippiTrisha Arnold, Laura Whiteley, Rani A Elwy, et al.
American Journal of Medical Genetics. Part A|March 7, 2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndromePeer Arts, Jessica Garland, Alicia B Byrne, et al.
JMIR Research Protocols|June 20, 2025
Acceptance-Based Pre-Exposure Prophylaxis Intervention (ACTPrEP) to Engage Young Black Men Who Have Sex With Men in the Southern United States: Protocol for a Pilot Randomized Controlled TrialTrisha Arnold, Kayla K Giorlando, Andrew P Barnett, et al.
Human Mutation|April 3, 2016
Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.
Journal of Medical Genetics|January 29, 2020
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesisAlicia B Byrne, Shuji Mizumoto, Peer Arts, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2009
Incorporating model quality information in climate change detection and attribution studiesB D Santer, K E Taylor, P J Gleckler, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Science (New York, N.Y.)|November 25, 2010
Glucose and weight control in mice with a designed ghrelin O-acyltransferase inhibitorBrad P Barnett, Yousang Hwang, Martin S Taylor, et al.
Journal of Vitreoretinal Diseases|July 5, 2021
Rationale for American Society of Retina Specialists Best Practice Recommendations for Conducting Vitreoretinal Surgery during the COVID-19 EraDaniel L Chao, Jayanth Sridhar, Ajay E Kuriyan, et al.
Pageof 51

Showing results (471-480 of 501) with videos related to

Sort By:
Pageof 51
Molecular Vision|October 26, 2022
The phenotypic spectrum of <i>ADAMTSL4-</i>associated ectopia lentis: Additional cases, complications, and review of literatureLachlan S W Knight, Sean Mullany, Deepa A Taranath, et al.
Journal of Racial and Ethnic Health Disparities|November 17, 2022
Mapping Implementation Science with Expert Recommendations for Implementing Change (MIS-ERIC): Strategies to Improve PrEP Use among Black Cisgender Women Living in MississippiTrisha Arnold, Laura Whiteley, Rani A Elwy, et al.
American Journal of Medical Genetics. Part A|March 7, 2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndromePeer Arts, Jessica Garland, Alicia B Byrne, et al.
JMIR Research Protocols|June 20, 2025
Acceptance-Based Pre-Exposure Prophylaxis Intervention (ACTPrEP) to Engage Young Black Men Who Have Sex With Men in the Southern United States: Protocol for a Pilot Randomized Controlled TrialTrisha Arnold, Kayla K Giorlando, Andrew P Barnett, et al.
Human Mutation|April 3, 2016
Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.
Journal of Medical Genetics|January 29, 2020
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesisAlicia B Byrne, Shuji Mizumoto, Peer Arts, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2009
Incorporating model quality information in climate change detection and attribution studiesB D Santer, K E Taylor, P J Gleckler, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Science (New York, N.Y.)|November 25, 2010
Glucose and weight control in mice with a designed ghrelin O-acyltransferase inhibitorBrad P Barnett, Yousang Hwang, Martin S Taylor, et al.
Journal of Vitreoretinal Diseases|July 5, 2021
Rationale for American Society of Retina Specialists Best Practice Recommendations for Conducting Vitreoretinal Surgery during the COVID-19 EraDaniel L Chao, Jayanth Sridhar, Ajay E Kuriyan, et al.
Pageof 51