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R Ali

Showing results (1021-1030 of 1,192) with videos related to

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Human Molecular Genetics|December 5, 2013
Hsp90 inhibition protects against inherited retinal degenerationMònica Aguilà, Dalila Bevilacqua, Caroline McCulley, et al.
The Journal of Cell Biology|September 19, 2022
Spatiotemporal control of actomyosin contractility by MRCKβ signaling drives phagocytosisCeniz Zihni, Anastasios Georgiadis, Conor M Ramsden, et al.
The Journal of Biological Chemistry|April 21, 2022
mTORC1 regulates high levels of protein synthesis in retinal ganglion cells of adult micePatrice E Fort, Mandy K Losiewicz, Lynda Elghazi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 19, 2007
Gene transfer of an engineered zinc finger protein enhances the anti-angiogenic defense systemKatsutoshi Yokoi, Huanda Steve Zhang, Shu Kachi, et al.
Human Genomics|September 26, 2022
Pharmacogenomics implementation in cardiovascular disease in a highly diverse population: initial findings and lessons learned from a pilot study in United Arab EmiratesZeina N Al-Mahayri, Lubna Q Khasawneh, Mais N Alqasrawi, et al.
The American Journal of Pathology|June 17, 2015
IL-4 regulates specific Arg-1(+) macrophage sFlt-1-mediated inhibition of angiogenesisWei-Kang Wu, Anastasios Georgiadis, David A Copland, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Clinical Microbiology|March 30, 2026
Evaluation of self-collection of nasal swab specimens for COVID-19 diagnostic testing in children in the United States, 2020-2023Zachary R Smith, Andrew Godoshian, Peter Boersma, et al.
Evidence-Based Practice in Child and Adolescent Mental Health|June 17, 2024
Validation of the Diagnostic Interview Schedule for Children (DISC-5) Tic Disorder and Attention-Deficit/Hyperactivity Disorder ModulesRebecca H Bitsko, Joseph R Holbrook, Prudence W Fisher, et al.
Journal of Medical Genetics|November 11, 2017
Defect in phosphoinositide signalling through a homozygous variant in <i>PLCB3</i> causes a new form of spondylometaphyseal dysplasia with corneal dystrophySalma Ben-Salem, Sarah M Robbins, Nara Lm Sobreira, et al.
Pageof 120

Showing results (1021-1030 of 1,192) with videos related to

Sort By:
Pageof 120
Human Molecular Genetics|December 5, 2013
Hsp90 inhibition protects against inherited retinal degenerationMònica Aguilà, Dalila Bevilacqua, Caroline McCulley, et al.
The Journal of Cell Biology|September 19, 2022
Spatiotemporal control of actomyosin contractility by MRCKβ signaling drives phagocytosisCeniz Zihni, Anastasios Georgiadis, Conor M Ramsden, et al.
The Journal of Biological Chemistry|April 21, 2022
mTORC1 regulates high levels of protein synthesis in retinal ganglion cells of adult micePatrice E Fort, Mandy K Losiewicz, Lynda Elghazi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 19, 2007
Gene transfer of an engineered zinc finger protein enhances the anti-angiogenic defense systemKatsutoshi Yokoi, Huanda Steve Zhang, Shu Kachi, et al.
Human Genomics|September 26, 2022
Pharmacogenomics implementation in cardiovascular disease in a highly diverse population: initial findings and lessons learned from a pilot study in United Arab EmiratesZeina N Al-Mahayri, Lubna Q Khasawneh, Mais N Alqasrawi, et al.
The American Journal of Pathology|June 17, 2015
IL-4 regulates specific Arg-1(+) macrophage sFlt-1-mediated inhibition of angiogenesisWei-Kang Wu, Anastasios Georgiadis, David A Copland, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Clinical Microbiology|March 30, 2026
Evaluation of self-collection of nasal swab specimens for COVID-19 diagnostic testing in children in the United States, 2020-2023Zachary R Smith, Andrew Godoshian, Peter Boersma, et al.
Evidence-Based Practice in Child and Adolescent Mental Health|June 17, 2024
Validation of the Diagnostic Interview Schedule for Children (DISC-5) Tic Disorder and Attention-Deficit/Hyperactivity Disorder ModulesRebecca H Bitsko, Joseph R Holbrook, Prudence W Fisher, et al.
Journal of Medical Genetics|November 11, 2017
Defect in phosphoinositide signalling through a homozygous variant in <i>PLCB3</i> causes a new form of spondylometaphyseal dysplasia with corneal dystrophySalma Ben-Salem, Sarah M Robbins, Nara Lm Sobreira, et al.
Pageof 120