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Showing results (801-810 of 854) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2010
Age-dependent maintenance of motor control and corticostriatal innervation by death receptor 3Jason Peter Twohig, Malcolm I Roberts, Nuria Gavalda, et al.
World Neurosurgery|November 28, 2022
Delays in Presentation After Traumatic Spinal Cord Injury-A Systematic ReviewTej D Azad, Sumil K Nair, Anita L Kalluri, et al.
Human Molecular Genetics|May 6, 2009
X-linked cataract and Nance-Horan syndrome are allelic disordersMargherita Coccia, Simon P Brooks, Tom R Webb, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
The Journal of Clinical Investigation|July 7, 2026
A peripheral subpopulation of retinal pigment epithelium resists oxidative damage through SERPINE3-mediated Caspase-1 inhibitionHuirong Li, Takerra Johnson-Stephenson, Vincent P Kunze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single centerThierry Vilboux, Daniel A Doherty, Ian A Glass, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2025
Endogenous LRRK2 and PINK1 function in a convergent neuroprotective ciliogenesis pathway in the brainEnrico Bagnoli, Yu-En Lin, Sophie Burel, et al.
JCI Insight|January 25, 2019
One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1BDavid R Adams, Supriya Menezes, Ramon Jauregui, et al.
Translational Vision Science & Technology|June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone StructureKatie M Litts, Erica N Woertz, Niamh Wynne, et al.
Plos One|November 22, 2022
Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmiaHildegard Nikki Hall, Hemant Bengani, Robert B Hufnagel, et al.
Pageof 86

Showing results (801-810 of 854) with videos related to

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Pageof 86
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2010
Age-dependent maintenance of motor control and corticostriatal innervation by death receptor 3Jason Peter Twohig, Malcolm I Roberts, Nuria Gavalda, et al.
World Neurosurgery|November 28, 2022
Delays in Presentation After Traumatic Spinal Cord Injury-A Systematic ReviewTej D Azad, Sumil K Nair, Anita L Kalluri, et al.
Human Molecular Genetics|May 6, 2009
X-linked cataract and Nance-Horan syndrome are allelic disordersMargherita Coccia, Simon P Brooks, Tom R Webb, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
The Journal of Clinical Investigation|July 7, 2026
A peripheral subpopulation of retinal pigment epithelium resists oxidative damage through SERPINE3-mediated Caspase-1 inhibitionHuirong Li, Takerra Johnson-Stephenson, Vincent P Kunze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single centerThierry Vilboux, Daniel A Doherty, Ian A Glass, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2025
Endogenous LRRK2 and PINK1 function in a convergent neuroprotective ciliogenesis pathway in the brainEnrico Bagnoli, Yu-En Lin, Sophie Burel, et al.
JCI Insight|January 25, 2019
One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1BDavid R Adams, Supriya Menezes, Ramon Jauregui, et al.
Translational Vision Science & Technology|June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone StructureKatie M Litts, Erica N Woertz, Niamh Wynne, et al.
Plos One|November 22, 2022
Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmiaHildegard Nikki Hall, Hemant Bengani, Robert B Hufnagel, et al.
Pageof 86