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Brian P Brooks

Showing results (51-60 of 158) with videos related to

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Molecular Vision|March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cellsEugenia Poliakov, Natalya V Strunnikova, Jian-kang Jiang, et al.
Biochemistry|March 9, 2005
Protein kinase C phosphorylation modulates N- and C-terminal regulatory activities of the PITX2 homeodomain proteinHerbert M Espinoza, Mrudula Ganga, Usha Vadlamudi, et al.
Frontiers in Genetics|December 12, 2022
Transcriptional mapping of the macaque retina and RPE-choroid reveals conserved inter-tissue transcription drivers and signaling pathwaysAmeera Mungale, David M McGaughey, Congxiao Zhang, et al.
Journal of the American Academy of Dermatology|July 17, 2010
Brittle hair, developmental delay, neurologic abnormalities, and photosensitivity in a 4-year-old girlXiaolong Zhou, Sikandar G Khan, Deborah Tamura, et al.
American Journal of Medical Genetics. Part A|May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to KhanDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Translational Vision Science & Technology|June 6, 2025
Electroretinography With the RM Electrode: Normative Reference Ranges, Variation With Age, and Comparison With the Burian-Allen ElectrodeBrett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Investigative Ophthalmology & Visual Science|February 28, 2014
Developing cellular therapies for retinal degenerative diseasesKapil Bharti, Mahendra Rao, Sara Chandros Hull, et al.
American Journal of Ophthalmology|November 17, 2025
The Developmental Landscape of Children With Uveal Coloboma and Its Relationship With Clinical Phenotype and GeneticsBrian P Brooks, Alexandra T Hehn, Delphine Blain, et al.
Journal of Ophthalmology|October 21, 2020
Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics CohortJasmine Y Serpen, Lev Prasov, Wadih M Zein, et al.
Human Mutation|June 1, 2010
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRLLorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Pageof 16

Showing results (51-60 of 158) with videos related to

Sort By:
Pageof 16
Molecular Vision|March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cellsEugenia Poliakov, Natalya V Strunnikova, Jian-kang Jiang, et al.
Biochemistry|March 9, 2005
Protein kinase C phosphorylation modulates N- and C-terminal regulatory activities of the PITX2 homeodomain proteinHerbert M Espinoza, Mrudula Ganga, Usha Vadlamudi, et al.
Frontiers in Genetics|December 12, 2022
Transcriptional mapping of the macaque retina and RPE-choroid reveals conserved inter-tissue transcription drivers and signaling pathwaysAmeera Mungale, David M McGaughey, Congxiao Zhang, et al.
Journal of the American Academy of Dermatology|July 17, 2010
Brittle hair, developmental delay, neurologic abnormalities, and photosensitivity in a 4-year-old girlXiaolong Zhou, Sikandar G Khan, Deborah Tamura, et al.
American Journal of Medical Genetics. Part A|May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to KhanDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Translational Vision Science & Technology|June 6, 2025
Electroretinography With the RM Electrode: Normative Reference Ranges, Variation With Age, and Comparison With the Burian-Allen ElectrodeBrett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Investigative Ophthalmology & Visual Science|February 28, 2014
Developing cellular therapies for retinal degenerative diseasesKapil Bharti, Mahendra Rao, Sara Chandros Hull, et al.
American Journal of Ophthalmology|November 17, 2025
The Developmental Landscape of Children With Uveal Coloboma and Its Relationship With Clinical Phenotype and GeneticsBrian P Brooks, Alexandra T Hehn, Delphine Blain, et al.
Journal of Ophthalmology|October 21, 2020
Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics CohortJasmine Y Serpen, Lev Prasov, Wadih M Zein, et al.
Human Mutation|June 1, 2010
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRLLorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Pageof 16