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Molecular Vision
|
March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cells
Eugenia 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 protein
Herbert 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 pathways
Ameera 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 girl
Xiaolong 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 Khan
Daniel 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 Electrode
Brett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Investigative Ophthalmology & Visual Science
|
February 28, 2014
Developing cellular therapies for retinal degenerative diseases
Kapil 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 Genetics
Brian 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 Cohort
Jasmine 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 NRL
Lorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
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of 16
Search research articles
Search
Showing results (51-60 of 158) with videos related to
Sort By:
Page
of 16
Molecular Vision
|
March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cells
Eugenia 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 protein
Herbert 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 pathways
Ameera 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 girl
Xiaolong 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 Khan
Daniel 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 Electrode
Brett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Investigative Ophthalmology & Visual Science
|
February 28, 2014
Developing cellular therapies for retinal degenerative diseases
Kapil 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 Genetics
Brian 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 Cohort
Jasmine 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 NRL
Lorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Page
of 16