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Mary C Whitman

Showing results (31-40 of 59) with videos related to

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Investigative Ophthalmology & Visual Science|July 10, 2025
Disrupted Motor Neuron and Neuromuscular Junction Development in an Albino Mice Model of Infantile NystagmusSampath Vemula, Abdikheyre Osman, Xiguang Yang, et al.
Genes|January 25, 2025
Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical NeuronsMayra Martinez-Sanchez, William Skarnes, Ashish Jain, et al.
Developmental Biology|August 9, 2022
TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouseMary C Whitman, Nicole M Gilette, Jessica L Bell, et al.
Investigative Ophthalmology & Visual Science|October 30, 2018
Loss of CXCR4/CXCL12 Signaling Causes Oculomotor Nerve Misrouting and Development of Motor Trigeminal to Oculomotor SynkinesisMary C Whitman, Elaine H Nguyen, Jessica L Bell, et al.
Investigative Ophthalmology & Visual Science|April 25, 2017
Ocular Motor Nerve Development in the Presence and Absence of Extraocular MuscleSuzanne M Michalak, Mary C Whitman, Jong G Park, et al.
The British Journal of Ophthalmology|January 27, 2026
Amblyopia and adult health: a comprehensive analysis of long-term systemic, sensory and mental health comorbidities in a national cohortKyoung A Viola Lee, Carsten Langholm, Trevor Lin, et al.
Ophthalmology|May 20, 2026
Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with StrabismusSarah MacKinnon, Rachael Zacks, Brenda Barry, et al.
Ophthalmology|January 22, 2025
Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research ProgramKyoung A Viola Lee, Inas F Aboobakar, Ashish Jain, et al.
Ophthalmic Genetics|July 31, 2025
Novel structural variant in <i>CACNA1F</i> causing congenital stationary night blindness identified with whole genome sequencingMayra Martinez Sanchez, Nafiza Meher, Hanna DeBruyn, et al.
JAMA Ophthalmology|February 15, 2024
Presence of Copy Number Variants Associated With Esotropia in Patients With ExotropiaMayra Martinez Sanchez, Wai-Man Chan, Sarah E MacKinnon, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Investigative Ophthalmology & Visual Science|July 10, 2025
Disrupted Motor Neuron and Neuromuscular Junction Development in an Albino Mice Model of Infantile NystagmusSampath Vemula, Abdikheyre Osman, Xiguang Yang, et al.
Genes|January 25, 2025
Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical NeuronsMayra Martinez-Sanchez, William Skarnes, Ashish Jain, et al.
Developmental Biology|August 9, 2022
TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouseMary C Whitman, Nicole M Gilette, Jessica L Bell, et al.
Investigative Ophthalmology & Visual Science|October 30, 2018
Loss of CXCR4/CXCL12 Signaling Causes Oculomotor Nerve Misrouting and Development of Motor Trigeminal to Oculomotor SynkinesisMary C Whitman, Elaine H Nguyen, Jessica L Bell, et al.
Investigative Ophthalmology & Visual Science|April 25, 2017
Ocular Motor Nerve Development in the Presence and Absence of Extraocular MuscleSuzanne M Michalak, Mary C Whitman, Jong G Park, et al.
The British Journal of Ophthalmology|January 27, 2026
Amblyopia and adult health: a comprehensive analysis of long-term systemic, sensory and mental health comorbidities in a national cohortKyoung A Viola Lee, Carsten Langholm, Trevor Lin, et al.
Ophthalmology|May 20, 2026
Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with StrabismusSarah MacKinnon, Rachael Zacks, Brenda Barry, et al.
Ophthalmology|January 22, 2025
Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research ProgramKyoung A Viola Lee, Inas F Aboobakar, Ashish Jain, et al.
Ophthalmic Genetics|July 31, 2025
Novel structural variant in <i>CACNA1F</i> causing congenital stationary night blindness identified with whole genome sequencingMayra Martinez Sanchez, Nafiza Meher, Hanna DeBruyn, et al.
JAMA Ophthalmology|February 15, 2024
Presence of Copy Number Variants Associated With Esotropia in Patients With ExotropiaMayra Martinez Sanchez, Wai-Man Chan, Sarah E MacKinnon, et al.
Pageof 6