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Anna Matynia

Showing results (31-40 of 37) with videos related to

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Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|March 7, 2024
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseasesDaniel C Brock, Meng Wang, Hafiz Muhammad Jafar Hussain, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2018
Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring miceKan Xie, Devon P Ryan, Brandon L Pearson, et al.
Investigative Ophthalmology & Visual Science|June 15, 2026
Corneal Innervation Research at a Crossroads: A Tool-Driven Roadmap for the FutureAnna Matynia, Ian D Meng, Brian M Davis, et al.
Biomolecules|March 28, 2024
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated GenesRebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomicsMubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
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Showing results (31-40 of 37) with videos related to

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You have reached the last page of results.This site can display upto 37 results.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|March 7, 2024
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseasesDaniel C Brock, Meng Wang, Hafiz Muhammad Jafar Hussain, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2018
Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring miceKan Xie, Devon P Ryan, Brandon L Pearson, et al.
Investigative Ophthalmology & Visual Science|June 15, 2026
Corneal Innervation Research at a Crossroads: A Tool-Driven Roadmap for the FutureAnna Matynia, Ian D Meng, Brian M Davis, et al.
Biomolecules|March 28, 2024
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated GenesRebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomicsMubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
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