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M Jablonski

Showing results (141-150 of 186) with videos related to

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Biorxiv : the Preprint Server for Biology|April 10, 2026
Comparison of Deep Learning Tools for Optic Nerve Axon Quantification Finds Limited Generalizability on Independent ValidationBenton Chuter, Noah Emmert, Min Young Kim, et al.
Neurobiology of Disease|November 9, 2021
Tau-tubulin kinase 1 phosphorylates TDP-43 at disease-relevant sites and exacerbates TDP-43 pathologyYuan Tian, Yi Wang, Angela M Jablonski, et al.
Radiation Research|January 27, 2026
Development of an Extended-release Formulation of Radioprotectin-1 for Mitigation of Gastrointestinal Acute Radiation SyndromeDerek D Norman, Sue Chin Lee, Yoojin Shin, et al.
Investigative Ophthalmology & Visual Science|March 15, 2011
Genetic dissection of the Gpnmb network in the eyeHong Lu, Xusheng Wang, Matthew Pullen, et al.
Molecular Vision|March 14, 2014
Varied manifestations of persistent hyperplastic primary vitreous with graded somatic mosaic deletion of a single geneMichelle N Mary-Sinclair, Xiaofei Wang, Douglas J Swanson, et al.
Molecular Vision|August 10, 2005
An ENU-induced mutation in Rs1h causes disruption of retinal structure and functionMonica M Jablonski, Claudia Dalke, XiaoFei Wang, et al.
Physiology & Behavior|October 9, 2018
Randomized trial of polychromatic blue-enriched light for circadian phase shifting, melatonin suppression, and alerting responsesJ P Hanifin, S W Lockley, K Cecil, et al.
Eye (London, England)|September 23, 2017
Comparison of effectiveness and safety between conbercept and ranibizumab for treatment of neovascular age-related macular degeneration. A retrospective case-controlled non-inferiority multiple center studyJ Cui, D Sun, H Lu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
The Journal of Endocrinology|February 7, 2008
Prolactin stimulates ubiquitination, initial internalization, and degradation of its receptor via catalytic activation of Janus kinase 2Gayathri Swaminathan, Bentley Varghese, Chellappagounder Thangavel, et al.
Pageof 19

Showing results (141-150 of 186) with videos related to

Sort By:
Pageof 19
Biorxiv : the Preprint Server for Biology|April 10, 2026
Comparison of Deep Learning Tools for Optic Nerve Axon Quantification Finds Limited Generalizability on Independent ValidationBenton Chuter, Noah Emmert, Min Young Kim, et al.
Neurobiology of Disease|November 9, 2021
Tau-tubulin kinase 1 phosphorylates TDP-43 at disease-relevant sites and exacerbates TDP-43 pathologyYuan Tian, Yi Wang, Angela M Jablonski, et al.
Radiation Research|January 27, 2026
Development of an Extended-release Formulation of Radioprotectin-1 for Mitigation of Gastrointestinal Acute Radiation SyndromeDerek D Norman, Sue Chin Lee, Yoojin Shin, et al.
Investigative Ophthalmology & Visual Science|March 15, 2011
Genetic dissection of the Gpnmb network in the eyeHong Lu, Xusheng Wang, Matthew Pullen, et al.
Molecular Vision|March 14, 2014
Varied manifestations of persistent hyperplastic primary vitreous with graded somatic mosaic deletion of a single geneMichelle N Mary-Sinclair, Xiaofei Wang, Douglas J Swanson, et al.
Molecular Vision|August 10, 2005
An ENU-induced mutation in Rs1h causes disruption of retinal structure and functionMonica M Jablonski, Claudia Dalke, XiaoFei Wang, et al.
Physiology & Behavior|October 9, 2018
Randomized trial of polychromatic blue-enriched light for circadian phase shifting, melatonin suppression, and alerting responsesJ P Hanifin, S W Lockley, K Cecil, et al.
Eye (London, England)|September 23, 2017
Comparison of effectiveness and safety between conbercept and ranibizumab for treatment of neovascular age-related macular degeneration. A retrospective case-controlled non-inferiority multiple center studyJ Cui, D Sun, H Lu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
The Journal of Endocrinology|February 7, 2008
Prolactin stimulates ubiquitination, initial internalization, and degradation of its receptor via catalytic activation of Janus kinase 2Gayathri Swaminathan, Bentley Varghese, Chellappagounder Thangavel, et al.
Pageof 19