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K Mullin

Showing results (31-40 of 50) with videos related to

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JCI Insight|June 8, 2023
Multimodal single-cell analysis of nonrandom heteroplasmy distribution in human retinal mitochondrial diseaseNathaniel K Mullin, Andrew P Voigt, Miles J Flamme-Wiese, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2019
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degenerationAndrew P Voigt, Kelly Mulfaul, Nathaniel K Mullin, et al.
The Journal of Clinical Investigation|April 23, 2024
NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal developmentNathaniel K Mullin, Laura R Bohrer, Andrew P Voigt, et al.
Human Molecular Genetics|September 30, 2021
Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptomsNathaniel K Mullin, Kristin R Anfinson, Megan J Riker, et al.
Journal of Veterinary Pharmacology and Therapeutics|February 1, 2018
Pharmacokinetics of cefquinome in healthy and Pasteurella multocida-infected rabbitsS T Elazab, D E Schrunk, R W Griffith, et al.
Human Molecular Genetics|May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profilesAndrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Science (New York, N.Y.)|December 23, 2000
Evidence for genetic linkage of Alzheimer's disease to chromosome 10qL Bertram, D Blacker, K Mullin, et al.
Investigative Ophthalmology & Visual Science|October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial TranscriptomicsAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICSAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Annals of Neurology|February 24, 2001
No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer diseaseL Bertram, S Guénette, J Jones, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
JCI Insight|June 8, 2023
Multimodal single-cell analysis of nonrandom heteroplasmy distribution in human retinal mitochondrial diseaseNathaniel K Mullin, Andrew P Voigt, Miles J Flamme-Wiese, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2019
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degenerationAndrew P Voigt, Kelly Mulfaul, Nathaniel K Mullin, et al.
The Journal of Clinical Investigation|April 23, 2024
NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal developmentNathaniel K Mullin, Laura R Bohrer, Andrew P Voigt, et al.
Human Molecular Genetics|September 30, 2021
Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptomsNathaniel K Mullin, Kristin R Anfinson, Megan J Riker, et al.
Journal of Veterinary Pharmacology and Therapeutics|February 1, 2018
Pharmacokinetics of cefquinome in healthy and Pasteurella multocida-infected rabbitsS T Elazab, D E Schrunk, R W Griffith, et al.
Human Molecular Genetics|May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profilesAndrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Science (New York, N.Y.)|December 23, 2000
Evidence for genetic linkage of Alzheimer's disease to chromosome 10qL Bertram, D Blacker, K Mullin, et al.
Investigative Ophthalmology & Visual Science|October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial TranscriptomicsAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICSAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Annals of Neurology|February 24, 2001
No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer diseaseL Bertram, S Guénette, J Jones, et al.
Pageof 5