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A S Jun

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Journal of Pharmacy & Pharmaceutical Sciences : a Publication of the Canadian Society for Pharmaceutical Sciences, Societe Canadienne Des Sciences Pharmaceutiques|December 12, 2001
High-performance liquid chromatography assay of amiodarone in rat plasmaA S Jun, D R Brocks
Eye (London, England)|November 25, 2003
Prospects for gene therapy in corneal diseaseA S Jun, D F P Larkin
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
Clear corneal cataract wound dehiscence during pneumatic retinopexyA S Jun, D J Pieramici, W Z Bridges
Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystoniaA S Jun, M D Brown, D C Wallace
Methods in Enzymology|January 1, 1996
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell linesI A Trounce, Y L Kim, A S Jun, et al.
Experimental Eye Research|August 9, 2021
Induction of the integrated stress response in the rat corneaC Peterson, Y C Kim, L M Ensign, et al.
Molecular and Cellular Biology|March 1, 1996
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystoniaA S Jun, I A Trounce, M D Brown, et al.
The Journal of Biological Chemistry|September 8, 2000
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutationM D Brown, I A Trounce, A S Jun, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Microarray analysis of gene expression in human donor corneasA S Jun, S H Liu, E H Koo, et al.
American Journal of Medical Genetics|January 22, 1996
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patientsM D Brown, J M Shoffner, Y L Kim, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Pharmacy & Pharmaceutical Sciences : a Publication of the Canadian Society for Pharmaceutical Sciences, Societe Canadienne Des Sciences Pharmaceutiques|December 12, 2001
High-performance liquid chromatography assay of amiodarone in rat plasmaA S Jun, D R Brocks
Eye (London, England)|November 25, 2003
Prospects for gene therapy in corneal diseaseA S Jun, D F P Larkin
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
Clear corneal cataract wound dehiscence during pneumatic retinopexyA S Jun, D J Pieramici, W Z Bridges
Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystoniaA S Jun, M D Brown, D C Wallace
Methods in Enzymology|January 1, 1996
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell linesI A Trounce, Y L Kim, A S Jun, et al.
Experimental Eye Research|August 9, 2021
Induction of the integrated stress response in the rat corneaC Peterson, Y C Kim, L M Ensign, et al.
Molecular and Cellular Biology|March 1, 1996
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystoniaA S Jun, I A Trounce, M D Brown, et al.
The Journal of Biological Chemistry|September 8, 2000
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutationM D Brown, I A Trounce, A S Jun, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Microarray analysis of gene expression in human donor corneasA S Jun, S H Liu, E H Koo, et al.
American Journal of Medical Genetics|January 22, 1996
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patientsM D Brown, J M Shoffner, Y L Kim, et al.
Pageof 2