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J M Shoffner

Showing results (21-30 of 50) with videos related to

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Biochimica Et Biophysica Acta|August 9, 1990
Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsiesX X Zheng, J M Shoffner, A S Voljavec, et al.
The Journal of Pediatrics|May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiencyK North, M S Korson, N Krawiecki, et al.
Nature Genetics|August 1, 1994
Mitochondrial diabetes revisitedS W Ballinger, J M Shoffner, S Gebhart, et al.
Annals of Neurology|September 1, 1991
Mitochondrial oxidative phosphorylation defects in Parkinson's diseaseJ M Shoffner, R L Watts, J L Juncos, et al.
Annals of Neurology|July 1, 1992
Mitochondrial oxidative phosphorylation defects in Parkinson's diseaseD C Wallace, J M Shoffner, R L Watts, et al.
Israel Journal of Medical Sciences|December 1, 1985
Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?Z Laron, M Kelijman, A Pertzelan, et al.
American Journal of Ophthalmology|February 1, 1997
Strabismus and mitochondrial defects in chronic progressive external ophthalmoplegiaJ A Sorkin, J M Shoffner, H E Grossniklaus, 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.
Kidney International|April 1, 1995
Renal amino acid transport in adults with oxidative phosphorylation diseasesJ M Shoffner, A S Voljavec, J Dixon, et al.
JAMA|October 2, 1991
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac diseaseM Corral-Debrinski, G Stepien, J M Shoffner, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Biochimica Et Biophysica Acta|August 9, 1990
Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsiesX X Zheng, J M Shoffner, A S Voljavec, et al.
The Journal of Pediatrics|May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiencyK North, M S Korson, N Krawiecki, et al.
Nature Genetics|August 1, 1994
Mitochondrial diabetes revisitedS W Ballinger, J M Shoffner, S Gebhart, et al.
Annals of Neurology|September 1, 1991
Mitochondrial oxidative phosphorylation defects in Parkinson's diseaseJ M Shoffner, R L Watts, J L Juncos, et al.
Annals of Neurology|July 1, 1992
Mitochondrial oxidative phosphorylation defects in Parkinson's diseaseD C Wallace, J M Shoffner, R L Watts, et al.
Israel Journal of Medical Sciences|December 1, 1985
Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?Z Laron, M Kelijman, A Pertzelan, et al.
American Journal of Ophthalmology|February 1, 1997
Strabismus and mitochondrial defects in chronic progressive external ophthalmoplegiaJ A Sorkin, J M Shoffner, H E Grossniklaus, 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.
Kidney International|April 1, 1995
Renal amino acid transport in adults with oxidative phosphorylation diseasesJ M Shoffner, A S Voljavec, J Dixon, et al.
JAMA|October 2, 1991
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac diseaseM Corral-Debrinski, G Stepien, J M Shoffner, et al.
Pageof 5