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K J Morten

Showing results (1-10 of 12) with videos related to

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Methods in Molecular Medicine|March 11, 2011
Diagnosis of mitochondrial disorders using the PCRK J Morten
Neurology|November 18, 1998
Stabilization of the pyruvate dehydrogenase E1alpha subunit by dichloroacetateK J Morten, M Caky, P M Matthews
FEBS Letters|November 18, 2005
Rapid rates of newly synthesized mitochondrial protein degradation are significantly affected by the generation of mitochondrial free radicalsA Basoah, P M Matthews, K J Morten
Neurology|November 18, 1998
Mechanisms of expression of pyruvate dehydrogenase deficiency caused by an E1alpha subunit mutationK J Morten, M Caky, P M Matthews
Diabetologia|July 1, 1995
Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndromeJ Poulton, S O'Rahilly, K J Morten, et al.
Neurology|August 17, 1999
Dichloroacetate stabilizes the mutant E1alpha subunit in pyruvate dehydrogenase deficiencyK J Morten, P Beattie, G K Brown, et al.
Human Molecular Genetics|June 1, 1994
Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?J Poulton, K J Morten, K Weber, et al.
Human Molecular Genetics|December 1, 1993
A new point mutation associated with mitochondrial encephalomyopathyK J Morten, J M Cooper, G K Brown, et al.
Muscle & Nerve. Supplement|January 1, 1995
Duplications of mitochondrial DNA in Kearns-Sayre syndromeJ Poulton, K J Morten, D Marchington, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
Loss of autophagy in erythroid cells leads to defective removal of mitochondria and severe anemia in vivoM Mortensen, D J P Ferguson, M Edelmann, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Methods in Molecular Medicine|March 11, 2011
Diagnosis of mitochondrial disorders using the PCRK J Morten
Neurology|November 18, 1998
Stabilization of the pyruvate dehydrogenase E1alpha subunit by dichloroacetateK J Morten, M Caky, P M Matthews
FEBS Letters|November 18, 2005
Rapid rates of newly synthesized mitochondrial protein degradation are significantly affected by the generation of mitochondrial free radicalsA Basoah, P M Matthews, K J Morten
Neurology|November 18, 1998
Mechanisms of expression of pyruvate dehydrogenase deficiency caused by an E1alpha subunit mutationK J Morten, M Caky, P M Matthews
Diabetologia|July 1, 1995
Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndromeJ Poulton, S O'Rahilly, K J Morten, et al.
Neurology|August 17, 1999
Dichloroacetate stabilizes the mutant E1alpha subunit in pyruvate dehydrogenase deficiencyK J Morten, P Beattie, G K Brown, et al.
Human Molecular Genetics|June 1, 1994
Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?J Poulton, K J Morten, K Weber, et al.
Human Molecular Genetics|December 1, 1993
A new point mutation associated with mitochondrial encephalomyopathyK J Morten, J M Cooper, G K Brown, et al.
Muscle & Nerve. Supplement|January 1, 1995
Duplications of mitochondrial DNA in Kearns-Sayre syndromeJ Poulton, K J Morten, D Marchington, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
Loss of autophagy in erythroid cells leads to defective removal of mitochondria and severe anemia in vivoM Mortensen, D J P Ferguson, M Edelmann, et al.
Pageof 2