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I J Holt

Showing results (11-20 of 46) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1988
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophyI J Holt, D H Miller, A E Harding
Nature|February 25, 1988
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesI J Holt, A E Harding, J A Morgan-Hughes
Nucleic Acids Research|June 26, 1989
Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanismsI J Holt, A E Harding, J A Morgan-Hughes
Human Molecular Genetics|April 1, 1996
Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?D R Marchington, J Poulton, A Sellar, et al.
Human Genetics|May 1, 1988
Mitochondrial DNA polymorphism in mitochondrial myopathyI J Holt, A E Harding, J A Morgan-Hughes
Human Molecular Genetics|March 1, 1997
Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutationF M Reid, A Rovio, I J Holt, et al.
Human Molecular Genetics|January 1, 1996
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybridsD R Dunbar, P A Moonie, M Zeviani, et al.
The Journal of Biological Chemistry|November 15, 2000
Impaired ATP synthase assembly associated with a mutation in the human ATP synthase subunit 6 geneL G Nijtmans, N S Henderson, G Attardi, et al.
Human Molecular Genetics|November 18, 1998
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutationA El Meziane, S K Lehtinen, I J Holt, et al.
EMBO Reports|November 20, 2001
Prominent mitochondrial DNA recombination intermediates in human heart muscleO A Kajander, P J Karhunen, I J Holt, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1988
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophyI J Holt, D H Miller, A E Harding
Nature|February 25, 1988
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesI J Holt, A E Harding, J A Morgan-Hughes
Nucleic Acids Research|June 26, 1989
Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanismsI J Holt, A E Harding, J A Morgan-Hughes
Human Molecular Genetics|April 1, 1996
Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?D R Marchington, J Poulton, A Sellar, et al.
Human Genetics|May 1, 1988
Mitochondrial DNA polymorphism in mitochondrial myopathyI J Holt, A E Harding, J A Morgan-Hughes
Human Molecular Genetics|March 1, 1997
Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutationF M Reid, A Rovio, I J Holt, et al.
Human Molecular Genetics|January 1, 1996
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybridsD R Dunbar, P A Moonie, M Zeviani, et al.
The Journal of Biological Chemistry|November 15, 2000
Impaired ATP synthase assembly associated with a mutation in the human ATP synthase subunit 6 geneL G Nijtmans, N S Henderson, G Attardi, et al.
Human Molecular Genetics|November 18, 1998
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutationA El Meziane, S K Lehtinen, I J Holt, et al.
EMBO Reports|November 20, 2001
Prominent mitochondrial DNA recombination intermediates in human heart muscleO A Kajander, P J Karhunen, I J Holt, et al.
Pageof 5