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E Holme

Showing results (41-50 of 111) with videos related to

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Biochemical and Molecular Medicine|June 1, 1995
Effect of short-term treatment with pivalic acid containing antibiotics on serum carnitine concentration--a risk irrespective of ageK Abrahamsson, E Holme, U Jodal, et al.
Biochemical and Biophysical Research Communications|May 16, 1994
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletionN G Larsson, A Oldfors, E Holme, et al.
Journal of Internal Medicine|January 1, 1990
Metabolic effects of controlled-release metoprolol in hypertensive men with impaired or diabetic glucose tolerance: a comparison with atenololB Fagerberg, A Berglund, E Holme, et al.
Muscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.
Journal of Reproduction and Fertility|September 1, 1982
Properties of intact and univalent (Fab) antibodies raised against isolated, solubilized, mouse zonae pellucidaeR J Aitken, E Holme, D W Richardson, et al.
Lancet (London, England)|October 3, 1992
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenaseS Lindstedt, E Holme, E A Lock, et al.
Journal of Assisted Reproduction and Genetics|April 1, 1997
Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?M Houshmand, E Holme, C Hanson, et al.
Human Mutation|March 25, 1999
A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspringM Houshmand, C Lindberg, A R Moslemi, et al.
Pediatric Research|August 1, 1990
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndromeN G Larsson, E Holme, B Kristiansson, et al.
Annals of Neurology|November 1, 1991
Leber's hereditary optic neuropathy and complex I deficiency in muscleN G Larsson, O Andersen, E Holme, et al.
Pageof 12

Showing results (41-50 of 111) with videos related to

Sort By:
Pageof 12
Biochemical and Molecular Medicine|June 1, 1995
Effect of short-term treatment with pivalic acid containing antibiotics on serum carnitine concentration--a risk irrespective of ageK Abrahamsson, E Holme, U Jodal, et al.
Biochemical and Biophysical Research Communications|May 16, 1994
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletionN G Larsson, A Oldfors, E Holme, et al.
Journal of Internal Medicine|January 1, 1990
Metabolic effects of controlled-release metoprolol in hypertensive men with impaired or diabetic glucose tolerance: a comparison with atenololB Fagerberg, A Berglund, E Holme, et al.
Muscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.
Journal of Reproduction and Fertility|September 1, 1982
Properties of intact and univalent (Fab) antibodies raised against isolated, solubilized, mouse zonae pellucidaeR J Aitken, E Holme, D W Richardson, et al.
Lancet (London, England)|October 3, 1992
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenaseS Lindstedt, E Holme, E A Lock, et al.
Journal of Assisted Reproduction and Genetics|April 1, 1997
Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?M Houshmand, E Holme, C Hanson, et al.
Human Mutation|March 25, 1999
A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspringM Houshmand, C Lindberg, A R Moslemi, et al.
Pediatric Research|August 1, 1990
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndromeN G Larsson, E Holme, B Kristiansson, et al.
Annals of Neurology|November 1, 1991
Leber's hereditary optic neuropathy and complex I deficiency in muscleN G Larsson, O Andersen, E Holme, et al.
Pageof 12