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N-G Larsson

Showing results (11-20 of 49) with videos related to

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Annual Review of Genetics|January 1, 1995
Molecular genetic aspects of human mitochondrial disordersN G Larsson, D A Clayton
Lakartidningen|November 29, 1989
[DNA diagnosis of mitochondrial diseases is now possible]N G Larsson, E Holme, M H Tulinius
Journal of Internal Medicine|August 14, 1999
Mitochondrial medicine--recent advancesC Graff, D A Clayton, N G Larsson
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 23, 2001
Downregulation of Tfam and mtDNA copy number during mammalian spermatogenesisA Rantanen, M Jansson, A Oldfors, et al.
Brain : a Journal of Neurology|April 1, 1993
Mitochondrial DNA deletions in inclusion body myositisA Oldfors, N G Larsson, C Lindberg, et al.
Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
Structure and chromosomal localization of the mouse mitochondrial transcription factor A gene (Tfam)N G Larsson, G S Barsh, D A Clayton
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.
Biochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, 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.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Annual Review of Genetics|January 1, 1995
Molecular genetic aspects of human mitochondrial disordersN G Larsson, D A Clayton
Lakartidningen|November 29, 1989
[DNA diagnosis of mitochondrial diseases is now possible]N G Larsson, E Holme, M H Tulinius
Journal of Internal Medicine|August 14, 1999
Mitochondrial medicine--recent advancesC Graff, D A Clayton, N G Larsson
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 23, 2001
Downregulation of Tfam and mtDNA copy number during mammalian spermatogenesisA Rantanen, M Jansson, A Oldfors, et al.
Brain : a Journal of Neurology|April 1, 1993
Mitochondrial DNA deletions in inclusion body myositisA Oldfors, N G Larsson, C Lindberg, et al.
Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
Structure and chromosomal localization of the mouse mitochondrial transcription factor A gene (Tfam)N G Larsson, G S Barsh, D A Clayton
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.
Biochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, 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.
Pageof 5