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K Majamaa

Showing results (21-30 of 67) with videos related to

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Mutation Research|June 19, 2001
Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding regionS Finnilä, I E Hassinen, K Majamaa
Journal of Molecular Medicine (Berlin, Germany)|November 21, 2001
A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASILS Finnilä, S Tuisku, R Herva, et al.
The Cochrane Database of Systematic Reviews|January 27, 2006
Treatment for mitochondrial disordersP Chinnery, K Majamaa, D Turnbull, et al.
Biochimica Et Biophysica Acta|March 20, 1992
Synthesis of structurally unstable type III procollagen in patients with cerebral artery aneurysmK Majamaa, E R Savolainen, V V Myllylä
The Biochemical Journal|September 15, 1982
Regulation of proline 3-hydroxylation and prolyl 3-hydroxylase and 4-hydroxylase activities in transformed cellsK Majamaa, R Myllylä, K Alitalo, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Metabolic interventions against complex I deficiency in MELAS syndromeK Majamaa, H Rusanen, A Remes, et al.
The Biochemical Journal|November 1, 1979
Partial purification and characterization of chick-embryo prolyl 3-hydroxylaseK Tryggvason, K Majamaa, J Risteli, et al.
Human Genetics|December 22, 1999
Haplotype-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNAM S Lehtonen, M Meinilä, I E Hassinen, et al.
Neurology|May 1, 1993
Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutationA M Remes, K Majamaa, R Herva, et al.
American Journal of Human Genetics|March 11, 2000
Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresisS Finnilä, I E Hassinen, L Ala-Kokko, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Mutation Research|June 19, 2001
Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding regionS Finnilä, I E Hassinen, K Majamaa
Journal of Molecular Medicine (Berlin, Germany)|November 21, 2001
A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASILS Finnilä, S Tuisku, R Herva, et al.
The Cochrane Database of Systematic Reviews|January 27, 2006
Treatment for mitochondrial disordersP Chinnery, K Majamaa, D Turnbull, et al.
Biochimica Et Biophysica Acta|March 20, 1992
Synthesis of structurally unstable type III procollagen in patients with cerebral artery aneurysmK Majamaa, E R Savolainen, V V Myllylä
The Biochemical Journal|September 15, 1982
Regulation of proline 3-hydroxylation and prolyl 3-hydroxylase and 4-hydroxylase activities in transformed cellsK Majamaa, R Myllylä, K Alitalo, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Metabolic interventions against complex I deficiency in MELAS syndromeK Majamaa, H Rusanen, A Remes, et al.
The Biochemical Journal|November 1, 1979
Partial purification and characterization of chick-embryo prolyl 3-hydroxylaseK Tryggvason, K Majamaa, J Risteli, et al.
Human Genetics|December 22, 1999
Haplotype-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNAM S Lehtonen, M Meinilä, I E Hassinen, et al.
Neurology|May 1, 1993
Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutationA M Remes, K Majamaa, R Herva, et al.
American Journal of Human Genetics|March 11, 2000
Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresisS Finnilä, I E Hassinen, L Ala-Kokko, et al.
Pageof 7