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Jukka S Moilanen

Showing results (1-10 of 47) with videos related to

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Clinical and Translational Medicine|June 11, 2015
Human Chromosome Y and Haplogroups; introducing YDHS DatabaseTimo Tiirikka, Jukka S Moilanen
Molecular Biology and Evolution|June 5, 2003
Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNAJukka S Moilanen, Kari Majamaa
Molecular Biology and Evolution|September 2, 2003
Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup JJukka S Moilanen, Saara Finnila, Kari Majamaa
BMJ Neurology Open|September 26, 2024
Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNAKari Majamaa, Mikko Kärppä, Jukka S Moilanen
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
BMC Medical Genetics|August 15, 2013
Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer familiesMaria Haanpää, Katri Pylkäs, Jukka S Moilanen, et al.
Journal of Genetic Counseling|September 30, 2015
The Quality of Genetic Counseling and Connected Factors as Evaluated by Male BRCA1/2 Mutation Carriers in FinlandOuti Kajula, Maria Kääriäinen, Jukka S Moilanen, et al.
Journal of Molecular Evolution|June 29, 2005
Sequence variation in the tRNA genes of human mitochondrial DNATiina Vilmi, Jukka S Moilanen, Saara Finnilä, et al.
BMC Neurology|August 1, 2025
Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNASatu Winqvist, Mikko Kärppä, Jukka S Moilanen, et al.
BMC Research Notes|July 12, 2012
Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitusHeidi K Soini, Jukka S Moilanen, Saara Finnila, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Clinical and Translational Medicine|June 11, 2015
Human Chromosome Y and Haplogroups; introducing YDHS DatabaseTimo Tiirikka, Jukka S Moilanen
Molecular Biology and Evolution|June 5, 2003
Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNAJukka S Moilanen, Kari Majamaa
Molecular Biology and Evolution|September 2, 2003
Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup JJukka S Moilanen, Saara Finnila, Kari Majamaa
BMJ Neurology Open|September 26, 2024
Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNAKari Majamaa, Mikko Kärppä, Jukka S Moilanen
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
BMC Medical Genetics|August 15, 2013
Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer familiesMaria Haanpää, Katri Pylkäs, Jukka S Moilanen, et al.
Journal of Genetic Counseling|September 30, 2015
The Quality of Genetic Counseling and Connected Factors as Evaluated by Male BRCA1/2 Mutation Carriers in FinlandOuti Kajula, Maria Kääriäinen, Jukka S Moilanen, et al.
Journal of Molecular Evolution|June 29, 2005
Sequence variation in the tRNA genes of human mitochondrial DNATiina Vilmi, Jukka S Moilanen, Saara Finnilä, et al.
BMC Neurology|August 1, 2025
Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNASatu Winqvist, Mikko Kärppä, Jukka S Moilanen, et al.
BMC Research Notes|July 12, 2012
Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitusHeidi K Soini, Jukka S Moilanen, Saara Finnila, et al.
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