Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Finnilä

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Journal of Human Genetics|April 3, 2001
Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish populationS Finnilä, K Majamaa
Human Heredity|October 6, 2001
Evidence for mtDNA admixture between the Finns and the SaamiM Meinilä, S Finnilä, K Majamaa
American Journal of Human Genetics|May 12, 2001
Phylogenetic network for European mtDNAS Finnilä, M S Lehtonen, K Majamaa
Mutation Research|September 10, 1999
Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutationsS Finnilä, I E Hassinen, K Majamaa
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.
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.
Journal of Neurology|October 15, 2013
Variations of mitochondrial DNA polymerase γ in patients with Parkinson's diseaseS Ylönen, P Ylikotila, A Siitonen, et al.
Biochimica Et Biophysica Acta|August 24, 1999
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the ratJ Sajanti, A S Björkstrand, S Finnilä, et al.
Neurology|July 28, 2004
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathyA M Remes, S Finnilä, H Mononen, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Human Genetics|April 3, 2001
Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish populationS Finnilä, K Majamaa
Human Heredity|October 6, 2001
Evidence for mtDNA admixture between the Finns and the SaamiM Meinilä, S Finnilä, K Majamaa
American Journal of Human Genetics|May 12, 2001
Phylogenetic network for European mtDNAS Finnilä, M S Lehtonen, K Majamaa
Mutation Research|September 10, 1999
Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutationsS Finnilä, I E Hassinen, K Majamaa
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.
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.
Journal of Neurology|October 15, 2013
Variations of mitochondrial DNA polymerase γ in patients with Parkinson's diseaseS Ylönen, P Ylikotila, A Siitonen, et al.
Biochimica Et Biophysica Acta|August 24, 1999
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the ratJ Sajanti, A S Björkstrand, S Finnilä, et al.
Neurology|July 28, 2004
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathyA M Remes, S Finnilä, H Mononen, et al.
Pageof 2