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

Juha Saharinen

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Gene|December 3, 2002
cDNA cloning, expression profile and genomic structure of a novel human transcript on chromosome 10q24, and its analyses as a candidate gene for infantile onset spinocerebellar ataxiaKaisu Nikali, Juha Saharinen, Leena Peltonen
Journal of Cell Science|August 3, 2002
Secretion of human latent TGF-beta-binding protein-3 (LTBP-3) is dependent on co-expression of TGF-betaCarita Penttinen, Juha Saharinen, Krista Weikkolainen, et al.
Nature|February 24, 2006
Identification of pathways regulating cell size and cell-cycle progression by RNAiMikael Björklund, Minna Taipale, Markku Varjosalo, et al.
Nucleic Acids Research|October 13, 2007
CanGEM: mining gene copy number changes in cancerIlari Scheinin, Samuel Myllykangas, Ioana Borze, et al.
The European Journal of Neuroscience|April 14, 2010
Gene expression patterns in a rodent model for depressionMarkus Lagus, Natalia Gass, Juha Saharinen, et al.
Journal of Neurogenetics|July 13, 2012
Inter-tissue networks between the basal forebrain, hippocampus, and prefrontal cortex in a model for depression caused by disturbed sleepMarkus Lagus, Natalia Gass, Juha Saharinen, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 5, 2008
Critical immunological pathways are downregulated in APECED patient dendritic cellsNora Pöntynen, Mari Strengell, Niko Sillanpää, et al.
Journal of Neurobiology|September 13, 2005
Indicative oligodendrocyte dysfunction in spinal cords of human fetuses suffering from a lethal motoneuron diseaseNiklas Pakkasjärvi, Massimiliano Gentile, Juha Saharinen, et al.
Human Molecular Genetics|September 2, 2005
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and TwinkyKaisu Nikali, Anu Suomalainen, Juha Saharinen, et al.
BMC Genomics|March 29, 2008
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseasesCarina von Schantz, Juha Saharinen, Outi Kopra, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Gene|December 3, 2002
cDNA cloning, expression profile and genomic structure of a novel human transcript on chromosome 10q24, and its analyses as a candidate gene for infantile onset spinocerebellar ataxiaKaisu Nikali, Juha Saharinen, Leena Peltonen
Journal of Cell Science|August 3, 2002
Secretion of human latent TGF-beta-binding protein-3 (LTBP-3) is dependent on co-expression of TGF-betaCarita Penttinen, Juha Saharinen, Krista Weikkolainen, et al.
Nature|February 24, 2006
Identification of pathways regulating cell size and cell-cycle progression by RNAiMikael Björklund, Minna Taipale, Markku Varjosalo, et al.
Nucleic Acids Research|October 13, 2007
CanGEM: mining gene copy number changes in cancerIlari Scheinin, Samuel Myllykangas, Ioana Borze, et al.
The European Journal of Neuroscience|April 14, 2010
Gene expression patterns in a rodent model for depressionMarkus Lagus, Natalia Gass, Juha Saharinen, et al.
Journal of Neurogenetics|July 13, 2012
Inter-tissue networks between the basal forebrain, hippocampus, and prefrontal cortex in a model for depression caused by disturbed sleepMarkus Lagus, Natalia Gass, Juha Saharinen, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 5, 2008
Critical immunological pathways are downregulated in APECED patient dendritic cellsNora Pöntynen, Mari Strengell, Niko Sillanpää, et al.
Journal of Neurobiology|September 13, 2005
Indicative oligodendrocyte dysfunction in spinal cords of human fetuses suffering from a lethal motoneuron diseaseNiklas Pakkasjärvi, Massimiliano Gentile, Juha Saharinen, et al.
Human Molecular Genetics|September 2, 2005
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and TwinkyKaisu Nikali, Anu Suomalainen, Juha Saharinen, et al.
BMC Genomics|March 29, 2008
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseasesCarina von Schantz, Juha Saharinen, Outi Kopra, et al.
Pageof 3