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

Irene Pichler

Showing results (1-10 of 72) with videos related to

Pageof 8
Sort By:
Molecular Neurodegeneration|July 16, 2022
Crosstalk of organelles in Parkinson's disease - MiT family transcription factors as central players in signaling pathways connecting mitochondria and lysosomesMartin Lang, Peter P Pramstaller, Irene Pichler
Parkinson'S Disease|May 1, 2018
Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease PenetranceAlessandra Zanon, Peter P Pramstaller, Andrew A Hicks, et al.
Neural Regeneration Research|November 2, 2017
SLP-2: a potential new target for improving mitochondrial function in Parkinson's diseaseAlessandra Zanon, Andrew A Hicks, Peter P Pramstaller, et al.
Nature and Science of Sleep|April 26, 2013
Update on the management of restless legs syndrome: existing and emerging treatment optionsMaurizio F Facheris, Andrew A Hicks, Peter P Pramstaller, et al.
Cellular and Molecular Life Sciences : CMLS|May 5, 2022
A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid modelsMartin Lang, Anne Grünewald, Peter P Pramstaller, et al.
Hepatology (Baltimore, Md.)|March 19, 2013
Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasisChristine Schwienbacher, Alice Serafin, Alessandra Zanon, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypesIrene Pichler, Christian Fuchsberger, Christa Platzer, et al.
BMC Genetics|June 24, 2009
Genotyping human ancient mtDNA control and coding region polymorphisms with a multiplexed Single-Base-Extension assay: the singular maternal history of the Tyrolean IcemanPhillip Endicott, Juan J Sanchez, Irene Pichler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 15, 2024
Parkin R274W mutation affects muscle and mitochondrial physiologyMartina Sevegnani, Adriano Lama, Francesco Girardi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Exclusion of linkage to chromosome 14q in a large South Tyrolean family with Idiopathic Basal Ganglia Calcification (IBGC)Claudia Béu Volpato, Alessandro De Grandi, Ebba Buffone, et al.
Pageof 8

Showing results (1-10 of 72) with videos related to

Sort By:
Pageof 8
Molecular Neurodegeneration|July 16, 2022
Crosstalk of organelles in Parkinson's disease - MiT family transcription factors as central players in signaling pathways connecting mitochondria and lysosomesMartin Lang, Peter P Pramstaller, Irene Pichler
Parkinson'S Disease|May 1, 2018
Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease PenetranceAlessandra Zanon, Peter P Pramstaller, Andrew A Hicks, et al.
Neural Regeneration Research|November 2, 2017
SLP-2: a potential new target for improving mitochondrial function in Parkinson's diseaseAlessandra Zanon, Andrew A Hicks, Peter P Pramstaller, et al.
Nature and Science of Sleep|April 26, 2013
Update on the management of restless legs syndrome: existing and emerging treatment optionsMaurizio F Facheris, Andrew A Hicks, Peter P Pramstaller, et al.
Cellular and Molecular Life Sciences : CMLS|May 5, 2022
A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid modelsMartin Lang, Anne Grünewald, Peter P Pramstaller, et al.
Hepatology (Baltimore, Md.)|March 19, 2013
Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasisChristine Schwienbacher, Alice Serafin, Alessandra Zanon, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypesIrene Pichler, Christian Fuchsberger, Christa Platzer, et al.
BMC Genetics|June 24, 2009
Genotyping human ancient mtDNA control and coding region polymorphisms with a multiplexed Single-Base-Extension assay: the singular maternal history of the Tyrolean IcemanPhillip Endicott, Juan J Sanchez, Irene Pichler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 15, 2024
Parkin R274W mutation affects muscle and mitochondrial physiologyMartina Sevegnani, Adriano Lama, Francesco Girardi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Exclusion of linkage to chromosome 14q in a large South Tyrolean family with Idiopathic Basal Ganglia Calcification (IBGC)Claudia Béu Volpato, Alessandro De Grandi, Ebba Buffone, et al.
Pageof 8