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

Peter Vangheluwe

Showing results (31-40 of 82) with videos related to

Pageof 9
Sort By:
Autophagy|April 5, 2019
<i>LRRK2</i> mutations impair depolarization-induced mitophagy through inhibition of mitochondrial accumulation of RAB10Fieke Wauters, Tom Cornelissen, Dorien Imberechts, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|December 12, 2023
The lipid flippase ATP10B enables cellular lipid uptake under stress conditionsRosanne Wouters, Igor Beletchi, Chris Van den Haute, et al.
Frontiers in Molecular Neuroscience|June 7, 2014
Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disordersSarah van Veen, Danny M Sørensen, Tine Holemans, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|June 16, 2022
The alkalinizing, lysosomotropic agent ML-9 induces a pH-dependent depletion of ER Ca<sup>2+</sup> stores in celluloMartijn Kerkhofs, Tamara Vervloessem, Tomas Luyten, et al.
Human Molecular Genetics|February 19, 2020
CHCHD2 harboring Parkinson's disease-linked T61I mutation precipitates inside mitochondria and induces precipitation of wild-type CHCHD2Tom Cornelissen, Marco Spinazzi, Shaun Martin, et al.
The Journal of Biological Chemistry|April 25, 2012
Transmembrane helix 11 is a genuine regulator of the endoplasmic reticulum Ca2+ pump and acts as a functional parallel of β-subunit on α-Na+,K+-ATPasePrzemek A Gorski, Catharine A Trieber, Els Larivière, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Structural basis for the high Ca2+ affinity of the ubiquitous SERCA2b Ca2+ pumpIlse Vandecaetsbeek, Mieke Trekels, Marc De Maeyer, et al.
International Journal of Molecular Sciences|April 3, 2021
ATP13A2 Regulates Cellular α-Synuclein Multimerization, Membrane Association, and ExternalizationJianmin Si, Chris Van den Haute, Evy Lobbestael, et al.
Frontiers in Neuroscience|July 8, 2022
Inter-organellar Communication in Parkinson's and Alzheimer's Disease: Looking Beyond Endoplasmic Reticulum-Mitochondria Contact SitesStephanie Vrijsen, Céline Vrancx, Mara Del Vecchio, et al.
International Journal of Molecular Sciences|February 25, 2023
Identification and Characterization of p300-Mediated Lysine Residues in Cardiac SERCA2aPrzemek A Gorski, Ahyoung Lee, Philyoung Lee, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Autophagy|April 5, 2019
<i>LRRK2</i> mutations impair depolarization-induced mitophagy through inhibition of mitochondrial accumulation of RAB10Fieke Wauters, Tom Cornelissen, Dorien Imberechts, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|December 12, 2023
The lipid flippase ATP10B enables cellular lipid uptake under stress conditionsRosanne Wouters, Igor Beletchi, Chris Van den Haute, et al.
Frontiers in Molecular Neuroscience|June 7, 2014
Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disordersSarah van Veen, Danny M Sørensen, Tine Holemans, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|June 16, 2022
The alkalinizing, lysosomotropic agent ML-9 induces a pH-dependent depletion of ER Ca<sup>2+</sup> stores in celluloMartijn Kerkhofs, Tamara Vervloessem, Tomas Luyten, et al.
Human Molecular Genetics|February 19, 2020
CHCHD2 harboring Parkinson's disease-linked T61I mutation precipitates inside mitochondria and induces precipitation of wild-type CHCHD2Tom Cornelissen, Marco Spinazzi, Shaun Martin, et al.
The Journal of Biological Chemistry|April 25, 2012
Transmembrane helix 11 is a genuine regulator of the endoplasmic reticulum Ca2+ pump and acts as a functional parallel of β-subunit on α-Na+,K+-ATPasePrzemek A Gorski, Catharine A Trieber, Els Larivière, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Structural basis for the high Ca2+ affinity of the ubiquitous SERCA2b Ca2+ pumpIlse Vandecaetsbeek, Mieke Trekels, Marc De Maeyer, et al.
International Journal of Molecular Sciences|April 3, 2021
ATP13A2 Regulates Cellular α-Synuclein Multimerization, Membrane Association, and ExternalizationJianmin Si, Chris Van den Haute, Evy Lobbestael, et al.
Frontiers in Neuroscience|July 8, 2022
Inter-organellar Communication in Parkinson's and Alzheimer's Disease: Looking Beyond Endoplasmic Reticulum-Mitochondria Contact SitesStephanie Vrijsen, Céline Vrancx, Mara Del Vecchio, et al.
International Journal of Molecular Sciences|February 25, 2023
Identification and Characterization of p300-Mediated Lysine Residues in Cardiac SERCA2aPrzemek A Gorski, Ahyoung Lee, Philyoung Lee, et al.
Pageof 9