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

Guenter Schwarz

Showing results (61-70 of 73) with videos related to

Pageof 8
Sort By:
Cell Reports|February 7, 2025
The endocytic adaptor AP-2 maintains Purkinje cell function by balancing cerebellar parallel and climbing fiber synapsesMarianna Tolve, Janine Tutas, Ebru Özer-Yildiz, et al.
Antioxidants & Redox Signaling|October 15, 2014
Sulfite Oxidase Catalyzes Single-Electron Transfer at Molybdenum Domain to Reduce Nitrite to Nitric OxideJun Wang, Sabina Krizowski, Katrin Fischer-Schrader, et al.
Human Molecular Genetics|October 7, 2021
Biallelic gephyrin variants lead to impaired GABAergic inhibition in a patient with developmental and epileptic encephalopathyArthur Macha, Filip Liebsch, Steffen Fricke, et al.
Pediatrics|September 19, 2012
Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMPMarrit M Hitzert, Arend F Bos, Klasien A Bergman, et al.
Clinical Pharmacology and Therapeutics|May 11, 2022
Molybdenum Cofactor Catabolism Unravels the Physiological Role of the Drug Metabolizing Enzyme Thiopurine S-MethyltransferaseJulika Pristup, Elke Schaeffeler, Sita Arjune, et al.
Nature Metabolism|January 15, 2025
Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activityJanine Tutas, Marianna Tolve, Ebru Özer-Yildiz, et al.
EMBO Molecular Medicine|November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine|December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
The Journal of Clinical Investigation|November 3, 2025
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide releaseChun-Yu Fu, Joshua B Kohl, Filip Liebsch, et al.
The EMBO Journal|July 21, 2022
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Cell Reports|February 7, 2025
The endocytic adaptor AP-2 maintains Purkinje cell function by balancing cerebellar parallel and climbing fiber synapsesMarianna Tolve, Janine Tutas, Ebru Özer-Yildiz, et al.
Antioxidants & Redox Signaling|October 15, 2014
Sulfite Oxidase Catalyzes Single-Electron Transfer at Molybdenum Domain to Reduce Nitrite to Nitric OxideJun Wang, Sabina Krizowski, Katrin Fischer-Schrader, et al.
Human Molecular Genetics|October 7, 2021
Biallelic gephyrin variants lead to impaired GABAergic inhibition in a patient with developmental and epileptic encephalopathyArthur Macha, Filip Liebsch, Steffen Fricke, et al.
Pediatrics|September 19, 2012
Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMPMarrit M Hitzert, Arend F Bos, Klasien A Bergman, et al.
Clinical Pharmacology and Therapeutics|May 11, 2022
Molybdenum Cofactor Catabolism Unravels the Physiological Role of the Drug Metabolizing Enzyme Thiopurine S-MethyltransferaseJulika Pristup, Elke Schaeffeler, Sita Arjune, et al.
Nature Metabolism|January 15, 2025
Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activityJanine Tutas, Marianna Tolve, Ebru Özer-Yildiz, et al.
EMBO Molecular Medicine|November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
EMBO Molecular Medicine|December 3, 2017
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
The Journal of Clinical Investigation|November 3, 2025
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide releaseChun-Yu Fu, Joshua B Kohl, Filip Liebsch, et al.
The EMBO Journal|July 21, 2022
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Pageof 8