Search research articles
Contact Us
Filters
Showing results (61-70 of 73) with videos related to
Page
of 8
Sort By:
Cell Reports
|
February 7, 2025
The endocytic adaptor AP-2 maintains Purkinje cell function by balancing cerebellar parallel and climbing fiber synapses
Marianna 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 Oxide
Jun 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 encephalopathy
Arthur Macha, Filip Liebsch, Steffen Fricke, et al.
Pediatrics
|
September 19, 2012
Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMP
Marrit 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-Methyltransferase
Julika Pristup, Elke Schaeffeler, Sita Arjune, et al.
Nature Metabolism
|
January 15, 2025
Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activity
Janine 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 encephalopathy
Borislav 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 encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
The Journal of Clinical Investigation
|
November 3, 2025
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide release
Chun-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 NDUFS5
Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
Cell Reports
|
February 7, 2025
The endocytic adaptor AP-2 maintains Purkinje cell function by balancing cerebellar parallel and climbing fiber synapses
Marianna 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 Oxide
Jun 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 encephalopathy
Arthur Macha, Filip Liebsch, Steffen Fricke, et al.
Pediatrics
|
September 19, 2012
Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMP
Marrit 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-Methyltransferase
Julika Pristup, Elke Schaeffeler, Sita Arjune, et al.
Nature Metabolism
|
January 15, 2025
Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activity
Janine 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 encephalopathy
Borislav 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 encephalopathy
Borislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
The Journal of Clinical Investigation
|
November 3, 2025
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide release
Chun-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 NDUFS5
Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Page
of 8