Related references
Note: Only part of the references are listed.DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
Jason R. Vanstone et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2016)
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
Grace Yoon et al.
JOURNAL OF PEDIATRICS (2016)
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission
Rojeen Shahni et al.
BRAIN (2015)
Mutations in Fis1 disrupt orderly disposal of defective mitochondria
Qinfang Shen et al.
MOLECULAR BIOLOGY OF THE CELL (2014)
A novel Drp1 inhibitor diminishes aberrant mitochondrial fission and neurotoxicity
Xin Qi et al.
JOURNAL OF CELL SCIENCE (2013)
The clinical maze of mitochondrial neurology
Salvatore DiMauro et al.
NATURE REVIEWS NEUROLOGY (2013)
Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes
Hanan E. Shamseldin et al.
JOURNAL OF MEDICAL GENETICS (2012)
Role of Drp1, a Key Mitochondrial Fission Protein, in Neuropathic Pain
Luiz F. Ferrari et al.
JOURNAL OF NEUROSCIENCE (2011)
Screening for Active Small Molecules in Mitochondrial Complex I Deficient Patient's Fibroblasts, Reveals AICAR as the Most Beneficial Compound
Anna Golubitzky et al.
PLOS ONE (2011)
A Lethal de Novo Mutation in the Middle Domain of the Dynamin-related GTPase Drp1 Impairs Higher Order Assembly and Mitochondrial Division
Chuang-Rung Chang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
A mitochondrial protein compendium elucidates complex I disease biology
David J. Pagliarini et al.
CELL (2008)
A lethal defect of mitochondrial and peroxisomal fission
Hans R. Waterham et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene
Atsushi Tanaka et al.
EXPERIMENTAL CELL RESEARCH (2006)
Share Paper
