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Mitochondrial dynamics and neurodegeneration

https://doi.org/10.1007/s11910-009-0032-7
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50/50 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

The 50 checked references that resolve
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A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
resolves10.1146/annurev.genet.38.072902.093019
Mitochondrial Morphology and Dynamics in Yeast and Multicellular Eukaryotes
resolves10.1083/jcb.151.2.367
Dnm1p Gtpase-Mediated Mitochondrial Fission Is a Multi-Step Process Requiring the Novel Integral Membrane Component Fis1p
resolves10.1242/jcs.02415
The mitochondrial protein MTP18 contributes to mitochondrial fission in mammalian cells
resolves10.1126/science.1099793
Structural Basis of Mitochondrial Tethering by Mitofusin Complexes
resolves10.1073/pnas.0407043101
OPA1 requires mitofusin 1 to promote mitochondrial fusion
resolves10.1074/jbc.M607279200
Mitotic Phosphorylation of Dynamin-related GTPase Drp1 Participates in Mitochondrial Fission
resolves10.1038/sj.embor.7401062
Reversible phosphorylation of Drp1 by cyclic AMP‐dependent protein kinase and calcineurin regulates mitochondrial fission and cell death
resolves10.1074/jbc.C700083200
Cyclic AMP-dependent Protein Kinase Phosphorylation of Drp1 Regulates Its GTPase Activity and Mitochondrial Morphology
resolves10.1016/j.cub.2004.02.004
Sumo1 Conjugates Mitochondrial Substrates and Participates in Mitochondrial Fission
resolves10.1083/jcb.200611064
The mitochondrial E3 ubiquitin ligase MARCH5 is required for Drp1 dependent mitochondrial division
resolves10.1038/nature01633
Mitochondrial membrane remodelling regulated by a conserved rhomboid protease
resolves10.1073/pnas.0604983103
Phosphorylation and cleavage of presenilin-associated rhomboid-like protein (PARL) promotes changes in mitochondrial morphology
resolves10.1242/jcs.03381
Mitochondrial bioenergetics and structural network organization
resolves10.1016/j.mad.2005.03.002
Morpho-dynamic changes of mitochondria during ageing of human endothelial cells
resolves10.1016/j.bbagen.2006.05.012
Regulation of mitochondrial morphology and cell survival by Mitogenin I and mitochondrial single-stranded DNA binding protein
resolves10.1093/jb/mvm245
An RNAi Screen for Mitochondrial Proteins Required to Maintain the Morphology of the Organelle in Caenorhabditis elegans
resolves10.1091/mbc.e05-07-0678
Role of Essential Genes in Mitochondrial Morphogenesis in<i>Saccharomyces cerevisiae</i>
resolves10.1016/S1534-5807(01)00055-7
The Role of Dynamin-Related Protein 1, a Mediator of Mitochondrial Fission, in Apoptosis
resolves10.1016/j.molcel.2004.09.026
Drp-1-Dependent Division of the Mitochondrial Network Blocks Intraorganellar Ca2+ Waves and Protects against Ca2+-Mediated Apoptosis
resolves10.1016/j.ejcb.2007.04.002
Mitochondrial clustering induced by overexpression of the mitochondrial fusion protein Mfn2 causes mitochondrial dysfunction and cell death
resolves10.1038/nrm1697
Mitochondrial fission in apoptosis
resolves10.1007/s00439-004-1199-2
Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2A
resolves10.1038/79944
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
resolves10.1056/NEJMoa064436
A Lethal Defect of Mitochondrial and Peroxisomal Fission
resolves10.1038/ng796
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
resolves10.1083/jcb.200611080
Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations
resolves10.1523/JNEUROSCI.4798-06.2007
Altered Axonal Mitochondrial Transport in the Pathogenesis of Charcot-Marie-Tooth Disease from Mitofusin 2 Mutations
resolves10.1038/nature07534
Mitofusin 2 tethers endoplasmic reticulum to mitochondria
resolves10.1016/S1353-8020(08)70008-7
Genetics of parkinsonism
resolves10.1073/pnas.0602493103
Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of <i>Drosophila</i> Pink1 is rescued by Parkin
resolves10.1038/nature04788
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
resolves10.1038/nature04779
Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
resolves10.1073/pnas.0711845105
Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery
resolves10.1016/j.bbrc.2008.10.104
PINK1 controls mitochondrial localization of Parkin through direct phosphorylation
resolves10.1523/JNEUROSCI.0719-07.2007
Loss-of-Function of Human PINK1 Results in Mitochondrial Pathology and Can Be Rescued by Parkin
resolves10.1038/ncb1644
The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1
resolves10.1242/dmm.000109
Rhomboid-7 and HtrA2/Omi act in a common pathway with the Parkinson’s disease factors Pink1 and Parkin
resolves10.1016/j.freeradbiomed.2008.03.009
6-Hydroxydopamine (6-OHDA) induces Drp1-dependent mitochondrial fragmentation in SH-SY5Y cells
resolves10.1074/jbc.M800989200
The Spinocerebellar Ataxia 12 Gene Product and Protein Phosphatase 2A Regulatory Subunit Bβ2 Antagonizes Neuronal Survival by Promoting Mitochondrial Fission
resolves10.1073/pnas.0804871105
Amyloid-β overproduction causes abnormal mitochondrial dynamics via differential modulation of mitochondrial fission/fusion proteins
resolves10.1074/jbc.M509806200
Interaction of Huntingtin-associated Protein-1 with Kinesin Light Chain
resolves10.1242/jcs.01299
Cytoplasmic dynein regulates the subcellular distribution of mitochondria by controlling the recruitment of the fission factor dynamin-related protein-1
resolves10.1016/j.nbd.2005.05.029
Over-expression of tau results in defective synaptic transmission in Drosophila neuromuscular junctions
resolves10.1016/j.cell.2004.11.003
The Importance of Dendritic Mitochondria in the Morphogenesis and Plasticity of Spines and Synapses
resolves10.1016/S0896-6273(02)01094-2
Axonal Transport of Mitochondria to Synapses Depends on Milton, a Novel Drosophila Protein
resolves10.1016/j.neuron.2005.06.027
The GTPase dMiro Is Required for Axonal Transport of Mitochondria to Drosophila Synapses
resolves10.1073/pnas.261560998
Different responses of astrocytes and neurons to nitric oxide: The role of glycolytically generated ATP in astrocyte protection
resolves10.1016/j.expneurol.2006.08.015
Mitochondria mass is low in mouse substantia nigra dopamine neurons: Implications for Parkinson's disease
resolves10.1038/sj.emboj.7601963
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
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