(Q37965012)

26 August 2017

Neurodegeneration as a consequence of failed mitochondrial maintenance (English)

1 reference

26 August 2017

1 reference

2

1 reference

26 August 2017

Mariusz Karbowski

1

1 reference

26 August 2017

7 December 2011

1 reference

26 August 2017

Acta Neuropathologica

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26 August 2017

123

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26 August 2017

2

1 reference

26 August 2017

157-171

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-011-0921-0

26 August 2017

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cites work

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

A mutation associated with CMT2A neuropathy causes defects in Fzo1 GTP hydrolysis, ubiquitylation, and protein turnover.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondria, oxidants, and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

IBRDC2, an IBR-type E3 ubiquitin ligase, is a regulatory factor for Bax and apoptosis activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Paraquat and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

DNA repair in organelles: Pathways, organization, regulation, relevance in disease and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The layered structure of human mitochondrial DNA nucleoids

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

MAPL is a new mitochondrial SUMO E3 ligase that regulates mitochondrial fission

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial free radical generation, oxidative stress, and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial dysfunction as a cause of optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial dysfunction and spinocerebellar degenerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Cyclic AMP-dependent protein kinase phosphorylation of Drp1 regulates its GTPase activity and mitochondrial morphology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The complexities of p97 function in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial fusion protects against neurodegeneration in the cerebellum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

S-nitrosylation of Drp1 mediates beta-amyloid-related mitochondrial fission and neuronal injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The ubiquitin system: from basic mechanisms to the patient bed.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

OPA1 requires mitofusin 1 to promote mitochondrial fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Enzymes of triacylglycerol synthesis and their regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Protein carbonyl groups as biomarkers of oxidative stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Protein carbonylation, cellular dysfunction, and disease progression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitofusin 2 tethers endoplasmic reticulum to mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mutation spectrum and splicing variants in the OPA1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Bioenergetic dysfunction in Huntington's disease human cybrids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Scission, spores, and apoptosis: a proposal for the evolutionary origin of mitochondria in cell death induction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The novel tail-anchored membrane protein Mff controls mitochondrial and peroxisomal fission in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Iron-dependent functions of mitochondria--relation to neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

21 January 2018

Mitochondrial evolution

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Aging: a theory based on free radical and radiation chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Regulation of mitochondrial morphology by APC/CCdh1-mediated control of Drp1 stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Pathological consequences of VCP mutations on human striated muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Dnm1 forms spirals that are structurally tailored to fit mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

hFis1, a novel component of the mammalian mitochondrial fission machinery

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The mitochondrial E3 ubiquitin ligase MARCH5 is required for Drp1 dependent mitochondrial division

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Regulating mitochondrial outer membrane proteins by ubiquitination and proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Selective degradation of mitochondria by mitophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Gene-environment interactions in Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Impairing the mitochondrial fission and fusion balance: a new mechanism of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Structural basis of mitochondrial tethering by mitofusin complexes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

ALS-linked mutant superoxide dismutase 1 (SOD1) alters mitochondrial protein composition and decreases protein import.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Ubiquitin-proteasome system and mitochondria - reciprocity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Increasing organismal healthspan by enhancing mitochondrial protein quality control.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Emerging roles of mitochondrial proteases in neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Axonal mitochondrial transport and potential are correlated

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Controlling metabolism and cell death: at the heart of mitochondrial calcium signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Direct membrane association drives mitochondrial fission by the Parkinson disease-associated protein alpha-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Cargo-selected transport from the mitochondria to peroxisomes is mediated by vesicular carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Instability of the mitofusin Fzo1 regulates mitochondrial morphology during the mating response of the yeast Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Importance of the lon protease in mitochondrial maintenance and the significance of declining lon in aging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Molecular mechanisms and physiologic functions of mitochondrial dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

A mitochondrial protein compendium elucidates complex I disease biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

MiD49 and MiD51, new components of the mitochondrial fission machinery

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The dynamin-like protein DLP1 is essential for normal distribution and morphology of the endoplasmic reticulum and mitochondria in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Iron-sulphur cluster biogenesis and mitochondrial iron homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

On the origin of mitosing cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Genetic mouse models for Parkinson's disease display severe pathology in glial cell mitochondria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondria: the next (neurode)generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial dynamics and division in budding yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Supply and demand in cerebral energy metabolism: the role of nutrient transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitofusin 2 regulates STIM1 migration from the Ca2+ store to the plasma membrane in cells with depolarized mitochondria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The role of mitochondria in reactive oxygen species metabolism and signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Supercomplex organization of the oxidative phosphorylation enzymes in yeast mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

A mitochondrial ubiquitin ligase MITOL controls cell toxicity of polyglutamine-expanded protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitotic phosphorylation of dynamin-related GTPase Drp1 participates in mitochondrial fission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Quality control of mitochondria: protection against neurodegeneration and ageing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Genotype-phenotype correlations in Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial formation of reactive oxygen species

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Misfolded SOD1 associated with motor neuron mitochondria alters mitochondrial shape and distribution prior to clinical onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The role of mitochondria in apoptosis*.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Effects of overexpression of huntingtin proteins on mitochondrial integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Amyloid-beta overproduction causes abnormal mitochondrial dynamics via differential modulation of mitochondrial fission/fusion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Molecular machinery of mitochondrial fusion and fission

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The AAA-ATPase p97 is essential for outer mitochondrial membrane protein turnover

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial ubiquitin ligase MITOL ubiquitinates mutant SOD1 and attenuates mutant SOD1-induced reactive oxygen species generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

The BCL-2 protein family: opposing activities that mediate cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

GIDE is a mitochondrial E3 ubiquitin ligase that induces apoptosis and slows growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

Visual Recovery Patterns in Children with Leber's Hereditary Optic Neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-011-0921-0

10.1007/S00401-011-0921-0

21 January 2018

Identifiers

DOI

1 reference

26 August 2017

1 reference

PubMed ID

22143516