(Q48742196)

15 February 2018

title

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism (English)

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15 February 2018

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5

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15 February 2018

Laura Silvestri

Laura Silvestri

1

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Giorgio Casari

Giorgio Casari

7

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Enza Maria Valente

Enza Maria Valente

6

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Emanuele Bellacchio

3

Emanuele Bellacchio

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15 February 2018

Viviana Caputo

2

Viviana Caputo

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15 February 2018

author name string

Luigia Atorino

4

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15 February 2018

publication date

5 October 2005

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15 February 2018

published in

Human Molecular Genetics

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15 February 2018

volume

14

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15 February 2018

issue

22

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15 February 2018

page(s)

3477-3492

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15 February 2018

Parkinson's disease: mechanisms and models

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Hereditary early-onset Parkinson's disease caused by mutations in PINK1

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PINK1 mutations are associated with sporadic early-onset parkinsonism

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Novel PINK1 mutations in early-onset parkinsonism

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Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism

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Growth-suppressive effects of BPOZ and EGR2, two genes involved in the PTEN signaling pathway.

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The protein kinase complement of the human genome

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Parkin phosphorylation and modulation of its E3 ubiquitin ligase activity

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Alpha-synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease

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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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Rotenone neurotoxicity: a new window on environmental causes of Parkinson's disease and related brain amyloidoses

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alpha-synuclein promotes mitochondrial deficit and oxidative stress

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Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis

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The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization

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21 January 2018

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Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

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A simple method for displaying the hydropathic character of a protein

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Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.

21 January 2018

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Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability

21 January 2018

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Proteomic analysis of the mouse liver mitochondrial inner membrane

21 January 2018

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Lipid microdomains contribute to apoptosis-associated modifications of mitochondria in T cells.

21 January 2018

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The conformational plasticity of protein kinases

21 January 2018

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Kinase signaling cascades in the mitochondrion: a matter of life or death.

21 January 2018

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Cyclic adenosine monophosphate-dependent phosphorylation of mammalian mitochondrial proteins: enzyme and substrate characterization and functional role.

21 January 2018

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Protein kinase Cdelta activation induces apoptosis in response to cardiac ischemia and reperfusion damage: a mechanism involving BAD and the mitochondria

21 January 2018

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Sulfonylurea-sensitive potassium current evoked by sodium-loading in rat midbrain dopamine neurons

21 January 2018

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The role of oxidative stress, impaired glycolysis and mitochondrial respiratory redox failure in the cytotoxic effects of 6-hydroxydopamine in vitro

21 January 2018

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Molecular mechanisms of caspase regulation during apoptosis

21 January 2018

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Identification and functional analysis of human Tom22 for protein import into mitochondria

21 January 2018

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Loss of the intermembrane space protein Mgm1/OPA1 induces swelling and localized constrictions along the lengths of mitochondria

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDI377

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI377

1 reference

15 February 2018

1 reference

15 February 2018