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Literature DB >> 18687903

PINK1 in mitochondrial function.

Helene Plun-Favreau¹, John Hardy.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 2008 PMID： 18687903 PMCID： PMC2516263 DOI： 10.1073/pnas.0805908105

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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23 in total

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

Authors: Rosa M Canet-Avilés; Mark A Wilson; David W Miller; Rili Ahmad; Chris McLendon; Sourav Bandyopadhyay; Melisa J Baptista; Dagmar Ringe; Gregory A Petsko; Mark R Cookson
Journal: Proc Natl Acad Sci U S A Date: 2004-06-04 Impact factor: 11.205

2. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Authors: T Kitada; S Asakawa; N Hattori; H Matsumine; Y Yamamura; S Minoshima; M Yokochi; Y Mizuno; N Shimizu
Journal: Nature Date: 1998-04-09 Impact factor: 49.962

Review 3. Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia.

Authors: A H Schapira
Journal: Biochim Biophys Acta Date: 1999-02-09

4. Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin.

Authors: Ira E Clark; Mark W Dodson; Changan Jiang; Joseph H Cao; Jun R Huh; Jae Hong Seol; Soon Ji Yoo; Bruce A Hay; Ming Guo
Journal: Nature Date: 2006-05-03 Impact factor: 49.962

5. Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin.

Authors: Jeehye Park; Sung Bae Lee; Sungkyu Lee; Yongsung Kim; Saera Song; Sunhong Kim; Eunkyung Bae; Jaeseob Kim; Minho Shong; Jin-Man Kim; Jongkyeong Chung
Journal: Nature Date: 2006-05-03 Impact factor: 49.962

6. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

Authors: Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; Cornelia M van Duijn; Ben A Oostra; Peter Heutink
Journal: Science Date: 2002-11-21 Impact factor: 47.728

7. 1-Methyl-4-phenylpyridinium-induced apoptosis in cerebellar granule neurons is mediated by transferrin receptor iron-dependent depletion of tetrahydrobiopterin and neuronal nitric-oxide synthase-derived superoxide.

Authors: Tiesong Shang; Srigiridhar Kotamraju; Shasi V Kalivendi; Cecilia J Hillard; B Kalyanaraman
Journal: J Biol Chem Date: 2004-01-29 Impact factor: 5.157

Review 8. Expanding insights of mitochondrial dysfunction in Parkinson's disease.

Authors: Patrick M Abou-Sleiman; Miratul M K Muqit; Nicholas W Wood
Journal: Nat Rev Neurosci Date: 2006-03 Impact factor: 34.870

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

Authors: Enza Maria Valente; Patrick M Abou-Sleiman; Viviana Caputo; Miratul M K Muqit; Kirsten Harvey; Suzana Gispert; Zeeshan Ali; Domenico Del Turco; Anna Rita Bentivoglio; Daniel G Healy; Alberto Albanese; Robert Nussbaum; Rafael González-Maldonado; Thomas Deller; Sergio Salvi; Pietro Cortelli; William P Gilks; David S Latchman; Robert J Harvey; Bruno Dallapiccola; Georg Auburger; Nicholas W Wood
Journal: Science Date: 2004-04-15 Impact factor: 47.728

PINK1 in mitochondrial function.

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

2. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Review 3. Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia.

4. Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin.

5. Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin.

6. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

7. 1-Methyl-4-phenylpyridinium-induced apoptosis in cerebellar granule neurons is mediated by transferrin receptor iron-dependent depletion of tetrahydrobiopterin and neuronal nitric-oxide synthase-derived superoxide.

Review 8. Expanding insights of mitochondrial dysfunction in Parkinson's disease.

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

10. PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1.

Review 1. Gene-environment interactions: key to unraveling the mystery of Parkinson's disease.

Review 2. Culprit or Bystander: Defective Mitophagy in Alzheimer's Disease.

Review 3. Mitochondrial Kinases and the Role of Mitochondrial Protein Phosphorylation in Health and Disease.

Review 4. PINK1 function in health and disease.