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Literature DB >> 9973274

The yeast connection to Friedreich ataxia.

S A Knight¹, R Kim, D Pain, A Dancis.

Abstract

Entities: Disease Species

Mesh：

Substances：

Year: 1999 PMID： 9973274 PMCID： PMC1377746 DOI： 10.1086/302270

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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27 in total

1. Requirement for hsp70 in the mitochondrial matrix for translocation and folding of precursor proteins.

Authors: P J Kang; J Ostermann; J Shilling; W Neupert; E A Craig; N Pfanner
Journal: Nature Date: 1990-11-08 Impact factor: 49.962

2. A study of iron metabolism in neuropsychiatric patients. Hallervorden-Spatz disease.

Authors: J Szanto; F Gallyas
Journal: Arch Neurol Date: 1966-04

3. Characterization of yeast methyl sterol oxidase (ERG25) and identification of a human homologue.

Authors: L Li; J Kaplan
Journal: J Biol Chem Date: 1996-07-12 Impact factor: 5.157

4. A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.

Authors: P Smeyers; E Monrós; J Vílchez; J Lopez-Arlandis; F Prieto; F Palau
Journal: Hum Genet Date: 1996-06 Impact factor: 4.132

5. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.

Authors: K Ouahchi; M Arita; H Kayden; F Hentati; M Ben Hamida; R Sokol; H Arai; K Inoue; J L Mandel; M Koenig
Journal: Nat Genet Date: 1995-02 Impact factor: 38.330

6. Molecular cloning of mtp70, a mitochondrial member of the hsp70 family.

Authors: D M Engman; L V Kirchhoff; J E Donelson
Journal: Mol Cell Biol Date: 1989-11 Impact factor: 4.272

7. The cardiomyopathy of Friedreich's ataxia morphological observations in 3 cases.

Authors: J B Lamarche; M Côté; B Lemieux
Journal: Can J Neurol Sci Date: 1980-11 Impact factor: 2.104

8. The cold sensitivity of a mutant of Saccharomyces cerevisiae lacking a mitochondrial heat shock protein 70 is suppressed by loss of mitochondrial DNA.

Authors: B Schilke; J Forster; J Davis; P James; W Walter; S Laloraya; J Johnson; B Miao; E Craig
Journal: J Cell Biol Date: 1996-08 Impact factor: 10.539

9. Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.

Authors: F Palau; G De Michele; J J Vilchez; M Pandolfo; E Monrós; S Cocozza; P Smeyers; J Lopez-Arlandis; G Campanella; S Di Donato
Journal: Ann Neurol Date: 1995-03 Impact factor: 10.422

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

Authors: V Campuzano; L Montermini; M D Moltò; L Pianese; M Cossée; F Cavalcanti; E Monros; F Rodius; F Duclos; A Monticelli; F Zara; J Cañizares; H Koutnikova; S I Bidichandani; C Gellera; A Brice; P Trouillas; G De Michele; A Filla; R De Frutos; F Palau; P I Patel; S Di Donato; J L Mandel; S Cocozza; M Koenig; M Pandolfo
Journal: Science Date: 1996-03-08 Impact factor: 47.728

12 in total

Review 1. Yeast as a model for human mtDNA replication.

Authors: G S Shadel
Journal: Am J Hum Genet Date: 1999-11 Impact factor: 11.025

2. Antioxidant enzymes in blood of patients with Friedreich's ataxia.

Authors: G Tozzi; M Nuccetelli; M Lo Bello; S Bernardini; L Bellincampi; S Ballerini; L M Gaeta; C Casali; A Pastore; G Federici; E Bertini; F Piemonte
Journal: Arch Dis Child Date: 2002-05 Impact factor: 3.791

3. Self-association and precursor protein binding of Saccharomyces cerevisiae Tom40p, the core component of the protein translocation channel of the mitochondrial outer membrane.

Authors: D M Gordon; J Wang; B Amutha; D Pain
Journal: Biochem J Date: 2001-05-15 Impact factor: 3.857

The yeast connection to Friedreich ataxia.

1. Requirement for hsp70 in the mitochondrial matrix for translocation and folding of precursor proteins.

2. A study of iron metabolism in neuropsychiatric patients. Hallervorden-Spatz disease.

3. Characterization of yeast methyl sterol oxidase (ERG25) and identification of a human homologue.

4. A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.

5. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.

6. Molecular cloning of mtp70, a mitochondrial member of the hsp70 family.

7. The cardiomyopathy of Friedreich's ataxia morphological observations in 3 cases.

8. The cold sensitivity of a mutant of Saccharomyces cerevisiae lacking a mitochondrial heat shock protein 70 is suppressed by loss of mitochondrial DNA.

9. Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.

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

Review 1. Yeast as a model for human mtDNA replication.

2. Antioxidant enzymes in blood of patients with Friedreich's ataxia.

3. Self-association and precursor protein binding of Saccharomyces cerevisiae Tom40p, the core component of the protein translocation channel of the mitochondrial outer membrane.

Review 4. Protein fate in neurodegenerative proteinopathies: polyglutamine diseases join the (mis)fold.

Review 5. Mitochondrial involvement in cell death of non-mammalian eukaryotes.

6. GTP in the mitochondrial matrix plays a crucial role in organellar iron homoeostasis.

Review 7. Molecular genetics approaches in yeast to study amyloid diseases.

8. A dynamic model of the proteins that form the initial iron-sulfur cluster biogenesis machinery in yeast mitochondria.

Review 9. Making yeast tremble: yeast models as tools to study neurodegenerative disorders.

Review 10. Modeling Huntington disease in yeast: perspectives and future directions.