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Literature DB >> 9090376

Frataxin fracas.

M Cossée, V Campuzano, H Koutnikova, K Fischbeck, J L Mandel, M Koenig, S I Bidichandani, P I Patel, M D Moltè, J Cañizares, R De Frutos, L Pianese, F Cavalcanti, A Monticelli, S Cocozza, L Montermini, M Pandolfo.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 1997 PMID： 9090376 DOI： 10.1038/ng0497-337

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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Cited

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15 in total

1. Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.

Authors: S I Bidichandani; T Ashizawa; P I Patel
Journal: Am J Hum Genet Date: 1997-05 Impact factor: 11.025

2. Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model.

Authors: Belén Mollá; Diana C Muñoz-Lasso; Pablo Calap; Angel Fernandez-Vilata; María de la Iglesia-Vaya; Federico V Pallardó; Maria Dolores Moltó; Francesc Palau; Pilar Gonzalez-Cabo
Journal: Neurotherapeutics Date: 2019-04 Impact factor: 7.620

3. Triple therapy with darbepoetin alfa, idebenone, and riboflavin in Friedreich's ataxia: an open-label trial.

Authors: Javier Arpa; Irene Sanz-Gallego; Francisco J Rodríguez-de-Rivera; Francisco J Domínguez-Melcón; Daniel Prefasi; Javier Oliva-Navarro; Mar Moreno-Yangüela; Samuel I Pascual-Pascual
Journal: Cerebellum Date: 2013-10 Impact factor: 3.847

4. The GAA*TTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner.

Authors: E Grabczyk; K Usdin
Journal: Nucleic Acids Res Date: 2000-07-15 Impact factor: 16.971

5. Iron in neurodegenerative disorders.

Authors: D. Berg; G. Becker; P. Riederer; O. Riess
Journal: Neurotox Res Date: 2002 Nov-Dec Impact factor: 3.911

6. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.

Authors: S I Bidichandani; T Ashizawa; P I Patel
Journal: Am J Hum Genet Date: 1998-01 Impact factor: 11.025

Frataxin fracas.

1. Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.

2. Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model.

3. Triple therapy with darbepoetin alfa, idebenone, and riboflavin in Friedreich's ataxia: an open-label trial.

4. The GAA*TTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner.

5. Iron in neurodegenerative disorders.

6. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.

Review 7. Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities.

8. Alleviating transcript insufficiency caused by Friedreich's ataxia triplet repeats.

Review 9. Potential therapeutic benefits of strategies directed to mitochondria.

10. Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen.