The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells-Reference-Cited by-同舟云学术

The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells

Published:2014-01-10 Issue:2 Volume:6 Page:169-182
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Perli Elena¹²,Giordano Carla¹,Pisano Annalinda¹³,Montanari Arianna¹²⁴,Campese Antonio F⁵,Reyes Aurelio⁶,Ghezzi Daniele⁷,Nasca Alessia⁷,Tuppen Helen A⁸,Orlandi Maurizia¹⁵,Di Micco Patrizio⁹,Poser Elena⁹,Taylor Robert W⁸,Colotti Gianni¹⁰,Francisci Silvia²⁴,Morea Veronica¹⁰,Frontali Laura²⁴,Zeviani Massimo⁶,d'Amati Giulia¹²

Affiliation:

1. Department of Radiology, Oncology and Pathology Sapienza University of Rome Rome Italy

2. Pasteur Institute‐Cenci Bolognetti Foundation Rome Italy

3. Department of Internal Medicine and Medical Specialties Sapienza University of Rome Rome Italy

4. Department of Biology and Biotechnologies ‘Charles Darwin’ Sapienza University of Rome Rome Italy

5. Department of Molecular Medicine Sapienza University of Rome Rome Italy

6. MRC‐Mitochondrial Biology Unit Cambridge UK

7. Unit of Molecular Neurogenetics The Foundation “Carlo Besta” Institute of Neurology IRCCS Milan Italy

8. Wellcome Trust Center for Mitochondrial Research Institute for Ageing and Health Newcastle University Newcastle upon Tyne UK

9. Department of Biochemical Sciences “A. Rossi Fanelli” Sapienza University of Rome Rome Italy

10. National Research Council of Italy Institute of Molecular Biology and Pathology Rome Italy

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/emmm.201303198

Reference52 articles.

1. The Role of Aminoacyl-tRNA Synthetases in Genetic Diseases

2. Notch3 and Canonical NF-κB Signaling Pathways Cooperatively Regulate Foxp3 Transcription

3. Mutations in the Mitochondrial Seryl-tRNA Synthetase Cause Hyperuricemia, Pulmonary Hypertension, Renal Failure in Infancy and Alkalosis, HUPRA Syndrome

4. The Protein Data Bank

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