(Q28481587)

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Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans

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Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans (English)

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1 reference

based on heuristic

inferred from title

neurodegeneration

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based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

19

object named as

Bernard Brais

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Jean-Pierre Bouchard

12

object named as

Jean-Pierre Bouchard

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object named as

Vafa Bayat

1

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object named as

Manish Jaiswal

3

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object named as

Brett H Graham

18

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object named as

Hugo J Bellen

20

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10

object named as

Jean Mathieu

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Geneviève Bernard

7

object named as

Geneviève Bernard

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11

object named as

Michel Vanasse

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author name string

Isabelle Thiffault

2

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Martine Tétreault

4

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Taraka Donti

5

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Florin Sasarman

6

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Julie Demers-Lamarche

8

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Marie-Josée Dicaire

9

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Marie-France Rioux

13

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Charles M Lourenco

14

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Zhihong Li

15

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Claire Haueter

16

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Eric A Shoubridge

17

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language of work or name

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publication date

2012

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10

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3

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e1001288

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Creative Commons Attribution 4.0 International

20 March 2012

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April 2022 Public Data File from Crossref

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3308940/fullTextXML

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2 June 2018

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21 January 2018

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21 January 2018

DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis.

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

Regulation of postsynaptic structure and protein localization by the Rho-type guanine nucleotide exchange factor dPix

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21 January 2018

Genetic analysis of growth cone guidance in Drosophila: fasciclin II functions as a neuronal recognition molecule

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21 January 2018

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.

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21 January 2018

Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome.

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21 January 2018

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21 January 2018

Mitochondrial DNA mutations in disease and aging.

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Mapping of mutation causing Friedreich's ataxia to human chromosome 9

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21 January 2018

Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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12 December 2020

based on heuristic

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12 December 2020

based on heuristic

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1371/JOURNAL.PBIO.1001288

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