(Q33571798)

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A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Laurence Faivre

6

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Laurence Faivre

1 reference

Europe PubMed Central

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28 July 2017

Christel Thauvin-Robinet

2

object named as

Christel Thauvin-Robinet

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28 July 2017

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Philippe Latour

1

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Europe PubMed Central

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28 July 2017

Chantal Baudelet-Méry

3

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28 July 2017

Pierre Soichot

4

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Europe PubMed Central

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28 July 2017

Veronica Cusin

5

1 reference

Europe PubMed Central

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28 July 2017

Marie-Claire Locatelli

7

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Europe PubMed Central

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28 July 2017

Martine Mayençon

8

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Europe PubMed Central

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28 July 2017

Annie Sarcey

9

1 reference

Europe PubMed Central

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28 July 2017

Emmanuel Broussolle

10

1 reference

Europe PubMed Central

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28 July 2017

William Camu

11

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Europe PubMed Central

PubMed publication ID

28 July 2017

Albert David

12

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Europe PubMed Central

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28 July 2017

Robert Rousson

13

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28 July 2017

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publication date

31 December 2009

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28 July 2017

American Journal of Human Genetics

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28 July 2017

86

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28 July 2017

1

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28 July 2017

77-82

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

The C-Ala Domain Brings Together Editing and Aminoacylation Functions on One tRNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

The structure of alanyl-tRNA synthetase with editing domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

The role of aminoacyl-tRNA synthetases in genetic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Distinct domains of tRNA synthetase recognize the same base pair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Trans-editing of mischarged tRNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Elucidation of tRNA-dependent editing by a class II tRNA synthetase and significance for cell viability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Comparing bound and unbound protein structures using energy calculation and rotamer statistics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Origin of mitochondria in relation to evolutionary history of eukaryotic alanyl-tRNA synthetase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Universal rules and idiosyncratic features in tRNA identity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Functional analysis of peptide motif for RNA microhelix binding suggests new family of RNA-binding domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

14 July 2018

Phenotype of Charcot-Marie-Tooth disease Type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

31 October 2018

Alanyl-tRNA synthetase crystal structure and design for acceptor-stem recognition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

31 October 2018

Free energies of amino acid side-chain rotamers in alpha-helices, beta-sheets and alpha-helix N-caps.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801750

31 October 2018

The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/20045102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

https://pubmed.ncbi.nlm.nih.gov/20045102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modular design of components of the operational RNA code for alanine in evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/20045102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2009.12.005

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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