(Q37408197)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19732863%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Acute infantile liver failure due to mutations in the TRMU gene (English)

1 reference

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7 February 2020

1 reference

5

1 reference

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7 February 2020

Agnès Rötig

12

1 reference

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7 February 2020

Ivan Tarassov

13

1 reference

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7 February 2020

author name string

Avraham Zeharia

1

1 reference

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7 February 2020

Avraham Shaag

2

1 reference

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7 February 2020

Orit Pappo

3

1 reference

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7 February 2020

Anne-Marie Mager-Heckel

4

1 reference

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7 February 2020

Marine Beinat

6

1 reference

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7 February 2020

Olga Karicheva

7

1 reference

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7 February 2020

Hanna Mandel

8

1 reference

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7 February 2020

Noa Ofek

9

1 reference

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7 February 2020

Reeval Segel

10

1 reference

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7 February 2020

Daphna Marom

11

1 reference

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7 February 2020

Orly Elpeleg

14

1 reference

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7 February 2020

language of work or name

English

0 references

publication date

1 September 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19732863%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

7 February 2020

published in

1 reference

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7 February 2020

volume

85

1 reference

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7 February 2020

issue

3

1 reference

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7 February 2020

page(s)

401-407

1 reference

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Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia

7 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

mtDNA depletion myopathy: elucidation of the tissue specificity in the mitochondrial thymidine kinase (TK2) deficiency

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Interaction of tRNAs and of phosphorothioate-substituted nucleic acids with an organomercurial. Probing the chemical environment of thiolated residues by affinity electrophoresis

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Conserved bases in the TPsi C loop of tRNA are determinants for thermophile-specific 2-thiouridylation at position 54.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Modified nucleoside dependent Watson-Crick and wobble codon binding by tRNALysUUU species

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

Single atom modification (O-->S) of tRNA confers ribosome binding.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2771591

The development of cystathionase activity during the first year of life

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19732863

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hepatic metallothionein as a source of zinc and cysteine during the first year of life

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19732863

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2009.08.004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19732863%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

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7 February 2020

PubMed publication ID

19732863

1 reference