A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. (Q37073167)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27161322%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

title

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function (English)

1 reference

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4 April 2020

main subject

arterial hypertension

0 references

1 reference

13

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4 April 2020

author name string

Pingping Jiang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27161322%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Meng Wang

2

1 reference

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4 April 2020

Ling Xue

3

1 reference

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4 April 2020

Yun Xiao

4

1 reference

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4 April 2020

Jialing Yu

5

1 reference

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4 April 2020

Hui Wang

6

1 reference

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4 April 2020

Juan Yao

7

1 reference

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4 April 2020

Hao Liu

8

1 reference

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4 April 2020

Yanyan Peng

9

1 reference

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4 April 2020

Hanqing Liu

10

1 reference

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4 April 2020

Haiying Li

11

1 reference

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4 April 2020

Ye Chen

12

1 reference

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4 April 2020

language of work or name

English

0 references

publication date

29 June 2016

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Molecular and Cellular Biology

4 April 2020

published in

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4 April 2020

volume

36

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4 April 2020

issue

14

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4 April 2020

page(s)

1920-1930

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Creative Commons Attribution 4.0 International

4 April 2020

copyright license

start time

1 July 2016

1 reference

April 2023 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageQuant

object named as

ImageQuant

2 references

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4936059/fullTextXML

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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29 September 2017

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Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families

27 June 2018

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Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4936059

Mitochondrial tRNA mutations associated with deafness

4 September 2018

1 reference

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Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.

4 September 2018

1 reference

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4 September 2018

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4 September 2018

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The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation

4 September 2018

1 reference

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4 September 2018

1 reference

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4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4936059

Mitochondrial Genetics and Human Systemic Hypertension

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27161322

12 December 2020

inferred from PubMed ID database lookup

The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27161322

12 December 2020

inferred from PubMed ID database lookup

Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27161322

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1128/MCB.00199-16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27161322%20AND%20SRC:MED&resulttype=core&format=json

release_yvqv2ujk4zdcxb33gqq6ukaojq

4 April 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yvqv2ujk4zdcxb33gqq6ukaojq

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27161322%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

PubMed publication ID

27161322

1 reference