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Mitochondrial DNA 7908-8816 region mutations in maternally inherited essential hypertensive subjects in China.

Ye Zhu | Xiang Gu | Chao Xu
BMC medical genomics | 2018

Nuclear genes or family-based mitochondrial screening have been the focus of genetic studies into essential hypertension. Studies into the role of mitochondria in sporadic Chinese hypertensives are lacking. The objective of the study was to explore the relationship between mitochondrial DNA (mtDNA) variations and the development of maternally inherited essential hypertension (MIEH) in China.

Pubmed ID: 30326913

Research resources used in this publication

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Associated grants

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This is a list of tools and resources that we have found mentioned in this publication.


mtDB - Human Mitochondrial Genome Database (tool)

RRID:SCR_002945

A database of human mitochondrial genomes containing mtDNA sequences, polymorphic sites, and the ability to search for specific variants. It contains 1865 complete sequences and 839 coding region sequences.

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MITOMAP - A human mitochondrial genome database (tool)

RRID:SCR_002996

Database of polymorphisms and mutations of the human mitochondrial DNA. It reports published and unpublished data on human mitochondrial DNA variation. All data is curated by hand. If you would like to submit published articles to be included in mitomap, please send them the citation and a pdf.

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SPSS (tool)

RRID:SCR_002865

Software package used for interactive, or batched, statistical analysis in social science, health sciences and marketing. Software platform offers advanced statistical analysis, a library of machine-learning algorithms, text analysis, open-source extensibility, integration with big data and deployment into applications.Versions that were produced by SPSS Inc. before the IBM acquisition (Versions 18 and earlier) would be given origin or publisher of SPSS Inc. in Chicago.

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Applied Biosystems (tool)

RRID:SCR_005039

An Antibody supplier

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