Three Nonsynonymous Single Nucleotide Polymorphisms in theRhitHGene Cause Reduction of the Repression Activity That Leads to Upregulation of M-LPH, a Participant in Mitochondrial Function-Reference-Cited by-同舟云学术

Three Nonsynonymous Single Nucleotide Polymorphisms in theRhitHGene Cause Reduction of the Repression Activity That Leads to Upregulation of M-LPH, a Participant in Mitochondrial Function

Published:2013-12 Issue:6 Volume:2 Page:440-447
ISSN:2164-7860
Container-title:BioResearch Open Access
language:en
Short-container-title:BioResearch Open Access

Author:

Iida Reiko¹²,Ueki Misuzu³,Fujihara Junko⁴,Takeshita Haruo⁴,Kimura-Kataoka Kaori⁴,Yasuda Toshihiro²³

Affiliation:

1. Division of Life Science, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

2. Research and Education Program for Life Science, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

3. Division of Medical Genetics & Biochemistry, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

4. Department of Legal Medicine, Center for Integrated Research in Science, Shimane University School of Medicine, Izumo, Japan.

Publisher

Mary Ann Liebert Inc

Subject

General Biochemistry, Genetics and Molecular Biology

Link

http://www.liebertpub.com/doi/pdf/10.1089/biores.2013.0042

Reference27 articles.

2. Cloning, Mapping, Genomic Organization, and Expression of Mouse M-LP, a New Member of the Peroxisomal Membrane Protein Mpv17 Domain Family

3. M-LP, Mpv17-like Protein, Has a Peroxisomal Membrane Targeting Signal Comprising a Transmembrane Domain and a Positively Charged Loop and Up-regulates Expression of the Manganese Superoxide Dismutase Gene

4. Transgenic mouse model of kidney disease: Insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome

5. Inner ear defect similar to Alport's syndrome in the glomerulosclerosis mouse model Mpv17

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1. Deficiency of M-LP/Mpv17L leads to development of β-cell hyperplasia and improved glucose tolerance via activation of the Wnt and TGF-β pathways;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2022-03

2. Knockout of Mpv17-Like Protein (M-LPH) Gene in Human Hepatoma Cells Results in Impairment of mtDNA Integrity through Reduction of TFAM, OGG1, and LIG3 at the Protein Levels;Oxidative Medicine and Cellular Longevity;2018-09-17

3. Identification of interacting partners of Human Mpv17-like protein with a mitigating effect of mitochondrial dysfunction through mtDNA damage;Free Radical Biology and Medicine;2015-10