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Knockout of M-LP/Mpv17L, a newly identified atypical PDE, alleviates diabetic conditions in mice

Acta diabetologica, 2024-10, Vol.61 (10), p.1327-1331

2024

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High-fat diets cause insulin resistance despite an increase in muscle mitochondria

Proceedings of the National Academy of Sciences - PNAS, 2008-06, Vol.105 (22), p.7815-7820

2008

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Discrimination Between Infant and Adult Bloodstains Using Micro‐Raman Spectroscopy: A Preliminary Study

Journal of forensic sciences, 2019-05, Vol.64 (3), p.698-701

2019

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Survey of single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 2 producing loss of function potentially implicated in the pathogenesis of parakeratosis

PloS one, 2017-04, Vol.12 (4), p.e0175083

2017

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Evaluation of the functional effects of genetic variants‒missense and nonsense SNPs, indels and copy number variations‒in the gene encoding human deoxyribonuclease I potentially implicated in autoimmunity

Scientific reports, 2019-09, Vol.9 (1), p.13660-11, Article 13660

2019

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Low genetic heterogeneity of copy number variations (CNVs) in the genes encoding the human deoxyribonucleases 1-like 3 and II potentially relevant to autoimmunity

PloS one, 2019-04, Vol.14 (4), p.e0215479-e0215479

2019

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Association of SNPs in genes encoding zinc transporters on blood zinc levels in humans

Legal medicine (Tokyo, Japan), 2018-01, Vol.30, p.28-33

2018

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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, Vol.2018 (2018), p.1-14

2018

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Distribution and toxicity evaluation of ZnO dispersion nanoparticles in single intravenously exposed mice

The Journal of Medical Investigation, 2015, Vol.62(1.2), pp.45-50

2015

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Analysis of copy number variation in the NEDD4L gene potentially implicated in body height in the Japanese population

Legal medicine (Tokyo, Japan), 2019-03, Vol.37, p.83-85

2019

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Association of SNPs in transferrin and transferrin receptor genes with blood iron levels in human

Legal medicine (Tokyo, Japan), 2019-02, Vol.36, p.17-20

2019

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Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.2917-2927

2013

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Worldwide Distribution of Four SNPs in X‐Ray and Repair and Cross‐Complementing Group 1 (XRCC1)

Clinical and translational science, 2015-08, Vol.8 (4), p.347-350

2015

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Identification of functional SNPs potentially served as a genetic risk factor for the pathogenesis of parakeratosis in the gene encoding human deoxyribonuclease I-like 2 (DNase 1L2) implicated in terminal differentiation of keratinocytes

Gene, 2015-04, Vol.561 (1), p.15-22

2015

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Accuracy and Usefulness of the AVOXimeter 4000 as Routine Analysis of Carboxyhemoglobin

Journal of forensic sciences, 2013-07, Vol.58 (4), p.1047-1049

2013

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Evaluation of all nonsynonymous single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 1, possibly implicated in the blocking of endocytosis-mediated foreign gene transfer

DNA and cell biology, 2014-02, Vol.33 (2), p.79-87

2014

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Comparative biochemical properties of vertebrate deoxyribonuclease I

Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 2012-11, Vol.163 (3-4), p.263-273

2012

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Evaluation of all non‐synonymous single nucleotide polymorphisms (SNPs) in the genes encoding human deoxyribonuclease I and I‐like 3 as a functional SNP potentially implicated in autoimmunity

The FEBS journal, 2014-01, Vol.281 (1), p.376-390

2014

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Identification of the functional alleles of the nonsynonymous single-nucleotide polymorphisms potentially implicated in systemic lupus erythematosus in the human deoxyribonuclease I gene

DNA and cell biology, 2014-08, Vol.33 (8), p.492-502

2014

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Simple screening method for copy number variations associated with physical features

Legal medicine (Tokyo, Japan), 2017-03, Vol.25, p.71-74

2017

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Functional Single Nucleotide Polymorphisms (SNPs) in the Genes Encoding the Human Deoxyribonuclease (DNase) Family Potentially Relevant to Autoimmunity

Immunological investigations, 2016-07, Vol.45 (5), p.406-419

2016

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Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme

Clinica chimica acta, 2009-09, Vol.407 (1), p.20-24

2009

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Seven nonsynonymous SNPs in the gene encoding human deoxyribonuclease II may serve as a functional SNP potentially implicated in autoimmune dysfunction

Electrophoresis, 2013-12, Vol.34 (24), p.3361-3369

2013

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An autopsy case of spontaneous esophageal perforation (Boerhaave syndrome)

Legal medicine (Tokyo, Japan), 2016-11, Vol.23, p.5-9

2016

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Five non-synonymous SNPs in the gene encoding human deoxyribonuclease I-like 2 implicated in terminal differentiation of keratinocytes reduce or abolish its activity

Electrophoresis, 2013-02, Vol.34 (3), p.456-462

2013

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Knockout of M-LP/Mpv17L, a newly identified atypical PDE, alleviates diabetic conditions in mice

High-fat diets cause insulin resistance despite an increase in muscle mitochondria

Discrimination Between Infant and Adult Bloodstains Using Micro‐Raman Spectroscopy: A Preliminary Study

Survey of single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 2 producing loss of function potentially implicated in the pathogenesis of parakeratosis

Evaluation of the functional effects of genetic variants‒missense and nonsense SNPs, indels and copy number variations‒in the gene encoding human deoxyribonuclease I potentially implicated in autoimmunity

Low genetic heterogeneity of copy number variations (CNVs) in the genes encoding the human deoxyribonucleases 1-like 3 and II potentially relevant to autoimmunity

Association of SNPs in genes encoding zinc transporters on blood zinc levels in humans

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

Distribution and toxicity evaluation of ZnO dispersion nanoparticles in single intravenously exposed mice

Analysis of copy number variation in the NEDD4L gene potentially implicated in body height in the Japanese population

Association of SNPs in transferrin and transferrin receptor genes with blood iron levels in human

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual

Worldwide Distribution of Four SNPs in X‐Ray and Repair and Cross‐Complementing Group 1 (XRCC1)

Identification of functional SNPs potentially served as a genetic risk factor for the pathogenesis of parakeratosis in the gene encoding human deoxyribonuclease I-like 2 (DNase 1L2) implicated in terminal differentiation of keratinocytes

Accuracy and Usefulness of the AVOXimeter 4000 as Routine Analysis of Carboxyhemoglobin

Evaluation of all nonsynonymous single-nucleotide polymorphisms in the gene encoding human deoxyribonuclease I-like 1, possibly implicated in the blocking of endocytosis-mediated foreign gene transfer

Comparative biochemical properties of vertebrate deoxyribonuclease I

Evaluation of all non‐synonymous single nucleotide polymorphisms (SNPs) in the genes encoding human deoxyribonuclease I and I‐like 3 as a functional SNP potentially implicated in autoimmunity

Identification of the functional alleles of the nonsynonymous single-nucleotide polymorphisms potentially implicated in systemic lupus erythematosus in the human deoxyribonuclease I gene

Simple screening method for copy number variations associated with physical features

Functional Single Nucleotide Polymorphisms (SNPs) in the Genes Encoding the Human Deoxyribonuclease (DNase) Family Potentially Relevant to Autoimmunity

Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme

Seven nonsynonymous SNPs in the gene encoding human deoxyribonuclease II may serve as a functional SNP potentially implicated in autoimmune dysfunction

An autopsy case of spontaneous esophageal perforation (Boerhaave syndrome)

Five non-synonymous SNPs in the gene encoding human deoxyribonuclease I-like 2 implicated in terminal differentiation of keratinocytes reduce or abolish its activity

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