Kaori Kimura-Kataoka

发表

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

T. Yasuda, H. Takeshita, J. Fujihara, 2015, Clinical and translational science.

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

R. Iida, T. Yasuda, M. Ueki, 2019, Scientific Reports.

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

R. Iida, T. Yasuda, M. Ueki, 2019, PloS one.

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

R. Iida, T. Yasuda, M. Ueki, 2019, Legal medicine.

Simple screening method for copy number variations associated with physical features.

Toshihiro Yasuda, Kaori Kimura-Kataoka, Misuzu Ueki, 2017, Legal medicine.

Cell-free DNA Release in the Plasma of Patients with Cardiac Disease is Associated with Cell Death Processes

H. Takeshita, J. Fujihara, Yasuyuki Kawai, 2022, Indian Journal of Clinical Biochemistry.

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.

R. Iida, T. Yasuda, M. Ueki, 2014, DNA and cell biology.

Genetic and expression analysis of all non‐synonymous single nucleotide polymorphisms in the human deoxyribonuclease I‐like 1 and 2 genes

R. Iida, T. Yasuda, I. Yuasa, 2010, Electrophoresis.

Implementation of a personal identification system using alveolar bone images.

H. Fujimoto, H. Takeshita, Y. Kurihara, 2023, Forensic science international.

Circulating cell-free DNA fragment analysis by microchip electrophoresis and its relationship with DNase I in cardiac diseases.

T. Yasuda, M. Ueki, H. Takeshita, 2019, Clinica chimica acta; international journal of clinical chemistry.

Blood identification and discrimination between human and nonhuman blood using portable Raman spectroscopy

T. Yasuda, H. Takeshita, J. Fujihara, 2017, International Journal of Legal Medicine.

Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution.

R. Iida, T. Yasuda, I. Yuasa, 2012, Legal medicine.

Confirmation that SNPs in the high mobility group‐A2 gene (HMGA2) are associated with adult height in the Japanese population; wide‐ranging population survey of height‐related SNPs in HMGA2

R. Iida, T. Yasuda, Y. Koda, 2011, Electrophoresis.

First survey of the three gene polymorphisms (PON1 Q192R, eNOS E298D and eNOS C‐786T) potentially associated with coronary artery spasm in African populations and comparison with worldwide data

T. Yasuda, Y. Koda, H. Takeshita, 2011, Cell biochemistry and function.

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

R. Iida, T. Yasuda, M. Ueki, 2016, Immunological investigations.

Distribution and haplotype analysis of all the non-synonymous and autoimmunity-related single nucleotide polymorphisms in the human deoxyribonuclease II gene using worldwide populations.

R. Iida, T. Yasuda, M. Ueki, 2013, Legal medicine.

Ethnic variation in genotype frequencies of delta-aminolevulinic acid dehydratase (ALAD).

T. Yasuda, Y. Koda, A. Panduro, 2009, Toxicology letters.

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

R. Iida, T. Yasuda, M. Hasegawa, 2017, PloS one.

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.

R. Iida, T. Yasuda, M. Ueki, 2015, Gene.

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

R. Iida, T. Yasuda, M. Ueki, 2013, Electrophoresis.

Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I‐like 1 and 2 genes

R. Iida, T. Yasuda, Y. Koda, 2010, Electrophoresis.

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

T. Yasuda, H. Takeshita, J. Fujihara, 2015, The journal of medical investigation : JMI.

Comparison of Acute Toxicity of ZnO and Silica-coated ZnO Nanoparticles in Mice after Single Intravenous Injection: Preliminary Experiment to Apply to Biological Imaging

Hideki Hashimoto, Takaya Yamada, Miki Tongu, 2014 .

Global analysis of genetic variations in a 56-bp variable number of tandem repeat polymorphisms within the human deoxyribonuclease I gene.

R. Iida, T. Yasuda, M. Ueki, 2015, Legal medicine.

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

R. Iida, T. Yasuda, M. Ueki, 2014, DNA and cell biology.

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

R. Iida, T. Yasuda, M. Ueki, 2014, The FEBS journal.

Functional and genetic survey of all known single-nucleotide polymorphisms within the human deoxyribonuclease I gene in wide-ranging ethnic groups.

R. Iida, T. Yasuda, Y. Koda, 2011, DNA and cell biology.

A biochemical and genetic study on all non-synonymous single nucleotide polymorphisms of the gene encoding human deoxyribonuclease I potentially relevant to autoimmunity.

R. Iida, E. Tsubota, T. Yasuda, 2010, The international journal of biochemistry & cell biology.

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

T. Yasuda, H. Takeshita, J. Fujihara, 2018, Legal medicine.

Comparison of serum cell-free DNA between postmortem and living samples.

H. Takeshita, J. Fujihara, Y. Takinami, 2021, Clinica chimica acta; international journal of clinical chemistry.

An autopsy case of spontaneous esophageal perforation (Boerhaave syndrome).

T. Yasuda, Ken Inoue, H. Takeshita, 2016, Legal medicine.

Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populations.

R. Iida, T. Yasuda, I. Yuasa, 2011, Legal medicine.