Authors : Ihara F; Department of Immunoparasitology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, 565-0871, Japan.; Laboratory of Immunoparasitology, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, 565-0871, Japan.

Subjects: Toxoplasma*/Toxoplasma*/Toxoplasma*/genetics ; Toxoplasma*/Toxoplasma*/Toxoplasma*/classification ; Phylogeny*

Source: Nature communications [Nat Commun] 2024 May 22; Vol. 15 (1), pp. 4278. Date of Electronic Publication: 2024 May 22.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium:

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Characterizing rare and low-frequency height-associated variants in the Japanese population.

Authors : Akiyama M; Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Yokohama, 230-0045, Japan.; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, 812-8582, Japan.

Subjects: Genetic Variation*; Body Height/Body Height/Body Height/*genetics ; Genome-Wide Association Study/Genome-Wide Association Study/Genome-Wide Association Study/*methods

Source: Nature communications [Nat Commun] 2019 Sep 27; Vol. 10 (1), pp. 4393. Date of Electronic Publication: 2019 Sep 27.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium:

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Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.

Authors : Takata A; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan. .; Nakashima M

Subjects: Genetic Variation*; Spasms, Infantile/Spasms, Infantile/Spasms, Infantile/*genetics; Adaptor Proteins, Vesicular Transport/Adaptor Proteins, Vesicular Transport/Adaptor Proteins, Vesicular Transport/genetics Epileptic Encephalopathy, Early Infantile, 3; Infantile Epileptic-Dyskinetic Encephalopathy

Source: Nature communications [Nat Commun] 2019 Jun 07; Vol. 10 (1), pp. 2506. Date of Electronic Publication: 2019 Jun 07.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium:

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Construction of full-length Japanese reference panel of class I HLA genes with single-molecule, real-time sequencing.

Authors : Mimori T; Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.; Graduate School of Medicine, Tohoku University, Sendai, Japan.

Subjects: Genetic Variation* ; High-Throughput Nucleotide Sequencing*; Genome, Human/Genome, Human/Genome, Human/*genetics

Source: The pharmacogenomics journal [Pharmacogenomics J] 2019 Apr; Vol. 19 (2), pp. 136-146. Date of Electronic Publication: 2018 Jan 19.Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101083949 Publication Model: Print-Electronic

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Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy.

Authors : Hayashi T; Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University (TMDU), Tokyo, Japan. .; Department of Cardiology, Keio University School of Medicine, 35 Shinanomachi, Shinjyuku-ku, Tokyo, 160-8582, Japan. .

Subjects: Genetic Variation*; Cardiomegaly/Cardiomegaly/Cardiomegaly/*genetics ; Cardiomyopathy, Restrictive/Cardiomyopathy, Restrictive/Cardiomyopathy, Restrictive/*genetics

Source: Journal of human genetics [J Hum Genet] 2018 Sep; Vol. 63 (9), pp. 989-996. Date of Electronic Publication: 2018 Jun 15.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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Y chromosome analysis for common surnames in the Japanese male population.

Authors : Ochiai E; Department of Forensic Medicine, Tokai University School of Medicine, Isehara, Japan.; Osawa M

Subjects: Genetics, Population* ; Phylogeny*; Chromosomes, Human, Y/Chromosomes, Human, Y/Chromosomes, Human, Y/*genetics

Source: Journal of human genetics [J Hum Genet] 2021 Jul; Vol. 66 (7), pp. 731-738. Date of Electronic Publication: 2021 Feb 01.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.

Authors : Li Y; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.; Ikeda A

Subjects: Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/*genetics ; Parkinson Disease/Parkinson Disease/Parkinson Disease/*genetics

Source: Journal of human genetics [J Hum Genet] 2020 Sep; Vol. 65 (9), pp. 771-781. Date of Electronic Publication: 2020 May 13.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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Extreme genetic signatures of local adaptation during Lotus japonicus colonization of Japan.

Authors : Shah N; Department of Molecular Biology and Genetics, Aarhus University, 8000, Aarhus C, Denmark.; Wakabayashi T

Subjects: Acclimatization/Acclimatization/Acclimatization/*genetics ; Lotus/Lotus/Lotus/*genetics; Biological Evolution

Source: Nature communications [Nat Commun] 2020 Jan 14; Vol. 11 (1), pp. 253. Date of Electronic Publication: 2020 Jan 14.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium:

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Genetic variants of calcium and vitamin D metabolism in kidney stone disease.

Authors : Howles SA; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK. .; Academic Endocrine Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. .

Subjects: Calcium/Calcium/Calcium/*metabolism ; Kidney Calculi/Kidney Calculi/Kidney Calculi/*genetics ; Vitamin D/Vitamin D/Vitamin D/*metabolism

Source: Nature communications [Nat Commun] 2019 Nov 15; Vol. 10 (1), pp. 5175. Date of Electronic Publication: 2019 Nov 15.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium:

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Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women.

Authors : Hotta K; EBM Research Center, Kyoto University Graduate School of Medicine, Yoshida-Konoecho, Sakyo-ku, Kyoto, Japan. ; Kitamoto A

Subjects: Genetic Association Studies* ; Genetic Variation*; 5'-Nucleotidase/5'-Nucleotidase/5'-Nucleotidase/*genetics

Source: Journal of human genetics [J Hum Genet] 2012 Jan; Vol. 57 (1), pp. 46-51. Date of Electronic Publication: 2011 Nov 10.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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