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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Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women.

Authors : Omasu F; Department of Molecular Biology, Institute of Gerontology, Nippon Medical School, 1-396 Kosugi-cho, Nakahara-ku, Kawasaki 211-8533, Japan.; Ezura Y

Subjects: Bone Density* ; Chromosomes, Human, Pair 5* ; Genetic Variation*

Source: Journal of human genetics [J Hum Genet] 2003; Vol. 48 (7), pp. 342-5. Date of Electronic Publication: 2003 Jun 06.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women.

Authors : Hirano H; Dentistry and Oral Surgery, Tokyo Metropolitan Geriatric Medical Center, Tokyo, Japan.; Ezura Y

Subjects: Extracellular Matrix Proteins* ; Genetic Variation*; Calcium-Binding Proteins/Calcium-Binding Proteins/Calcium-Binding Proteins/*genetics

Source: Journal of human genetics [J Hum Genet] 2003; Vol. 48 (6), pp. 288-292. Date of Electronic Publication: 2003 Apr 29.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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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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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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Complex divergence at a microsatellite marker C1_2_5 in the lineage of HLA-Cw/-B haplotype.

Authors : Shichi D; Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.; Ota M

Subjects: Genetic Variation* ; Phylogeny*; HLA-B Antigens/HLA-B Antigens/HLA-B Antigens/*genetics

Source: Journal of human genetics [J Hum Genet] 2009 Apr; Vol. 54 (4), pp. 224-9. Date of Electronic Publication: 2009 Feb 27.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis.

Authors : Mori S; Department of Internal Medicine, Tokyo Metropolitan Geriatric Hospital, 35-2 Sakae-cho, Itabashi-ku, Tokyo, 173-0015, Japan. .; Kou I

Subjects: Genetic Variation*; ADAM Proteins/ADAM Proteins/ADAM Proteins/*genetics ; Bone Density/Bone Density/Bone Density/*genetics

Source: Journal of human genetics [J Hum Genet] 2008; Vol. 53 (8), pp. 694-697. Date of Electronic Publication: 2008 May 17.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited

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