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Academic Journal

The Born in Guangzhou Cohort Study enables generational genetic discoveries.

Subjects: Cohort Studies* ; Gene-Environment Interaction* ; Phenotype*

  • Source: Nature [Nature] 2024 Feb; Vol. 626 (7999), pp. 565-573. Date of Electronic Publication: 2024 Jan 31.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic architecture of variation in Arabidopsis thaliana rosettes.

  • Authors : Morón-García O; The National Plant Phenomics Centre, Institute of Biological, Rural and Environmental Sciences (IBERS), Aberystwyth University, Aberystwyth, United Kingdom.; Garzón-Martínez GA

Subjects: Genetic Variation* ; Phenotype* ; Quantitative Trait Loci*

  • Source: PloS one [PLoS One] 2022 Feb 16; Vol. 17 (2), pp. e0263985. Date of Electronic Publication: 2022 Feb 16 (Print Publication: 2022).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome.

  • Authors : Skalníková M; Center of Molecular Medicine, Central European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic.; Department of Internal Medicine, Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, 625 00 Brno, Czech Republic.

Subjects: Alleles* ; Genetic Predisposition to Disease* ; Genetic Variation*

  • Source: International journal of molecular sciences [Int J Mol Sci] 2022 Jan 14; Vol. 23 (2). Date of Electronic Publication: 2022 Jan 14.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Novel CLTC variants cause new brain and kidney phenotypes.

  • Authors : Itai T; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa, Japan.; Miyatake S

Subjects: Brain* ; Genetic Variation* ; Kidney*

  • Source: Journal of human genetics [J Hum Genet] 2022 Jan; Vol. 67 (1), pp. 1-7. Date of Electronic Publication: 2021 Jul 07.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Pan-genome of Raphanus highlights genetic variation and introgression among domesticated, wild, and weedy radishes.

  • Authors : Zhang X; Key Laboratory of Biology and Genetic Improvement of Horticultural Crops, Ministry of Agriculture, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China.; Liu T

Subjects: Domestication* ; Gene Flow* ; Genetic Variation*

  • Source: Molecular plant [Mol Plant] 2021 Dec 06; Vol. 14 (12), pp. 2032-2055. Date of Electronic Publication: 2021 Aug 10.Publisher: Cell Press Country of Publication: England NLM ID: 101465514 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Structural and numerical Y chromosomal variations in elderly men identified through multiplex ligation-dependent probe amplification.

  • Authors : Ogiwara Y; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.; Department of Advanced Pediatric Medicine, Tohoku University School of Medicine, Tokyo, Japan.

Subjects: Chromosome Aberrations* ; Genetic Variation* ; Phenotype*

  • Source: Journal of human genetics [J Hum Genet] 2021 Dec; Vol. 66 (12), pp. 1181-1184. Date of Electronic Publication: 2021 Jun 09.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A supergene underlies linked variation in color and morphology in a Holarctic songbird.

  • Authors : Funk ER; Department of Ecology and Evolutionary Biology, University of Colorado, Boulder, CO, 80309, USA. .; Mason NA

Subjects: Evolution, Molecular* ; Genetic Variation* ; Genotype*

  • Source: Nature communications [Nat Commun] 2021 Nov 25; Vol. 12 (1), pp. 6833. Date of Electronic Publication: 2021 Nov 25.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Identification of Two Variants of Acinetobacter baumannii Strain ATCC 17978 with Distinct Genotypes and Phenotypes.

  • Authors : Wijers CDM; Department of Pathology, Microbiology, and Immunology, Vanderbilt Universitygrid.152326.1 Medical Center, Nashville, Tennessee, USA.; Vanderbilt Institute for Infection, Immunology, and Inflammation, Vanderbilt Universitygrid.152326.1 Medical Center, Nashville, Tennessee, USA.

Subjects: Genetic Variation* ; Genotype* ; Phenotype*

  • Source: Infection and immunity [Infect Immun] 2021 Nov 16; Vol. 89 (12), pp. e0045421. Date of Electronic Publication: 2021 Aug 30.Publisher: American Society For Microbiology Country of Publication: United States NLM ID: 0246127 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.

  • Authors : Gigli M; Cardiothoracovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI), University of Trieste, Trieste, Italy (M.G., D.S., M.M., M.D.F., A.P., G.D.A., F.B., G.S.).; Stolfo D

Subjects: Genetic Predisposition to Disease* ; Genetic Variation* ; Phenotype*

  • Source: Circulation [Circulation] 2021 Nov 16; Vol. 144 (20), pp. 1600-1611. Date of Electronic Publication: 2021 Sep 30.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0147763 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.

  • Authors : Ghesh L; Service de Génétique Médicale, CHU Nantes, Nantes, France.; UF de Fœtopathologie et Génétique, CHU de Nantes, Nantes, France.

Subjects: Genetic Predisposition to Disease* ; Genetic Variation* ; Phenotype*Hydrolethalus syndrome

  • Source: Clinical genetics [Clin Genet] 2021 Oct; Vol. 100 (4), pp. 462-467. Date of Electronic Publication: 2021 Jul 13.Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004

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