Works about HUMAN genetics
Results: 5000
Editorial: Challenges and prospects for conservation genetics at XXI century.
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- Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1554590
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- Article
Effects of Particulate Matter Exhaust on Functional Parameters of Organ Systems and Reactive Oxygen Species: A Cross-Sectional Study.
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- Asia Pacific Journal of Medical Toxicology, 2024, v. 13, n. 4, p. 151
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- Article
THE NEW GENETICS / GENOMICS REVOLUTION IN HEALTH CARE.
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- Malaysian Journal of Medical Sciences, 2006, v. 13, p. 6
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- Article
True, New, and Important: An Introduction to the Special Issue.
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- Journal of Sex Research, 2004, v. 41, n. 1, p. 2, doi. 10.1080/00224490409552208
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- Article
Using Museum Guests as Crowdsourced Participants in Human Subject Research.
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- Curator, 2020, v. 63, n. 3, p. 407, doi. 10.1111/cura.12371
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- Article
Development of a Sleeping Beauty-Based Telomerase Gene Delivery System for Hepatocytes.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 2, p. 227, doi. 10.1271/bbb.100403
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- Article
Cajón de sastre.
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- istor, 2016, n. 66, p. 287
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- Article
Age Matters.
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- Organization Studies, 2014, v. 35, n. 11, p. 1719, doi. 10.1177/0170840614553771
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- Article
Good genes, complementary genes and human mate preferences.
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- Genetica, 2008, v. 134, n. 1, p. 31, doi. 10.1007/s10709-008-9254-x
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- Article
Good genes, complementary genes and human mate preferences.
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- Genetica, 2008, v. 132, n. 3, p. 309, doi. 10.1007/s10709-007-9174-1
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- Article
Genetic diversity and variety composition of cassava on small-scale farms in Uganda: an interdisciplinary study using genetic markers and farmer interviews.
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- Genetica, 2007, v. 130, n. 3, p. 301
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- Article
Severe Infantile Carnitine Palmitoyltransferase II Deficiency in 19-Week Fetal Sibs.
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- Pediatric & Developmental Pathology, 2009, v. 12, n. 6, p. 481, doi. 10.2350/08-10-0548.1
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- Article
Gelehrte als Identifikationsfiguren? Vom Umgang mit fachkultureller Erinnerung in medizinischen Fächern.
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- Berichte zur Wissenschafts-Geschichte, 2024, v. 47, n. 1/2, p. 77, doi. 10.1002/bewi.202300018
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- Article
Pascal Germann, Laboratorien der Vererbung. Rassenforschung und Humangenetik in der Schweiz, 1900-1970, Göttingen: Wallstein 2016. 490 S., € 54,00. ISBN 978-3-8353-1950-9.
- Published in:
- 2017
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- Publication type:
- Book Review
Multiplex FISH and three-dimensional DNA imaging with near infrared femtosecond laser pulses.
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- Histochemistry & Cell Biology, 2000, v. 114, n. 4, p. 337, doi. 10.1007/s004180000185
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- Article
Genome studies at the PAG 2011 conference.
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- Functional & Integrative Genomics, 2011, v. 11, n. 1, p. 1, doi. 10.1007/s10142-011-0215-6
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- Article
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
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- Archives of Dermatological Research, 2006, v. 298, n. 3, p. 135, doi. 10.1007/s00403-006-0671-3
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- Article
Tuberous sclerosis complex genes: from flies to human genetics.
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- Archives of Dermatological Research, 2001, v. 293, n. 8, p. 383
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- Article
Recovery of cell-free mRNA and microRNA from human semen based on their physical nature.
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- Biotechnology & Applied Biochemistry, 2014, v. 61, n. 3, p. 342, doi. 10.1002/bab.1172
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- Publication type:
- Article
Results and Perspectives of Modern Developmental Biology with Reference to Fundamental Research and Medicine.
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- Russian Journal of Developmental Biology, 2003, v. 34, n. 6, p. 403, doi. 10.1023/B:RUDO.0000007896.34717.59
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- Publication type:
- Article
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease.
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- Nature Immunology, 2011, v. 12, n. 3, p. 213, doi. 10.1038/ni.1992
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- Article
Riding technology waves.
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- Nature Immunology, 2001, v. 2, n. 3, p. 181, doi. 10.1038/85222
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- Article
Study the expression of Neogene TIGD3 that derived from DNA transposons in colorectal cancer cell lines.
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- Al-Yarmouk Journal, 2019, v. 11, n. 1, p. 24
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- Publication type:
- Article
Chromatinopathies – from discovery to clinical diagnosis in the real world.
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- 2024
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- Editorial
H2A monoubiquitination: insights from human genetics and animal models.
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- Human Genetics, 2024, v. 143, n. 4, p. 511, doi. 10.1007/s00439-023-02557-x
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- Article
Editorial for the Neurogenetics and Neurogenomics special issue.
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- 2023
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- Publication type:
- Editorial
Comparative neurogenetics of dog behavior complements efforts towards human neuropsychiatric genetics.
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- Human Genetics, 2023, v. 142, n. 8, p. 1231, doi. 10.1007/s00439-023-02580-y
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- Publication type:
- Article
Correction: VIsoQLR: an interactive tool for the detection, quantification and fine-tuning of isoforms in selected genes using long-read sequencing.
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- 2023
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- Correction Notice
Special issue: the genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders.
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- Human Genetics, 2023, v. 142, n. 5, p. 595, doi. 10.1007/s00439-023-02566-w
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- Article
Publisher Correction: Predicting functional consequences of mutations using molecular interaction network features.
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- 2022
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- Correction Notice
Publisher Correction: Revealing modifier variations characterizations for elucidating the genetic basis of human phenotypic variations.
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- 2022
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- Correction Notice
Editorial to the Special Issue on "The molecular genetics of hearing and deafness".
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- 2022
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- Publication type:
- Editorial
Correction to: Genetic etiology of non-syndromic hearing loss in Latin America.
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- 2022
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- Correction Notice
Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan.
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- 2022
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- Correction Notice
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant.
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- 2022
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- Correction Notice
Correction to: Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.
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- 2021
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- Correction Notice
Correction to: Causal influences of neuroticism on mental health and cardiovascular disease.
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- 2021
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- Correction Notice
Peter S. Harper: obituary.
- Published in:
- 2021
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- Editorial
The human genetic determinism of life-threatening infectious diseases: genetic heterogeneity and physiological homogeneity?
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- 2020
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- Publication type:
- Editorial
Human genetics of Buruli ulcer.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 847, doi. 10.1007/s00439-020-02163-1
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- Publication type:
- Article
Human genetics and malaria resistance.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 801, doi. 10.1007/s00439-020-02142-6
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- Publication type:
- Article
Human genetics of HCV infection phenotypes in the era of direct-acting antivirals.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 855, doi. 10.1007/s00439-020-02136-4
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- Article
Incomplete penetrance in primary immunodeficiency: a skeleton in the closet.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 745, doi. 10.1007/s00439-020-02131-9
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- Article
Human genetics of leishmania infections.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 813, doi. 10.1007/s00439-020-02130-w
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- Article
Human genetics of meningococcal infections.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 961, doi. 10.1007/s00439-020-02128-4
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- Article
The monogenic basis of human tuberculosis.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 1001, doi. 10.1007/s00439-020-02126-6
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- Article
Susceptibility to infection in early life: a growing role for human genetics.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 733, doi. 10.1007/s00439-019-02109-2
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- Publication type:
- Article
Human genetics of life-threatening influenza pneumonitis.
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- Human Genetics, 2020, v. 139, n. 6/7, p. 941, doi. 10.1007/s00439-019-02108-3
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- Article
Identifying causal variants and genes using functional genomics in specialized cell types and contexts.
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- Human Genetics, 2020, v. 139, n. 1, p. 95, doi. 10.1007/s00439-019-02044-2
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- Publication type:
- Article
Long-read sequencing in deciphering human genetics to a greater depth.
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- Human Genetics, 2019, v. 138, n. 11/12, p. 1201, doi. 10.1007/s00439-019-02064-y
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- Publication type:
- Article