Showing 7,761 - 7,780 results of 14,077 for search '"genetics"', query time: 0.09s Refine Results
  1. 7761

    Diversité génétique de l’allèle O dans des populations berbères by Silvayn Amory, Jean-Michel Dugoujon, Stéphanie Despiau, Francis Roubinet, Farha El-Chennawi, Antoine Blancher

    Published 2005-12-01
    “…The results show an important genetic diversity considering the limited number of individuals under study. …”
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    Article
  2. 7762

    Neurogenetic Algorithm for Solving Combinatorial Engineering Problems by M. Jalali Varnamkhasti, Nasruddin Hassan

    Published 2012-01-01
    “…Diversity of the population in a genetic algorithm plays an important role in impeding premature convergence. …”
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    Article
  3. 7763

    Duchenne muscular dystrophy: recent insights in brain related comorbidities by Cyrille Vaillend, Yoshitsugu Aoki, Eugenio Mercuri, Jos Hendriksen, Konstantina Tetorou, Aurelie Goyenvalle, Francesco Muntoni

    Published 2025-02-01
    “…This suggests that future genetic therapies could address both muscle and brain dysfunction in DMD patients.…”
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    Article
  4. 7764

    Osteopetrosis and Its Relevance for the Discovery of New Functions Associated with the Skeleton by Amélie E. Coudert, Marie-Christine de Vernejoul, Maurizio Muraca, Andrea Del Fattore

    Published 2015-01-01
    “…Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. …”
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    Article
  5. 7765

    Dilated cardiomyopathy and myocarditis: a clinical case by O.V. Onyshchenko, D.V. Riabenko, O.A. Yepanchintseva

    Published 2023-12-01
    “…This clinical case emphasizes the importance of a complete diagnostic examination with the use of genetic testing in certain cases. …”
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    Article
  6. 7766

    Applications of piggyBac Transposons for Genome Manipulation in Stem Cells by Yi Sun, Guang Liu, Yue Huang

    Published 2021-01-01
    “…Transposons are mobile genetic elements in the genome. The piggyBac (PB) transposon system is increasingly being used for stem cell research due to its high transposition efficiency and seamless excision capacity. …”
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    Article
  7. 7767

    Identification of Novel Causal FBN1 Mutations in Pedigrees of Marfan Syndrome by Yueli Wang, Xiaoyan Li, Rongjuan Li, Ya Yang, Jie Du

    Published 2018-01-01
    “…Marfan syndrome (MFS) is an autosomal dominant genetic disorder of the connective tissue, typically characteristic of cardiovascular manifestations, valve prolapse, left ventricle enlargement, and cardiac failure. …”
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    Article
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  11. 7771

    Evaluation of the Frequency of HLA-DQ2/DQ8 Genes Among Patients with Celiac Disease and Those on a Gluten-Free Diet by Marek K. Kowalski, Danuta Domżał-Magrowska, Ewa Małecka-Wojciesko

    Published 2025-01-01
    “…Background: Celiac disease (CD) is a chronic, permanent, gluten-dependent disease that manifests itself with inflammation of the small intestine and malabsorption in genetically predisposed individuals with HLA-DQ2 and -DQ8 (human leukocyte antigen) histocompatibility antigens. …”
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    Article
  12. 7772

    Associations between lipid-lowering drugs and urate and gout outcomes: a Mendelian randomization study by Min Liu, Na Yin, Yuhang Zhu, Aili Du, Chunyuan Cai, Pengyuan Leng

    Published 2025-01-01
    “…The aim of this study was to investigate the genetic association between lipid-lowering drugs and urate and gout.MethodsIn this study, two genetic proxies were employed to approximate lipid-lowering drug exposure: expression quantitative trait loci (eQTL) associated with drug-target genes and genetic variations proximal to or within genes targeted by these drugs, which are linked to low-density lipoprotein cholesterol (LDL-C) levels. …”
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    Article
  13. 7773

    IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice by Tingwenyi Hu, Xiangrong Tang, Tiechao Ruan, Shunhua Long, Guicen Liu, Jing Ma, Xueqi Li, Ruoxuan Zhang, Guoning Huang, Ying Shen, Tingting Lin

    Published 2025-01-01
    “…Abstract Background Asthenozoospermia (ASZ) accounts for about 20-40% of male infertility, and genetic factors, contributing to 30-40% of the causes of ASZ, still need further exploration. …”
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    Article
  14. 7774
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  17. 7777

    DIVERSITY OF THE PUMPKIN COLLECTION AND ITS HEREDITARY POTENTIAL. RESULTS AND PROSPECTS OF BREEDING PRACTICE by A. G. Elatskova

    Published 2019-10-01
    “…The Kuban Experiment Station of VIR, where the collection of pumpkin genetic resources is maintained and regenerated for long-term storage in the genebank, conducts comprehensive research work to analyze the genetic diversity of pumpkin accessions and disclose the potential of its hereditary variation.Objective. …”
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    Article
  18. 7778

    Inheritance of scald resistance in four barley landraces by G. S. Konovalova, E. E. Radchenko

    Published 2019-01-01
    “…The goal of the present work was to study genetic control to the dangerous pathogen in four other barley landraces.Materials and methods. …”
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  19. 7779

    Identifcation and fine mapping of qHSW1, a major QTL for hundred-seed weight in mungbean by Xuesong Han, Xuesong Han, Long Zhao, Juan Yu, Xingmin Wang, Shilong Zhang, Li Li, Li Li, Changyan Liu, Changyan Liu

    Published 2025-01-01
    “…This study employed a recombinant inbred line (RIL) population of 200 lines that were genotyped via whole-genome resequencing to exploit genetic potential in the identification of HSW-associated quantitative trait loci (QTLs) across four environments. …”
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    Article
  20. 7780