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Microbial diversity and biogeography across gastrointestinal tracts of Takifugu pufferfish revealed by full-length 16S amplicon sequencing
Published 2025-01-01“…Our findings reveal a compositional and functional biogeography of pufferfish gut microbiota along the GIT and between host genetics. Additionally, the differential abundance of specific amplicon sequence variants and their correlation with host genetic backgrounds and intestinal sections highlight the role of environmental filtering in shaping microbial communities, with certain bacterial taxa exhibiting strong preferences for particular intestinal sites or genetic backgrounds, suggesting potential localized adaptation or functional specialization. …”
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3762
Development of new SSR markers for homoeologous WFZP loci based on the study of structure and location of microsatellites in gene-rich regions of chromosomes 2AS , 2BS, 2DS
Published 2015-07-01“…The structure and location of SSR loci determine their potential as molecular genetic markers and may have impact on the potential function of microsatellites in important biological processes. …”
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3763
Clinical manifestations in Egyptian Pompe disease patients: Molecular variability and enzyme replacement therapy (ERT) outcomes
Published 2025-01-01“…Abstract Background Pompe disease is a rare genetic disorder caused by a deficiency of the enzyme acid alpha-glucosidase. …”
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Species identification of spider mites (Tetranychidae: Tetranychinae): a review of methods
Published 2023-06-01“…In this regard, biochemical and molecular genetic methods such as allozyme analysis, DNA barcoding, restriction fragment length polymorphism (PCR-RFLP), selection of species-specific primers and real-time PCR are becoming important. …”
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3766
Case Report: The first Korean familial case of BCAP31-related deafness, dystonia, and cerebral hypomyelination
Published 2025-01-01“…Deafness, dystonia, and central hypomyelination (DDCH) syndrome (OMIM #300475) is a rare X-linked genetic disorder characterized by developmental delays, deafness, central hypomyelination, and dystonia. …”
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3767
p104 Binds to Rac1 and Reduces Its Activity during Myotube Differentiation of C2C12 Cell
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3768
Bisphosphonate Treatment in a Patient Affected by MPS IVA with Osteoporotic Phenotype
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3769
Learning-induced sensory plasticity of mouse olfactory epithelium
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3770
ПОЛИПЛОИДИЯ И МЕЖВИДОВАЯ ГИБРИДИЗАЦИЯ В ЭВОЛЮЦИИ ЦВЕТКОВЫХ РАСТЕНИЙ
Published 2015-01-01“…Бэтсон, президент конференции, в своем обращении к участникам, названном «The Progress of Genetic Research», ярко и убедительно продемонстрировал, что уже появилась наука, направленная на изучение явлений наследственности и изменчивости, подразумевающая выходы на проблемы эволюции и систематики, на решение практических проблем селекции животных и растений – новая наука, у которой еще нет короткого и ясного названия, – и предложил назвать ее «genetics». …”
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3771
A Drosophila melanogaster mitotype may have an adaptive meaning
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Mitochondrial-ER Contact Sites and Tethers Influence the Biosynthesis and Function of Coenzyme Q
Published 2025-02-01Get full text
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3775
Disomic chromosome 3R(3B) substitution causes a complex of meiotic abnormalities in bread wheat <i>Triticum aestivum</i> L.
Published 2024-07-01“…Triticum aestivum L. lines introgressed with alien chromosomes create a new genetic background that changes the gene expression of both wheat and donor chromosomes. …”
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Human Transcriptome and Chromatin Modifications: An ENCODE Perspective
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Molecular Mechanisms Regulating Hepcidin Revealed by Hepcidin Disorders
Published 2011-01-01“…Disruption of these regulatory loops leads to genetic diseases characterized by iron deficiency (iron-refractory iron-deficiency anemia) or iron overload (hemochromatosis). …”
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