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8621
Inhibition of Notch Signaling Promotes the Differentiation of Epicardial Progenitor Cells into Adipocytes
Published 2021-01-01“…There was EAT located at the atrial–ventricular groove in mouse. By using genetic lineage tracing methods, we found that EPCs were a source of epicardial adipocytes. …”
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8622
The Role of Oral Biomarkers in the Assessment of Noncommunicable Diseases
Published 2024-12-01“…<b>Methods</b>: This narrative review synthesizes the current literature on biochemical, immunological, genetic, and microbiological oral biomarkers, with a focus on their sources, types, and clinical applications. …”
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8623
The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?
Published 2016-01-01“…He had hypocalcemia, hyperphosphatemia, and elevated Parathyroid Hormone levels. Genetic testing revealed a known mutation of GNAS gene, confirming the diagnosis of Pseudohypoparathyroidism Type Ia (PHP-Ia) (c.34C>T (p.G1n12X)). …”
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8624
Is there anybody (new) out there? Seven new species of Ligidium (Isopoda, Oniscidea, Ligiidae) from the Southern Appalachians, eastern North America
Published 2025-02-01“…Together these genes reveal considerable genetic divergence among the new species and from previously described ones. …”
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8625
Transcriptional engineering for value enhancement of oilseed crops: a forward perspective
Published 2025-01-01“…Recent genomic, transcriptomic, and metabolomics research has expanded our understanding of the genetic and physiological control of fatty acid biosynthesis and composition. …”
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8626
Eating Problems and Overlap with ADHD and Autism Spectrum Disorders in a Nationwide Twin Study of 9- and 12-Year-Old Children
Published 2013-01-01“…The cross-twin, cross-trait correlations suggested low correlations between EAT-P and ADHD or EAT-P and ASD. Genetic effects accounted for 44% of the variation in liability for eating problems. …”
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8627
Audiological alterations in resistance to thyroid hormone syndrome: emphasizing lifelong assessment
Published 2025-02-01“…Subjects with RTH from the same family, carrying a THRB gene variant, underwent detailed clinical evaluation and serum biochemistry analysis. The genetic assessment involved sequencing of the THRB gene. …”
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8628
Aquatic Invertebrate Antimicrobial Peptides in the Fight Against Aquaculture Pathogens
Published 2025-01-01“…These AMPs could serve as feed additives, therapeutic agents, or in genetic engineering approaches like CRISPR/Cas9-mediated transgenesis to enhance resilience of farmed species. …”
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8629
Responsive afatinib treatment in high-grade salivary gland ductal carcinoma and NSCLC with uncommon EGFR mutations: Treatment outcomes
Published 2024-06-01“…The success of afatinib in both malignancies underscores the importance of personalized medicine. Targeting specific genetic alterations with afatinib offers tailored treatment strategies, potentially improving outcomes and quality of life. …”
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8630
Mineral Composition of Traditional Non-GMO Soybean Cultivars in relation to Nitrogen Fertilization
Published 2020-01-01“…Soybean is widely used as food. Genetic factors, as well as agrotechnical procedures, affect the yield and quality of soybeans. …”
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8631
New aspects of non-alcoholic fatty liver disease
Published 2015-09-01“…To analyze modern data on pathogenesis and principles of treatment of non-alcoholic fatty liver disease (NAFLD).Key points. Now concepts on genetic determinants of NAFLD and diagnostics methods develop rapidly. …”
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8632
Dysphagia and Neck Swelling in a Case of Undiagnosed Lhermitte-Duclos Disease and Cowden Syndrome
Published 2015-01-01“…Additional imaging subsequently revealed the presence of thyroid nodules and bilateral breast cancers. Genetic testing later confirmed the diagnosis of Cowden syndrome. …”
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8633
Newborn with Extensive Bart Syndrome
Published 2024-12-01“…Bart syndrome is a rare genetic disorder characterized by the presence of mechanical fragility and a congenital localized absence of the skin. …”
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8634
CRISPR Gene Editing in Strawberry
Published 2018-02-01“… Because cultivated strawberries are genetically complex, conventional breeding of strawberry can be difficult. …”
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8635
On the discovery of the multibracteate Silver-leaved linden in Mostar, Bosnia and Herzegovina
Published 2022-12-01“… In the scope of the genetic, morphological and phenological research of the genus Tilia in Bosnia and Herzegovina, with control populations in Germany, multibracteate silver-leaved linden (T. tomentosa Moench.) was discovered in Mostar. …”
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8636
Orques tolkienesques : entre OGM et androïdes posthumains ?
Published 2022-07-01“…Tolkien’s Orcs, and more specifically, his Uruk-hai, are genetically modified organisms, which are studded with metal to improve them and could have been inspired by Asimovian robots. …”
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8637
NETWORK MODELS OF INSTITUTIONALIZATION IN EDUCATION FOR THE KNOWLEDGE SOCIETY (BY THE EXAMPLE OF "THE STEP INTO THE FUTURE" PROGRAMME)
Published 2016-12-01“…The development of integrated and network systems is becoming a genetic feature of the educational institution of the research type, and the study of their opportunities and configurations provides the key to effective forms of modern education organization. …”
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8638
TEC Data Forecasting Using a Novel Nonlinear Model
Published 2015-01-01“…A novel nonlinear TEC forecasting model is proposed in the paper; the main produces of the model are as follows: first the EOF decomposition of TEC data is made, then the genetic algorithm is used to establish the nonlinear time field model, and finally the decomposed space field and the predicted time field are reconstructed to achieve the purpose of forecasting the TEC data. …”
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8639
La densité des mots dans Bouvard et Pécuchet
Published 2012-11-01“…In the wake of many Flaubertian genetic studies, we will try once again to ponder the meaning of this encyclopedic novel’s textual opacity which reflects both its own genesis and the cultural context of that period. …”
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8640
The Complexity of Pain Management in Children Affected by Mucopolysaccharidoses
Published 2017-01-01“…Mucopolysaccharidoses (MPSs) are a group of rare, genetic lysosomal storage disorders. They are caused by deficiencies of the lysosomal enzymes involved in the degradation of glycosaminoglycans (GAGs). …”
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