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961
FoxA1 knockdown promotes BMSC osteogenesis in part by activating the ERK1/2 signaling pathway and preventing ovariectomy-induced bone loss
Published 2025-02-01“…Osteoporosis is a significant global health issue, and the current treatment options are highly restricted. Transplanting genetically engineered MSCs has been acknowledged as a highly promising therapy for osteoporosis. …”
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962
Clinical and endoscopical and morphofunctional scores in evaluation of development of gastroesophageal reflux disease in various age groups
Published 2012-09-01“…Its development at patients of all age groups is observed on a background of gastritis with, probably, genetically determined hyperplasia of gastric epithelial cells producing NO-synthase and endothelin-1. …”
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963
Diversity in Adaptive Evolution of Methicillin-Resistant Staphylococcus aureus Clinical Isolates Under Exposure to Continuous Linezolid Stress in vitro
Published 2025-02-01“…Tala Han,1 Ting Jia,1 Junrui Wang1,2 1Department of Laboratory Medicine, Affiliated Hospital of Inner Mongolian Medical University, Hohhot, 010050, People’s Republic of China; 2Inner Mongolia Key Laboratory of Clinical Pathogenic Microorganism, The Affiliated Hospital of Inner Mongolian Medical University, Hohhot, 010050, People’s Republic of ChinaCorrespondence: Junrui Wang, Clinical Laboratory, Affiliated hospital of Inner Mongolian Medical University, Hohhot, 010050, People’s Republic of China, Tel +86 04713451315, Email [email protected]: Linezolid resistance in methicillin-resistant Staphylococcus aureus (MRSA) was reported frequently in recent years, but the mechanism underlying this process was less reported, especially for clinical isolates with different genetic background. Thus, this study aims to explore the adaptive evolution characteristics underlying linezolid resistance in MRSA clinical isolates exposed to continuous induction stress of linezolid in vitro.Methods: The in vitro susceptibility of 1032 MRSA clinical isolates to linezolid was detected using commercial VITEK-2 equipment via broth microdilution. …”
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964
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965
Structural insights into dynamics of the BMV TLS aminoacylation
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966
Understanding and reducing delayed dental care for early childhood caries: a structural equation model approach
Published 2025-02-01“…Multi-factor analysis revealed key factors affecting treatment delay, including permanent residence, medical insurance type, oral health habits, reasons for visit, first symptoms, the time of first discovery of oral problems, brushing teeth before bedtime every day, a genetic history of dental caries and the staging of dental caries. …”
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967
Carbapenem-resistant Enterobacterales (CRE) colonisation as a predictor for subsequent CRE infection: A retrospective surveillance study
Published 2025-01-01“…Contribution: This study reports higher CRE colonization rates in South Africa than previously documented, highlighting the urgent need to reduce colonization. The close genetic link between CRE colonization and subsequent infection suggests that knowledge of prior colonization can guide clinicians in selecting effective antibiotics, particularly for infections occurring within 30 days. …”
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968
Clinical, genomic, and histopathologic diversity in cerebral cavernous malformations
Published 2025-02-01“…This study aimed to clarify the clinical, genetic, and pathological features of CCMs using a multicenter cohort across three Chinese centers. …”
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969
Comparative analysis of chloroplast genomes reveals molecular evolution and phylogenetic relationships within the Papilionoideae of Fabaceae
Published 2025-02-01“….), and Caragana (Car.) are grouped within the Inverted Repeat-Lacking Clade (IRLC). Genetic characteristic analysis revealed a plentiful presence of SSR loci, with single-nucleotide repeats and dinucleotide (A/T) repeats being the most predominant. …”
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970
Causal role of plasma liposome in diabetic retinopathy: mendelian randomization (MR) study
Published 2025-02-01“…Conclusion In summary, genetic evidence suggests a causal relationship between the levels of specific lipid levels and DR. …”
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971
Trisomy 21 screening with αlpha software and the Fetal Medicine Foundation algorithm
Published 2023-11-01“…Data from the three largest laboratories collected between 2010 and 2015 were linked with genetic tests to assess screen positive and detection rates. …”
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972
Implementasi Algoritma Genetika dalam optimasi Performa Truk Sampah Menggunakan Aplikasi Trash Queen
Published 2023-02-01“…Trash Queen utilizes genetic algorithm to run simulations repeatedly until an optimal solution is obtained. …”
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973
A novel early stage drip irrigation system cost estimation model based on management and environmental variables
Published 2025-02-01“…Then, different machine learning models such as Multivariate Linear Regression, Support Vector Regression, Artificial Neural Networks, Gene Expression Programming, Genetic Algorithms, Deep Learning, and Decision Trees, were used to estimate the costs of each of the of the aforementioned sections. …”
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974
RNA editing-based biomarker blood test for the diagnosis of bipolar disorder: protocol of the EDIT-B study
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975
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976
Advances in machine learning applications to resource technology for organic solid waste
Published 2025-03-01“…A key focus of this work is the combination of ML models with optimization algorithms like Genetic Algorithm, which improves the performance of ML models by optimizing hyperparameters and enhancing prediction accuracy. …”
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977
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978
Evaluation of in-vitro and in-silico antidiabetic potential, glucose metabolism, antioxidant, cytotoxicity and phytochemical content of Ipomoea bolusiana Schinz and Ipomoea crassip...
Published 2025-02-01“…Background: Diabetes Mellitus is a chronic metabolic disorder caused by genetic disorders and other factors such as the use of certain medications, pancreatic injury, and autoimmune diseases such as rheumatoid arthritis and high blood pressure. …”
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979
Impaired cognitive function and decreased monoamine neurotransmitters in the DNAJC12 gene knockout mouse model
Published 2025-02-01“…Methods We thoroughly examined the clinical features and genetic mutations evident in two patients with biallelic mutations in the DNAJC12 gene. …”
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980