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11141
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11142
PLCG2 and IFNAR1: The Potential Biomarkers Mediated by Immune Infiltration and Osteoclast Differentiation of Ankylosing Spondylitis in the Peripheral Blood
Published 2024-01-01“…The objective was to investigate the interaction between genetic and clinical features and to identify the essential relationships underlying coexpression modules. …”
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11143
The Association Between Adiponectin Gene Polymorphism (rs1501299) and Metabolic Syndrome
Published 2025-01-01“…The APN levels in the GT (14.3 ± 5.3 mg/L) and TT (13.4 ± 5.4 mg/L) genotypes of the study subjects were lower than those of the GG genotype (15.5 ± 4.8 mg/L, p < 0.05).Conclusion: The occurrence of Mets may be associated with genetic variants at the rs1501299 locus, especially for individuals with G to T variants that reduce APN levels and lead to a higher risk of developing Mets.Keywords: adiponectin, gene polymorphism, metabolic syndrome…”
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11144
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11145
First report of Haemaphysalis bispinosa, molecular-geographic relationships of Ixodes granulatus and a new Dermacentor species from Vietnam
Published 2025-01-01“…Conclusions Haemaphysalis bispinosa shows genetic homogeneity in the whole of South and Southeast Asia, probably owing to its frequent association with domestic ruminants and dogs (i.e. frequently transported hosts). …”
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11146
Evaluating the Effectiveness of Cyclin-Dependent Kinase 4/6 Inhibitors in Early- and Very Early-Onset Metastatic Breast Cancer: A Multicenter Study
Published 2025-01-01“…The findings underscore the urgent need for personalized treatment strategies, routine genetic testing, and dedicated clinical trials designed to address the specific needs of these high-risk subgroups. …”
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11147
Biodesulfurization of high-sulfur oil from the Karazhanbas field of Kazakhstan with deep eutectic solvents
Published 2025-01-01“…The research methodology was based on the application of the Koch methods to determine the total number of microorganisms; light microscopy – for the study of microbiological preparations; genetic identification of bacteria based on the analysis of the nucleotide sequence of a fragment of the 16S rRNA gene; synthesis of deep eutectic solvents; testing of isolated bacteria – for sensitivity to Cr (VI), for the ability of microorganisms to use hydrocarbons of high-sulfur oil, for activity in sulfur-containing crude oil, for determination of the mass fraction of sulfur. …”
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11148
Exploring sex differences in Alzheimer’s disease: a comprehensive analysis of a large patient cohort from a memory unit
Published 2025-01-01“…To enhance our understanding of how sex influences the characteristics of AD patients and its potential impact on the disease trajectory, we conducted a comprehensive analysis of demographic, clinical, cognitive, and genetic data from a sizable and well-characterized cohort of AD dementia patients at a memory clinic in Barcelona, Spain. …”
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11149
Effect of trace elements and nutrients on 21 autoimmune diseases: a Mendelian randomization study
Published 2025-01-01“…However, whether there is a genetic causal effect between serum trace elements, nutrients, and autoimmune diseases remains unclear.ObjectiveThis study aims to investigate the causal effects of serum trace elements and nutrients on 21 autoimmune diseases using Mendelian randomization (MR).MethodsSingle nucleotide polymorphisms for the exposure factors (serum trace elements and vitamins) were obtained from the published UK Biobank database and genome-wide association study (GWAS) public databases. …”
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11150
Dissemination of Staphylococcus epidermidis in Swedish bovine dairy herds: minimal overlap with human isolates
Published 2025-02-01“…The primary aim of this study was to assess the genetic relatedness of S. epidermidis isolates from bovine subclinical mastitis (SCM), bovine milk filters, healthy dairy farmers or farm personnel, and human hospital patients in Sweden, and to detect and compare genes encoding antimicrobial resistance (AMR) and virulence factors. …”
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11151
Novel loci for triglyceride/HDL-C ratio longitudinal change among subjects without T2D
Published 2025-01-01“…Triglyceride (TG)/HDL-C ratio (THR) is a surrogate predictor of hyperinsulinemia. To identify novel genetic loci for THR change over time (ΔTHR), we conducted genome-wide association study (GWAS) and genome-wide linkage scan (GWLS) among nondiabetic Europeans from the Long Life Family Study (n = 1,384). …”
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11152
Induction of Somatic Embryogenesis and Organogenesis in Zimbabwean Sweet Potato (cv Brondal)
Published 2021-01-01“…Somatic embryogenesis (SE) and organogenesis are crucial in the development of disease free plants and genetic engineering. An investigation was conducted on the ability of treatments containing a combination of 2,4-D and Kinetin to induce either SE or organogenesis from cultured sweet potato cv Brondal leaves. …”
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11153
N1-methylnicotinamide promotes age-related cochlear damage via the overexpression of SIRT1
Published 2025-01-01“…Age-related hearing loss (ARHL) is a complex condition with genetic, aging, and environmental influences. Sirtuins, particularly SIRT1, are NAD-dependent protein deacetylases critical to aging and stress responses. …”
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11154
Influence of minor hydrocarbon seepage on sulfur cycling in marine subsurface sediments
Published 2025-02-01“…</p> <p>Overall, our study demonstrates that the gradient in pore water geochemistry, the rates of sulfate reduction processes, and the genetic features of microbial populations actively involved in sulfate-driven AOM processes are all affected by low and often unnoticed upward HC fluxes. …”
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11155
Selective expression and significance of ACKR2 in lung aerocytes
Published 2025-01-01“…Previous findings suggest that the genetic absence of ACKR2 leads to heightened tumor growth in inflammation-driven models. …”
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11156
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry
Published 2016-01-01“…Objectives Facioscapulohumeral muscular dystrophy type 1 (FSHD1) has been genetically linked to reduced numbers (≤8) of D4Z4 repeats at 4q35. …”
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11157
Mutational Landscape of Bone Marrow CD19 and CD138 Cells in Waldenström Macroglobulinemia (WM) and IgM Monoclonal Gammopathy of Undetermined Significance (IgM MGUS)
Published 2024-12-01“…ABSTRACT Background Despite recurrent and activating mutations, including MYD88, CXCR4, ARID1A, KMT2D, and CD79B were identified, the genetic basis for Waldenström's Macroglobulinemia (WM) and the risk of progression of IgM MGUS to WM remain to be fully elucidated. …”
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11158
Characterisation of EfbA from the Endodontic Pathogen Enterococcus faecalis and Prediction of Immunodominant EfbA Epitope Peptides: An In-vitro and In-silico Study
Published 2025-01-01“…Total of 20 carious scrapings were collected from patients with root caries and were phenotypically characterised for E. faecalis and the EfbA genetic determinant by Polymerase Chain Reaction (PCR) amplification. …”
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11159
Significance of KLK7 expression, polymorphisms, and function in sheep horn growth
Published 2025-01-01“…This study aims to elucidate the relationship between KLK7 and sheep horns by analyzing the expression, genetic polymorphisms, and potential functions of KLK7 in sheep horns. …”
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11160
Bariatric Surgery as a Molecular Modulator: The Role of FSHR Polymorphisms in Enhancing eNOS Expression and Reproductive Hormone Dynamics in Women with Severe Obesity
Published 2024-12-01“…These findings indicate the possibility of combining genetic testing and bariatric therapies to improve infertility treatment in obese women.…”
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