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8961
Cyclophosphamide Pharmacogenomic Variation in Cancer Treatment and Its Effect on Bioactivation and Pharmacokinetics
Published 2024-01-01“…Previous studies have shown the effect of the enzymes’ genetic polymorphisms on Cy kinetics and its clinical outcome. …”
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8962
ZBiotics ameliorates T2DM-induced histopathological damage in liver, kidney and adipose tissues by modulating the NOD-like receptor signaling in Wistar rats
Published 2025-02-01“…In silico analysis was performed to construct a genetic-epigenetic network linked to STING-NOD pathway and autophagy signaling. …”
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8963
A Mutation in IL4RA Is Associated with the Degree of Pathology in Human TB Patients
Published 2016-01-01“…Together, our genetic association study in human TB patients further supports the assumption that IL-13/IL-4Rα-dependent mechanisms are involved in mediating tissue pathology of human TB.…”
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8964
Multi-Host of Ectomycorrhizal Fungi on Dipterocarpaceae in Tropical Rain Forests
Published 2019-05-01“…The most ectomycorrhizal fungi that play a role in multi-host are those with genetic relationship to the orders of Thelephorales, Russulales, and Sebacinales. …”
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8965
Causal relationship between affect disorders and endometrial cancer: a Mendelian randomisation study
Published 2024-12-01“…Inverse variance-weighted, MR-Egger and weighted median MR analyses were performed, together with a range of sensitivity analyses.Results Mendelian randomisation analysis showed no statistically significant genetic responsibility effect of anxiety and stress-related disorders on any pathological type of endometrial cancer. …”
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8966
A Boy With KIF11-Associated Disorder Along With ADHD and ASD: Collaboration Between Paediatrics and Child Psychiatry
Published 2024-01-01“…Moreover, gaining a deeper understanding of the higher prevalence of ASD and ADHD in individuals with KIF11 mutations could offer valuable insights into the genetic mechanisms underlying neurodevelopmental disorders.…”
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8967
Effects of Single-Nucleotide Polymorphisms in Cytokine, Toll-Like Receptor, and Progesterone Receptor Genes on Risk of Miscarriage
Published 2018-01-01“…Spontaneous abortion is a complex, multifactorial pathology, where various genetic, neural, endocrine, and immunological factors are involved. …”
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8968
Constitutive expression of Cas9 and rapamycin-inducible Cre recombinase facilitates conditional genome editing in Plasmodium berghei
Published 2025-01-01“…Conventional reverse genetic tools cannot be used to study essential genes of the asexual blood stages, thereby necessitating the development of conditional strategies. …”
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8969
Auditory evoked-potential abnormalities in a mouse model of 22q11.2 Deletion Syndrome and their interactions with hearing impairment
Published 2025-01-01“…We exploited large inter-individual variation in hearing ability among Df1/+ mice to distinguish effects of genetic background from effects of hearing impairment. …”
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8970
Evaluating the impact of smoking on the risk of dry eye disease: a two-sample Mendelian randomization study
Published 2024-12-01“…Adhering to STROBE-MR guidelines, a MR analysis was conducted using genetic instrumental variables from Genome-wide association studies (GWAS). …”
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8971
Assessment of Developmental Prosopagnosia in an Individual with Tourette Syndrome and Attention Deficit Hyperactivity Disorder: A Case Report
Published 2025-01-01“…While ON’s DP, Tourette syndrome, and ADHD may have distinct genetic origins, impairment in face identity recognition has been observed across several neurodevelopmental conditions and is likely more common than currently thought.…”
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8972
Oral phenotype and scoring of vascular Ehlers–Danlos syndrome: a case–control study
Published 2012-04-01“…Objective Vascular Ehlers–Danlos syndrome (vEDS) is a rare genetic condition related to mutations in the COL3A1 gene, responsible of vascular, digestive and uterine accidents. …”
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8973
Congenital malformations in children of epileptic pregnant women in the Cienfuegos province (2008-2018)
Published 2022-12-01“…<br /><strong>Conclusion</strong>: the risk factors associated with congenital malformations in children of epileptic mothers were: maternal age over 35 years, history of previous pregnancy with malformation and genetic interruption of pregnancy.</p>…”
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8974
Impact of Rs657152 Gene Polymorphisms on Inflammatory Markers in COVID-19 Patients With Type 2 Diabetes Mellitus
Published 2024-11-01“…Understanding this genetic relationship is crucial for improving treatment strategies and predicting outcomes in this high-risk group. …”
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8975
Multifaceted taxonomy of two Dactylogyrus species on Enteromius paludinosus: Integrating light microscopy, scanning electron microscopy and molecular approaches
Published 2025-01-01“…Soft tissues of SEM analysed specimens were genetically characterised using CO1 mtDNA, 18S-ITS1-5.8S rDNA and partial 28S rDNA fragments. …”
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8976
Assessing the authenticity and purity of a commercial Bacillus thuringiensis bioinsecticide through whole genome sequencing and metagenomics approaches
Published 2025-01-01“…., the absence of any undesired genetic material) of commercial Bacillus thuringiensis bioinsecticides. …”
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8977
Identification of key regulators in pancreatic ductal adenocarcinoma using network theoretical approach.
Published 2025-01-01“…The disease's development involves complex interactions among immunological, genetic, and environmental factors, yet its molecular mechanism remains elusive. …”
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8978
Association between dietary components and gut microbiota: a Mendelian randomization study
Published 2025-01-01“…Conclusion: There are potential genetic and causal associations between dietary components and gut microbiota.…”
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8979
A novel TGFBR2 mutation causes Loeys-Dietz syndrome in a Chinese infant: A case report
Published 2025-01-01“…Conclusions: Our comprehensive genetic analysis suggested that the p.Glu335_Tyr336delinsAsp variant of TGFBR2 caused aberrant TGF-β signaling and contributed to LDS in the patient.…”
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8980
Examining the Formalin Fixation Method for Maintaining High RNA Quality in Surgical Lung Specimens
Published 2025-01-01“…ABSTRACT Background Multiplex genetic testing is recommended when treating nonsmall cell lung cancer. …”
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