Results 61 to 70 of about 17,479 (163)
Possible Association of IL-4 VNTR Polymorphism with Susceptibility to Preeclampsia
BioMed Research International, 2014 Preeclampsia (PE) is a pregnancy-specific disorder that results in maternal mortality and morbidity. Growing evidence indicated that cytokines are involved in the pathogenesis of PE and interleukin-4 VNTR polymorphism could be implicated in altering the ...
S. Salimi +4 more
semanticscholar +1 more source
Genetic Heterogeneity of Francisella tularensis Subspecies mediasiatica Strains
Проблемы особо опасных инфекцийThe aim of the study was to conduct comparative phylogenetic analysis of Francisella tularensis subsp. mediasiatica strains isolated in different territories of contemporary Republics of Kazakhstan, Uzbekistan, Altai Territory, and the Altai Republic in ...
V. M. Sorokin +5 more
doaj +1 more source
İstanbul Medical Journal, 2019 Introduction:It has been shown that the host immune response and chronic inflammation could play a role as important risk factors for cancer. Oral squamous cell carcinoma (OSCC) is a common cancer worldwide. In this study, we aimed to evaluate the impact
Özge Gümüşay +4 more
doaj +1 more source
Инфекция и иммунитет, 2018 . Background. Mycobacterium avium subsp. hominissuis (MAH) is an important pathogen responsible for most of the human-associated nontuberculous mycobacteria infections.
M. Menichini +3 more
doaj +1 more source
Identification of Potential Vaccine Strains of Escherichia coli Isolates From Diarrhoeic Calves
Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.This study aimed to identify vaccine candidate Escherichia coli strains isolated from diarrheic calves. Faecal samples collected from 500 calves were analysed, and E. coli strains were isolated and characterized phenotypically and genotypically. Antibiotic resistance profiles, virulence‐associated genes and MLVA genotyping were used to select 20 ...
Yasemin Erdoğan +16 more
wiley +1 more source
Nature Genetics, 2013 Although genetic lesions responsible for some mendelian disorders can be rapidly discovered through massively parallel sequencing of whole genomes or exomes, not all diseases readily yield to such efforts.
Andrew W. Kirby +42 more
semanticscholar +1 more source
Cluster plot obtained after the HRM analysis using the VNTR-4bis and VNTR-Lb5.
, 2015 Cluster plot obtained after the HRM analysis using the VNTR-4bis and VNTR-Lb5.
Amélie Desvars (219115) +4 more
core +1 more source
A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations
Annals of Clinical and Translational Neurology, Volume 13, Issue 8, Page 1726-1732, August 2026.ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley +1 more source
Проблемы особо опасных инфекцийThe aim of the study was to conduct spatio-temporal retrospective and operational genetic analysis of the tularemia agent population in the Rostov Region, Donetsk People’s Republic (DPR), Lugansk PR and Ukraine in the period of 1943–2023.
V. M. Sorokin +6 more
doaj +1 more source
Animal Genetics, Volume 57, Issue 4, August 2026.ABSTRACT Canine mammary tumours (CMTs) are one of the most frequently observed malignancies in female dogs. Many studies have investigated epigenetic changes in CMT at the nuclear level, yet the role of mtDNA methylation, particularly in the D‐loop region, remains largely unexplored.
Krzysztof Kowal +5 more
wiley +1 more source