Results 71 to 80 of about 29,122 (264)
Genetic Heterogeneity of Francisella tularensis Subspecies mediasiatica Strains
The 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
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
Genome-wide prediction of human VNTRs
Polymorphic minisatellites, also known as variable number of tandem repeats (VNTRs), are tandem repeat regions that show variation in the number of repeat units among chromosomes in a population. Currently, there are no general methods for predicting which minisatellites have a high probability of being polymorphic, given their sequence characteristics.
Karl, Näslund +5 more
openaire +2 more sources
Placental Site Trophoblastic Tumor Acquires Immune Functions by Incorporating Host Maternal Genes
PSTT cells, through cell fusion with B cells, incorporate abundant non‐inherited maternal genes that are detectable by DNIMA. These hybrid cells acquire immunotherapy‐resistant genetic changes and increase the expression of B cell‐derived immune‐related molecules such as Ig, HLA, LILRB, SIGLEC10, and so on, creating an immunotolerant environment around
Kyosuke Kagami +15 more
wiley +1 more source
Discriminatory powers of VNTR-9 and VNTR-15 among six field sites and their concordance for defining clustered and unique strains.
Yanlin Zhao (251552) +5 more
core +1 more source
. 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
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
Per3 VNTR polymorphism and chronic heart failure [PDF]
The aim of this study was to investigate the relationship between gene Period3 (Per3) variable number tandem repeat (VNTR) polymorphism and chronic heart failure (CHF).The study subjects (372 patients of Caucasian origin with CHF and 332 healthy controls) were genotyped for Per3 VNTR polymorphism using an allele-specific PCR.No significant differences ...
Jolana, Lipkova +8 more
openaire +2 more sources
Technologies for engineering repetitive DNA
Abstract Repetitive DNA, a fundamental architectural element of genomes, is widespread across organisms and comprises about 54% of the human genome. With advances in long‐read sequencing and bioinformatics approaches, highly repetitive sequences can now be characterized in depth.
Shuting Ma, Yali Cui, Yi Wu
wiley +1 more source
The 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

