Results 21 to 30 of about 122,711 (274)

Polymorphisms of MicroRNA-146a Gene in Behcet’s Disease in Iraqi Patients

open access: yesJournal of Pure and Applied Microbiology, 2018
The present study was carried out to detect the association of miR-146a haplotypes polymorphisms with Behcet’s Disease in Iraqi patients, PCR-SSCP technique used in present study, blood was used to DNA extraction, the results show that there was strong
Israa Harjan Mohsen   +4 more
doaj   +1 more source

Origin and Distribution of the VRN-A1 Exon 4 and Exon 7 Haplotypes in Domesticated Wheat Species

open access: yesAgronomy, 2018
The high adaptive potential of modern wheat to a wide range of environmental conditions is determined by genetic changes during domestication. Genetic diversity in VRN1 genes is a key contributor to this adaptability.
Alexandr Muterko, Elena Salina
doaj   +1 more source

Haplotypes of [‐794(CATT)5–8/‐173G>C] MIF gene polymorphisms and its soluble levels in cutaneous squamous cell carcinoma in western Mexican population

open access: yesMolecular Genetics & Genomic Medicine, 2023
Background Some cytokines are strongly implicated in the development of squamous cell carcinoma (SCC) such as the Macrophage migration inhibitory factor (MIF).
Elizabeth Guevara‐Gutiérrez   +9 more
doaj   +1 more source

The mitochondrial DNA HVI and HVII sequences and haplogroup distribution in a population sample from Vietnam

open access: yesAnnals of Human Biology, 2022
Background Mitochondrial DNA (mtDNA) analysis has been used in forensics and requires well-established population databases for statistical interpretations. However, high-quality mtDNA data from Vietnamese population samples have been limited.
Nam Ngoc Nguyen   +7 more
doaj   +1 more source

Amplification of Cherimoya (Annona cherimola Mill.) with Chloroplast-Specific Markers: Geographical Implications on Diversity and Dispersion Studies

open access: yesHorticulturae, 2022
Previously developed Annona cherimola specific primers based on the plant barcode gene matK were tested in 546 cherimoya accessions. Of those, 296 belong to an ex situ world reference germplasm collection maintained at the IHSM La Mayora-CSIC-UMA in ...
Nerea Larranaga   +4 more
doaj   +1 more source

Pattern Recognition Molecules of Lectin Complement Pathway in Ischemic Stroke

open access: yesPharmacogenomics and Personalized Medicine, 2021
Gohar Tsakanova,1,2 Ani Stepanyan,1 Rudi Steffensen,3 Armine Soghoyan,4 Jens Christian Jensenius,5 Arsen Arakelyan1 1Institute of Molecular Biology NAS RA, Yerevan, Armenia; 2CANDLE Synchrotron Research Institute, Yerevan, Armenia; 3Department of ...
Tsakanova G   +5 more
doaj  

Genetic Differentiation and Population Structure of Threatened Prunus africana Kalm. in Western Cameroon Using Molecular Markers

open access: yesDiversity, 2020
Genetic diversity of species is an important baseline for the domestication process. In Cameroon, Prunus africana, an important and threatened medicinal tree, is among the priority species for domestication.
Justine G. Nzweundji   +4 more
doaj   +1 more source

ASA Status, NPPA/NPPB Haplotype and Coronary Artery Disease Have an Impact on BNP/NT-proBNP Plasma Levels

open access: yesCells, 2022
Plasma concentrations of natriuretic peptides (NP) contribute to risk stratification and management of patients undergoing non-cardiac surgery. However, genetically determined variability in the levels of these biomarkers has been described previously ...
Markus Hahn   +5 more
doaj   +1 more source

SHIELD: Secure Haplotype Imputation Employing Local Differential Privacy [PDF]

open access: yesarXiv, 2023
We introduce Secure Haplotype Imputation Employing Local Differential privacy (SHIELD), a program for accurately estimating the genotype of target samples at markers that are not directly assayed by array-based genotyping platforms while preserving the privacy of donors to public reference panels.
arxiv  

Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study

open access: yesHepatology, EarlyView., 2022
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan   +19 more
wiley   +1 more source

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