Results 51 to 60 of about 12,118 (162)

Per3 VNTR polymorphism and chronic heart failure [PDF]

open access: yesBiomedical Papers, 2014
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

X‐Linked Hypophosphatemia Caused by a New Partial Insertion of LINE‐1 in the PHEX Gene

open access: yesHuman Mutation, Volume 2026, Issue 1, 2026.
X‐linked hypophosphatemia (XLH), primarily caused by mutations of the PHEX gene, is the most common cause of genetic rickets. Pediatric cases of XLH typically present with elevated levels of serum fibroblast growth factor 23 (FGF23), hypophosphatemia, rickets, and impaired growth.
Dongmei Li   +6 more
wiley   +1 more source

Variable-number tandem-repeat markers for typing Mycobacterium intracellulare strains isolated in humans

open access: yesBMC Microbiology, 2010
Background Mycobacterium intracellulare, a species of the Mycobacterium avium complex, may be the cause of severe lung, lymphatic node, skin and bone/joint infections, as well as bacteriemia.
Dauchy Frédéric-Antoine   +6 more
doaj   +1 more source

Genetic Heterogeneity of Francisella tularensis Subspecies mediasiatica Strains

open access: yesПроблемы особо опасных инфекций
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

Epidemiological links between tuberculosis cases identified twice as efficiently by whole genome sequencing than conventional molecular typing: A population-based study.

open access: yesPLoS ONE, 2018
BackgroundPatients with Mycobacterium tuberculosis isolates sharing identical DNA fingerprint patterns can be epidemiologically linked. However, municipal health services in the Netherlands are able to confirm an epidemiological link in only around 23 ...
Rana Jajou   +8 more
doaj   +1 more source

The Psychiatric‐Metabolic Interface: Exploring the Interplay Between Mental Disorders and Metabolic Syndrome

open access: yesMental Illness, Volume 2026, Issue 1, 2026.
Psychiatric disorders affect a person′s mental health, causing emotional and physical disturbances. Metabolic syndrome (MetS) is a medical condition characterized by metabolic abnormalities and health complications. Research suggests that individuals with specific psychiatric conditions are more likely to develop MetS.
Linda Elias   +11 more
wiley   +1 more source

Abstract Supplement

open access: yesPulmonary Medicine, Volume 2026, Issue 1, 2026.

Marzia Folegani, Semonti Nandi
wiley   +1 more source

Spatio-Temporal Analysis of the Tularemia Agent Population in the Rostov Region, DPR, LPR and Ukraine from 1943 to 2023

open access: yesПроблемы особо опасных инфекций
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

Integrated phenotypic and proteomic screening identifies top‐tier Alzheimer's disease therapeutic targets

open access: yesAlzheimer's &Dementia, Volume 21, Issue 12, December 2025.
Abstract INTRODUCTION Alzheimer's disease (AD) is a complex neurodegenerative disorder. Hundreds of therapeutic targets have been nominated through genetic and multi‐omic studies, but effective prioritization remains a major bottleneck. METHODS We applied an integrative screening framework to assess 29 candidate targets from risk‐enriched biological ...
Gregory A. Cary   +12 more
wiley   +1 more source

LINE-1 ORF1p does not determine substrate preference for human/orangutan SVA and gibbon LAVA

open access: yesMobile DNA, 2020
Background Non-autonomous VNTR (Variable Number of Tandem Repeats) composite retrotransposons – SVA (SINE-R-VNTR-Alu) and LAVA (L1-Alu-VNTR-Alu) – are specific to hominoid primates. SVA expanded in great apes, LAVA in gibbon.
Annette Damert
doaj   +1 more source

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