Results 41 to 50 of about 14,132 (209)

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

Genome-wide prediction of human VNTRs

open access: yesGenomics, 2005
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

A Mycobacterium leprae VNTR database

open access: yesLeprosy Review, 2010
A great deal of the last quarter of a century’s astonishing progress in understanding and treating human disease is attributable to the existence of public databases where information about DNA sequences, protein sequences, protein structures, human variation, etc. is stored and is freely available to all interested investigators.
openaire   +2 more sources

Genome-wide investigation of VNTR motif polymorphisms in 8,222 genomes: Implications for biological regulation and human traits

open access: yesCell Genomics
Summary: Variable number tandem repeat (VNTR) is a pervasive and highly mutable genetic feature that varies in both length and repeat sequence. Despite the well-studied copy-number variants, the functional impacts of repeat motif polymorphisms remain ...
Sijia Zhang   +13 more
doaj   +1 more source

GENETIC DIVERSITY OF MYCOBACTERIUM AVIUM subsp. HOMINISSUIS STRAINS ISOLATED IN ITALY BASED ON VNTR LOCI ANALYSIS

open access: yesИнфекция 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

vamos: VNTR annotation using efficient motif sets

open access: yes, 2022
AbstractMotivationRoughly 3% of the human genome is composed of variable-number tandem repeats (VNTRs): tandemly repeated arrays of motifs at least six bases. These loci are highly polymorphic: over 61% of insertion and deletion variants at least 50 bases found from long-read assemblies are inside VNTRs.
Jingwen Ren, Bida Gu, Chaisson, Mark JP
openaire   +1 more source

Unveiling Aging and Alzheimer's Disease–Associated Dynamics of LINE1 DNA Content and Protein Expression in Mouse Brains

open access: yesAging Cell, Volume 24, Issue 12, December 2025.
A fundamental understanding of the Alzheimer’s disease (AD) specific trajectory of LINE1 has been limited. This study reveals an unanticipated U‐shaped trajectory of LINE1 content and expression in both wild‐type and AD mouse brains, and discerns specific changes in LINE1 content and expression tied to AD neuropathology in a sex‐different manner.
Minyan Jiang   +9 more
wiley   +1 more source

Evolutionary history of the PER3 variable number of tandem repeats (VNTR): idiosyncratic aspect of primate molecular circadian clock. [PDF]

open access: yesPLoS ONE, 2014
The PER3 gene is one of the clock genes, which function in the core mammalian molecular circadian system. A variable number of tandem repeats (VNTR) locus in the 18th exon of this gene has been strongly associated to circadian rhythm phenotypes and sleep
Flávia Cal Sabino   +7 more
doaj   +1 more source

Long‐read sequencing reveals genomic and epigenomic variation in the dark genome of human Alzheimer's disease

open access: yesAlzheimer's &Dementia, Volume 21, Issue 11, November 2025.
Abstract INTRODUCTION Faulty DNA repair and epigenetic regulation contribute to neurodegeneration in Alzheimer's disease. Long‐read sequencing enables analysis of “dark regions” that are difficult to study via traditional sequencing methodologies.
Paulino Ramirez   +8 more
wiley   +1 more source

Home - About - Disclaimer - Privacy