Results 21 to 30 of about 17,479 (163)

VNTR sequence and genotyping.

open access: yes, 2022
Sequence of the 33 bp VNTR is shown, with the 8 bp T-box protein consensus sequence in underlined red text. IGV screenshot displays homozygosity for alleles 1 (top), 2 (middle; reference allele), and 3 (bottom) of the VNTR.
Jacquelyn M. Evans (3716872)   +7 more
core   +1 more source

New Genetic Markers for Molecular Typing of Bacillus anthracis Strains

open access: yesПроблемы особо опасных инфекций, 2019
Objective: Identification of new markers for the molecular typing of Bacillus anthracis. Materials and methods. The genomes of 16 B. anthracis strains from the collection of the Stavropol Research Anti-Plague Institute, 11 B.
E. I. Eremenko   +13 more
doaj   +1 more source

A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia

open access: yesScientific Reports, 2019
The MIR137HG gene encoding microRNA-137 (miR-137) is genome-wide associated with schizophrenia (SZ), however, the underlying molecular mechanisms remain unknown.
Ashley Pacheco   +3 more
semanticscholar   +1 more source

Analysis of Vibrio cholerae Genotype Stability at Low Temperature and Nutrients Deficiency

open access: yesПроблемы особо опасных инфекций, 2016
Objective is an experimental study of the low temperature and nutrient deficiency effects on the stability of Vibrio cholerae El Tor genetic loci complex.Materials and methods. The stability of the genetic loci (i.e. the basic pathogenicity genes; genome
L. V. Mironova   +5 more
doaj   +1 more source

Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations

open access: yesScientific Reports, 2018
Recently, the Mucin-1 (MUC1) gene has been identified as a causal gene of autosomal dominant tubulointerstitial kidney disease (ADTKD). Most causative mutations are buried within a GC-rich 60 basepair variable number of tandem repeat (VNTR), which ...
A. Wenzel   +17 more
semanticscholar   +1 more source

A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression

open access: yesFrontiers in Molecular Neuroscience, 2022
We describe the characterisation of a variable number tandem repeat (VNTR) domain within intron 1 of the amyotrophic lateral sclerosis (ALS) risk gene CFAP410 (Cilia and flagella associated protein 410) (previously known as C21orf2), providing insight ...
Jack N. G. Marshall   +19 more
doaj   +1 more source

MOLECULAR CHARACTERIZATION OF MYCOBACTERIUM TUBERCULOSIS STRAINS CIRCULATING IN THE URAL REGION, RUSSIA

open access: yesИнфекция и иммунитет, 2014
. Overall 178 Mycobacterium tuberculosis isolates recovered in 2009–2011 from newly diagnosed epidemiologically unlinked to TB patients in the Ural region of Russia have been studied.
T. V. Umpeleva   +4 more
doaj   +1 more source

Role of MIRU-VNTR and spoligotyping in assessing the genetic diversity of Mycobacterium tuberculosis in Henan Province, China

open access: yesBMC Infectious Diseases, 2018
BackgroundTuberculosis remains a serious threat to human health as an infectious disease in China. Henan, a most populated province in China, has a high incidence of tuberculosis (TB).
Jie Shi   +6 more
semanticscholar   +1 more source

Copy number variants and VNTR length polymorphisms of the carboxyl-ester lipase (CEL) gene as risk factors in pancreatic cancer.

open access: yesPancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2017
BACKGROUND/OBJECTIVES We have recently described copy number variants (CNVs) of the human carboxyl-ester lipase (CEL) gene, including a recombined deletion allele (CEL-HYB) that is a genetic risk factor for chronic pancreatitis.
M. Dalva   +15 more
semanticscholar   +1 more source

Data_Sheet_1_Characterisation of the Function of a SINE-VNTR-Alu Retrotransposon to Modulate Isoform Expression at the MAPT Locus.PDF

open access: yes, 2022
SINE-VNTR-Alu retrotransposons represent one class of transposable elements which contribute to the regulation and evolution of the primate genome and have the potential to be involved in genetic instability and disease progression.
Vivien J. Bubb (9642066)   +4 more
core   +1 more source

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