Results 111 to 120 of about 17,479 (163)
Genotyping of strains by Multilocus VNTR Analysis
International audience(C.) is the causative agent of ovine enzootic abortion with zoonotic potential whose epidemiology has been held back because of the obligate intracellular habitat of the bacterium.
Maingourd, Cyril +24 more
core +1 more source
Comparison of VNTR-based clustering with WGS.
Comparison of VNTR-based clustering with WGS.
Timothy Brown (3191448) +5 more
core +1 more source
VNTR DNA Variation in Siberian Indigenous Populations [PDF]
This is the published version. Copyright 1995 Wayne State University Press.The VNTR loci D7S104, D11S129, D18S17, D20S15, and D21S112 in three indigenous Siberian populations were analyzed to determine the populations' genetic structure.
Leonard, William R. +6 more
core +1 more source
There are conflicting results concerning DC-SIGN and DC-SIGNR VNTR polymorphisms. The present study aimed to evaluate the possible association between DC-SIGN as well as DC-SIGNR VNTR polymorphisms and pulmonary tuberculosis (PTB) in a sample of Iranian ...
Mohammad Naderi +4 more
doaj
MIRU-VNTR Mtbc Kinshasa 2005-2010
MIRU-VNTR patterns for retreatment cases in Kinshasa, DRC 2005 ...
Bouke C. de Jong (20655) +1 more
core +1 more source
Laith N AL-Eitan,1,2 Ayah Y Almasri,1 Sahar O Al-Habahbeh1 1Department of Applied Biological Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan; 2Department of Biotechnology and Genetic Engineering, Jordan University of Science ...
AL-Eitan LN, Almasri AY, Al-Habahbeh SO
doaj
Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD). [PDF]
Although there is evidence for the involvement of genes of serotonergic and dopaminergic systems in the manifestation of the Behavioural and Psychological Symptoms in Dementia (BPSD), genetic association studies are contradictory.
Belinda Martin +12 more
core
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
Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene
Usher syndrome type IC is a rare, autosomal recessive sensorineural disorder caused by mutations in the USH1C gene, which encodes a PDZ-domain protein named harmonin. The Acadian-specific 216G--\u3eA mutation in exon 3 and a variant 9-repeat VNTR allele (
Keats, Bronya J +9 more
core +1 more source
Background: Recently it is shown that Mycobacterium tuberculosis Beijing genotype are associated with drug resistance. Thus a simple and rapid method is required for identification and differentiation of Beijing family isolates. Therefore the aim of this
Mohaddese Mozafari +6 more
doaj

