Results 81 to 90 of about 29,122 (264)

Identification of Potential Vaccine Strains of Escherichia coli Isolates From Diarrhoeic Calves

Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.
This study aimed to identify vaccine candidate Escherichia coli strains isolated from diarrheic calves. Faecal samples collected from 500 calves were analysed, and E. coli strains were isolated and characterized phenotypically and genotypically. Antibiotic resistance profiles, virulence‐associated genes and MLVA genotyping were used to select 20 ...
Yasemin Erdoğan, Ediz Kağan Özgen, Murat Özmen, Elif Karadeniz Pütür, Nebahat Polat, Ersan Pütür, Mücahit Harmancı, Ercan Atalay, Ahmet Temur, Meryem Güloğlu, Lütfullah Celep, Seyda Cengiz, Mehmet Cemal Adıgüzel, Cihan Öz, Timur Gülhan, Alper Çiftci, Erhan Çiftgül   +16 more
wiley   +1 more source

Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene

, 2004
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, Bronya J.B Keats, Deininger, Prescott L, Mark A Batzer, Prescott L Deininger, Savas, Sevtap, Frischhertz, Ben, Ben Frischhertz, Batzer, Mark A, Sevtap Savas   +9 more
core   +1 more source

A VNTR immediately adjacent to the human pseudoautosomal telomere [PDF]

Nucleic Acids Research, 1990
The probe 29C1 detects a hypervariable locus 18kb from the telomere of the human X and Y chromosomes, in the pseudoautosomal region. Here we report that hypervariability of fragments containing this sequence in the human population arises by loss or gain of a 31 base pair GC rich repeat. Labelled 29C1 does not detect a DNA fingerprint at low stringency,
C F, Inglehearn, H J, Cooke
openaire   +2 more sources

A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations

Annals of Clinical and Translational Neurology, Volume 13, Issue 8, Page 1726-1732, August 2026.
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley   +1 more source

DRD4 VNTR Allele and Genotype Frequencies.

, 2013
DRD4 VNTR Allele and Genotype Frequencies.
Shirley Y. Hill (333445), Robert E. Ferrell (47106), Kasey G. Creswell (333443), Stephen B. Manuck (124689), Michael A. Sayette (333444), John D. Dimoff (333446)   +5 more
core   +1 more source

Preliminary Analysis of CpG, CHG and CHH Methylation in the Mitochondrial Control Region of Dogs With Malignant Mammary Gland Tumours

Animal Genetics, Volume 57, Issue 4, August 2026.
ABSTRACT Canine mammary tumours (CMTs) are one of the most frequently observed malignancies in female dogs. Many studies have investigated epigenetic changes in CMT at the nuclear level, yet the role of mtDNA methylation, particularly in the D‐loop region, remains largely unexplored.
Krzysztof Kowal, Kaja Ziółkowska‐Twarowska, Angelika Tkaczyk‐Wlizło, Carlos Vaamonde‐García, Mercedes Fernández‐Moreno, Brygida Ślaska   +5 more
wiley   +1 more source

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

PLoS 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, Albert de Neeling, Rianne van Hunen, Gerard de Vries, Henrieke Schimmel, Arnout Mulder, Richard Anthony, Wim van der Hoek, Dick van Soolingen   +8 more
doaj   +1 more source

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

BMC 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, Dégrange Sébastien, Charron Alain, Dupon Michel, Xin Yi, Bébéar Cécile, Maugein Jeanne   +6 more
doaj   +1 more source

Development and analytical validation of a targeted short‐read next generation sequencing‐based pharmacogenetic panel for comprehensive variant detection

British Journal of Pharmacology, Volume 183, Issue 16, Page 4735-4760, August 2026.
Abstract Background and Purpose Genomic profiling of patients for genetic variants that modify the effect of specific medications has many benefits, including the possibility of avoiding toxicities and ensuring an adequate effect of the medication. Our intention was to develop a comprehensive, high‐quality pharmacogenetic test panel for clinical use ...
Anna Gréen, Nils Johan Fredriksson, Michael Andresen, Jon Jonasson, Malin Lindqvist Appell, Henrik Gréen   +5 more
wiley   +1 more source

Meta-analysis of the DRD5 VNTR in persistent ADHD [PDF]

European Neuropsychopharmacology, 2016
Attention-Deficit/Hyperactivity Disorder (ADHD) is a common neuropsychiatric disorder with a complex genetic background. DRD5, the gene encoding the dopamine receptor D5, was recently confirmed as a candidate gene for ADHD in children through meta-analysis.
Klein, M., Berger, S., Hoogman, M., Hoogman, M., Dammers, J.T., Makkinje, R.R., Makkinje, R.R., Heister, A., Heister, A., Galesloot, T.E., Kiemeney, L.A., Kiemeney, L.A., Weber, H., Kittel-Schneider, S., Lesch, K.P., Reif, A., Ribases, M., Ramos-Quiroga, J.A., Cormand, B., Zayats, T., Hegvik, T.A., Jacobsen, K.K., Johansson, S., Haavik, J., Mota, N.R., Bau, C.H., Grevet, E.H., Doyle, A., Faraone, S.V, Arias-Vasquez, A., Arias-Vasquez, A., Arias-Vasquez, A., Franke, B., Franke, B.   +33 more
openaire   +3 more sources