Results 101 to 110 of about 17,479 (163)

INTERLEUKIN 1 AND INTERLEUKIN 4 GENES POLYMORPHISM ASSOCIATED WITH EARLY AND PRESCHOOL AGE CHILDREN SENSITIZATION TO STREPTOCOCCUS PYOGENES

Инфекция и иммунитет, 2016
Background. Streptococcus pyogenes infection and sensitization to its antigens is considered to be an unfavorable factor for the induction of rheumatic pathology. The search for genetic predictors of rheumatic diseases in general, and sensitization to S.
A. V. Shabaldin, E. V. Shabaldina, S. V. Ryazantsev, A. S. Simbirtsev   +3 more
doaj   +1 more source

Long‐read sequencing reveals SVA insertion in AP3B1 causing Hermansky–Pudlak syndrome 2

Pediatric Allergy and Immunology, Volume 37, Issue 7, July 2026.
Naomi Baba, Ahmed Elashy, Oliver Wegehaupt, Barbara Zieger, Melisa Felek, Micol Ferro, Kimberly Gilmour, Ute Fischer, Arndt Borkhardt, Stephan Ehl, David Koppstein, Sujal Ghosh   +11 more
wiley   +1 more source

Origins and evolution of VNTR loci: The apolipoprotein B 3\u27 VNTR

, 1993
I studied the apolipoprotein (apo) B 3$\sp\prime$ variable number tandem repeat (VNTR) and did computer simulations of the stepwise mutation model to address four questions: (1) How did the apo B VNTR originate?
Shriver, Mark David
core   +1 more source

VNTR analysis of environmental samples.

, 2015
UA, unassigned, OTS, genotypic designation of unidentified MPM, NP, none positive. ND, not done, 0, no amplification. BAF-3 was confirmed as M. marinum from BLAST searches. Two water bodies (Wro-Offin and Mon-Offin) are not shown because no VNTR loci was
Dziedzom K. de Souza (417272), Bassirou Bonfoh (424496), Charles A. Narh (586900), Samuel C. K. Tay (685483), Lydia Mosi (549898), Daniele O. Konan (685482), Charles Quaye (272214), Daniel A. Boakye (90294), Christelle Dassi (685481)   +8 more
core   +1 more source

Direct PCR‐Based VNTR Analysis of TPO Intron 10 for Rapid Detection of Maternal Cell Contamination in Prenatal Diagnosis

Clinical and Translational Science
Maternal cell contamination (MCC) in fetal specimens poses a major risk for misdiagnosis in prenatal genetic testing. Standard variable number tandem repeat (VNTR) analysis of the thyroid peroxidase (TPO) gene intron 10 is informative for MCC detection ...
Phongsathorn Wichian, Apisit Pattrakorn, Supan Fucharoen, Hataichanok Srivorakun, Simaporn Prommetta, Supawadee Yamsri   +5 more
doaj   +1 more source

VNTR Raw data

, 2014
This file contains the numbers of the repeats obtained from the sequenced VNTR loci. These data were implemented to generated the Minimum Spanning Network using BioNumerics software (version 7 ...
Anibal Tapiero (3314844), Nathalia Arias-Rojas (3314847), César A. Trujillo (3314853), César A. Medina (3314850), Bernal, Adriana J., Trujillo, César A., Medina, César A., Silvia Restrepo (204944), Adriana J. Bernal (662033), Lucie Poulin (488933), Koebnik, Ralf, Restrepo, Silvia, Poulin, Lucie, Tapiero, Anibal, Arias-Rojas, Nathalia, Ralf Koebnik (93571)   +15 more
core   +1 more source

The dopaminergic midbrain participates in human episodic memory formation: Evidence from genetic imaging [PDF]

, 2006
Recent data from animal studies raise the possibility that dopaminergic neuromodulation promotes the encoding of novel stimuli. We investigated a possible role for the dopaminergic midbrain in human episodic memory by measuring how polymorphisms in ...
Heinze, HJ, Bunzeck, N, Bernstein, HG, Gundelfinger, ED, Tischmeyer, W, Lauer, CJ, Duzel, E, Schott, BH, Seidenbecher, CI, Fenker, DB   +9 more
core  

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

Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR

Genome Medicine
Background Repetitive genome regions, such as variable number of tandem repeats (VNTR) or short tandem repeats (STR), are major constituents of the uncharted dark genome and evade conventional sequencing approaches. The protein-coding LPA kringle IV type-
Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Lukas Forer, Silvia Di Maio, Hansi Weissensteiner, Bernhard Paulweber, Sebastian Schönherr, Florian Kronenberg, Stefan Coassin   +9 more
doaj   +1 more source

VNTR: Application to prenatal diagnosis

, 1997
Purpose: In prenatal diagnosis maternal DNA contamination of the CVS (chorionic villus sample) must be excluded for obtaining reliable results.
Evruke C., Ozgunen F.T., Curuk A., Aksoy K., Attila G., Arpaci A., Yuregir G.   +6 more
core   +1 more source