Results 61 to 70 of about 29,122 (264)
Haplotype network of the genotyped strains SNP7614, VNTR 27–5 and VNTR 12–5.
, 2015 Haplotype network of the genotyped strains SNP7614, VNTR 27–5 and VNTR 12–5.
Gabriel Bedoya (36821) +5 more
core +1 more source
International Journal of Cancer, Volume 159, Issue 10, Page 2512-2524, 15 November 2026.Pre‐treatment DPYD and UGT1A1 genotyping is increasingly used to prevent fluoropyrimidine‐ and irinotecan‐related toxicity, but variant‐specific real‐world effects remain unclear. In an unselected cohort of cancer patients with actionable genotypes, genotype‐driven dosing improved safety while preserving treatment exposure in high‐risk DPYD c.1905+1G>A
Martina Gambron +12 more
wiley +1 more source
A Nelore Cattle Structural Variant Catalog
Animal Genetics, Volume 57, Issue 5, October 2026.ABSTRACT Structural variants (SVs) contribute more nucleotide divergence between mammalian genomes than single nucleotide polymorphisms, yet no population‐scale, long‐read‐validated SV catalog has been available for Bos indicus cattle. Nelore, the most numerically important indicine breed worldwide, diverges substantially from the taurine‐derived ...
Thales de Lima Silva +10 more
wiley +1 more source
Annals of Neurology, Volume 100, Issue 4, Page 751-767, October 2026.Objective Initially described in 1976, X‐linked dystonia parkinsonism (XDP) is a neurodegenerative disease that can be characterized by the presentation of dystonia and parkinsonism symptoms. Although this disease bears some resemblance to other neurodegenerative diseases in terms of symptomatology, the pathological signature of XDP is still unclear ...
Adelie Y.S. Tan +19 more
wiley +1 more source
BMC Genomics, 2015 VNTR (Variable Number of Tandem Repeats) composite retrotransposons - SVA (SINE-R-VNTR-Alu), LAVA (LINE-1-Alu-VNTR-Alu), PVA (PTGR2-VNTR-Alu) and FVA (FRAM-VNTR-Alu) - are specific to hominoid primates.
I. Lupan +3 more
semanticscholar +1 more source
European Journal of Haematology, Volume 117, Issue 4, Page 1052-1060, October 2026.ABSTRACT Background Sickle cell disease (SCD) is a chronic and life‐limiting hemoglobin and systemic vascular disease. While over 1000 people have undergone hematopoietic cell transplantation (HCT) over the last 40 years, long‐term disease‐specific and health‐related quality of life data are lacking.
Gregory M. T. Guilcher +20 more
wiley +1 more source
VNTR genotypes among 40 genomes.
, 2012 VNTR genotypes among 40 genomes.
Alison P. Klein (173817) +7 more
core +1 more source
Possible Association of IL-4 VNTR Polymorphism with Susceptibility to Preeclampsia
BioMed Research International, 2014 Preeclampsia (PE) is a pregnancy-specific disorder that results in maternal mortality and morbidity. Growing evidence indicated that cytokines are involved in the pathogenesis of PE and interleukin-4 VNTR polymorphism could be implicated in altering the ...
S. Salimi +4 more
semanticscholar +1 more source
A Mycobacterium leprae VNTR database
Leprosy 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
Genomic Medicine Sweden: Advancing precision medicine at the national level
Journal of Internal Medicine, Volume 300, Issue 4, Page 397-419, October 2026.Abstract High‐throughput sequencing has transformed clinical diagnostics of rare diseases (RD), cancer and infectious diseases by enabling the identification of disease‐causing genetic alterations and facilitating individualised treatment and care.
Anders Edsjö +58 more
wiley +1 more source