Deficiency in homozygous haplotypes reveals recessive lethal variants affecting fertility and viability in the Friesian horse. [PDF]
Steensma MJ +5 more
europepmc +1 more source
ABSTRACT Background The Testicular Cancer Consortium (TECAC) was established in 2012 and is comprised of researchers from over 25 centers in Europe and North America. TECAC's overarching goal is to investigate the genetic susceptibility of testicular germ cell tumors (TGCT) to better understand their biology, impact prevention strategies, and inform ...
Peter A. Kanetsky +28 more
wiley +1 more source
Genetic Basis Analysis for Candidate QTLs and Functional Genes Controlling Four-Seeded Pods at Lower-Node in Soybean (<i>Glycine max</i>) Plant. [PDF]
Raja R +6 more
europepmc +1 more source
Tubulointerstitial nephritis and uveitis syndrome in children: What to keep an eye on
Abstract Purpose The purpose of this study was to determine the disease course in patients with tubulointerstitial nephritis and uveitis (TINU) syndrome, focusing on long‐term outcome and the incidence of complications such as chronic kidney disease (CKD).
Jytte Hendrikse +4 more
wiley +1 more source
Haplotype-based genome-wide association study uncovers QTL for fruit-related traits in the 287 tomato accessions. [PDF]
Nguyen TTN, Heo J, Lim B, Sim SC.
europepmc +1 more source
Abstract Purpose Inherited retinal diseases (IRDs) are a clinically and genetically heterogeneous group of disorders, with ~30% of cases remaining genetically unsolved. Complete congenital stationary night blindness (cCSNB) is a subtype of IRD, usually associated with reduced visual acuity, nystagmus and high myopia.
Filip Spanic +10 more
wiley +1 more source
A haplotype-phased male genome sequence of the stinging nettle, Urtica dioica ssp. dioica. [PDF]
Hirabayashi K +5 more
europepmc +1 more source
Genetic diversity of mitochondrial DNA D-loop sequences in UAE native chickens. [PDF]
Kullan ARK +3 more
europepmc +1 more source
Decoding immune‐driven erythroid failure in pure red cell aplasia
Pure red cell aplasia (PRCA) is increasingly recognised as a T‐cell‐mediated bone marrow failure syndrome, yet its immunogenetic drivers remain poorly defined. In their paper, Yamashita et al. integrate human leucocyte antigen (HLA) typing, T‐cell receptor repertoire analysis and mutational profiling to reveal enriched HLA alleles, signal transducer ...
Federico Spataro +2 more
wiley +1 more source
Strongyloides Genetic Diversity among Humans, Dogs, and Nonhuman Primates, Central African Republic, 2016-2022. [PDF]
Nosková E +9 more
europepmc +1 more source

