Polymorphisms in the genes of citohrom oxidase P450 2D6 (CYP2D6), paraoxonase 1 (PON1) and apolipoproteine E (APOE) as risk factors for Parkinson's disease [PDF]
Vojnosanitetski Pregled, 2007 Background/Aim. The presence of Parkinson's disease (PD) among the members of a family is a clear indication of the significance of genetics in its development.
Đurić Gordana +5 more
doaj +1 more source
Molecular characterization of a species in the genus Rubus in Boyacá, Colombia [PDF]
Revista Brasileira de Fruticultura, 2021 Colombia is home to blackberry genetic resources which present a morphological diversity. The relevant characteristics related to its diversity are the presence of prickles, the shape of its leaves, the number and color of its fruits, and its enormous ...
Brigitte Liliana Moreno–Medina +1 more
doaj +1 more source
Differential coupling of gibberellin responses by Rht-B1c suppressor alleles and Rht-B1b in wheat highlights a unique role for the DELLA N-terminus in dormancy [PDF]
, 2017 During the Green Revolution, substantial increases in wheat (Triticum aestivum) yields were realized, at least in part, through the introduction of the Reduced height (Rht)-B1b and Rht-D1b semi-dwarfing alleles.
Chandler, Peter Michael +3 more
core +1 more source
KIR2DL2/2DL3-E(35) alleles are functionally stronger than -Q(35) alleles. [PDF]
, 2016 KIR2DL2 and KIR2DL3 segregate as alleles of a single locus in the centromeric motif of the killer cell immunoglobulin-like receptor (KIR) gene family. Although KIR2DL2/L3 polymorphism is known to be associated with many human diseases and is an important
Bao, Ju +5 more
core +1 more source
Revista Mexicana de Ciencias Pecuarias, 2020 The porcine reproductive and respiratory syndrome (PRRS) is a viral disease that decreases the reproductive performance in breeding sows and leads to economic losses to the swine industry.
Carlos Martín Aguilar-Trejo +9 more
doaj +1 more source
Diagnostics, 2021 Background: Polycystic ovary syndrome (PCOS) is the most common endocrinopathy in women. Depending on the diagnostic criteria applied, it occurs in up to 16.6% of the general female population. Congenital adrenal hyperplasia includes a group of autosomal
Lasma Lidaka +5 more
doaj +1 more source
Selection responses of means and inbreeding depression for female fecundity in Drosophila melanogaster suggest contributions from intermediate-frequency alleles to quantitative trait variation [PDF]
, 2007 The extent to which quantitative trait variability is caused by rare alleles maintained by mutation, versus intermediate-frequency alleles maintained by balancing selection, is an unsolved problem of evolutionary genetics.
Borthwick, Helen +2 more
core +1 more source
The AGTR2 (RS11091046) Gene Polymorphism is Associated with Cycling Performance in Korean Cyclists [PDF]
운동과학, 2022 Purpose This study aimed to investigate the association between AGTR2 (rs11091046 A>C) gene polymorphism and athletic performance. Methods The Korean national team cyclists enrolled in the study performed 30-second Wingate test (peak power, mean power ...
Seok-ki Min +5 more
doaj +1 more source
Cytological characterization and allelism testing of anther developmental mutants identified in a screen of maize male sterile lines. [PDF]
, 2013 Proper regulation of anther differentiation is crucial for producing functional pollen, and defects in or absence of any anther cell type result in male sterility.
Cande, William Zacheus +7 more
core +2 more sources
Prediction of HLA class II alleles using SNPs in an African population [PDF]
, 2012 BACKGROUND: Despite the importance of the human leukocyte antigen (HLA) gene locus in research and clinical practice, direct HLA typing is laborious and expensive.
Adeyemo, Adebowale +7 more
core +4 more sources