Authors: Odilon P. Morais J?ºnior, Jo?£o Batista Duarte, Fl?¡vio Breseghello, Alexandre S. G. Coelho, Tereza C. O. Borba, Jordene T. Aguiar, P?©ricles C. F. Neves, and Orlando P. Morais
In genomic recurrent selection programs of self-pollinated crops, additive genetic effects (breeding values) are effectively relevant for selection of superior progenies as new parents. However, considering additive and nonadditive genetic effects can improve the prediction of genome-enhanced breeding values (GEBV) of progenie.. Read More»
Authors: K.B. Penteado, C.I.S. Gressler, A.D. Da Cruz, T.C. Vieira, & M.A. D. Gigonzac
X-Fragile Syndrome (FXS) is the most common cause of inherited intellectual disability and the second of genetic origin, with an estimated prevalence of 1/4000 men and 1/6000 women. The etiology is associated with a trinucleotide expansion of CGG sequences and hypermethylation of the promoter region of the FMR1 (Fragile-X Ment.. Read More»
Authors: Q.D. Jiang, X.G. Zhou, Xiao.Z, X.P. Li and F.R. Nie
This study effects of Echinacea polysaccharide(EPS) to Lipopolysaccharides(LPS) injure RAW264.7 cell NF-κB and MAPK signaling pathway. The test was divided into blank groupã?LPS group and 100 mu g/mL EPS + LPS group, The respectively extract Cytoplasm protein and nucleoprotein. After Gel electrophoresis, the Western .. Read More»
Authors: Fehmida Bibi, Peter Natesan Pushparaj, Muhammad I. Naseer, Muhammad yasir, Esam I. Azhar
MicroRNAs (miRNAs) are non-coding small RNA molecules that regulate the differential expression of genes. The expression of miRNAs is dysregulated in various types of cancers, including Gastric Cancer (GC), and has both prognostic and diagnostic potential. To interpret the role of miRNA expression in GC, we evaluated the expre.. Read More»
Authors: Diana Rojas M?¡laga, Ana C. Brusius-Facchin, Kristiane Michelin-Tirelli, T?ªmis M. F?©lix, Jaqueline Schulte, Jamile Pereira, Eurico Camargo Neto, Claudio Sampaio Filho, Roberto Giugliani.
When a low activity of acid α-glucosidase (GAA) is found, particularly in newborn screening programs, to differentiate α-glucosidase pseudo deficiency from true Pompe disease is important and urgent, as the result generates parental stress and also because this differentiation drives decisions related to the manage.. Read More»
Authors: S. Mizell, S.L. Miller, A.M. Royer, K.J. Thornton, and M.D. Garcia
The objective of the current study was to evaluate single nucleotide polymorphisms (SNP) for potential growth and carcass trait associations located in two previously described quantitative trait loci (QTL) regions associated with bovine respiratory disease. A population of 323 crossbred steers sired by five purebred sire bree.. Read More»
Authors: Kum Chol Ri*, Jong Su Kim, Chol Kim
The Klf6 gene is a tumor suppressor gene belonging to the family of the Klf gene and closely associated with tumor formation. Recently, super enhancers(SEs) have been shown to play a particularly important role in regulating cell identity and are attempting to evaluate the in vivo function of SEs. But direct functional evidenc.. Read More»
Authors: Xiaomeng Ren, Xin Zhang, Yanyan Zhu, Yaser Gamallat, Abdo Meyiah, Shenhao Ma, Yi Xin
Antibiotic-induced disruption of the intestinal microbiota has serious consequences for human physiology. We conducted a microbial dysbiosis animal model to study and directly provide evidence for microbial dysbiosis contribution to malignant melanoma animal model. Females C57BL/6 wild-type (WT) mice injected with a limiting t.. Read More»
Authors: R.S. Mascarenhas, F.R.B. Oliveira, J.F. Corr?ªa, K.S.F. e Silva, I.R. Costa, A.M. Barbosa, M.H. Lagares, F.L. Campedelli, M.P. de Morais, J.V.M. Martins, D.A. Rodrigues, e K.K.V.O. Moura
Atherosclerosis is a chronic inflammatory condition and originates due to the accumulation of lipids in the innermost layer of the arteries. It is often related due to other underlying diseases, such as systemic arterial hypertension and type 2 diabetes mellitus, which may be the cause or may contribute to a worse prognosis of.. Read More»
Authors: Walid Zammiti, Sarra Said, Amani Shaman, Faisel Mohammed Abu-Duhier
Background: Protein Z (PZ) is a vitamin K-dependent plasma glycoprotein, it plays a key role in the physiologic inhibition of coagulation by acting as a cofactor in the inactivation of factor Xa. The relationship between PZ gene polymorphisms and pregnancy loss is controversial. To address this, we investigate the association .. Read More»