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Carotenoids gene markers for sweetpotato (Ipomoea batatas L. Lam): applications in genetic mapping, diversity evaluation and cross‑species transference
(Springer, 2014-04)
Carotenoids play essential biological roles in plants, and genes involved in the carotenoid biosynthesis pathway are evolutionarily conserved. Orange sweetpotato is an important source of β-carotene, a precursor of vitamin ...
Chromosomal imbalances in successive moments of human bladder urothelial carcinoma
(2013-08-01)
Objective: To understand developmental characteristics of urinary bladder carcinomas (UBC) by evaluating genomic alterations and p53 protein expression in primary tumors, their recurrences, and in the morphologically normal ...
Chromosomal imbalances in successive moments of human bladder urothelial carcinoma
(2013-08-01)
Objective: To understand developmental characteristics of urinary bladder carcinomas (UBC) by evaluating genomic alterations and p53 protein expression in primary tumors, their recurrences, and in the morphologically normal ...
Gene amplification is a mechanism of SW overexpression in breast cancer
(Amer Assoc Cancer ResearchPhiladelphiaEUA, 2005)
Quantitative real-time polymerase Chain reaction for enteropathogenic escherichia coli: A tool for investigation of asymptomatic versus symptomatic infections
(Oxford University Press, 2011)
Background. Enteropathogenic Escherichia coli (EPEC) strains are pediatric pathogens commonly isolated from both healthy and sick children with diarrhea in areas of endemicity. The aim of this study was to compare the ...
A comprehensive analysis of gene expression alterations in newly synthesized Paspalum notatum autotetraploid
(Elsevier Ireland, 2005-12)
Although the causes of novel variation in polyploids are not well understood, they could involve changes in gene expression through dosage-regulation, altered regulatory interactions and rapid genetic/epigenetic changes. ...
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1
(WILEY-BLACKWELL PUBLISHING, INC, 2010)
P>Objective Congenital hypogonadotropic hypogonadism with anosmia (Kallmann syndrome) or with normal sense of smell is a heterogeneous genetic disorder caused by defects in the synthesis, secretion and action of ...
Partial-AZFc deletions in Chilean men with primary spermatogenic impairment: gene dosage and Y-chromosome haplogroups
(Springer, 2020)
Purpose To investigate the association of partial-AZFc deletions in Chilean men with primary spermatogenic failure and their testicular histopathological phenotypes, analyzing the contribution ofDAZdosage,CDY1copies, and ...