Publications by authors named "A El-Seedy"

Cystic fibrosis (CF) is inherited by CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations. A variety of mutations have been identified in the CFTR gene that may be associated with cystic fibrosis, and these mutations demonstrate extensive molecular genetic heterogeneity in this disease. Little is known about the molecular mechanism by which mutations affect CFTR function, and only a minority of mutations have been characterized by functional studies.

View Article and Find Full Text PDF

Background And Aim: There is a limited amount of research conducted on quail breeding domestically and internationally, particularly at the molecular level. This study aimed to detect single-nucleotide polymorphisms in the growth hormone (GH) and insulin-like growth factor-1 (IGF-1) genes across two quail varieties and their hybrids correlate these genetic factors with body weight (BW) and growth rate at 0 and 6 weeks, and assess crossing effects.

Materials And Methods: White and Japanese quail were crossed.

View Article and Find Full Text PDF

The monocarboxylate transporter 4 (MCT4; Slc16a3) is expressed in the central nervous system, notably by astrocytes. It is implicated in lactate release and the regulation of glycolytic flux. Whether its expression varies during normal and/or pathological aging is unclear.

View Article and Find Full Text PDF

Environmental contamination by complex mixtures of pesticides and metals is a major health problem in agriculture and industry. In real life scenarios, we are exposed to mixtures of chemicals rather than single chemicals, and therefore it is critical to assess their toxicity. The current work was conducted to assess the toxic effects of a low dose (2% median lethal dose) of ethoprophos (Etho, 0.

View Article and Find Full Text PDF
Article Synopsis
  • * This study aimed to identify complex alleles with the N1303K mutation among patients from Lebanon, Egypt, and France by using PCR amplification and DNA sequencing.
  • * Results indicate that N1303K, along with associated polymorphisms, leads to abnormal CFTR mRNA splicing, affecting the protein's quality and quantity, which may influence the severity of Cystic Fibrosis symptoms.
View Article and Find Full Text PDF