Cystic fibrosis is a fatal human genetic disease caused by mutations in the CFTR gene
encoding a cAMP-activated chloride channel. It is characterized by abnormal fluid transport …

The most common mutation in the cystic fibrosis transmembrane conductance regulator (CFTR)
gene, ΔF508, causes retention of ΔF508-CFTR in the endoplasmic reticulum and leads …

Cystic fibrosis (CF) is a frequent autosomal recessive disorder caused by mutation of a
gene encoding a multifunctional transmembrane protein, the cystic fibrosis transmembrane …

Numerous factors, other than mutations in the CFTR gene, affect the phenotypic variability of
cystic fibrosis (CF). With a two-dimensional electrophoresis (2-DE) analysis of total protein …

Membrane proteins play a large variety of functions in life and represent 30% of all genomes
sequenced. Due to their hydrophobic nature, they are tightly bound to their biological …

Hepatocellular carcinoma (HCC) is a major cause of cancer worldwide. Proteomic studies
provide opportunities to uncover targets for the diagnosis and treatment of this disease. …

… Ali Belabbes Ikrame Belamfedel Alaoui Sadek Benattou Mohammed Benazza Hussain
Benhdech Adil Benhlima Said Benouini Rachid Ben Yakhlef Majid Benzekki Kamal Berrada …

Automatic segmentation of biological image is an important step to understand a biological
process. Moreover, the task is difficult due to ambiguous boundaries and intensity …

This paper is focused on the examination of the bonding properties of a series of [M(NHC) 2
X 2 ] (M = nd 8 transition metal; X = Cl, Br and I) complexes in normal, abnormal and mixed …

Starch is the most important carbohydrate in the human diet. Depending on botanical origin
and genetic background, starch has different chemical structures, and so different functional …