𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Neutrophils in the Innate Immunity Conundrum of Cystic Fibrosis: A CFTR-Related Matter?

✍ Scribed by Witko-Sarsat, Véronique

Book ID
120090503
Publisher
S. Karger AG
Year
2013
Tongue
English
Weight
56 KB
Volume
5
Category
Article
ISSN
1662-811X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Disrupted posttranscriptional regulation
Disrupted posttranscriptional regulation of the cystic fibrosis transmembrane conductance regulator (CFTR) by a 5′UTR mutation is associated with a cftr-related disease
✍ Samuel W. Lukowski; Cristina Bombieri; Ann E. O. Trezise 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 502 KB

Cystic fibrosis (CF) is characterised as a single-gene disorder with a simple, autosomal recessive mode of inheritance. However, translation of CFTR genotype into CF phenotype is influenced by nucleotide sequence variations at multiple genetic loci, and individuals heterozygous for CFTR mutations ar

The spectrum of CFTR mutations in south-
The spectrum of CFTR mutations in south-west German cystic fibrosis patients
✍ M. Lindner; A. Wolf; B. Moh; P. Steinbach; E. Kleihauer; C. R. Bartram; A. E. Ku 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 298 KB

The cystic fibrosis transmembrane conductance regulator (CFTR) gene of 110 cystic fibrosis (CF) patients from the south-west of Germany was screened for 12 different mutations. This analysis resulted in an identification of 79% of all CF mutations and a complete genotype in 66% of the families. The