نتایج جستجو برای: ivs8 polyt

تعداد نتایج: 142  

Journal: :Respiratory Research 2008
Isabelle Fajac Marion Viel Sébastien Sublemontier Dominique Hubert Thierry Bienvenu

BACKGROUND Bronchiectasis is defined as a permanent dilation of the airways arising from chronic bronchial inflammation/infection. In 50% of cases, no etiology can be identified. Recently, the role of the epithelial sodium channel ENaC has been pointed out in the pathophysiology of cystic fibrosis, a disease due to mutations in the CFTR gene and causing bronchiectasis in the airways. Moreover, ...

2015
Yong-jia Yang Yuan Hu Rui Zhao Xinyu He Liu Zhao Ming Tu Lijun Zhou Jihong Guo Linqian Wu Tantai Zhao Yi-min Zhu

Infantile cystinosis (IC) is a rare autosomal recessive disorder characterized by a defect in the lysosomal-membrane transport protein, cystinosin. It serves as a prototype for lysosomal transport disorders. To date, several CTNS mutations have been identified as the cause of the prototypic disease across different ethnic populations worldwide. However, in Asia, the CTNS mutation is very rarely...

Journal: :American journal of human genetics 2002
Lodewijk IJlst Ference J Loupatty Jos P N Ruiter Marinus Duran Willy Lehnert Ronald J A Wanders

3-Methylglutaconic aciduria type I is an autosomal recessive disorder clinically characterized by various symptoms ranging from delayed speech development to severe neurological handicap. This disorder is caused by a deficiency of 3-methylglutaconyl-CoA hydratase, one of the key enzymes of leucine degradation. This results in elevated urinary levels of 3-methylglutaconic acid, 3-methylglutaric ...

Journal: :Protein engineering 1997
P Yao Y Xie Y H Wang Y L Sun Z X Huang G T Xiao S D Wang

Phenylalanine-35, which is a residue of the hydrophobic patch on the surface of cytochrome b5, has been mutated into Tyr35, His35 and Leu35 to elucidate the functions of the Phe35 and give further insight into the roles of the hydrophobic patch and/or aromatic network. The effects of these mutations on the heme environment, denaturation towards heating and the denaturant urea, redox potential a...

Journal: :Genetics and molecular research : GMR 2002
Gerardo Luzardo Isabel Aznarez Beatriz Crispino Adriana Mimbacas Liria Martínez Rossana Poggio Julian Zielenski Lap-Chee Tsui Horacio Cardoso

We conducted clinical and genetic analyses of 52 cystic fibrosis (CF) patients in Uruguay, which is about half of the known affected individuals in the country. A relatively high proportion had a mild presentation, characterized by pancreatic sufficiency (28%), a strong pulmonary component (97%), and borderline sweat electrolyte measurements (25%). Mutational analysis of CF chromosomes demonstr...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید