| #17118644 in Books | 2009-08-04 | Original language:English | PDF # 1 | 8.66 x.39 x5.91l,.57 | File type: PDF | 172 pages||About the Author|Ph.D. in Chemical Biology from Stevens Institute of Technology, Hoboken, NJ, USA. Currently employed at Johnson & Johnson Consumer Companies Inc., NJ. Recipient of multiple academic awards; author and co-author on several publications in peer re
Cystic fibrosis (CF) is caused by the dysfunction of cystic fibrosis transmembrane conductance regulator (CFTR). The predominant mutation found in CF patients (delta F508) results in a mislocalized channel, which is unable to reach the plasma membrane. Rab proteins are small GTPases involved in vesicle transport. The regulation of CFTR by Rab GTPases-4 and 27a was evaluated in multiple cell systems: the colorectal HT-29 cells, bronchial epithelial IB3-1 and S9 cells. Ove...
You can specify the type of files you want, for your device.Cystic Fibrosis Transmembrane Conductance Regulator: Regulation by Rab GTPases | Simarna Kaur. I have read it a couple of times and even shared with my family members. Really good. Couldnt put it down.
