Cystic fibrosis : diagnosis and protocols, Volume I, Approaches to study and correct CFTR defects, edited by Margarida D. Amaral, Karl Kunzelmann, (electronic book)

Resource Information

The instance Cystic fibrosis : diagnosis and protocols, Volume I, Approaches to study and correct CFTR defects, edited by Margarida D. Amaral, Karl Kunzelmann, (electronic book) represents a material embodiment of a distinct intellectual or artistic creation found in University of Liverpool. This resource is a combination of several types including: Instance, Electronic.

Image

http://covers.openlibrary.org/b/isbn/9781617791178-M.jpg?default=false

Label

Cystic fibrosis : diagnosis and protocols, Volume I, Approaches to study and correct CFTR defects, edited by Margarida D. Amaral, Karl Kunzelmann, (electronic book)

Title remainder

diagnosis and protocols

Title number

Volume I

Title part

Approaches to study and correct CFTR defects

Medium

electronic book

Statement of responsibility

edited by Margarida D. Amaral, Karl Kunzelmann

Instantiates

• Cystic fibrosis : diagnosis and protocols, Volume I, Approaches to study and correct CFTR defects

Publication

• New York, Springer, 2011

Bibliography note

Includes bibliographical references and index

Color

multicolored

Contents

• Design of gene therapy trials in CF patients
• Jane C. Davies and Eric W.F.W. Alton
• Nasal potential difference measurements to assess CFTR ion channel activity / Steven M. Rowe, John Paul Clancy, and Michael Wilschanski
• Measurement of ion transport function in rectal biopsies
• Martin J. Hug ... [et al.]
• Introduction to section II: RNA Methods to approach CFTR expression
• Ann Harris
• Quantification of CFTR transcripts
• Anabela S. Ramalho, Luka A. Clarke, and Margarida D. Amaral
• Nonsense-mediated mRNA decay and cystic fibrosis
• Introduction to section I : the relevance of CF diagnostic tools for measuring restoration of CFTR function after therapeutic interventions in human clinical trials
• Liat Linde and Batsheva Kerem
• Approaches to study CFTR Pre-mRNA splicing defects
• Elisa Goina, Eugenio Fernandez-Alanis, and Franco Pagani
• Impact of microRNA in normal and pathological respiratory epithelia
• Lisa Giovannini-Chami ... [et al.]
• Genomic approaches to studying CFTR transcriptional regulation
• Christopher J. Ott and Ann Harris
• Introduction to section III : biochemical methods to study CFTR protein
• Margarida D. Amaral and Gergely L. Lukacs
• Analysis of CFTR folding and degradation in transiently transfected cells
• Kris De Boeck and Melissa Ashlock
• Diane E. Grove ... [et al.]
• In vitro methods for CFTR biogenesis
• Yoshihiro Matsumura, LeeAnn Rooney, and William R. Skach
• Analysis of CFTR interactome in the macromolecular complexes
• Chunying Li and Anjaparavanda P. Naren
• Methods to monitor cell surface expression and endocytic trafficking of CFTR in polarized epithelial cells
• Jennifer M. Bomberger, William B. Guggino, and Bruce A. Stanton
• Segmental and subcellular distribution of CFTR in the kidney
• Francois Jouret, Pierre J. Courtoy, and Olivier Devuyst
• Endocytic sorting of CFTR variants monitored by single-cell fluorescence ratiometric image analysis (FRIA) in living cells
• High-throughput screening of libraries of compounds to identify CFTR modulators
• Herve Barriere ... [et al.]
• Introduction to section IV: biophysical methods to approach CFTR structure
• Juan L. Mendoza, Andre Schmidt, and Philip J. Thomas
• CFTR three-dimensional structure
• Robert C. Ford ... [et al.]
• Molecular modeling tools and approaches for CFTR and cystic fibrosis
• Adrian W.R. Serohijos, Patrick H. Thibodeau, and Nikolay V. Dokholyan
• Biochemical and biophysical approaches to probe CFTR structure
• Andre Schmidt, Juan L. Mendoza, and Philip J. Thomas
• NMR spectroscopy to study the dynamics and interactions of CFTR
• Nicoletta Pedemonte, Olga Zegarra-Moran, and Luis J.V. Galietta
• Voula Kanelis, P. Andrew Chong, and Julie D. Forman-Kay
• Introduction to section V : assessment of CFTR function
• Karl Kunzelmann
• Application of high-resolution single-channel recording to functional studies of cystic fibrosis mutants
• Zhiwei Cai ... [et al.]
• Electrophysiological, biochemical, and bioinformatic methods for studying CFTR channel gating and its regulation
• Laszlo Csanady ... [ et al.]
• CFTR regulation by phosphorylation
• Rodrigo Alzamora, J Darwin King, and Kenneth R. Hallows
• How to measure CFTR-dependent bicarbonate transport : from single channels to the intact epithelium
• Repair of CFTR folding defects with correctors that function as pharmacological chaperones
• Martin J. Hug, Lane L. Clarke, and Michael A. Gray
• Tip W. Loo and David M. Clarke
• Use of primary cultures of human bronchial epithelial cells isolated from cystic fibrosis patients for the pre-clinical testing of CFTR modulators
• Timothy Neuberger ... [et al.]

Control code

SPR729873935

Dimensions

unknown

Extent

1 online resource (xvi, 528 p.)

Form of item

online

Isbn

9781617791178

Other physical details

ill. (some col.)

Record ID

b2588430

Specific material designation

remote