Cystic fibrosis methods and protocols

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Sprache:English
Veröffentlicht: Totowa, N.J. Humana Press 2002
Schriftenreihe:Methods in molecular medicine 70
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Datensatz im Suchindex

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adam_text Contents Preface v Contributors xi Part I Genetics of Cystic Fibrosis 1 CFTR Mutation Detection by Multiplex Heteroduplex (mHET) Analysis on MDE Gel Julian Zielenski, Isabel Aznarez, Tuncer Onay, John Tzounzouris, Danuta Markiewicz, and Lap Chee Tsui 3 2 cDNA Microarrays for Pharmacogenomic Analysis of Cystic Fibrosis Meera Srivastava, Ofer Eidelman, and Harvey B. Pollard 21 3 Natural Animal Models of Human Genetic Diseases Jeffrey J. Wine, Michael Dean, and Damjan Glavac 31 Part II CFTR Structure and Function: Structure, Gating, and Regulation 4 Electrophysiological Approach to Studying CFTR Horst Fischer 49 5 Quantitative Analysis of ATP Dependent Gating of CFTR Allan Powe, Zhen Zhou, Tzyh Chang Hwang, and Georg Nagel ...67 6 CFTR Regulation by Phosphorylation Tang Zhu, Deborah A. R. Hinkson, David Dahan, Alexandra Evagelidis, and John W. Hanrahan 99 7 Transepithelial Measurements of Bicarbonate Secretion in Calu 3 Cells Robert J. Bridges 111 8 Transepithelial Impedance Analysis of Chloride Secretion Ashvani K. Singh, Sangeeta Singh, Daniel C. Devor, Raymond A. Frizzell, Willy van Driessche, and Robert J. Bridges 129 9 Studies of the Molecular Basis for Cystic Fibrosis Using Purified Reconstituted CFTR Protein liana Kogan, Mohabir Ramjeesingh, Canhui Li, and Christine E. Bear 143 vii 10 Probing CFTR Channel Structure and Function Using the Substituted Cysteine Accessibility Method Myles H. Akabas 159 11 Methods for the Study of intermolecular and Intramolecular Interactions Regulating CFTR Function Anjaparavanda P. Naren 175 12 Fluorescent Indicator Methods to Assay Functional CFTR Expression in Cells Alan S. Verkman and Sujatha Jayaraman 187 Expression, Folding, and Degradation 13 Immunolocalization of CFTR in Intact Tissue and Cultured Cells Christopher R. Marino 199 14 Analysis of CFTR Trafficking and Polarization Using Green Fluorescent Protein and Confocal Microscopy Bryan D. Moyer and Bruce A. Stanton 217 15 CFTR Folding and Maturation in Cells Mohamed Benharouga, Manu Sharma, and Gergely L. Lukacs 229 16 Isolation of CFTR: Chaperone Complexes by Co lmmunoprecipitation Geoffrey C. Meacham and Douglas M. Cyr 245 17 CFTR Expression and ER Associated Degradation in Yeast Yimao Zhang, Susan Michaelis, and Jeffrey L. Brodsky 257 18 Manipulating the Folding Pathway of AF508 CFTR Using Chemical Chaperones Marybeth Howard and William J. Welch 267 19 CFTR Degradation and Aggregation Michael J. Corboy, Philip J. Thomas, and W. Christian Wigley.. 277 20 In Vitro Reconstitution of CFTR Biogenesis and Degradation Jon Oberdorf and William R. Skach 295 21 In Vitro CFTR Folding Assays Rhesa D. Stidham, W. Christian Wigley, and Philip J. Thomas... 311 22 Analysis of CFTR Endocytosis by Cell Surface Biotinylation Kelly Weixel and Neil A. Bradbury 323 Regulatory Complexes 23 CFTR Regulation of ENaC Scott H. Donaldson, Elaine G. Poligone, and M. Jackson Stutts.... 343 24 Yeast Two Hybrid Identification and Analysis of Protein Interactions with CFTR Viswanathan Raghuram, Kenneth R. Hallows, and J. Kevin Foskett 365 25 Biochemical Assays for Studying Indirect Interactions Between CFTR and the Cytoskeleton Peter J. Mohler, Patricia L. Kultgen, M. Jackson Stutts, and Sharon L. Milgram 383 26 CFTR Associated ATP Transport and Release Marie E. Egan 395 Part III Pathophysiology of Cystic Fibrosis 27 Inflammatory Mediators in CF Patients Jay B. Hilliard, Michael W. Konstan, and Pamela B. Davis 409 28 Bacterial Colonization and Infection in the CF Lung Scott D. Sagel, Elaine B. Dowell, and Frank J. Accurso 433 29 Antimicrobial Peptides and Proteins in the CF Airway Alexander M. Cole and Tomas Gam 447 30 Bacterial Epithelial Interactions Ruth Bryan and Alice Prince 465 31 Thin Film Measurements of Airway Surface Liquid Volume/Composition and Mucus Transport Rates In Vitro Robert Tarran and Richard C. Boucher 479 Animal Models of Cystic Fibrosis 32 Murine Models of CF Airway Infection and Inflammation James F. Chmiel, Michael W. Konstan, and Melvin Berger 495 33 Analysis of Lipid Abnormalities in CF Mice Steven D. Freedman, Paola G. Blanco, Julie C. Shea, and Juan G. Alvarez 517 34 Bioelectric Measurement of CFTR Function in Mice Barbara R. Grubb 525 35 Xenograft Model of the CF Airway Mohammed Filali, Yulong Zhang, Teresa C. Ritchie, and John F. Engelhardt 537 36 Development of Conditionally Immortalized Epithelial Cell Lines from CF and Non CF Mice Calvin U. Cotton 551 37 Technical Approaches to Analyze the In Vivo Ion Composition of Airway Surface Liquid Jean Marie Zahm, Sonia Baconnais, Gerard Balossier, and Edith Puchelle 563 Part IV Novel Therapeutic Approaches for Cystic Fibrosis 38 Design of Gene Therapy Clinical Trials in CF Patients Kimberly V. Curlee and Eric J. Sorscher 575 39 Formulation of Synthetic Vectors for Cystic Fibrosis Gene Therapy John Marshall and Seng H. Cheng 585 40 Adeno Associated Viral Vectors for CF Gene Therapy Terence R. Flotte, Isabel Virella Lowell, and Kye A. Chesnut 599 Index 609
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record_format marc
series Methods in molecular medicine
series2 Methods in molecular medicine
spelling Cystic fibrosis methods and protocols ed. by William R. Skach
Totowa, N.J. Humana Press 2002
XVI, 631 S. Ill., graph. Darst.
txt rdacontent
n rdamedia
nc rdacarrier
Methods in molecular medicine 70
Includes bibliographical references and index
Kystische fibrose gtt
Mucoviscidose - Manuels de laboratoire
Wetenschappelijke technieken gtt
Wissenschaftliches Arbeiten
Cystic Fibrosis Transmembrane Conductance Regulator Laboratory Manuals
Cystic Fibrosis genetics Laboratory Manuals
Cystic fibrosis Laboratory manuals
Mukoviszidose (DE-588)4040669-6 gnd rswk-swf
Molekulare Medizin (DE-588)4543844-4 gnd rswk-swf
Mukoviszidose (DE-588)4040669-6 s
Molekulare Medizin (DE-588)4543844-4 s
DE-604
Skach, William R. Sonstige oth
Methods in molecular medicine 70 (DE-604)BV011334960 70
HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009890253&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle Cystic fibrosis methods and protocols
Methods in molecular medicine
Kystische fibrose gtt
Mucoviscidose - Manuels de laboratoire
Wetenschappelijke technieken gtt
Wissenschaftliches Arbeiten
Cystic Fibrosis Transmembrane Conductance Regulator Laboratory Manuals
Cystic Fibrosis genetics Laboratory Manuals
Cystic fibrosis Laboratory manuals
Mukoviszidose (DE-588)4040669-6 gnd
Molekulare Medizin (DE-588)4543844-4 gnd
subject_GND (DE-588)4040669-6
(DE-588)4543844-4
title Cystic fibrosis methods and protocols
title_auth Cystic fibrosis methods and protocols
title_exact_search Cystic fibrosis methods and protocols
title_full Cystic fibrosis methods and protocols ed. by William R. Skach
title_fullStr Cystic fibrosis methods and protocols ed. by William R. Skach
title_full_unstemmed Cystic fibrosis methods and protocols ed. by William R. Skach
title_short Cystic fibrosis methods and protocols
title_sort cystic fibrosis methods and protocols
topic Kystische fibrose gtt
Mucoviscidose - Manuels de laboratoire
Wetenschappelijke technieken gtt
Wissenschaftliches Arbeiten
Cystic Fibrosis Transmembrane Conductance Regulator Laboratory Manuals
Cystic Fibrosis genetics Laboratory Manuals
Cystic fibrosis Laboratory manuals
Mukoviszidose (DE-588)4040669-6 gnd
Molekulare Medizin (DE-588)4543844-4 gnd
topic_facet Kystische fibrose
Mucoviscidose - Manuels de laboratoire
Wetenschappelijke technieken
Wissenschaftliches Arbeiten
Cystic Fibrosis Transmembrane Conductance Regulator Laboratory Manuals
Cystic Fibrosis genetics Laboratory Manuals
Cystic fibrosis Laboratory manuals
Mukoviszidose
Molekulare Medizin
url http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009890253&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
volume_link (DE-604)BV011334960
work_keys_str_mv AT skachwilliamr cysticfibrosismethodsandprotocols