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Despite the many milestones in cystic fibrosis (CF) research,
progress toward curing the disease has been slow, and it is
increasingly difficult to grasp and use the already wide and still
growing range of diverse methods currently employed to study CF so
as to understand it in its multidisciplinary nature. Cystic
Fibrosis: Diagnosis and Protocols aims to provide the CF research
community and related researchers with a very wide range of
high-quality experimental tools, as an easy way to grasp and use
classical and novel methods applied to cystic fibrosis. Volume II:
Methods and Resources to Understand Cystic Fibrosis focuses on
pathophysiology, Omics approaches, and a variety of key resources
recently made available for CF research. Written in the highly
successful Methods in Molecular Biology (TM) series format,
chapters include introductions to their respective topics, lists of
the necessary materials and reagents, step-by-step, readily
reproducible laboratory protocols, and tips on troubleshooting and
avoiding known pitfalls. Comprehensive and practical, Cystic
Fibrosis: Diagnosis and Protocols will provide readers with optimal
working tools to address pressing questions in the best technical
way, while helping all of us, as a research and clinical community,
to move faster hand-in-hand toward unravelling the secrets of this
challenging disorder and cure it.
Despite the many milestones in cystic fibrosis (CF) research,
progress towards curing the disease has been slow, and it is
increasingly difficult to grasp and use the already wide and still
growing range of diverse methods currently employed to study CF so
as to understand it in its multidisciplinary nature. Cystic
Fibrosis: Diagnosis and Protocols aims to provide the CF research
community and related researchers with a very wide range of
high-quality experimental tools, as an easy way to grasp and use
classical and novel methods applied to cystic fibrosis. Volume I:
Approaches to Study and Correct CFTR Defects focuses on the cystic
fibrosis transmembrane conductance regulator (CFTR) and its
expression, biogenesis, structure, and function in terms of the
defects causing CF. Written in the highly successful Methods in
Molecular Biology (TM) series format, chapters include
introductions to their respective topics, lists of the necessary
materials and reagents, step-by-step, readily reproducible
laboratory protocols, and tips on troubleshooting and avoiding
known pitfalls. Comprehensive and practical, Cystic Fibrosis:
Diagnosis and Protocols will provide readers with optimal working
tools to address pressing questions in the best technical way,
while helping all of us, as a research and clinical community, to
move faster hand-in-hand toward unravelling the secrets of this
challenging disorder and cure it.
Despite the many milestones in cystic fibrosis (CF) research,
progress towards curing the disease has been slow, and it is
increasingly difficult to grasp and use the already wide and still
growing range of diverse methods currently employed to study CF so
as to understand it in its multidisciplinary nature. Cystic
Fibrosis: Diagnosis and Protocols aims to provide the CF research
community and related researchers with a very wide range of
high-quality experimental tools, as an easy way to grasp and use
classical and novel methods applied to cystic fibrosis. Volume I:
Approaches to Study and Correct CFTR Defects focuses on the cystic
fibrosis transmembrane conductance regulator (CFTR) and its
expression, biogenesis, structure, and function in terms of the
defects causing CF. Written in the highly successful Methods in
Molecular Biology (TM) series format, chapters include
introductions to their respective topics, lists of the necessary
materials and reagents, step-by-step, readily reproducible
laboratory protocols, and tips on troubleshooting and avoiding
known pitfalls. Comprehensive and practical, Cystic Fibrosis:
Diagnosis and Protocols will provide readers with optimal working
tools to address pressing questions in the best technical way,
while helping all of us, as a research and clinical community, to
move faster hand-in-hand toward unravelling the secrets of this
challenging disorder and cure it.
Despite the many milestones in cystic fibrosis (CF) research,
progress toward curing the disease has been slow, and it is
increasingly difficult to grasp and use the already wide and still
growing range of diverse methods currently employed to study CF so
as to understand it in its multidisciplinary nature. Cystic
Fibrosis: Diagnosis and Protocols aims to provide the CF research
community and related researchers with a very wide range of
high-quality experimental tools, as an easy way to grasp and use
classical and novel methods applied to cystic fibrosis. Volume II:
Methods and Resources to Understand Cystic Fibrosis focuses on
pathophysiology, Omics approaches, and a variety of key resources
recently made available for CF research. Written in the highly
successful Methods in Molecular Biology (TM) series format,
chapters include introductions to their respective topics, lists of
the necessary materials and reagents, step-by-step, readily
reproducible laboratory protocols, and tips on troubleshooting and
avoiding known pitfalls. Comprehensive and practical, Cystic
Fibrosis: Diagnosis and Protocols will provide readers with optimal
working tools to address pressing questions in the best technical
way, while helping all of us, as a research and clinical community,
to move faster hand-in-hand toward unravelling the secrets of this
challenging disorder and cure it.
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