The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /

Cystic Fibrosis — A Strategy for the Future -- Molecular Genetics of Cystic Fibrosis -- The CF Gene Product as a Member of a Membrane Transporter (TM6-NBF) Super Family -- Genetic Analysis of Cystic Fibrosis -- Molecular and Genetic Analyses at the CF Locus -- Identification of Cystic Fibrosis Mutations -- Mutation Analysis for Cystic Fibrosis in a North American Population -- Toward a Geographical History of the Predominant and Secondary Mutations in Europe -- Origin and Diffusion of the Major CF Mutation in Europe -- Present State of DNA-Diagnosis for Cystic Fibrosis and Attitudes Concerning a Heterozygote Screening in the GDR -- Pros and Cons of Neonatal Screening for Cystic Fibrosis -- Genotype-Phenotype Correlations in Cystic Fibrosis Patients -- Ion Transport in Normal and CF Airway Epithelia -- Aerosolized Amiloride as Treatment of Cystic Fibrosis Lung Disease: A Pilot Study -- Some Properties of Sodium and Chloride Channels in Respiratory Epithelia of CF- and Non-CF-Patients -- Roles of Ca and cAMP on Cl Channel Activity in Cystic Fibrosis Sweat Clear Cells as Studied by Microsuperfusion and Cell Volume Analysis -- Regulation of Absorption in the Human Sweat Duct -- Altered Biochemical Regulation of Secretion in Cystic Fibrosis Epithelial Cells -- Chloride Ion Transport in Transformed Normal and Cystic Fibrosis Epithelial Cells -- Conductance Pathways Involved in Chloride Secretion and Their Regulation -- Regulation of Epithelial Chloride Channels: Roles of Protein Kinases and Arachidonic Acid -- Cytosolic Inhibition and Excision Activation of Epithelial Chloride Channels -- Purification of the Epithelial Cl Channel -- Regulation of Expression of CFTR in Human Intestinal Epithelial Cells -- Cystic Fibrosis, the CFTR, and Rectifying Cl- Channels -- Regulation of Ion Conductance in Human Skin Fibroblasts -- Chloride Transport in the Cystic Fibrosis Enterocyte -- Chloride Transport Pathways in Human Keratinocytes -- A Chloride Conductance Evoked by Hypotonic Shock in Epithelial Cells -- Regulation of Lymphocyte Chloride Channels -- Guanine Nucleotide Binding Proteins Regulate Epithelial Na+ Channels -- Attitudes of Parents of Cystic Fibrosis Children Towards Neonatal Screening and Antenatal Diagnosis -- DNA Analysis in CF Families by Biotinylated Probes and Polymerase Chain Reaction Technique -- Prevalence of the Major Mutation of the CF Gene in Belgian Patients -- Cystic Fibrosis in the Sicilian Population: Linkage Disequilibrium and Prenatal Diagnosis by Polimerase Chain Reaction -- Study of Reconstitution of the Rabbit Parotid Na+/K+/2Cl-Cotransporter -- Human Placental Membrane Vesicles as Models for Investigation of Cystic Fibrosis -- The DeltaF508 Mutation in Israeli CF Families -- The DeltaF508-Deletion in 99 CF Patients of Switzerland -- The Prevalence of the Deletion F508 in a Belgian Cystic Fibrosis Population -- Cystic Fibrosis Delta F508 Mutation in a French Population -- Frequency of the Delta-F508 Mutation and Flanking Marker Haplotypes at the Cystic Fibrosis Locus from 167 Czech Families -- The Response of Chloride Transport to Cyclic AMP, Calcium and Hypotonic Shock in Normal and Cystic Fibrosis Fibroblasts -- 2D-Electrophoresis of Mitochondrial Proteins from Cystic Fibrosis Patients -- Frequency of Cystic Fibrosis Mutations and Associated Haplotype Distribution in Slovak CF Patients -- Frequency of Cystic Fibrosis Mutations Among Italian Patients -- Cultured Human Placental Trophoblasts as Models for Investigating Defective Regulation of Chloride Transport and Protein Secretion in Cystic Fibrosis -- A Deletion Mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Locus: DeltaI507 -- DNA Technology for Prenatal Diagnosis of Cystic Fibrosis in Italy -- Incidence of Cystic Fibrosis at the Faroe Islands.

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Bibliographic Details
Main Authors: Tsui, Lap-Chee. editor., Romeo, Giovanni. editor., Greger, Rainer. editor., Gorini, Sergio. editor., SpringerLink (Online service)
Format: Texto biblioteca
Language:eng
Published: Boston, MA : Springer US : Imprint: Springer, 1991
Subjects:Life sciences., Human genetics., Biochemistry., Plant science., Botany., Animal anatomy., Life Sciences., Biochemistry, general., Human Genetics., Animal Anatomy / Morphology / Histology., Plant Sciences.,
Online Access:http://dx.doi.org/10.1007/978-1-4684-5934-0
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id KOHA-OAI-TEST:217278
record_format koha
institution COLPOS
collection Koha
country México
countrycode MX
component Bibliográfico
access En linea
En linea
databasecode cat-colpos
tag biblioteca
region America del Norte
libraryname Departamento de documentación y biblioteca de COLPOS
language eng
topic Life sciences.
Human genetics.
Biochemistry.
Plant science.
Botany.
Animal anatomy.
Life Sciences.
Biochemistry, general.
Human Genetics.
Animal Anatomy / Morphology / Histology.
Plant Sciences.
Life sciences.
Human genetics.
Biochemistry.
Plant science.
Botany.
Animal anatomy.
Life Sciences.
Biochemistry, general.
Human Genetics.
Animal Anatomy / Morphology / Histology.
Plant Sciences.
spellingShingle Life sciences.
Human genetics.
Biochemistry.
Plant science.
Botany.
Animal anatomy.
Life Sciences.
Biochemistry, general.
Human Genetics.
Animal Anatomy / Morphology / Histology.
Plant Sciences.
Life sciences.
Human genetics.
Biochemistry.
Plant science.
Botany.
Animal anatomy.
Life Sciences.
Biochemistry, general.
Human Genetics.
Animal Anatomy / Morphology / Histology.
Plant Sciences.
Tsui, Lap-Chee. editor.
Romeo, Giovanni. editor.
Greger, Rainer. editor.
Gorini, Sergio. editor.
SpringerLink (Online service)
The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
description Cystic Fibrosis — A Strategy for the Future -- Molecular Genetics of Cystic Fibrosis -- The CF Gene Product as a Member of a Membrane Transporter (TM6-NBF) Super Family -- Genetic Analysis of Cystic Fibrosis -- Molecular and Genetic Analyses at the CF Locus -- Identification of Cystic Fibrosis Mutations -- Mutation Analysis for Cystic Fibrosis in a North American Population -- Toward a Geographical History of the Predominant and Secondary Mutations in Europe -- Origin and Diffusion of the Major CF Mutation in Europe -- Present State of DNA-Diagnosis for Cystic Fibrosis and Attitudes Concerning a Heterozygote Screening in the GDR -- Pros and Cons of Neonatal Screening for Cystic Fibrosis -- Genotype-Phenotype Correlations in Cystic Fibrosis Patients -- Ion Transport in Normal and CF Airway Epithelia -- Aerosolized Amiloride as Treatment of Cystic Fibrosis Lung Disease: A Pilot Study -- Some Properties of Sodium and Chloride Channels in Respiratory Epithelia of CF- and Non-CF-Patients -- Roles of Ca and cAMP on Cl Channel Activity in Cystic Fibrosis Sweat Clear Cells as Studied by Microsuperfusion and Cell Volume Analysis -- Regulation of Absorption in the Human Sweat Duct -- Altered Biochemical Regulation of Secretion in Cystic Fibrosis Epithelial Cells -- Chloride Ion Transport in Transformed Normal and Cystic Fibrosis Epithelial Cells -- Conductance Pathways Involved in Chloride Secretion and Their Regulation -- Regulation of Epithelial Chloride Channels: Roles of Protein Kinases and Arachidonic Acid -- Cytosolic Inhibition and Excision Activation of Epithelial Chloride Channels -- Purification of the Epithelial Cl Channel -- Regulation of Expression of CFTR in Human Intestinal Epithelial Cells -- Cystic Fibrosis, the CFTR, and Rectifying Cl- Channels -- Regulation of Ion Conductance in Human Skin Fibroblasts -- Chloride Transport in the Cystic Fibrosis Enterocyte -- Chloride Transport Pathways in Human Keratinocytes -- A Chloride Conductance Evoked by Hypotonic Shock in Epithelial Cells -- Regulation of Lymphocyte Chloride Channels -- Guanine Nucleotide Binding Proteins Regulate Epithelial Na+ Channels -- Attitudes of Parents of Cystic Fibrosis Children Towards Neonatal Screening and Antenatal Diagnosis -- DNA Analysis in CF Families by Biotinylated Probes and Polymerase Chain Reaction Technique -- Prevalence of the Major Mutation of the CF Gene in Belgian Patients -- Cystic Fibrosis in the Sicilian Population: Linkage Disequilibrium and Prenatal Diagnosis by Polimerase Chain Reaction -- Study of Reconstitution of the Rabbit Parotid Na+/K+/2Cl-Cotransporter -- Human Placental Membrane Vesicles as Models for Investigation of Cystic Fibrosis -- The DeltaF508 Mutation in Israeli CF Families -- The DeltaF508-Deletion in 99 CF Patients of Switzerland -- The Prevalence of the Deletion F508 in a Belgian Cystic Fibrosis Population -- Cystic Fibrosis Delta F508 Mutation in a French Population -- Frequency of the Delta-F508 Mutation and Flanking Marker Haplotypes at the Cystic Fibrosis Locus from 167 Czech Families -- The Response of Chloride Transport to Cyclic AMP, Calcium and Hypotonic Shock in Normal and Cystic Fibrosis Fibroblasts -- 2D-Electrophoresis of Mitochondrial Proteins from Cystic Fibrosis Patients -- Frequency of Cystic Fibrosis Mutations and Associated Haplotype Distribution in Slovak CF Patients -- Frequency of Cystic Fibrosis Mutations Among Italian Patients -- Cultured Human Placental Trophoblasts as Models for Investigating Defective Regulation of Chloride Transport and Protein Secretion in Cystic Fibrosis -- A Deletion Mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Locus: DeltaI507 -- DNA Technology for Prenatal Diagnosis of Cystic Fibrosis in Italy -- Incidence of Cystic Fibrosis at the Faroe Islands.
format Texto
topic_facet Life sciences.
Human genetics.
Biochemistry.
Plant science.
Botany.
Animal anatomy.
Life Sciences.
Biochemistry, general.
Human Genetics.
Animal Anatomy / Morphology / Histology.
Plant Sciences.
author Tsui, Lap-Chee. editor.
Romeo, Giovanni. editor.
Greger, Rainer. editor.
Gorini, Sergio. editor.
SpringerLink (Online service)
author_facet Tsui, Lap-Chee. editor.
Romeo, Giovanni. editor.
Greger, Rainer. editor.
Gorini, Sergio. editor.
SpringerLink (Online service)
author_sort Tsui, Lap-Chee. editor.
title The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
title_short The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
title_full The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
title_fullStr The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
title_full_unstemmed The Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies /
title_sort identification of the cf (cystic fibrosis) gene [electronic resource] : recent progress and new research strategies /
publisher Boston, MA : Springer US : Imprint: Springer,
publishDate 1991
url http://dx.doi.org/10.1007/978-1-4684-5934-0
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spelling KOHA-OAI-TEST:2172782018-07-30T23:53:05ZThe Identification of the CF (Cystic Fibrosis) Gene [electronic resource] : Recent Progress and New Research Strategies / Tsui, Lap-Chee. editor. Romeo, Giovanni. editor. Greger, Rainer. editor. Gorini, Sergio. editor. SpringerLink (Online service) textBoston, MA : Springer US : Imprint: Springer,1991.engCystic Fibrosis — A Strategy for the Future -- Molecular Genetics of Cystic Fibrosis -- The CF Gene Product as a Member of a Membrane Transporter (TM6-NBF) Super Family -- Genetic Analysis of Cystic Fibrosis -- Molecular and Genetic Analyses at the CF Locus -- Identification of Cystic Fibrosis Mutations -- Mutation Analysis for Cystic Fibrosis in a North American Population -- Toward a Geographical History of the Predominant and Secondary Mutations in Europe -- Origin and Diffusion of the Major CF Mutation in Europe -- Present State of DNA-Diagnosis for Cystic Fibrosis and Attitudes Concerning a Heterozygote Screening in the GDR -- Pros and Cons of Neonatal Screening for Cystic Fibrosis -- Genotype-Phenotype Correlations in Cystic Fibrosis Patients -- Ion Transport in Normal and CF Airway Epithelia -- Aerosolized Amiloride as Treatment of Cystic Fibrosis Lung Disease: A Pilot Study -- Some Properties of Sodium and Chloride Channels in Respiratory Epithelia of CF- and Non-CF-Patients -- Roles of Ca and cAMP on Cl Channel Activity in Cystic Fibrosis Sweat Clear Cells as Studied by Microsuperfusion and Cell Volume Analysis -- Regulation of Absorption in the Human Sweat Duct -- Altered Biochemical Regulation of Secretion in Cystic Fibrosis Epithelial Cells -- Chloride Ion Transport in Transformed Normal and Cystic Fibrosis Epithelial Cells -- Conductance Pathways Involved in Chloride Secretion and Their Regulation -- Regulation of Epithelial Chloride Channels: Roles of Protein Kinases and Arachidonic Acid -- Cytosolic Inhibition and Excision Activation of Epithelial Chloride Channels -- Purification of the Epithelial Cl Channel -- Regulation of Expression of CFTR in Human Intestinal Epithelial Cells -- Cystic Fibrosis, the CFTR, and Rectifying Cl- Channels -- Regulation of Ion Conductance in Human Skin Fibroblasts -- Chloride Transport in the Cystic Fibrosis Enterocyte -- Chloride Transport Pathways in Human Keratinocytes -- A Chloride Conductance Evoked by Hypotonic Shock in Epithelial Cells -- Regulation of Lymphocyte Chloride Channels -- Guanine Nucleotide Binding Proteins Regulate Epithelial Na+ Channels -- Attitudes of Parents of Cystic Fibrosis Children Towards Neonatal Screening and Antenatal Diagnosis -- DNA Analysis in CF Families by Biotinylated Probes and Polymerase Chain Reaction Technique -- Prevalence of the Major Mutation of the CF Gene in Belgian Patients -- Cystic Fibrosis in the Sicilian Population: Linkage Disequilibrium and Prenatal Diagnosis by Polimerase Chain Reaction -- Study of Reconstitution of the Rabbit Parotid Na+/K+/2Cl-Cotransporter -- Human Placental Membrane Vesicles as Models for Investigation of Cystic Fibrosis -- The DeltaF508 Mutation in Israeli CF Families -- The DeltaF508-Deletion in 99 CF Patients of Switzerland -- The Prevalence of the Deletion F508 in a Belgian Cystic Fibrosis Population -- Cystic Fibrosis Delta F508 Mutation in a French Population -- Frequency of the Delta-F508 Mutation and Flanking Marker Haplotypes at the Cystic Fibrosis Locus from 167 Czech Families -- The Response of Chloride Transport to Cyclic AMP, Calcium and Hypotonic Shock in Normal and Cystic Fibrosis Fibroblasts -- 2D-Electrophoresis of Mitochondrial Proteins from Cystic Fibrosis Patients -- Frequency of Cystic Fibrosis Mutations and Associated Haplotype Distribution in Slovak CF Patients -- Frequency of Cystic Fibrosis Mutations Among Italian Patients -- Cultured Human Placental Trophoblasts as Models for Investigating Defective Regulation of Chloride Transport and Protein Secretion in Cystic Fibrosis -- A Deletion Mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Locus: DeltaI507 -- DNA Technology for Prenatal Diagnosis of Cystic Fibrosis in Italy -- Incidence of Cystic Fibrosis at the Faroe Islands.Life sciences.Human genetics.Biochemistry.Plant science.Botany.Animal anatomy.Life Sciences.Biochemistry, general.Human Genetics.Animal Anatomy / Morphology / Histology.Plant Sciences.Springer eBookshttp://dx.doi.org/10.1007/978-1-4684-5934-0URN:ISBN:9781468459340