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.
Main Authors: | , , , , |
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Format: | Texto biblioteca |
Language: | eng |
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Boston, MA : Springer US : Imprint: Springer,
1991
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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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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. |
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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 |