Molecular and Cell Biology of Muscular Dystrophy

Inbunden, Engelska, 1993

Del i serien Molecular and Cell Biology of Human Diseases Series

2 271 kr

Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

Beskrivning

Molecular and Cell Biology of Muscular Dystrophy gives a series of accounts of various aspects of the remarkable breakthrough which has been achieved in our understanding of the Duchenne/Becker muscular dystrophies and of the consequences and ramifications of this breakthrough.

Produktinformation

Utgivningsdatum:1993-07-31
Mått:155 x 235 x 25 mm
Vikt:711 g
Format:Inbunden
Språk:Engelska
Serie:Molecular and Cell Biology of Human Diseases Series
Antal sidor:344
Upplaga:1993
Förlag:Chapman and Hall
ISBN:9780412434402

Utforska kategorier

Innehållsförteckning

1 Molecular human genetics and the Duchenne/Becker muscular dystrophy gene.- 1.1 Introduction.- 1.2 DMD and BMD phenotype.- 1.3 Localization to Xp21.- 1.4 Isolation of Xp21 sequences.- 1.5 Chromosome walking and jumping in Xp21.- 1.6 Identification of expressed sequences.- 1.7 Gene sequence and organization.- 1.8 Genotype and phenotype.- 1.9 Dystrophin.- 1.10 Conclusions.- References.- 2 Genotype/phenotype correlations in Duchenne/Becker dystrophy.- 2.1 Introduction.- 2.2 Duchenne muscular dystrophy.- 2.3 Dystrophinopathy in girls and women.- 2.4 Becker muscular dystrophy.- 2.5 Conclusion.- References.- 3 Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy.- 3.1 Introduction.- 3.2 Duchenne and Becker muscular dystrophy.- 3.3 Genetic counselling for Duchenne and Becker muscular dystrophy: prior to molecular genetics.- 3.4 Genetic counselling of Duchenne and Becker muscular dystrophy post molecular genetics.- 3.5 Genetic counselling of Duchenne and Becker muscular dystrophy: Future.- 3.6 Conclusion.- Acknowledgements.- References.- 4 Inheritance and pathogenicity of myotonic dystrophy.- 4.1 Introduction.- 4.2 The clinical picture.- 4.3 Biochemical, electrophysiological and histological findings.- 4.4 Genetic mapping of the myotonic locus.- 4.5 Physical mapping.- 4.6 Isolation of the DM region as a series of overlapping genomic clones.- 4.7 Identifying candidate genes.- 4.8 Future prospects.- Acknowledgements.- References.- 5 Genetic mapping of facioscapulohumeral muscular dystrophy.- 5.1 Introduction.- 5.2 Positional cloning.- 5.3 Facioscapulohumeral muscular dystrophy: clinical features.- 5.4 FSHD: Linkage analysis and positional cloning.- Acknowledgements.- References.- 6 Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy.- 6.1 Introduction.- 6.2 Membrane properties of dystrophin.- 6.3 Dystrophin—glycoprotein complex.- 6.4 Structure and function of dystroglycan (43/156 dystrophin-associated glycoprotein).- 6.5 Molecular pathogenesis of Duchenne muscular dystrophy.- 6.6 Summary.- Acknowledgements.- References.- 7 PCR analysis of muscular dystrophy in mdx mice.- 7.1 Introduction.- 7.2 Mouse dystrophin cDNA clones.- 7.3 mdx mice.- 7.4 PCR analysis of mouse dystrophin expression.- 7.5 Summary.- Acknowledgements.- References.- 8 Cell biology of the satellite cell.- 8.1 Introduction.- 8.2 Satellite cells in normal muscle.- 8.3 Behaviour of satellite cells in damaged muscle.- 8.4 Satellite cells, myoblasts and implant therapy.- References.- 9 Molecular and cell biology of skeletal muscle regeneration.- 9.1 Introduction.- 9.2 Developmental origin of satellite cells and their identification in vivo.- 9.3 Replication during postnatal growth.- 9.4 Numbers and proliferative capacity of mpc from animals of different ages.- 9.5 The influence of growth factors and extracellular matrix components on the proliferation and differentiation of mpc.- Acknowledgements.- References.- 10 Molecular mechanisms of muscle damage.- 10.1 Introduction.- 10.2 The mechanisms of damage to normal skeletal muscle subjected to various damaging stresses.- 10.3 Mechanisms of damage in dystrophin-deficient muscle.- 10.4 Conclusions.- Acknowledgements.- References.- 11 Human dystrophin gene transfer: Genetic correction of dystrophin deficiency.- 11.1 Somatic gene therapy: An introduction.- 11.2 Therapeutic targets in Duchenne muscular dystrophy.- 11.3 Recombinant dystrophin genes: Their nature and availability.- 11.4 Physical gene transfer techniques.- 11.5 Viral-mediated gene transferstrategies.- 11.6 Studies in transgenic animals: Germ line gene transfer.- 11.7 Dystrophin: Structure and function.- 11.8 Gene therapy for Duchenne muscular dystrophy: Future prospects.- References.- 12 Myoblast transplantation in inherited myopathies.- 12.1 Introduction.- 12.2 Myoblast transplantation in animal models of inherited myopathies.- 12.3 Problems associated with myoblast transfer.- Acknowledgements.- References.

Du kanske också är intresserad av

Nyhet

L’amour toujours : Berättelsen om Tidö

Maggie Strömberg, Torbjörn Nilsson

Inbunden, 2026

275 kr

Molecular and Cell Biology of Muscular Dystrophy

T. Partridge

Häftad, 2012

2 271 kr

Molecular and Cell Biology of Muscular Dystrophy

T. Partridge

E-bok

2012

2 948 kr

Biological Functions of Carbohydrates

D.J. Candy

Häftad, 2013

557 kr

Molecular and Cell Biology of Neuropsychiatric Diseases

F. Owen, R. Itzhaki

Häftad, 2012

1 139 kr

Molecular Biology of Neuropsychiatric Disease

F. Owen, F. Owen, R. Itzhaki

Inbunden, 1993

1 252 kr

Nyhet

Del 11

Medusa

Lars Kepler

Inbunden, 2026

269 kr

Molecular and Cell Biology of Sexually Transmitted Diseases

D.J. Wright, L.C. Archard

Inbunden, 1992

1 139 kr

Molecular and Cell Biology of Human Gene Therapeutics

G. Dickson

Inbunden, 1995

2 271 kr

Molecular and Cell Biology of Sexually Transmitted Diseases

D.J. Wright, L.C. Archard

Häftad, 2012

1 139 kr

Molecular and Cell Biology of Muscular Dystrophy

AvT. Partridge

Inbunden, Engelska, 1993

Del i serien Molecular and Cell Biology of Human Diseases Series

2 271 kr

Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

Beskrivning

Produktinformation

Utgivningsdatum:1993-07-31
Mått:155 x 235 x 25 mm
Vikt:711 g
Format:Inbunden
Språk:Engelska
Serie:Molecular and Cell Biology of Human Diseases Series
Antal sidor:344
Upplaga:1993
Förlag:Chapman and Hall
ISBN:9780412434402

Utforska kategorier

Innehållsförteckning

1 Molecular human genetics and the Duchenne/Becker muscular dystrophy gene.- 1.1 Introduction.- 1.2 DMD and BMD phenotype.- 1.3 Localization to Xp21.- 1.4 Isolation of Xp21 sequences.- 1.5 Chromosome walking and jumping in Xp21.- 1.6 Identification of expressed sequences.- 1.7 Gene sequence and organization.- 1.8 Genotype and phenotype.- 1.9 Dystrophin.- 1.10 Conclusions.- References.- 2 Genotype/phenotype correlations in Duchenne/Becker dystrophy.- 2.1 Introduction.- 2.2 Duchenne muscular dystrophy.- 2.3 Dystrophinopathy in girls and women.- 2.4 Becker muscular dystrophy.- 2.5 Conclusion.- References.- 3 Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy.- 3.1 Introduction.- 3.2 Duchenne and Becker muscular dystrophy.- 3.3 Genetic counselling for Duchenne and Becker muscular dystrophy: prior to molecular genetics.- 3.4 Genetic counselling of Duchenne and Becker muscular dystrophy post molecular genetics.- 3.5 Genetic counselling of Duchenne and Becker muscular dystrophy: Future.- 3.6 Conclusion.- Acknowledgements.- References.- 4 Inheritance and pathogenicity of myotonic dystrophy.- 4.1 Introduction.- 4.2 The clinical picture.- 4.3 Biochemical, electrophysiological and histological findings.- 4.4 Genetic mapping of the myotonic locus.- 4.5 Physical mapping.- 4.6 Isolation of the DM region as a series of overlapping genomic clones.- 4.7 Identifying candidate genes.- 4.8 Future prospects.- Acknowledgements.- References.- 5 Genetic mapping of facioscapulohumeral muscular dystrophy.- 5.1 Introduction.- 5.2 Positional cloning.- 5.3 Facioscapulohumeral muscular dystrophy: clinical features.- 5.4 FSHD: Linkage analysis and positional cloning.- Acknowledgements.- References.- 6 Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy.- 6.1 Introduction.- 6.2 Membrane properties of dystrophin.- 6.3 Dystrophin—glycoprotein complex.- 6.4 Structure and function of dystroglycan (43/156 dystrophin-associated glycoprotein).- 6.5 Molecular pathogenesis of Duchenne muscular dystrophy.- 6.6 Summary.- Acknowledgements.- References.- 7 PCR analysis of muscular dystrophy in mdx mice.- 7.1 Introduction.- 7.2 Mouse dystrophin cDNA clones.- 7.3 mdx mice.- 7.4 PCR analysis of mouse dystrophin expression.- 7.5 Summary.- Acknowledgements.- References.- 8 Cell biology of the satellite cell.- 8.1 Introduction.- 8.2 Satellite cells in normal muscle.- 8.3 Behaviour of satellite cells in damaged muscle.- 8.4 Satellite cells, myoblasts and implant therapy.- References.- 9 Molecular and cell biology of skeletal muscle regeneration.- 9.1 Introduction.- 9.2 Developmental origin of satellite cells and their identification in vivo.- 9.3 Replication during postnatal growth.- 9.4 Numbers and proliferative capacity of mpc from animals of different ages.- 9.5 The influence of growth factors and extracellular matrix components on the proliferation and differentiation of mpc.- Acknowledgements.- References.- 10 Molecular mechanisms of muscle damage.- 10.1 Introduction.- 10.2 The mechanisms of damage to normal skeletal muscle subjected to various damaging stresses.- 10.3 Mechanisms of damage in dystrophin-deficient muscle.- 10.4 Conclusions.- Acknowledgements.- References.- 11 Human dystrophin gene transfer: Genetic correction of dystrophin deficiency.- 11.1 Somatic gene therapy: An introduction.- 11.2 Therapeutic targets in Duchenne muscular dystrophy.- 11.3 Recombinant dystrophin genes: Their nature and availability.- 11.4 Physical gene transfer techniques.- 11.5 Viral-mediated gene transferstrategies.- 11.6 Studies in transgenic animals: Germ line gene transfer.- 11.7 Dystrophin: Structure and function.- 11.8 Gene therapy for Duchenne muscular dystrophy: Future prospects.- References.- 12 Myoblast transplantation in inherited myopathies.- 12.1 Introduction.- 12.2 Myoblast transplantation in animal models of inherited myopathies.- 12.3 Problems associated with myoblast transfer.- Acknowledgements.- References.