Robert Rhoads
Progress in Molecular and Subcellular Biology 3
Robert Rhoads
Progress in Molecular and Subcellular Biology 3
- Broschiertes Buch
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Produktdetails
- Progress in Molecular and Subcellular Biology .3
- Verlag: Springer / Springer Berlin Heidelberg / Springer, Berlin
- Artikelnr. des Verlages: 978-3-642-65580-7
- Softcover reprint of the original 1st ed. 1973
- Seitenzahl: 268
- Erscheinungstermin: 8. Dezember 2011
- Englisch
- Abmessung: 244mm x 170mm x 15mm
- Gewicht: 468g
- ISBN-13: 9783642655807
- ISBN-10: 3642655807
- Artikelnr.: 36120124
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Reverse Transcription and the Central Dogma.- I. Introduction.- II. Cryptology and the Central Dogma.- III. Reverse Transcription: Experimental Evidence.- IV. Reverse Transcription and Cancer.- V. Is There Reverse Transcription in Bacteria?.- VI. Biological Significance of Reverse Transcription.- VII. Cryptography and the Central Dogma.- VIII. Conclusion.- IX. Glossary of Terms.- X. Addendum.- The Isolation of Genes: A Review of Advances in the Enrichment, Isolation and in vitro Synthesis of Specific Cistrons.- I. Introduction.- II. Procedures for the Preparation of Specific Cistrons.- III. Conclusion.- Mechanism of Protein Synthesis and the Use of Inhibitors in the Study of Protein Synthesis.- I. Introduction.- II. Initiation of Protein Synthesis.- III. Chain Elongation.- IV. Chain Termination.- V. Epilogue.- Structural Features of Immunoglobulin Light Chains.- I. Introduction.- II. Association of Light Chains.- III. Thermal Behavior of Bence-Jones Proteins.- IV. Distribution of Polar and Apolar Residues in Amino Acid Sequences of Light Chains.- V. Criteria of Purity in the Bence-Jones Protein Used in the Crystallographic Study.- VI. Crystallography of the Mcg Bence-Jones Protein.- VII. Discussion.- VIII. Summary.- The Thalassemia Syndromes: Genetically Determined Disorders of the Regulation of Protein Synthesis in Eukaryotic Cells.- I. Introduction.- II. The Beta Thalassemias: Clinical Picture and Pathogenesis of Anemia.- III. The Molecular Basis of the Suppression of Beta Chain Synthesis in Severe Beta Thalassemia.- The Mitochondrial DNA of Malignant Cells.- I. Introduction.- II. Morphology of Mitochondria in Malignant Cells.- III. Size and Structure of Mitochondrial DNA in Malignant Cells.- IV. Synthesis of Mitochondrial DNA in Malignant Cells: Content, Rate and Mechanism.- V. Is the Informational Content of Mitochondrial DNA Modified in Malignant Cells?.- VI. Are the Changes in Mitochondrial DNA in Malignant Cells Under Genetic Control?.- VII. Are the Changes in Mitochondrial DNA Related to Some Energy Imbalance in Mitochondria of Malignant Cells?.- VIII. Are the Changes Observed in Mitochondrial DNA of Malignant Cells Specific of Malignancy?.- IX. Concluding Remarks.- References.
Reverse Transcription and the Central Dogma.- I. Introduction.- II. Cryptology and the Central Dogma.- III. Reverse Transcription: Experimental Evidence.- IV. Reverse Transcription and Cancer.- V. Is There Reverse Transcription in Bacteria?.- VI. Biological Significance of Reverse Transcription.- VII. Cryptography and the Central Dogma.- VIII. Conclusion.- IX. Glossary of Terms.- X. Addendum.- The Isolation of Genes: A Review of Advances in the Enrichment, Isolation and in vitro Synthesis of Specific Cistrons.- I. Introduction.- II. Procedures for the Preparation of Specific Cistrons.- III. Conclusion.- Mechanism of Protein Synthesis and the Use of Inhibitors in the Study of Protein Synthesis.- I. Introduction.- II. Initiation of Protein Synthesis.- III. Chain Elongation.- IV. Chain Termination.- V. Epilogue.- Structural Features of Immunoglobulin Light Chains.- I. Introduction.- II. Association of Light Chains.- III. Thermal Behavior of Bence-Jones Proteins.- IV. Distribution of Polar and Apolar Residues in Amino Acid Sequences of Light Chains.- V. Criteria of Purity in the Bence-Jones Protein Used in the Crystallographic Study.- VI. Crystallography of the Mcg Bence-Jones Protein.- VII. Discussion.- VIII. Summary.- The Thalassemia Syndromes: Genetically Determined Disorders of the Regulation of Protein Synthesis in Eukaryotic Cells.- I. Introduction.- II. The Beta Thalassemias: Clinical Picture and Pathogenesis of Anemia.- III. The Molecular Basis of the Suppression of Beta Chain Synthesis in Severe Beta Thalassemia.- The Mitochondrial DNA of Malignant Cells.- I. Introduction.- II. Morphology of Mitochondria in Malignant Cells.- III. Size and Structure of Mitochondrial DNA in Malignant Cells.- IV. Synthesis of Mitochondrial DNA in Malignant Cells: Content, Rate and Mechanism.- V. Is the Informational Content of Mitochondrial DNA Modified in Malignant Cells?.- VI. Are the Changes in Mitochondrial DNA in Malignant Cells Under Genetic Control?.- VII. Are the Changes in Mitochondrial DNA Related to Some Energy Imbalance in Mitochondria of Malignant Cells?.- VIII. Are the Changes Observed in Mitochondrial DNA of Malignant Cells Specific of Malignancy?.- IX. Concluding Remarks.- References.