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Aggiungi al carrelloCondizione: New. The variability of clinical symptoms in mitochondrial diseases calls for a systematic presentation of the full range of protocols used in their assessment. This volume provides cutting-edge methods of analysis as well as expert guidance on how to apply them. Editor(s): Wong, Lee-Jun C. Series: Methods in Molecular Biology. Num Pages: 353 pages, 36 black & white tables, biography. BIC Classification: MFN. Category: (P) Professional & Vocational. Dimension: 261 x 184 x 26. Weight in Grams: 838. . 2012. 2012. Hardback. . . . .
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Condizione: New. The variability of clinical symptoms in mitochondrial diseases calls for a systematic presentation of the full range of protocols used in their assessment. This volume provides cutting-edge methods of analysis as well as expert guidance on how to apply them. Editor(s): Wong, Lee-Jun C. Series: Methods in Molecular Biology. Num Pages: 353 pages, 36 black & white tables, biography. BIC Classification: MFN. Category: (P) Professional & Vocational. Dimension: 261 x 184 x 26. Weight in Grams: 838. . 2012. 2012. Hardback. . . . . Books ship from the US and Ireland.
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Neuware -Due to the complexity of the mitochondrial system and the myriad genes involved in their function, the clinical manifestations of mitochondrial diseases are remarkably variable and heterogeneous. The laboratory and clinical methodologies used to evaluate dysfunction may vary widely, and thusly a systematic presentation of the numerous protocols that are applied to the assessment of these clinically and genetically heterogeneous disorders has proven to be essential. Mitochondrial Disorders: Biochemical and Molecular Analysis strives to fill this need with a collection of key protocols provided by leading experts in the field. Beginning with overviews of complexity of mitochondrial and nuclear genome disorders, the book continues with a section devoted to current biochemical protocols and a part focused on the DNA-based approaches used to identify molecular defects. Written in the highly successful Methods in Molecular Biology(TM) series format, chapters contain 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. Detailed and authoritative, Mitochondrial Disorders: Biochemical and Molecular Analysis serves as a vital guide to researchers seeking to understand this incredibly complicated type of breakdown in cellular biology. 364 pp. Englisch.
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Aggiungi al carrelloCondizione: New. 2016. Softcover reprint of the original 1st ed. 2012. paperback. . . . . .
Da: Books Puddle, New York, NY, U.S.A.
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Mitochondrial Disorders | Biochemical and Molecular Analysis | Lee-Jun C. Wong | Taschenbuch | xi | Englisch | 2016 | Humana | EAN 9781493959501 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Mitochondrial Disorders Caused by Nuclear Genes | Lee-Jun C. Wong | Taschenbuch | xii | Englisch | 2014 | Springer | EAN 9781489992413 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders | Lee-Jun C. Wong | Taschenbuch | viii | Englisch | 2018 | Springer | EAN 9783319859095 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Lingua: Inglese
Editore: Springer New York, Springer New York, 2012
ISBN 10: 1461437210 ISBN 13: 9781461437215
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Aggiungi al carrelloBuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are encoded by both mitochondrial and nuclear genomes and are essential in all cells. In addition, the biogenesis, structure and function of mitochondria, including DNA replication, transcription, and translation, all require nuclear encoded genes. Since mitochondria are present in every cell, every tissue, mitochondrial disorder usually affects multiple organs.
Lingua: Inglese
Editore: Springer New York, Springer New York, 2014
ISBN 10: 1489992413 ISBN 13: 9781489992413
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 168,73
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are encoded by both mitochondrial and nuclear genomes and are essential in all cells. In addition, the biogenesis, structure and function of mitochondria, including DNA replication, transcription, and translation, all require nuclear encoded genes. Since mitochondria are present in every cell, every tissue, mitochondrial disorder usually affects multiple organs.