Trinucleotide repeat protocols (20 Ergebnisse)

Zustand: New. pp. 356 52:B&W 6.14 x 9.21in or 234 x 156mm (Royal 8vo) Case Laminate on White w/Gloss Lam.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. In English.

Zustand: New. In English.

Taschenbuch. Zustand: Neu. Trinucleotide Repeat Protocols | Yoshinori Kohwi | Taschenbuch | Einband - flex.(Paperback) | Englisch | 2010 | Humana Press | EAN 9781617374463 | Verantwortliche Person für die EU: Springer Heidelberg, Tiergartenstr. 17, 69121 Heidelberg, buchhandel-buch[at]springer[dot]com | Anbieter: preigu. …

Zustand: New. In English.

Zustand: New. Editor(s): Kohwi, Yoshinori. Series: Methods in Molecular Biology. Num Pages: 342 pages, biography. BIC Classification: PSF. Category: (P) Professional & Vocational. Dimension: 229 x 152 x 20. Weight in Grams: 523. . 2010. 1st ed. Softcover of orig. ed. 2004. Paperback. . . . . Books ship from the US and Ireland.…

Gebunden. Zustand: New. Trinucleotide repeats are relatively common in the human genome. These simple repeats have received much attention since epoch-making discoveries were made that particular trinucleotide repeats are expanded in the causal genes of human hereditary neurologic.

Zustand: New. Describes techniques for studying trinucleotide pathology at the molecular level. This book features protocols covering targets ranging from DNA and RNA, to proteins and whole animals. It utilizes techniques, including gel electrophoresis, quantitative RT-PCR, and immunological analysis, antibody usage and its applications. Series: Methods in Molecular Biology. Num Pages: 342 pages, biography. BIC Classification: PSAK. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 20. Weight in Grams: 690. . 2004. Hardback. . . . . Books ship from the US and Ireland.…

Zustand: New. Trinucleotide repeats are relatively common in the human genome. These simple repeats have received much attention since epoch-making discoveries were made that particular trinucleotide repeats are expanded in the causal genes of human hereditary neurologic.

Zustand: New. In English.

Taschenbuch. Zustand: Neu. Trinucleotide Repeat Protocols | Yoshinori Kohwi (u. a.) | Taschenbuch | xiii | Englisch | 2016 | Humana | EAN 9781493959716 | 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. …

Paperback. Zustand: Brand New. 2nd reprint edition. 309 pages. 10.00x7.01x0.74 inches. In Stock.

Zustand: New. Coverage in this volume includes an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome. Editor(s): Kohwi, Yoshinori; McMurray, Cynthia T. Series: Methods in Molecular Biology. Num Pages: 309 pages, 40 black & white illustrations, 24 colour illustrations, biography. BIC Classification: MBGR; MFN. Category: (P) Professional & Vocational. Dimension: 254 x 178 x 17. Weight in Grams: 596. . 2016. Softcover reprint of the original 2nd ed. 2013. Paperback. . . . . Books ship from the US and Ireland. …

Zustand: Sehr gut. Zustand: Sehr gut | Seiten: 312 | Sprache: Englisch | Produktart: Bücher | Two decades have passed since trinucleotide repeat expansion was first discovered in genes responsible for certain neurological diseases. Since then, new technologies have developed and innovative concepts have emerged, which may prove useful in devising therapeutic approaches to neurological diseases. Divided into six convenient sections, Trinucleotide Repeat Protocols, Second Edition covers a wide range of topics such as an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome.  This edition focuses not only on direct analysis of trinucleotide repeat diseases but also on alternative approaches for the analysis of trinucleotide repeat diseases, with the hope that this will result in a better understanding of the mechanisms and future therapeutic prospects for treatment of these diseases. Written in the successful Methods in Molecular Biology¿ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.   Authoritative and easily accessible, Trinucleotide Repeat Protocols, Second Edition seeks to serve researchers with its thorough methodologies on this expanding field.…

Hardcover. Zustand: Brand New. 2nd edition. 280 pages. 10.00x7.00x0.80 inches. In Stock.

Zustand: New. Coverage in this volume includes an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome. Editor(s): Kohwi, Yoshinori; McMurray, Cynthia T. Series: Methods in Molecular Biology. Num Pages: 296 pages, 40 black & white illustrations, 24 colour illustrations, biography. BIC Classification: MBGR; MFN; MJN. Category: (P) Professional & Vocational. Dimension: 254 x 178 x 23. Weight in Grams: 783. . 2013. 2nd ed. 2013. Hardback. . . . . Books ship from the US and Ireland. …

Buch. Zustand: Neu. Neuware - Trinucleotide repeats are relatively common in the human genome. These simple repeats have received much attention since epoch-making discoveries were made that particular trinucleotide repeats are expanded in the causal genes of human hereditary neurological disorders. For example, the CGG repeat is expanded in fragile X syndrome at the 5' untranslated region (UTR) of its causal gene. In myotonic dystrophy, it is the CTG repeat that is expanded at the 3' UTR of its causal gene. The CAG repeat was also found expanded in coding regions of the genes responsible for X-linked spinal and bulbar muscular atrophy, Huntington's disease, spinocerebellar ataxia, and other disorders. On the other hand, expansion of the GAA repeat was identified in the intron of the gene responsible for the Friedreich's ataxia. For these trinucleotide repeat diseases, the longer the trinucleotide expansion, the earlier the age of onset and the more severe the syndrome. Thus, these findings that showed the intriguing link between a particular trinucleotide expansion and its associated neurological disorders have led to a new field of intensive study. Active research addressing the underlying mechanisms for trinucleotide repeat diseases has employed various approaches ranging from DNA biochemistry to animal models for the diseases. In particular, animal models for the triplet repeat diseases have provided excellent resources not only for understanding the mechanisms but also for exploring therapeutic interventions. …