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Stem Cell Proliferation and Differentiation, Volume 138 [Hardback]

Volume editor (University of Massachusetts, USA)
  • Formāts: Hardback, 258 pages, height x width: 229x152 mm, weight: 480 g
  • Sērija : Current Topics in Developmental Biology
  • Izdošanas datums: 25-Mar-2020
  • Izdevniecība: Academic Press Inc
  • ISBN-10: 0128128909
  • ISBN-13: 9780128128909
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  • Cena: 204,27 €
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  • Formāts: Hardback, 258 pages, height x width: 229x152 mm, weight: 480 g
  • Sērija : Current Topics in Developmental Biology
  • Izdošanas datums: 25-Mar-2020
  • Izdevniecība: Academic Press Inc
  • ISBN-10: 0128128909
  • ISBN-13: 9780128128909
Citas grāmatas par šo tēmu:

Stem Cell Proliferation and Differentiation, Volume 138, the latest release in the Current Topics in Developmental Biology series, highlights new advances in the field, with this new volume presenting interesting chapters. Each chapter is written by an international board of authors.

  • Provides the authority and expertise of leading contributors from an international board of authors
  • Presents the latest release in the Current Topics in Developmental Biology series
  • Includes the latest information on stem cell proliferation and differentiation
Contributors ix
Preface xi
1 Chromatin regulation and dynamics in stem cells
1(72)
David C. Klein
Sarah J. Hainer
1 Chromatin compaction, structure, and function
3(5)
2 Chromatin dynamics regulate gene expression
8(1)
3 ATP-dependent nucleosome remodeling complexes establish and maintain chromatin state
9(9)
4 Histone modifications provide an additional layer of gene regulation
18(7)
5 Histone chaperones and histone variants regulate chromatin structure
25(4)
6 Histone H2A variants
29(2)
7 Histone H3 variants
31(1)
8 Histone chaperones
32(4)
9 Chromatin structure is dynamic and highly regulated
36(1)
10 Stem cell chromatin is dynamic and tuned to regulate cell fate
36(1)
11 ES cells carefully regulate their chromatin via specialized transcription factors
37(2)
12 Embryonic stem cell chromatin is poised for action
39(1)
13 Histone modifications are specifically regulated in stem cells to maintain pluripotency and facilitate differentiation
39(3)
14 Chromatin state is precisely regulated by nucleosome remodeling factors in ES cells
42(9)
15 Long-range chromatin interactions are critical for regulation of luripotency
51(3)
16 ES cells regulate chromatin by common processes to preserve pluripotency
54(19)
Acknowledgments
55(1)
References
55(18)
2 Role of IncRNAs in stem cell maintenance and differentiation
73(40)
Meghali Aich
Debojyoti Chakraborty
1 Introduction
74(1)
2 Origin of noncoding RNAs
75(1)
3 Core regulatory circuit in ESCs
76(2)
4 LncRNAs: New determinants of ES cell fate
78(1)
5 Long noncoding RNAs (IncRNAs) and their biological function
78(2)
6 Discovery of IncRNAs: From sequences to function
80(1)
7 Long noncoding RNAs and epigenetic regulation
80(1)
8 Dissecting functional IncRNAs from transcriptional noise
81(1)
9 LncRNAs in ESC pluripotency and somatic cell reprogramming
81(6)
10 LncRNAs play a role in the differentiation of pluripotent stem cells
87(1)
11 LncRNAs regulating the epigenome
88(1)
12 The role of IncRNAs in dosage composition
89(1)
13 LncRNAs implicated in imprinting developmentally associated genes
90(1)
14 LncRNAs regulating signaling pathways in ESCs
91(1)
15 LncRNAs regulating organ development
92(1)
16 LncRNAs affecting neural development
93(1)
17 LncRNAs regulating organogenesis
94(1)
18 Cellular localization and maturation of IncRNAs
95(1)
19 LncRNAs regulating the stability and functions of other RNAs
95(1)
20 LncRNAs functioning in protein modification pathways
96(1)
21 Mechanisms of lncRNA:DNA/RNA interaction
96(2)
22 Allosteric regulation of proteins by IncRNAs
98(1)
23 Single cell analysis of IncRNA functions
99(1)
24 LncRNAs in disease progression
100(1)
25 LncRNA knockouts often show lack of phenotype: The importance of context and redundancy
101(1)
26 Conclusions
102(9)
References
102(9)
Further reading
111(2)
3 Regulation of pluripotency and reprogramming by RNA binding proteins
113(26)
Dan Li
Mohamed S. Kishta
Jianlong Wang
1 Pluripotency and reprogramming
114(1)
2 RNA binding proteins
115(9)
3 RNA helicases and DEAD-box helicase family
124(6)
4 Conclusions
130(9)
Acknowledgments
130(1)
References
130(9)
4 Generating primed pluripotent epiblast stem cells: A methodology chapter
139(36)
Milan Samanta
Sundeep Kalantry
1 Introduction
140(1)
2 Materials
141(8)
3 Methods
149(17)
4 Discussion
166(1)
5 Recipes
166(5)
6 Notes
171(4)
Acknowledgments
173(1)
References
173(2)
5 Differentiation of human pluripotent stem cells toward pharyngeal endoderm derivatives: Current status and potential
175(34)
Margaret E. Magaletta
Richard Siller
Rene Maehr
1 Introduction
176(2)
2 Overview of the pharyngeal apparatus formation within the gut tube
178(2)
3 Pharyngeal endoderm development and lineage specification within the pharyngeal pouches
180(2)
4 Pharynx derivative pluripotent stem cell differentiation protocols: Current status
182(13)
5 Applications of hPSCs for studying pharyngeal endoderm development and disease
195(1)
6 Future directions for hPSC differentiation approaches toward pharyngeal derivatives
196(3)
7 Concluding remarks
199(10)
Acknowledgments
199(1)
References
199(10)
6 Epigenetic metabolites license stem cell states
209
Logeshwaran Somasundaram
Shiri Levy
Abdiasis M. Hussein
Devon D. Ehnes
Julie Mathieu
Hannele Ruohola-Baker
1 Introduction
210(1)
2 Stem cell energetics
210(2)
3 Metabolism of quiescent stem cells
212(5)
4 Metabolism of active stem cells
217(5)
5 HIF, the master regulator of metabolism
222(2)
6 Epigenetic signatures and epigenetic metabolites
224(5)
7 Conclusion
229
Acknowledgments
230(1)
References
230(10)
Further reading
240
Thomas Fazzio is Associate Professor in the Department of Molecular, Cell, and Cancer Biology at the University of Massachusetts, USA