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Relevant bibliographies by topics / Hemopoietic stem cells and induced pluripotent stem cells / Books

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Books on the topic 'Hemopoietic stem cells and induced pluripotent stem cells'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Yildirim, Sibel. Induced Pluripotent Stem Cells. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-2206-8.

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2

Sullivan, Patrick J. Induced stem cells. Nova Science, 2011.

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3

Sullivan, Patrick J. Induced stem cells. Nova Science, 2011.

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4

Nagy, Andras, and Kursad Turksen, eds. Induced Pluripotent Stem (iPS) Cells. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2119-6.

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5

Turksen, Kursad, and Andras Nagy, eds. Induced Pluripotent Stem (iPS) Cells. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3055-5.

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6

Ding, Baojin, and Yu Tang, eds. Human Induced Pluripotent Stem Cells. Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3999-3.

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7

Zhao, Xiaoyang. Studies of Pluripotency in Embryonic Stem Cells and Induced Pluripotent Stem Cells. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8819-9.

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8

Turksen, Kursad, ed. Induced Pluripotent Stem Cells and Human Disease. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2585-9.

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9

Ye, Kaiming, and Sha Jin, eds. Human Embryonic and Induced Pluripotent Stem Cells. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-267-0.

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10

Heine, Vivi M., Stephanie Dooves, Dwayne Holmes, and Judith Wagner. Induced Pluripotent Stem Cells in Brain Diseases. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-2816-5.

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11

Amit, M., and Joseph Itskovitz-Eldor. Atlas of human pluripotent stem cells: Derivation and culturing. Humana Press, 2012.

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12

Friedrich, Schuening, ed. Radiation-induced hemopoietic and immune dysfunction. Defense Nuclear Agency, 1991.

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13

Friedrich, Schuening, ed. Radiation-induced hemopoietic and immune dysfunction. Defense Nuclear Agency, 1991.

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14

Sha, Jin, and SpringerLink (Online service), eds. Human Embryonic and Induced Pluripotent Stem Cells: Lineage-Specific Differentiation Protocols. Springer Science+Business Media, LLC, 2012.

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15

Song, Loujin. Development of Novel Therapeutics for Timothy Syndrome Using Human Induced Pluripotent Stem Cells. [publisher not identified], 2017.

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16

Yildirim, Sibel. Induced Pluripotent Stem Cells. Springer, 2012.

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17

Induced Pluripotent Stem Cells Springerbriefs in Stem Cells. Springer, 2011.

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18

Ding, Baojin. Human Induced Pluripotent Stem Cells. Springer, 2024.

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19

Zhao, Xiaoyang. Studies of Pluripotency in Embryonic Stem Cells and Induced Pluripotent Stem Cells. Springer, 2016.

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20

Zhao, Xiaoyang. Studies of Pluripotency in Embryonic Stem Cells and Induced Pluripotent Stem Cells. Springer, 2014.

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21

Zhao, Xiaoyang. Studies of Pluripotency in Embryonic Stem Cells and Induced Pluripotent Stem Cells. Springer London, Limited, 2014.

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22

Turksen, Kursad, and Andras Nagy. Induced Pluripotent Stem Cells: Methods and Protocols. Springer, 2022.

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23

Turksen, Kursad, and Andras Nagy. Induced Pluripotent Stem Cells: Methods and Protocols. Springer New York, 2019.

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24

Induced Pluripotent Stem Cells: Methods and Protocols. Springer, 2023.

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25

Update on Induced Pluripotent Stem Cells [Working Title]. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.82950.

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26

Ahmed Al-Anazi, Khalid, ed. Update on Mesenchymal and Induced Pluripotent Stem Cells. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.77857.

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27

Update on Mesenchymal and Induced Pluripotent Stem Cells. IntechOpen, 2020.

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28

Turksen, Kursad, and Andras Nagy. Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization. Springer New York, 2016.

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29

Turksen, Kursad, and Andras Nagy. Patient-Specific Induced Pluripotent Stem Cell Models: Generation and Characterization. Springer New York, 2015.

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30

Itskovitz-Eldor, Joseph, and Michal Amit. Atlas of Human Pluripotent Stem Cells: Derivation and Culturing. Humana, 2016.

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31

Itskovitz-Eldor, Joseph, and Michal Amit. Atlas of Human Pluripotent Stem Cells: Derivation and Culturing. Springer, 2011.

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32

Induced Pluripotent Stem Cells and Human Disease: Methods and Protocols. Springer, 2023.

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33

Turksen, Kursad. Induced Pluripotent Stem Cells and Human Disease: Methods and Protocols. Springer, 2022.

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34

Induced Pluripotent Stem Cells in Brain Diseases Springerbriefs in Neuroscience. Springer, 2011.

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35

Ye, Kaiming, and Sha Jin. Human Embryonic and Induced Pluripotent Stem Cells: Lineage-Specific Differentiation Protocols. Humana Press, 2016.

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36

Allsopp, Tim, and G. Sitta Sittampalam. Induced Pluripotent Stem Cells for Disease Modelling, Drug Discovery and Toxicology Testing: Regenerative Pharmacology, Drug Discovery and Development. Royal Society of Chemistry, The, 2017.

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37

Calcium Handling in HipscDerived Cardiomyocytes Springerbriefs in Stem Cells. Springer, 2012.

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38

iPS saibō no sangyōteki ōyō gijutsu: Industrial applied technology of induced pluripotent stem cells. Shī Emu Shī Shuppan, 2009.

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39

Brennand, Kristen. Application of Stem Cells to Understanding Psychiatric Disorders. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0005.

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Abstract:

While much has been learned through clinical post-mortem and neuroimaging studies of patients and animal models of autism spectrum disorder (ASD), bipolar disorder (BD) and schizophrenia (SZ), these classical approaches have yet to fully elucidate the interaction of complex genetic risk factors on disease predisposition. The derivation of human induced pluripotent stem cells (hiPSCs) from patients with psychiatric disorders permits the study of the full complement of risk variants (known and unknown) that underlie disease predisposition, precisely in the cell types relevant to disease. The fol

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40

Dooves, Stephanie, Dwayne Holmes, Judith Wagner, and Vivi M. Heine. Induced Pluripotent Stem Cells in Brain Diseases: Understanding the Methods, Epigenetic Basis, and Applications for Regenerative Medicine. Springer London, Limited, 2012.

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41

Nat, Roxana, and Andreas Eigentler. Cell Culture, iPS Cells and Neurodegenerative Diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190233563.003.0013.

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Somatic reprogramming technology, which enables the conversion of adult human non-neural cells into neurons, has progressed rapidly in recent years. The derivation of patient-specific induced pluripotent stem (iPS) cells has become routine. The inherent broad differentiation potential of iPS cells makes possible the generation of diverse types of human neurons. This constitutes a remarkable step in facilitating the development of more appropriate and comprehensive preclinical human disease models, as well as for high throughput drug screenings and cell therapy. This chapter reviews recent prog

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42

Drapeau, Elodie, Hala Harony-Nicolas, and Jacqueline N. Crawley. Animal and Cellular Models of Pediatric Psychiatric Disorders. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0061.

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The study of childhood psychiatric disorders is especially challenging, not only because of the difficulties in obtaining relevant human samples but also because of ethical considerations regarding the ability of children to provide informed consent. Models that can be experimentally manipulated are therefore indispensable to study those disorders. Traditionally, biological psychiatry research has extensively employed animal models and characterizations of rodent behavior. More recently, induced pluripotent stem cells (iPSCs), and induced differentiation of iPSCs into different types of brain

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43

Pletnikov, Mikhail V., Guo-Li Ming, and Christopher A. Ross. Animal and Cellular Models of Psychotic Disorders. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0015.

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Animal and cell models are experimental systems developed to study particular aspects of a disease, as no model can accurately reflect all features of the disease. In this critical review we mention some of the nongenetic models but focus on genetic mouse models, evaluate their advantages and limitations, and comment on potential new prospects for the field. The ability to reprogram somatic cells from patients and unaffected donors to induced pluripotent stem cells (iPSCs) has the potential to substantially enhance our knowledge of normal cellular development and disease pathogenesis. The use

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