Books on the topic 'Ependymal stem progenitor cells'

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1

Reynolds, Brent A., and Loic P. Deleyrolle. Neural progenitor cells: Methods and protocols. New York: Humana Press, 2013.

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2

American Association of Blood Banks. Progenitor Cell Standards Task Force., ed. Standards for hematopoietic progenitor cells. Bethesda, Md: American Association of Blood Banks, 1996.

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3

E, Brecher Mark, ed. Hematopoietic progenitor cells: Processing, standards, and practice. Bethesda, Md: American Association of Blood Banks, 1995.

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4

Atala, Anthony. Progenitor and stem cell technologies and therapies. Cambridge, UK: Woodhead Publishing, 2012.

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5

American Association of Blood Banks., ed. Standards for hematopoietic progenitor cell services. 2nd ed. Bethesda, Md: American Association of Blood Banks, 2000.

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6

Co, Business Communications, ed. Stem cell and progenitor cell therapy: Current uses and future possibilities. Norwalk, CT: Business Communications Co., 2002.

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7

Arturo, Álvarez-Buylla, and García-Verdugo José Manuel, eds. Identification and characterization of neural progenitor cells in the adult mammalian brain. Berlin: Springer, 2009.

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8

American Association of Blood Banks. Standards for hematopoietic progenitor cell and cellular product services. 3rd ed. Bethesda, Md: American Association of Blood Banks, 2002.

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9

Progenitor cell therapy for neurological injury. New York: Humana Press, 2011.

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10

I, Moldovan Nicanor, ed. Novel angiogenic mechanisms: Role of circulating progenitor endothelial cells. New York: Kluwer Academic/Plenum, 2003.

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11

International Workshop "Novel Angiogenic Mechanisms" (2002 Columbus, Ohio). Novel angiogenic mechanisms: Role of circulating progenitor endothelial cells. New York: Kluwer Academic/Plenum, 2003.

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12

Chu, Peter Pui Tak. Retroviral-mediated human adenosine deaminase gene transfer into human hematopoietic progenitor and stem cells. Ottawa: National Library of Canada, 1995.

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13

Progenitor Cells Methods And Protocols. Humana Press, 2012.

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14

Joglekar, Mugdha V., and Anandwardhan A. Hardikar. Progenitor Cells: Methods and Protocols. Springer New York, 2019.

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15

Joglekar, Mugdha V., and Anandwardhan A. Hardikar. Progenitor Cells: Methods and Protocols. Springer New York, 2020.

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16

Reynolds, Brent A., and Loic P. Deleyrolle. Neural Progenitor Cells: Methods and Protocols. Humana Press, 2016.

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17

Deleyrolle, Loic P. Neural Progenitor Cells: Methods and Protocols. Springer, 2021.

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18

Deleyrolle, Loic P. Neural Progenitor Cells: Methods and Protocols. Springer, 2022.

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19

Menitove, Jay E. Standards for Hematopoietic Progenitor Cells. American Association of Blood Banks (AABB), 2002.

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20

Horton, Patrick M., and Brett E. Lawrence. Progenitor Cells: Biology, Characterization and Potential Clinical Applications. Nova Science Publishers, Incorporated, 2014.

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21

Atala, Anthony. Progenitor and Stem Cell Technologies and Therapies. Elsevier Science & Technology, 2012.

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22

Hematopoietic Progenitor Cells: A Primer for Medical Professionals. American Association of Blood Banks, 2000.

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23

Pleniceanu, Oren, and Benjamin Dekel. Kidney stem cells. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0344.

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End-stage renal failure is a major cause of death with currently only dialysis and transplantation available as therapeutic options, each with its own limitations and drawbacks. To allow regenerative medicine-based kidney replacement therapies and due to the fact that neither haematopoietic stem cells nor mesenchymal stem cells, the most accessible human stem cells, can be used to derive genuine nephron progenitors, much attention has been given to finding adult renal stem cells. Several candidates for this have been described, but their true identity as stem or progenitor cells and their potential use in therapy has not yet been shown. However, the analysis of embryonic renal stem cells, specifically stem/progenitor cells that are induced into the nephrogenic pathway to form nephrons until the 34th week of gestation, has been much more conclusive.
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24

Doeppner, Thorsten R., and Dirk M. Hermann, eds. Stem Cells and Progenitor Cells in Ischemic Stroke – Fashion or Future? Frontiers Media SA, 2016. http://dx.doi.org/10.3389/978-2-88919-724-8.

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25

Stem and Progenitor Cells in the Central Nervous System. Muenchen: Karger, 2006.

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26

Progenitor Cell Therapy for Neurological Injury. Humana, 2012.

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27

Lehal, Rajwinder Singh. Evidence that Pten loss induces mammary tumours by targeting stem/progenitor cells. 2007.

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28

Nowakowski, R. S. Stem and Progenitor Cells in the Central Nervous System: Developmental Neuroscience 2004 No. 2-4. S Karger Pub, 2005.

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29

Seaberg, Raewyn M. Mammalian brain development: The role of distinct neural stem and progenitor cells from embryonic neural induction to adult neurogenesis. 2004.

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30

Madlambayan, Gerard James. Endogenously produced protein regulators provide feedback signals that regulate the ex vivo expansion of human hematopoietic stem and progenitor cells. 2004.

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31

Weller, Michael, Michael Brada, Tai-Tong Wong, and Michael A. Vogelbaum. Astrocytic tumours: diffuse astrocytoma, anaplastic astrocytoma, glioblastoma, and gliomatosis cerebri. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0003.

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Astrocytic gliomas are primary brain tumours thought to originate from neural stem or progenitor cells. They are assigned grades II, III, or IV by the World Health Organization according to degree of malignancy as defined by histology. The following molecular markers are increasingly used for diagnostic subclassification or clinical decision-making: 1p/19q co-deletion status, O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status, and isocitrate dehydrogenase 1 and 2 mutation status. Extent of resection is a favourable prognostic factor, but surgery is never curative. Radiotherapy prolongs progression-free survival across all astrocytic glioma entities. Alkylating agent chemotherapy is an active treatment in particular for patients with MGMT promoter-methylated tumours. Anti-angiogenic therapies have failed to improve survival, and the current focus of major clinical trials is on novel targeted agents or on immunotherapy.
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32

Douglas, Kenneth. Bioprinting. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190943547.001.0001.

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Abstract: This book describes how bioprinting emerged from 3D printing and details the accomplishments and challenges in bioprinting tissues of cartilage, skin, bone, muscle, neuromuscular junctions, liver, heart, lung, and kidney. It explains how scientists are attempting to provide these bioprinted tissues with a blood supply and the ability to carry nerve signals so that the tissues might be used for transplantation into persons with diseased or damaged organs. The book presents all the common terms in the bioprinting field and clarifies their meaning using plain language. Readers will learn about bioink—a bioprinting material containing living cells and supportive biomaterials. In addition, readers will become at ease with concepts such as fugitive inks (sacrificial inks used to make channels for blood flow), extracellular matrices (the biological environment surrounding cells), decellularization (the process of isolating cells from their native environment), hydrogels (water-based substances that can substitute for the extracellular matrix), rheology (the flow properties of a bioink), and bioreactors (containers to provide the environment cells need to thrive and multiply). Further vocabulary that will become familiar includes diffusion (passive movement of oxygen and nutrients from regions of high concentration to regions of low concentration), stem cells (cells with the potential to develop into different bodily cell types), progenitor cells (early descendants of stem cells), gene expression (the process by which proteins develop from instructions in our DNA), and growth factors (substances—often proteins—that stimulate cell growth, proliferation, and differentiation). The book contains an extensive glossary for quick reference.
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