Books on the topic 'Neural progenitor'

To see the other types of publications on this topic, follow the link: Neural progenitor.

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 15 books for your research on the topic 'Neural progenitor.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse books on a wide variety of disciplines and organise your bibliography correctly.

1

Deleyrolle, Loic P., ed. Neural Progenitor Cells. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1783-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Reynolds, Brent A., and Loic P. Deleyrolle, eds. Neural Progenitor Cells. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-574-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Garcia-Verdugo, Jose Manuel, Arturo Alvarez-Buylla, and Sara Gil-Perotín. Identification and Characterization of Neural Progenitor Cells in the Adult Mammalian Brain. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-88719-5.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Costa, Marcos R., Cecilia Hedin-Pereira, and Caroline Rouaux, eds. Progenitor Diversity and Neural Cell Specification in the Central Nervous System. Frontiers Media SA, 2015. http://dx.doi.org/10.3389/978-2-88919-683-8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
11

Neural crest cell lineage restricts skeletal muscle progenitor cell differentiation through Neuregulin1-ErbB3 signaling. Developmental Cell, 2011.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
12

Rammah, Mayyasa, Francesca Rochais, and Robert G. Kelly. Incorporation of myocardial progenitors at the arterial pole of the heart. Edited by José Maria Pérez-Pomares, Robert G. Kelly, Maurice van den Hoff, José Luis de la Pompa, David Sedmera, Cristina Basso, and Deborah Henderson. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757269.003.0007.

Full text
Abstract:
The arterial pole of the heart is a hotspot for life-threatening forms of congenital heart defects (CHDs). It is formed by progressive addition of myocardium from epithelial progenitor cells in the second heart field (SHF). SHF cells contribute successively to the right ventricle and proximal and distal outflow tract myocardial walls which, after neural crest influx and cardiac septation, give rise to myocardium at the base of the aorta and pulmonary trunk. SHF cells are characterized by continued proliferation and differentiation delay controlled by an array of transcriptional regulators and signalling pathways which define the SHF progenitor cell niche in pharyngeal mesoderm. Failure of normal SHF deployment leads to a shortened outflow tract and failure of ventriculo-arterial alignment, resulting in a spectrum of conotruncal CHD. We discuss the origins of the SHF in cardiopharyngeal mesoderm and focus on the mechanisms driving SHF deployment, summarizing current understanding of critical signalling pathways and transcription factors.
APA, Harvard, Vancouver, ISO, and other styles
13

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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
14

Zaffran, Stéphane. Cardiac growth II: Cardiomyocyte polarization. Edited by José Maria Pérez-Pomares, Robert G. Kelly, Maurice van den Hoff, José Luis de la Pompa, David Sedmera, Cristina Basso, and Deborah Henderson. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757269.003.0010.

Full text
Abstract:
During vertebrate embryogenesis, the planar cell polarity (PCP) signalling pathway is responsible for cell movements essential for convergent extension during gastrulation, neural tube closure, neural crest cell migration, and heart morphogenesis. In the heart, the non-canonical Wnt/PCP pathway regulates cell polarity, cell shape, and cell dynamics during formation of the cardiac crescent and deployment of second heart field cardiac progenitors to the poles of the heart tube. PCP signalling is also essential for the establishment of left–right patterning in the early embryo. This chapter reviews our current understanding of PCP signalling in heart morphogenesis and how it affects the pathogenesis of congenital heart diseases.
APA, Harvard, Vancouver, ISO, and other styles
15

Rolfs, A. Isolation and Induction of Neuronal Progenitor Cells: Rostock Spring School 2006 Contributions, Special Issue, Neurodegenerative Diseases 2007. S Karger Pub, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography