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Retinoic acid signaling and neuronal differentiation
by
Blumberg, Bruce
, Janesick, Amanda
, Wu, Stephanie Cherie
in
Acids
/ Amniota
/ Animals
/ Antigens, Neoplasm - metabolism
/ Antineoplastic Agents - therapeutic use
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell cycle
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Differentiation
/ Embryos
/ genes
/ Humans
/ In vivo methods and tests
/ in vivo studies
/ Life Sciences
/ Metabolites
/ Molecular modelling
/ molluscs
/ Mollusks
/ Neoplasms - drug therapy
/ Neoplasms - metabolism
/ Neoplasms - pathology
/ Neural stem cells
/ Neurogenesis
/ Neurology
/ Neurons
/ Neurons - metabolism
/ phenotype
/ Phenotypes
/ Progenitor cells
/ Receptors, Retinoic Acid - chemistry
/ Receptors, Retinoic Acid - metabolism
/ Retinene
/ Retinoic acid
/ Retinoic acid receptors
/ Review
/ Signal Transduction
/ Spatial distribution
/ Stem cells
/ Transcription factors
/ Tretinoin - metabolism
/ Tretinoin - therapeutic use
/ Vitamin A
/ vitamin deficiencies
/ Vitamin deficiency
2015
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Retinoic acid signaling and neuronal differentiation
by
Blumberg, Bruce
, Janesick, Amanda
, Wu, Stephanie Cherie
in
Acids
/ Amniota
/ Animals
/ Antigens, Neoplasm - metabolism
/ Antineoplastic Agents - therapeutic use
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell cycle
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Differentiation
/ Embryos
/ genes
/ Humans
/ In vivo methods and tests
/ in vivo studies
/ Life Sciences
/ Metabolites
/ Molecular modelling
/ molluscs
/ Mollusks
/ Neoplasms - drug therapy
/ Neoplasms - metabolism
/ Neoplasms - pathology
/ Neural stem cells
/ Neurogenesis
/ Neurology
/ Neurons
/ Neurons - metabolism
/ phenotype
/ Phenotypes
/ Progenitor cells
/ Receptors, Retinoic Acid - chemistry
/ Receptors, Retinoic Acid - metabolism
/ Retinene
/ Retinoic acid
/ Retinoic acid receptors
/ Review
/ Signal Transduction
/ Spatial distribution
/ Stem cells
/ Transcription factors
/ Tretinoin - metabolism
/ Tretinoin - therapeutic use
/ Vitamin A
/ vitamin deficiencies
/ Vitamin deficiency
2015
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Do you wish to request the book?
Retinoic acid signaling and neuronal differentiation
by
Blumberg, Bruce
, Janesick, Amanda
, Wu, Stephanie Cherie
in
Acids
/ Amniota
/ Animals
/ Antigens, Neoplasm - metabolism
/ Antineoplastic Agents - therapeutic use
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell cycle
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Differentiation
/ Embryos
/ genes
/ Humans
/ In vivo methods and tests
/ in vivo studies
/ Life Sciences
/ Metabolites
/ Molecular modelling
/ molluscs
/ Mollusks
/ Neoplasms - drug therapy
/ Neoplasms - metabolism
/ Neoplasms - pathology
/ Neural stem cells
/ Neurogenesis
/ Neurology
/ Neurons
/ Neurons - metabolism
/ phenotype
/ Phenotypes
/ Progenitor cells
/ Receptors, Retinoic Acid - chemistry
/ Receptors, Retinoic Acid - metabolism
/ Retinene
/ Retinoic acid
/ Retinoic acid receptors
/ Review
/ Signal Transduction
/ Spatial distribution
/ Stem cells
/ Transcription factors
/ Tretinoin - metabolism
/ Tretinoin - therapeutic use
/ Vitamin A
/ vitamin deficiencies
/ Vitamin deficiency
2015
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Journal Article
Retinoic acid signaling and neuronal differentiation
2015
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Overview
The identification of neurological symptoms caused by vitamin A deficiency pointed to a critical, early developmental role of vitamin A and its metabolite, retinoic acid (RA). The ability of RA to induce post-mitotic, neural phenotypes in various stem cells, in vitro, served as early evidence that RA is involved in the switch between proliferation and differentiation. In vivo studies have expanded this “opposing signal” model, and the number of primary neurons an embryo develops is now known to depend critically on the levels and spatial distribution of RA. The proneural and neurogenic transcription factors that control the exit of neural progenitors from the cell cycle and allow primary neurons to develop are partly elucidated, but the downstream effectors of RA receptor (RAR) signaling (many of which are putative cell cycle regulators) remain largely unidentified. The molecular mechanisms underlying RA-induced primary neurogenesis in anamniote embryos are starting to be revealed; however, these data have been not been extended to amniote embryos. There is growing evidence that bona fide RARs are found in some mollusks and other invertebrates, but little is known about their necessity or functions in neurogenesis. One normal function of RA is to regulate the cell cycle to halt proliferation, and loss of RA signaling is associated with dedifferentiation and the development of cancer. Identifying the genes and pathways that mediate cell cycle exit downstream of RA will be critical for our understanding of how to target tumor differentiation. Overall, elucidating the molecular details of RAR-regulated neurogenesis will be decisive for developing and understanding neural proliferation–differentiation switches throughout development.
Publisher
Springer-Verlag,Springer Basel,Springer Nature B.V
Subject
/ Amniota
/ Animals
/ Antigens, Neoplasm - metabolism
/ Antineoplastic Agents - therapeutic use
/ Biomedical and Life Sciences
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Embryos
/ genes
/ Humans
/ molluscs
/ Mollusks
/ Neurons
/ Receptors, Retinoic Acid - chemistry
/ Receptors, Retinoic Acid - metabolism
/ Retinene
/ Review
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