Tumor-suppressor p53 is expressed in proliferating and newly formed neurons of the embryonic and postnatal rat brain: comparison with expression of the cell cycle regulators p21Waf1/Cip1, p27Kip1, p57Kip2, p16Ink4a, cyclin G1, and the proto-oncogene (Q28576833)

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English	Tumor-suppressor p53 is expressed in proliferating and newly formed neurons of the embryonic and postnatal rat brain: comparison with expression of the cell cycle regulators p21Waf1/Cip1, p27Kip1, p57Kip2, p16Ink4a, cyclin G1, and the proto-oncogene	scientific journal article

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scholarly article

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PubMed publication ID

31 January 2017

Tumor-suppressor p53 is expressed in proliferating and newly formed neurons of the embryonic and postnatal rat brain: comparison with expression of the cell cycle regulators p21Waf1/Cip1, p27Kip1, p57Kip2, p16Ink4a, cyclin G1, and the proto-oncogene (English)

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PubMed publication ID

31 January 2017

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author name string

M. van Lookeren Campagne

1

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PubMed publication ID

31 January 2017

R. Gill

2

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31 January 2017

language of work or name

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publication date

27 July 1998

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PubMed publication ID

31 January 2017

The Journal of Comparative Neurology

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PubMed publication ID

31 January 2017

397

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PubMed publication ID

31 January 2017

2

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31 January 2017

181–198

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PubMed publication ID

31 January 2017

Autoradiographic and histological studies of postnatal neurogenesis. IV. Cell proliferation and migration in the anterior forebrain, with special reference to persisting neurogenesis in the olfactory bulb

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Postnatal development of the cerebellar cortex in the rat. I. The external germinal layer and the transitional molecular layer

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High-frequency developmental abnormalities in p53-deficient mice.

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BAX is required for neuronal death after trophic factor deprivation and during development

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Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control

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21 January 2018

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

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Identifiers

10.1002/(SICI)1096-9861(19980727)397:2<181::AID-CNE3>3.0.CO;2-X

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

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