Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors (Q29616203)

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30 April 2017

author name string

Nakayama K

1

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30 April 2017

Ishida N

2

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Shirane M

3

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Inomata A

4

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Inoue T

5

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Shishido N

6

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Horii I

7

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Loh DY

8

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30 April 2017

Nakayama K

9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8646779

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8646779

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language of work or name

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30 April 2017

publication date

31 May 1996

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30 April 2017

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volume

85

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page(s)

707-20

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issue

5

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Radiation-induced cell cycle arrest compromised by p21 deficiency

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Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

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Inherited retinal dystrophy in the RCS rat: prevention of photoreceptor degeneration by pigment epithelial cell transplantation.

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

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1372427

1372427

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8646779

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017