Drm/Gremlin transcriptionally activates p21(Cip1) via a novel mechanism and inhibits neoplastic transformation (Q28588333)

GOA release 2020-03-11

author name string

Bo Chen

1

1 reference

31 January 2017

Meropi Athanasiou

2

1 reference

31 January 2017

Qiuping Gu

3

1 reference

31 January 2017

Donald G. Blair

Biochemical and Biophysical Research Communications

4

1 reference

31 January 2017

language of work or name

English

0 references

publication date

2 August 2002

1 reference

31 January 2017

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31 January 2017

295

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31 January 2017

5

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31 January 2017

1135–1141

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31 January 2017

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Signal relay by BMP antagonism controls the SHH/FGF4 feedback loop in vertebrate limb buds.

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DRM/GREMLIN (CKTSF1B1) maps to human chromosome 15 and is highly expressed in adult and fetal brain

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Uncoupling of p21WAF1/CIP1/SDI1 mRNA and protein expression upon genotoxic stress

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Two posttranscriptional pathways that regulate p21(Cip1/Waf1/Sdi1) are identified by HPV16-E6 interaction and correlate with life span and cellular senescence.

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Oncogenic functions of tumour suppressor p21(Waf1/Cip1/Sdi1): association with cell senescence and tumour-promoting activities of stromal fibroblasts

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