(Q40817472)

English

Transcriptional cross-talk between Smad, ERK1/2, and p38 mitogen-activated protein kinase pathways regulates transforming growth factor-beta-induced aggrecan gene expression in chondrogenic ATDC5 cells

scientific article published on 29 January 2001

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scholarly article

1 reference

Europe PubMed Central

24 September 2017

Transcriptional cross-talk between Smad, ERK1/2, and p38 mitogen-activated protein kinase pathways regulates transforming growth factor-beta-induced aggrecan gene expression in chondrogenic ATDC5 cells (English)

1 reference

Europe PubMed Central

24 September 2017

author name string

H Watanabe

1

1 reference

Europe PubMed Central

24 September 2017

M P de Caestecker

2

1 reference

Europe PubMed Central

24 September 2017

Y Yamada

3

1 reference

Europe PubMed Central

24 September 2017

language of work or name

0 references

publication date

29 January 2001

1 reference

Europe PubMed Central

24 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

24 September 2017

276

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Europe PubMed Central

24 September 2017

17

1 reference

Europe PubMed Central

24 September 2017

14466-14473

1 reference

Europe PubMed Central

24 September 2017

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Formation of cartilage-like spheroids by micromass cultures of murine C3H10T1/2 cells upon treatment with transforming growth factor-beta 1.

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Sequential progression of the differentiation program by bone morphogenetic protein-2 in chondrogenic cell line ATDC5.

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Roles of aggrecan, a large chondroitin sulfate proteoglycan, in cartilage structure and function.

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Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene.

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Chondrogenic differentiation of clonal mouse embryonic cell line ATDC5 in vitro: differentiation-dependent gene expression of parathyroid hormone (PTH)/PTH-related peptide receptor

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TGFbeta signaling: receptors, transducers, and Mad proteins.

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TGF-beta signalling from cell membrane to nucleus through SMAD proteins

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Human Smad3 and Smad4 are sequence-specific transcription activators

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Crystal structure of a Smad MH1 domain bound to DNA: insights on DNA binding in TGF-beta signaling

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Synergistic signaling in fetal brain by STAT3-Smad1 complex bridged by p300

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Cooperative binding of Smad proteins to two adjacent DNA elements in the plasminogen activator inhibitor-1 promoter mediates transforming growth factor beta-induced smad-dependent transcriptional activation

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21 January 2018

ATF-2 is a common nuclear target of Smad and TAK1 pathways in transforming growth factor-beta signaling

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Smad4 and FAST-1 in the assembly of activin-responsive factor

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21 January 2018

Smad3 and Smad4 cooperate with c-Jun/c-Fos to mediate TGF-beta-induced transcription

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Interaction and functional cooperation of PEBP2/CBF with Smads. Synergistic induction of the immunoglobulin germline Calpha promoter

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Glucocorticoid receptor inhibits transforming growth factor-beta signaling by directly targeting the transcriptional activation function of Smad3

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Synergistic cooperation of TFE3 and smad proteins in TGF-beta-induced transcription of the plasminogen activator inhibitor-1 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005724200

21 January 2018

Transcriptional activating activity of Smad4: roles of SMAD hetero-oligomerization and enhancement by an associating transactivator

1 reference

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21 January 2018

The oncoprotein Evi-1 represses TGF-beta signalling by inhibiting Smad3

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Negative feedback regulation of TGF-beta signaling by the SnoN oncoprotein

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21 January 2018

Interaction of the Ski oncoprotein with Smad3 regulates TGF-beta signaling

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A Smad transcriptional corepressor

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The tumor suppressor Smad4/DPC4 and transcriptional adaptor CBP/p300 are coactivators for smad3 in TGF-beta-induced transcriptional activation

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Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes

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The Smad4 activation domain (SAD) is a proline-rich, p300-dependent transcriptional activation domain

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TGF beta signals through a heteromeric protein kinase receptor complex

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Identifiers

10.1074/JBC.M005724200

0 references

1 reference

Europe PubMed Central

24 September 2017

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