The MAD-related protein Smad7 associates with the TGFbeta receptor and functions as an antagonist of TGFbeta signaling (Q28243202)

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S Abdollah

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Y Qiu

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J Cai

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Y Y Xu

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B W Grinnell

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M A Richardson

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J N Topper

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M A Gimbrone

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J L Wrana

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D Falb

Signal transduction by members of the transforming growth factor-beta superfamily

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language of work or name

English

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publication date

27 June 1997

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published in

Cell

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volume

89

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page(s)

1165-73

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issue

7

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A transcriptional partner for MAD proteins in TGF-beta signalling

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MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

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Xenopus Mad proteins transduce distinct subsets of signals for the TGF beta superfamily.

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Serine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1

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Partnership between DPC4 and SMAD proteins in TGF-beta signalling pathways.

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A human Mad protein acting as a BMP-regulated transcriptional activator

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MADR2 is a substrate of the TGFbeta receptor and its phosphorylation is required for nuclear accumulation and signaling

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Tumor suppressor activity of the TGF-beta pathway in human cancers

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Caenorhabditis elegans genes sma-2, sma-3, and sma-4 define a conserved family of transforming growth factor beta pathway components

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Identification of vascular endothelial genes differentially responsive to fluid mechanical stimuli: cyclooxygenase-2, manganese superoxide dismutase, and endothelial cell nitric oxide synthase are selectively up-regulated by steady laminar shear str

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Vascular MADs: two novel MAD-related genes selectively inducible by flow in human vascular endothelium

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Complementation between kinase-defective and activation-defective TGF-beta receptors reveals a novel form of receptor cooperativity essential for signaling.

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Mechanism of activation of the TGF-beta receptor

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Mammalian dwarfins are phosphorylated in response to transforming growth factor beta and are implicated in control of cell growth

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Receptor-associated Mad homologues synergize as effectors of the TGF-beta response

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The tumor suppressor Smad4/DPC 4 as a central mediator of Smad function

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

995181

995181

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference