Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling (Q24337871)

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English	Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling	scientific article

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8 March 2020

Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling (English)

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8 March 2020

Family with sequence similarity 83 member G

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GOA release 2020-03-11

BMP signaling pathway

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GOA release 2020-03-11

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based on heuristic

inferred from title

1

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8 March 2020

James Cuthbert Smith

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8 March 2020

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Kevin S Dingwell

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8 March 2020

Lina Herhaus

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8 March 2020

Robert Gourlay

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8 March 2020

Thomas Macartney

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8 March 2020

David Campbell

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8 March 2020

Gopal P Sapkota

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8 March 2020

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19 February 2014

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8 March 2020

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8 March 2020

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8 March 2020

2

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130210

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8 March 2020

FAM83A confers EGFR-TKI resistance in breast cancer cells and in mice

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Nuclear CDKs drive Smad transcriptional activation and turnover in BMP and TGF-beta pathways

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BMP type I receptor inhibition reduces heterotopic [corrected] ossification

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FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

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Regulation of Smad degradation and activity by Smurf2, an E3 ubiquitin ligase

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BMP signaling regulates sympathetic nervous system development through Smad4-dependent and -independent pathways

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Bone morphogenetic proteins

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BMP type I receptor ALK2 is essential for proper patterning at late gastrulation during mouse embryogenesis

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OTUB1 enhances TGFβ signalling by inhibiting the ubiquitylation and degradation of active SMAD2/3.

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BMP signaling in development and diseases: a pharmacological perspective

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Quantitative proteomics with siRNA screening identifies novel mechanisms of trastuzumab resistance in HER2 amplified breast cancers

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Protein phosphatase 5 modulates SMAD3 function in the transforming growth factor-β pathway

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USP11 augments TGFβ signalling by deubiquitylating ALK5.

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Regulation of the transforming growth factor β pathway by reversible ubiquitylation

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BMP signaling in vascular diseases

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27 September 2017

Phosphatases in SMAD regulation

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27 September 2017

The specificities of small molecule inhibitors of the TGFß and BMP pathways

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Bone morphogenetic protein and growth differentiation factor cytokine families and their protein antagonists

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ActRIIA and BMPRII Type II BMP receptor subunits selectively required for Smad4-independent BMP7-evoked chemotaxis

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27 September 2017

Overexpression of bone morphogenetic protein 4 enhances the invasiveness of Smad4-deficient human colorectal cancer cells

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Ectodermal Smad4 and p38 MAPK are functionally redundant in mediating TGF-beta/BMP signaling during tooth and palate development

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BMP suppresses PTEN expression via RAS/ERK signaling

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Deficient Alk3-mediated BMP signaling causes prenatal omphalocele-like defect

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SANE, a novel LEM domain protein, regulates bone morphogenetic protein signaling through interaction with Smad1.

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10.1098/RSOB.130210

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Consolidated OpenCitations Corpus – April 2017

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8 March 2020

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