Temporary Disabled. :) please Go back Mechanism of TGFbeta receptor inhibition by FKBP12 - Wikidata www.fgks.org » Address: [go: up one dir, main page] Include Form Remove Scripts Accept Cookies Show Images Show Referer Rotate13 Base64 Strip Meta Strip Title Session Cookies Home Random Nearby Log in Settings Donate About Wikidata Disclaimers Search (Q41101968) Watch EnglishMechanism of TGFbeta receptor inhibition by FKBP12scientific article published on July 1997In more languageseditStatements instance of scholarly article 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 title Mechanism of TGFbeta receptor inhibition by FKBP12 (English) 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 author name string Y G Chen series ordinal 1 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 F Liu series ordinal 2 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 J Massague series ordinal 3 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 language of work or name English 0 references publication date 1 July 1997 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 published in The EMBO Journal 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 volume 16 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 issue 13 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 page(s) 3866-3876 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 cites work The TGF-beta family mediator Smad1 is phosphorylated directly and activated functionally by the BMP receptor kinase 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 MADR2 is a substrate of the TGFbeta receptor and its phosphorylation is required for nuclear accumulation and signaling 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 A transcriptional partner for MAD proteins in TGF-beta signalling 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of chordin to BMP-4. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 TGFbeta signaling: receptors, transducers, and Mad proteins. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Ligand-independent activation of transforming growth factor (TGF) beta signaling pathways by heteromeric cytoplasmic domains of TGF-beta receptors 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 MADR1, a MAD-related protein that functions in BMP2 signaling pathways 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Complementation between kinase-defective and activation-defective TGF-beta receptors reveals a novel form of receptor cooperativity essential for signaling. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 The p21(RAS) farnesyltransferase alpha subunit in TGF-beta and activin signaling 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Caenorhabditis elegans genes sma-2, sma-3, and sma-4 define a conserved family of transforming growth factor beta pathway components 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Interaction of the transforming growth factor-beta type I receptor with farnesyl-protein transferase-alpha 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Type I receptors specify growth-inhibitory and transcriptional responses to transforming growth factor beta and activin 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 A mammalian protein targeted by G1-arresting rapamycin-receptor complex 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Reconstitution and transphosphorylation of TGF-beta receptor complexes 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Biochemical evidence for the autophosphorylation and transphosphorylation of transforming growth factor beta receptor kinases 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Human type II receptor for bone morphogenic proteins (BMPs): extension of the two-kinase receptor model to the BMPs 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 GS domain mutations that constitutively activate T beta R-I, the downstream signaling component in the TGF-beta receptor complex 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Genetic characterization and cloning of mothers against dpp, a gene required for decapentaplegic function in Drosophila melanogaster 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 The transforming growth factor beta receptors types I, II, and III form hetero-oligomeric complexes in the presence of ligand 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Cloning, structure, and expression of the mitochondrial cytochrome P-450 sterol 26-hydroxylase, a bile acid biosynthetic enzyme 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 A receptor for the immunosuppressant FK506 is a cis-trans peptidyl-prolyl isomerase 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 The transforming growth factor-beta family 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Chemistry and Biology of the Immunophilins and Their Immunosuppressive Ligands 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 The cytosolic-binding protein for the immunosuppressant FK-506 is both a ubiquitous and highly conserved peptidyl-prolyl cis-trans isomerase 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Immunophilin-sensitive protein phosphatase action in cell signaling pathways 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 TGF beta signals through a heteromeric protein kinase receptor complex 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Substrate specificities of the peptidyl prolyl cis-trans isomerase activities of cyclophilin and FK-506 binding protein: evidence for the existence of a family of distinct enzymes 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Partnership between DPC4 and SMAD proteins in TGF-beta signalling pathways. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 The GS domain of the transforming growth factor-beta type I receptor is important in signal transduction 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Phosphorylation-dependent interaction of the cytoplasmic domains of the type I and type II transforming growth factor-beta receptors 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Signaling activity of homologous and heterologous transforming growth factor-beta receptor kinase complexes. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 Transforming growth factor-beta (TGF-beta)-induced down-regulation of cyclin A expression requires a functional TGF-beta receptor complex. Characterization of chimeric and truncated type I and type II receptors 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 26 September 2017 FKBP-12 recognition is dispensable for signal generation by type I transforming growth factor-beta receptors. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 17 June 2018 Betaglycan presents ligand to the TGF beta signaling receptor. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 17 June 2018 Concomitant loss of transforming growth factor (TGF)-beta receptor types I and II in TGF-beta-resistant cell mutants implicates both receptor types in signal transduction. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 17 June 2018 The immunophilin FKBP12 functions as a common inhibitor of the TGF beta family type I receptors. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 19 August 2018 The Xenopus dorsalizing factor noggin ventralizes Drosophila embryos by preventing DPP from activating its receptor. 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 19 August 2018 Xenopus Mad proteins transduce distinct subsets of signals for the TGF beta superfamily 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 19 August 2018 Stabilization of calcium release channel (ryanodine receptor) function by FK506-binding protein 1 reference stated in PubMed Central reference URL https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170011 retrieved 19 August 2018 Identification of receptors for type-beta transforming growth factor 1 reference stated in PubMed reference URL https://pubmed.ncbi.nlm.nih.gov/9233797 retrieved 12 December 2020 based on heuristic inferred from PubMed ID database lookup Graded changes in dose of a Xenopus activin A homologue elicit stepwise transitions in embryonic cell fate 1 reference stated in PubMed reference URL https://pubmed.ncbi.nlm.nih.gov/9233797 retrieved 12 December 2020 based on heuristic inferred from PubMed ID database lookup FK506 binding protein mutational analysis. Defining the surface residue contributions to stability of the calcineurin co-complex 1 reference stated in PubMed reference URL https://pubmed.ncbi.nlm.nih.gov/9233797 retrieved 12 December 2020 based on heuristic inferred from PubMed ID database lookup Characterization of the Interaction of FKBP12 with the Transforming Growth Factor-β Type I Receptorin Vivo 1 reference stated in PubMed reference URL https://pubmed.ncbi.nlm.nih.gov/9233797 retrieved 12 December 2020 based on heuristic inferred from PubMed ID database lookup Identifiers DOI 10.1093/EMBOJ/16.13.3866 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 PMC publication ID 1170011 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 PubMed publication ID 9233797 1 reference stated in Europe PubMed Central PMC publication ID 1170011 retrieved 26 September 2017 ResearchGate publication ID 232780375 0 references Sitelinks Wikipedia(0 entries) edit Wikibooks(0 entries) edit Wikinews(0 entries) edit Wikiquote(0 entries) edit Wikisource(0 entries) edit Wikiversity(0 entries) edit Wikivoyage(0 entries) edit Wiktionary(0 entries) edit Multilingual sites(0 entries) edit
scientific article published on July 1997