Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/51385
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degois.publication.issue332pt_PT
degois.publication.titleScience Signalingpt_PT
dc.relation.publisherversionhttps://www.science.org/journal/signalingpt_PT
dc.contributor.authorPulido, Rafael-
dc.contributor.authorBaker, Suzanne J.-
dc.contributor.authorBarata, João T.-
dc.contributor.authorCarracedo, Arkaitz-
dc.contributor.authorCid, Victor J.-
dc.contributor.authorChin-Sang, Ian D.-
dc.contributor.authorDavé, Vrushank-
dc.contributor.authorden Hertog, Jeroen-
dc.contributor.authorDevreotes, Peter-
dc.contributor.authorEickholt, Britta J.-
dc.contributor.authorEng, Charis-
dc.contributor.authorFurnari, Frank B.-
dc.contributor.authorGeorgescu, Maria-Magdalena-
dc.contributor.authorGericke, Arne-
dc.contributor.authorHopkins, Benjamin-
dc.contributor.authorJiang, Xeujun-
dc.contributor.authorLee, Seung-Rock-
dc.contributor.authorLösche, Mathias-
dc.contributor.authorMalaney, Prerna-
dc.contributor.authorMatias-Guiu, Xavier-
dc.contributor.authorMolina, María-
dc.contributor.authorPandolfi, Pier Paolo-
dc.contributor.authorParsons, Ramon-
dc.contributor.authorPinton, Paolo-
dc.contributor.authorRivas, Carmen-
dc.contributor.authorRocha, Rafael M.-
dc.contributor.authorRodríguez, Manuel S.-
dc.contributor.authorRoss, Alonzo H.-
dc.contributor.authorSerrano, Manuel-
dc.contributor.authorStambolic, Vuk-
dc.contributor.authorStiles, Bangyan-
dc.contributor.authorSuzuki, Akira-
dc.contributor.authorTan, Seong-Seng-
dc.contributor.authorTonks, Nicholas K.-
dc.contributor.authorTrotman, Lloyd C.-
dc.contributor.authorWolff, Nicolas-
dc.contributor.authorWoscholski, Rudiger-
dc.contributor.authorWu, Hong-
dc.contributor.authorLeslie, Nicholas R.-
dc.date.accessioned2022-02-17T15:57:45Z-
dc.date.available2022-02-17T15:57:45Z-
dc.date.issued2014-
dc.identifier.citationScience Signaling 7 (332), pe15.pt_PT
dc.identifier.issn1945-0877-
dc.identifier.urihttp://hdl.handle.net/10451/51385-
dc.description© Copyright 2015 by the American Association for the Advancement of Science; all rights reserved.pt_PT
dc.description.abstractThe tumor suppressor PTEN is a major brake for cell transformation, mainly due to its phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P3] phosphatase activity that directly counteracts the oncogenicity of phosphoinositide 3-kinase (PI3K). PTEN mutations are frequent in tumors and in the germ line of patients with tumor predisposition or with neurological or cognitive disorders, which makes the PTEN gene and protein a major focus of interest in current biomedical research. After almost two decades of intense investigation on the 403-residue-long PTEN protein, a previously uncharacterized form of PTEN has been discovered that contains 173 amino-terminal extra amino acids, as a result of an alternate translation initiation site. To facilitate research in the field and to avoid ambiguities in the naming and identification of PTEN amino acids from publications and databases, we propose here a unifying nomenclature and amino acid numbering for this longer form of PTEN.pt_PT
dc.language.isoengpt_PT
dc.publisherAmerican Association for the Advancement of Sciencept_PT
dc.rightsrestrictedAccesspt_PT
dc.titleA unified nomenclature and amino acid numbering for human PTENpt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume7pt_PT
dc.identifier.doi10.1126/scisignal.2005560pt_PT
dc.identifier.eissn1937-9145-
Aparece nas colecções:IMM - Artigos em Revistas Internacionais
FM - Artigos em Revistas Internacionais

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