Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/353600
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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authorunicampSoardi, Fernanda Carolinept_BR
dc.contributor.authorunicampMaciel-Guerra, Andrea Trevaspt_BR
dc.contributor.authorunicampGuerra Junior, Gilpt_BR
dc.contributor.authorunicampMello, Maricilda Palandi dept_BR
dc.typeArtigopt_BR
dc.titleFunctional impact of novel androgen receptor mutations on the clinical manifestation of androgen insensitivity syndromept_BR
dc.contributor.authorPetroli, Reginaldo J.pt_BR
dc.contributor.authorHiort, Olafpt_BR
dc.contributor.authorStruve, Dagmarpt_BR
dc.contributor.authorGesing, Julia K.pt_BR
dc.contributor.authorSoardi, Fernanda C.pt_BR
dc.contributor.authorSpinola-Castro, Angela M.pt_BR
dc.contributor.authorMelo, Karlapt_BR
dc.contributor.authorArnhold, Ivo J. Pradopt_BR
dc.contributor.authorMaciel-Guerra, Andrea T.pt_BR
dc.contributor.authorGuerra-Junior, Gilpt_BR
dc.contributor.authorWerner, Ralfpt_BR
dc.contributor.authorMello, Maricilda P. dept_BR
dc.subjectSíndrome de resistência a andrógenospt_BR
dc.subjectPré-escolarpt_BR
dc.subjectTécnicas do sistema de duplo-híbridopt_BR
dc.subjectAndrogen-insensitivity syndromept_BR
dc.subjectPreschool childpt_BR
dc.subjectTwo-hybrid system techniquespt_BR
dc.description.abstractAndrogens are responsible for the development and maintenance of male sex characteristics. Dysfunctions in androgen action due to mutations in the androgen receptor gene (AR) can lead to androgen insensitivity syndrome (AIS) that can be classified as mildpt_BR
dc.relation.ispartofSexual developmentpt_BR
dc.relation.ispartofabbreviationSex. dev.pt_BR
dc.publisher.cityBaselpt_BR
dc.publisher.countrySuiçapt_BR
dc.publisherKargerpt_BR
dc.date.issued2017pt_BR
dc.date.monthofcirculationpt_BR
dc.language.isoengpt_BR
dc.description.volume11pt_BR
dc.description.issuenumber5-6pt_BR
dc.description.firstpage238pt_BR
dc.description.lastpage247pt_BR
dc.rightsFechadopt_BR
dc.sourceWOSpt_BR
dc.identifier.issn1661-5425pt_BR
dc.identifier.eissn1661-5433pt_BR
dc.identifier.doi10.1159/000484882pt_BR
dc.identifier.urlhttps://www.karger.com/Article/Abstract/484882pt_BR
dc.description.sponsorshipFAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOpt_BR
dc.description.sponsorshipCNPQ - CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICOpt_BR
dc.description.sponsorship1FAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOpt_BR
dc.description.sponsorship1CNPQ - CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICOpt_BR
dc.description.sponsordocumentnumber2009/08320-9pt_BR
dc.description.sponsordocumentnumber2008/01964-5pt_BR
dc.description.sponsordocumentnumbersem informaçãopt_BR
dc.date.available2021-01-04T20:49:20Z-
dc.date.accessioned2021-01-04T20:49:20Z-
dc.description.provenanceMade available in DSpace on 2021-01-04T20:49:20Z (GMT). No. of bitstreams: 1 000424206100002.pdf: 4263871 bytes, checksum: aac89531278bce6c38f7c1fa8d3a2812 (MD5) Previous issue date: 2017en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/353600-
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentDepartamento de Genética Médicapt_BR
dc.contributor.departmentDepartamento de Pediatriapt_BR
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.unidadeCentro de Biologia Molecular e Engenharia Genéticapt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.contributor.unidadeCentro de Biologia Molecular e Engenharia Genéticapt_BR
dc.identifier.source000424206100002pt_BR
dc.creator.orcid0000-0003-4166-7242pt_BR
dc.creator.orcidsem informaçãopt_BR
dc.creator.orcid0000-0002-2991-7678pt_BR
dc.creator.orcid0000-0003-0521-9100pt_BR
dc.type.formArtigo originalpt_BR
Appears in Collections:IB - Artigos e Outros Documentos
FCM - Artigos e Outros Documentos
CBMEG - Artigos e Outros Documentos

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