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Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome

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dc.contributor.authorWoellner, Cristina
dc.contributor.authorGertz, M. E.
dc.contributor.authorSchaffer, Alejandro
dc.contributor.authorLagos, Macarena
dc.contributor.authorPerro, Mario
dc.contributor.authorGlocker, Erik-Oliver
dc.contributor.authorPietrogrande, Maria Cristina
dc.contributor.authorCossu, Fausto
dc.contributor.authorMarin Franco, Jose Luis
dc.contributor.authorMatamoros, N.
dc.contributor.authorPietrucha, Bernard
dc.contributor.authorHeropolitanska-Pliszka, Edyta
dc.contributor.authorYeganch, M.
dc.contributor.authorRezaei, Nima
dc.contributor.authorEspanol, Teresa
dc.contributor.authorEhl, Stephan
dc.contributor.authorGennery, Andrew R.
dc.contributor.authorAbinun, Mario
dc.contributor.authorBreborowicz, Anna
dc.contributor.authorNiehues, Tim
dc.contributor.authorJunker, Anne K.
dc.contributor.authorTurvey, Stuart E.
dc.contributor.authorPlebani, Alessandro
dc.contributor.authorSanchez, Berta Erika Luis
dc.contributor.authorGarty, Ben Zion
dc.contributor.authorPignata, Claudio
dc.contributor.authorCancrini, Caterina
dc.contributor.authorLitzman, Jiří
dc.contributor.authorSanal, Özden
dc.contributor.authorBatimann, U.
dc.contributor.authorBacchetta, Rosa
dc.contributor.authorHsu, Amy P.
dc.contributor.authorDavis, Joie N.
dc.contributor.authorHammarström, Lennart L.G.
dc.contributor.authorDavis, Edward Graham
dc.contributor.authorEren, Efrem
dc.contributor.authorArkwright, Peter D.
dc.contributor.authorMoilanen, Jukka S.
dc.contributor.authorViemann, Dorothee
dc.contributor.authorKhan, Sujoy
dc.contributor.authorMáródi, László D.R.
dc.contributor.authorCant, Andrew James
dc.contributor.authorFreeman, Alexandra F.
dc.contributor.authorPuck, Jennifer M.
dc.contributor.authorHolland, Steven M.
dc.contributor.authorGrimbacher, Bodo
dc.contributor.buuauthorKılıç, Sara Şebnem
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.contributor.researcheridAAH-1658-2021
dc.date.accessioned2022-09-06T07:36:56Z
dc.date.available2022-09-06T07:36:56Z
dc.date.issued2010-04
dc.descriptionBu çalışma, 29-27 Kasım 2009 tarihleri arasında Bath[İngiltere]’da düzenlenen United Kingdom Primary Immunodeficiency Network Immunology Forum’da bildiri olarak sunulmuştur.
dc.description.sponsorshipUK Primary Immunodeficiency Network
dc.identifier.citationWoellner, C. vd. (2010). "Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome". Clinical and Experimental Immunology, 160(Supplement 1), 4-4.
dc.identifier.endpage4
dc.identifier.issn0009-9104
dc.identifier.issn1365-2249
dc.identifier.issueSupplement 1
dc.identifier.startpage4
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878129/?report=reader
dc.identifier.urihttp://hdl.handle.net/11452/28492
dc.identifier.volume160
dc.identifier.wos000276805800010
dc.indexed.wosSCIE
dc.indexed.wosCPCIS
dc.language.isoen
dc.publisherWiley
dc.relation.collaborationYurt içi
dc.relation.collaborationYurt dışı
dc.relation.collaborationSanayi
dc.relation.journalClinical and Experimental Immunology
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectImmunology
dc.subject.wosImmunology
dc.titleMutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome
dc.typeOther
dc.type.subtypeMeeting Abstract
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
local.indexed.atWOS

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