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Impaired melanocortin pathway function in prader-willi syndrome gene-magel2 deficient mice

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dc.authorid0000-0001-9192-5014
dc.authorid0000-0003-4604-4765
dc.authorid0000-0002-5198-3559
dc.authorid0000-0002-3247-613X
dc.authorid0000-0002-3325-8820
dc.contributor.authorÖncül, Merve
dc.contributor.authorDilsiz, Pelin
dc.contributor.authorAteş Öz, Edanur
dc.contributor.authorAteş, Tayfun
dc.contributor.authorAklan, İltan
dc.contributor.authorÇelik, Eşref
dc.contributor.authorSayar Atasoy, Nilüfer
dc.contributor.authorAtasoy, Deniz
dc.date.accessioned2021-01-13T07:51:31Z
dc.date.available2021-01-13T07:51:31Z
dc.date.issued2018
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Rejeneratif ve Restoratif Tıp Araştırmaları Merkezi (REMER)
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Fizyoloji Ana Bilim Dalı
dc.description.abstract[Abstract Not Available]
dc.description.sponsorshipTurkish Neuroendocrinology Societyen_US
dc.identifier.citationÖncül, M., Dilsiz, P., Ateş Öz, E., Ateş, T., Aklan, İ., Çelik, E. ... Atasoy, D. (2018). Impaired melanocortin pathway function in prader-willi syndrome gene-magel2 deficient mice. 3rd International Congress of the Turkish-Neuroendocrinology-Society içinde (7-7. ss.). Malatya, Turkey, June 29-July 01, 2018.
dc.identifier.endpage7
dc.identifier.issn0028-3835
dc.identifier.issn1423-0194
dc.identifier.issueSupplement: 1
dc.identifier.startpage7
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6234
dc.identifier.volume107
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherKarger
dc.relation.ispartof3rd International Congress of the Turkish-Neuroendocrinology-Societyen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectWilli Syndrome Gene
dc.subjectPathway Function
dc.subjectMagel2
dc.titleImpaired melanocortin pathway function in prader-willi syndrome gene-magel2 deficient mice
dc.typeConference Object

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