ORCID "0000-0003-4604-4765" PubMed İndeksli Yayınlar Koleksiyonu için listeleme
-
Impaired melanocortin pathway function in prader-willi syndrome gene-magel2 deficient mice
Öncül, Merve; Dilsiz, Pelin; Ateş Öz, Edanur; Ateş, Tayfun; Aklan, İltan; Çelik, Eşref; Sayar Atasoy, Nilüfer; Atasoy, Deniz (Oxford University Press, 2018)Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder causing social and learning deficits, impaired satiety and severe childhood obesity. Genetic underpinning of PWS involves deletion of a chromosomal region with ... -
Inactivation of Magel2 suppresses oxytocin neurons through synaptic excitation-inhibition imbalance
Ateş, Tayfun; Öncül, Merve; Dilsiz, Pelin; Topçu, İskalen Cansu; Cıvaş, Cihan Civan; Alp, Muhammed İkbal; Aklan, İltan; Öz, Edanur Ateş; Yavuz, Yavuz; Yılmaz, Bayram; Atasoy, Nilüfer Sayar; Atasoy, Deniz (Academic Press Inc Elsevier Science, 2019)Prader-Willi and the related Schaaf-Yang Syndromes (PWS/SYS) are rare neurodevelopmental disorders characterized by overlapping phenotypes of high incidence of autism spectrum disorders (ASD) and neonatal feeding difficulties. ... -
MCH neuron activity ıs sufficient for reward and reinforces feeding
Dilsiz, Pelin; Aklan, İltan; Sayar Atasoy, Nilufer; Yavuz, Yavuz; Filiz, Gizem; Köksalar, Fulya; Ateş, Tayfun; Öncül, Merve; Çoban, İlknur; Ateş Öz, Edanur; Cebecioğlu, Utku; Alp, Muhammed İkbal; Yılmaz, Bayram; Atasoy, Deniz (Karger, 2020)Background: Melanin-concentrating hormone (MCH)-expressing neurons have been implicated in regulation of energy homeostasis and reward, yet the role of their electrical activity in short-term appetite and reward modulation ...