Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Duygu Dölen"'
Autor:
Doğan Güçlühan Güçlü, Duygu Dölen
Publikováno v:
Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy. 18:323-329
Autor:
Tuğrul Ünal, Metehan Öztürk, İlyas Dolaş, Musa Özata, Duygu Dölen, Ümmü Mutlu, Ayşe Ok, Nurdan Gül, Özlem Soyluk Selçukbiricik, Ayşe Kubat Üzüm, Sema Yarman, Pulat Sabancı, Yavuz Aras, Altay Sencer, Aydın Aydoseli
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi.
Autor:
Tugrul Cem Unal, Altay Sencer, Ilyas Dolas, Cafer Ikbal Gulsever, Duran Sahin, Duygu Dolen, Musa Samet Ozata, Metehan Ozturk, Yavuz Aras, Aydin Aydoseli
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/4cea9972673249c4a58d03734459f536
Autor:
Tugrul Cem Unal, Altay Sencer, Ilyas Dolas, Cafer Ikbal Gulsever, Duran Sahin, Duygu Dolen, Musa Samet Ozata, Metehan Ozturk, Yavuz Aras, Aydin Aydoseli
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
IntroductionColloid cysts (CCs) are rare benign lesions that usually arise from the roof of the third ventricle. They may present with obstructive hydrocephalus and cause sudden death. Treatment options include ventriculoperitoneal shunting, cyst asp
Externí odkaz:
https://doaj.org/article/798141d95cdd4a1b8f24463b2d02efb9
Autor:
Sinan Çomu, Hudson H. Freeze, Gozde Tugce Akgumus, Ketu Mishra-Gorur, Ahmet Okay Caglayan, Akdes Serin Harmanci, Murat Gunel, Jacob F Baranoski, Katsuhito Yasuno, Duygu Dölen, Emine Z. Erson-Omay, Caner Çağlar, Kaya Bilguvar, Hande Kaymakçalan, Yesim Parman
N-glycanase 1 (NGLY1) is a conserved enzyme that is responsible for the deglycosylation of misfolded N-glycosylated proteins in the cytoplasm prior to their proteasome-mediated degradation. Disruption of this degradation process has been associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a56412f106cd6f80a326f05ba957696b
http://hdl.handle.net/20.500.12645/29115
http://hdl.handle.net/20.500.12645/29115
Autor:
Jana Schroth, William B. Dobyns, Hülya Kayserili, Jean-Baptiste Rivière, Haig Keshishian, Murat Gunel, Katsuhito Yasuno, Neil C. Chi, Shrikant Mane, Duygu Dölen, Burçin Baran, Richard P. Lifton, Caner Çağlar, Ahmet Okay Caglayan, Heba A.A. Hossni, Hüseyin Per, Ashleigh E. Schaffer, E. Zeynep Erson-Omay, Octavian Henegariu, Sefer Kumandaş, Cengiz Dilber, Fernando Vonhoff, Chiswili Chabu, Jacob F Baranoski, Wenqi Han, Kaya Bilguvar, Tian Xu, Gozde Tugce Akgumus, Rasim Ozgur Rosti, Hakan Gümüş, Shu Tu, Ketu Mishra-Gorur, Sayoko Nishimura, Emily Spencer, Nenad Sestan, Frank J. Minja, Joseph G. Gleeson, Maha S. Zaki, Çağri Çağlar, Angeliki Louvi
SummaryExome sequencing analysis of over 2,000 children with complex malformations of cortical development identified five independent (four homozygous and one compound heterozygous) deleterious mutations in KATNB1, encoding the regulatory subunit of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa601c2692c65701d6fcc4dcbef7d0f9
http://hdl.handle.net/20.500.12645/29101
http://hdl.handle.net/20.500.12645/29101
Autor:
Sefa Ozturk, Duygu Dolen, Tugrulcem Unal, Ilyas Dolas, Pulatakin Sabanci, Yavuz Aras, Aydin Aydoseli, Altay Sencer
Publikováno v:
Brain and Spine, Vol 3, Iss , Pp 102288- (2023)
Externí odkaz:
https://doaj.org/article/a8b6b45fdb4247ce8ce38f3d44207154