Výsledky vyhledávání - "DURLU, YUSUF K."

Akademický článek

A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis.

Autor: Iseri, Sibel A. Ugur¹, Durlu, Yusuf K.², Tolun, Aslihan¹ tolun@boun.edu.tr

Publikováno v: European Journal of Human Genetics. Oct2010, Vol. 18 Issue 10, p1121-1126. 6p. 3 Diagrams, 2 Charts, 2 Graphs.

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Novel Recessive Cone-Rod Dystrophy Caused By Poc1B Mutation

Autor: Durlu, Yusuf K., Koroglu, Cigdem, Tolun, Aslihan

IMPORTANCE A new form of cone-rod dystrophy (CORD) is described and the gene responsible for the disease is identified.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::f554e0221019cfa9293c332e72fcc538
https://aperta.ulakbim.gov.tr/record/61637

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Akademický článek

Characteristics of the P100 wave in Behçet's disease.

Autor: Durlu, Yusuf K., Mudun, A. Baki, Tanik, Osman, Agaoglu, Jale, Bulut, Serpil, Arslan, M. Okan

Publikováno v: Neuro-Ophthalmology; 1997, Vol. 17 Issue 4, p201-209, 9p

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Periodical

Response of Müller cells following experimental lensectomy-vitrectomy

Autor: Durlu, Yusuf K., Ishiguro, Sei-ichi, Yoshida, Akiko, Mito, Takezo, Tsuchiya, Makio, Tamai, Makoto

Publikováno v: Graefe's Archive for Clinical and Experimental Ophthalmology; January 1990, Vol. 228 Issue: 1 p44-48, 5p

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Periodical

Transplantation of Retinal Pigment Epithelium Using Viable Cryopreserved Cells

Autor: Durlu, Yusuf K., Tamai, Makoto

Publikováno v: Cell Transplantation; March 1997, Vol. 6 Issue: 2 p149-162, 14p

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Periodical

The Properties of Retinal Pigment Epithelial Cells in Proliferative Vitreoretinopathy Compared with Cultured Retinal Pigment Epithelial Cells

Autor: ABE, TOSHIAKI, DURLU, YUSUF K., TAMAI, MAKOTO

Publikováno v: Experimental Eye Research; August, 1996, Vol. 63 Issue: 2 p201-210, 10p

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Periodical

Identification of a Novel Isoform of Microphthalmia-Associated Transcription Factor That Is Enriched in Retinal Pigment Epithelium

Autor: Amae, Shintaro, Fuse, Nobuo, Yasumoto, Ken-ichi, Sato, Shigeru, Yajima, Ichiro, Yamamoto, Hiroaki, Udono, Tetsuo, Durlu, Yusuf K., Tamai, Makoto, Takahashi, Kazuhiro, Shibahara, Shigeki

Publikováno v: Biochemical and Biophysical Research Communications; June 29, 1998, Vol. 247 Issue: 3 p710-715, 6p

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Akademický článek

Novel recessive cone-rod dystrophy caused by POC1B mutation.

Autor: Durlu YK; Makula Eye Health, Fahrettin Kerim Gökay caddesi Çamtepe sokak 2/5, Göztepe, Kadiköy 34724 Istanbul, Turkey., Köroğlu Ç; Department of Molecular Biology and Genetics, Bogaziçi University, Istanbul, Turkey., Tolun A; Department of Molecular Biology and Genetics, Bogaziçi University, Istanbul, Turkey.

Publikováno v: JAMA ophthalmology [JAMA Ophthalmol] 2014 Oct; Vol. 132 (10), pp. 1185-91.

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Akademický článek

A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis.

Autor: Ugur Iseri SA; Department of Molecular Biology and Genetics, Boğaziçi University, Istanbul, Turkey., Durlu YK, Tolun A

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Oct; Vol. 18 (10), pp. 1121-6. Date of Electronic Publication: 2010 Jun 02.

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