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Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome Patients.
Chiang SCC, Wood SM, Tesi B, Akar HH, Al-Herz W, Ammann S, Belen FB, Caliskan U, Kaya Z, Lehmberg K, Patiroglu T, Tokgoz H, Ünüvar A, Introne WJ, Henter JI, Nordenskjöld M, Ljunggren HG, Meeths M, Ehl S, Krzewski K, Bryceson YT. Chiang SCC, et al. Among authors: caliskan u. Front Immunol. 2017 Apr 18;8:426. doi: 10.3389/fimmu.2017.00426. eCollection 2017. Front Immunol. 2017. PMID: 28458669 Free PMC article.
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Yılmaz Karapınar D, Patıroğlu T, Metin A, Çalışkan Ü, Celkan T, Yılmaz B, Karakaş Z, Karapınar TH, Akıncı B, Özkınay F, Onay H, Yeşilipek MA, Akar HH, Tüysüz G, Tokgöz H, Özdemir GN, Aslan Kıykım A, Karaman S, Kılınç Y, Oymak Y, Küpesiz A, Olcay L, Keskin Yıldırım Z, Aydoğan G, Gökçe M, İleri T, Aral YZ, Bay A, Atabay B, Kaya Z, Söker M, Özdemir Karadaş N, Özbek U, Özsait Selçuk B, Özdemir HH, Uygun V, Tezcan Karasu G, Yılmaz Ş. Yılmaz Karapınar D, et al. Among authors: caliskan u. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
Three Novel Calreticulin Mutations in Two Turkish Patients.
Hançer VS, Tokgöz H, Güvenç S, Çalışkan Ü, Büyükdoğan M. Hançer VS, et al. Among authors: caliskan u. Turk J Haematol. 2017 Dec 1;34(4):360-361. doi: 10.4274/tjh.2017.0146. Epub 2017 Jul 27. Turk J Haematol. 2017. PMID: 28747287 Free PMC article. No abstract available.
Ophthalmic manifestations in recently diagnosed childhood leukemia.
Bitirgen G, Belviranli S, Caliskan U, Tokgoz H, Ozkagnici A, Zengin N. Bitirgen G, et al. Among authors: caliskan u. Eur J Ophthalmol. 2016 Jan-Feb;26(1):88-91. doi: 10.5301/ejo.5000647. Epub 2015 Jul 3. Eur J Ophthalmol. 2016. PMID: 26165325
81 results