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A highly efficient and faithful MDS patient-derived xenotransplantation model for pre-clinical studies
Song, Yuanbin, Rongvaux, Anthony, Taylor, Ashley, Jiang, Tingting, Tebaldi, Toma, Balasubramanian, Kunthavai, Bagale, Arun, Terzi, Yunus Kasim, Gbyli, Rana, Wang, Xiaman, Fu, Xiaoying, Gao, Yimeng, Zhao, Jun, Podoltsev, Nikolai, Xu, Mina, Neparidze, Natalia, Wong, Ellice, Torres, Richard, Bruscia, Emanuela M., Kluger, Yuval, Manz, Markus G., Flavell, Richard A., Halene, Stephanie
Published in Nature communications (21.01.2019)
Published in Nature communications (21.01.2019)
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Random X chromosome inactivation in female Charcot-Marie-Tooth disease type X1: insights from sural nerve biopsy analysis
Bekircan-Kurt, Can Ebru, Aksu-Menges, Evrim, Kumtepe, Eray Taha, Durmaz, Ceren Damla, Terzi, Yunus Kasim, Ergul-Ulger, Zeynep, Temucin, Çagri Mesut, Erdem-Ozdamar, Sevim, Tan, Ersin, Balci-Hayta, Burcu
Published in BMC neurology (04.08.2025)
Published in BMC neurology (04.08.2025)
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Associations between IL-1α, IL-1β, TNFα, and IL-6 variations, and susceptibility to transposition of the great arteries
Atasoy Karakas, Latife, Tugrul, Duygu, Sahin Uysal, Nihal, Esin, Sertac, Tokel, Niyazi Kursat, Terzi, Yunus Kasim
Published in BMC cardiovascular disorders (19.05.2022)
Published in BMC cardiovascular disorders (19.05.2022)
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Placental Maspin Gene Expression Pattern May Be Used to Distinguish Between Preeclampsia and Intrauterine Growth Restriction
Onalan, Gogsen, Terzi, Yunus Kasim, Tohma, Yusuf Aytac, Yurtcu, Erkan, Kuscu, Esra, Sahin, Feride Iffet, Zeyneloglu, Hulusi Bulent
Published in Gynecology, obstetrics & reproductive medicine : GORM (01.08.2021)
Published in Gynecology, obstetrics & reproductive medicine : GORM (01.08.2021)
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A newborn case diagnosed as ısolated TBX1 deletion with 22q11 deletion syndrome
TURAN, Özden, YILMAZ ÇELİK, Zerrin, ANUK INCE, Deniz, TERZİ, Yunus Kasım, ECEVİT, Ayşe
Published in Cukurova Medical Journal (01.01.2020)
Published in Cukurova Medical Journal (01.01.2020)
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Fractalkine receptor polymorphism and chronic tonsillitis
Babakurban, Seda Turkoglu, Erbek, Selim S., Terzi, Yunus Kasim, Arslan, Fatih, Sahin, Feride I.
Published in European archives of oto-rhino-laryngology (01.07.2014)
Published in European archives of oto-rhino-laryngology (01.07.2014)
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Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients
Terzi, Yunus Kasim, Oguzkan, Sibel, Anlar, Banu, Aysun, Sabiha, Ayter, Sukriye
Published in Pediatric neurology (01.12.2007)
Published in Pediatric neurology (01.12.2007)
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The differences in the expression of fractalkine and its receptor in conditions of tonsillar hypertrophy and chronic tonsillitis
Koclu Hetemoglu, Elif, Turkoglu Babakurban, Seda, Terzi, Yunus Kasım, Sahin, Feride Iffet, Erbek, Selim Sermed
Published in Auris, nasus, larynx (01.08.2019)
Published in Auris, nasus, larynx (01.08.2019)
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Associations between IL-1[alpha], IL-1[beta], TNF[alpha], and IL-6 variations, and susceptibility to transposition of the great arteries
Atasoy Karakas, Latife, Tugrul, Duygu, Sahin Uysal, Nihal, Esin, Sertac, Tokel, Niyazi Kursat, Terzi, Yunus Kasim
Published in BMC cardiovascular disorders (19.05.2022)
Published in BMC cardiovascular disorders (19.05.2022)
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Determination of the Frequency of BCL-2 Polymorphisms (c.-717C>A and c.2364G>A) and LIF Polymorphism (c.1414T>G) in Patients with Congenital Anomalies of the Kidney and Urinary Tract
Oztepe, Tugce, Sahin, Feride Iffet, Caltik Yilmaz, Aysun, Baskin, Esra, Haberal, Mehmet, Terzi, Yunus Kasim
Published in Molecular syndromology (01.10.2024)
Published in Molecular syndromology (01.10.2024)
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Coronin 1A inhibits neurite outgrowth in PC12 cells
Terzi, Yunus Kasim, Kocaefe, Yusuf Cetin, Ayter, Sukriye
Published in Neuroscience letters (17.10.2014)
Published in Neuroscience letters (17.10.2014)
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Impact of Matrix Metalloproteinases 2 and 9 and Tissue Inhibitor of Metalloproteinase 2 Gene Polymorphisms on Allograft Rejection in Pediatric Renal Transplant Recipients
Akad Dincer, Selin, Sahin, Feride Iffet, Terzi, Yunus Kasim, Gulleroglu, Kaan, Baskin, Esra, Haberal, Mehmet
Published in Experimental and clinical transplantation (01.04.2023)
Published in Experimental and clinical transplantation (01.04.2023)
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Rare STAT3 haplotypes cause a predisposition to developing congenital anomalies of the kidney and urinary tract disorder
Polat, Mert, Şahin, Feride İffet, Baskin, Esra, Toprak, Uğur, Gülleroğlu, Kaan Savaş, Haberal, Mehmet, Terzi, Yunus Kasım
Published in Turkish journal of medical sciences (01.01.2024)
Published in Turkish journal of medical sciences (01.01.2024)
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Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients
Terzi, Yunus Kasım, Bulakbaşı Balcı, Tuğçe, Boğa, Can, Koç, Zafer, Yılmaz Çelik, Zerrin, Özdoğu, Hakan, Karakuş, Sema, İffet Şahin, Feride
Published in Turkish journal of haematology (01.12.2016)
Published in Turkish journal of haematology (01.12.2016)
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