Screening of new antileukemic agents from essential oils of algae extracts and computational modeling of their interactions with intracellular signaling nodes B Atasever-Arslan, K Yilancioglu, Z Kalkan, AC Timucin, H Gür, FB Isik, ... European Journal of Pharmaceutical Sciences 83, 120-131, 2016 | 32 | 2016 |
Apoptotic effect of Nigella sativa on human lymphoma U937 cells BA Arslan, FB Isik, H Gur, F Ozen, T Catal Pharmacognosy magazine 13 (Suppl 3), S628, 2017 | 24 | 2017 |
High plasma pentraxin 3 levels in diabetic polyneuropathy patients with nociceptive pain C Salcini, B Atasever-Arslan, G Sunter, H Gur, FB Isik, CC Saylan, ... The Tohoku Journal of Experimental Medicine 239 (1), 73-79, 2016 | 13 | 2016 |
Extracellular vesicle microRNA-mediated transcriptional regulation may contribute to dementia with Lewy bodies molecular pathology FB Isik, HM Knight, AP Rajkumar Acta Neuropsychiatrica, 1-10, 2023 | 1 | 2023 |
Іn vitro ANTILEUKEMIC ACTIVITY OF Euphorbia echinus EXTRACT H Sbayou, H Gür, F Özen, FB Işik, S Amghar, A Elharti, M Konuk, ... Biotechnologia Acta 15 (6), 70-74, 2022 | | 2022 |
A novel homozygous nonsense mutation (p. R516X) in the SLC5A5 gene causing congenital hypothyroidism FB Isik, MD Sozuguzel, BK Aydin, C Parlayan, M Yildiz, H Cangul EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1248-1249, 2019 | | 2019 |
A novel candidate frameshift mutation for Catecholaminergic Polymorphic Ventricular Tachycardia FB Isik, MD Sozuguzel, N Genc, EF Caralan, Z Dogru, C Akdeniz, V Tuzcu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 143-143, 2019 | | 2019 |
A novel homozygous nonsense mutation (p. R516X) in the SLC5A5 gene causing congenital hypothyroidism FB Işık, MD Sözügüzel, B Kılıçoğlu Aydın, C Parlayan, M Yıldız, H Cangül 52nd Conference of the European-Society-of-Human-Genetics (ESHG), 2019 | | 2019 |
Akraba evliliği bulunan konjenital hipotiroidi hastalarında yeni varyasyonların keşfi FB Işık İstanbul Medipol Üniversitesi Sağlık Bilimleri Enstitüsü, 2019 | | 2019 |
The investigation of genetic etiology in familial cases with congenital hypothyroidism AD Kardelen Al, FB Işık, E Karakılıç Özturan, MD Sözügüzel, AP Öztürk, ... Hormone Research In Paediatrics, 2019 | | 2019 |
A novel candidate frameshift mutation for catecholaminergic polymorphic ventricular tchycardia FB Işık, MD Sözügüzel, NM Genç, EF Çaralan, Z Doğru, C Akdeniz, ... 51st Conference of the European-Society-of-Human-Genetics (ESHG) in …, 2019 | | 2019 |
A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome MD Sözügüzel, FB Işık, NM Genç, EF Çaralan, Z Doğru, C Akdeniz, ... 51st Conference of the European-Society-of-Human-Genetics (ESHG) in …, 2019 | | 2019 |
Antileukemic Drug Potentials of Essential Oils of Algea Extracts BA Arslan, K Yilancioglu, Z Kalkan, VE Atalay, H Gur, FB Isik, E Deniz, ... ACTA PHYSIOLOGICA 215, 15-15, 2015 | | 2015 |
Oral Communications BA Arslan, K Yılancıoğlu, Z Kalkan, VE Atalay, H Gür, FB Işık, E Deniz, ... | | |
The investigation of genetic etiology in familial cases with congenital hypothyroidism FB Isik, EK Ozturan, MD Sozuguzel, AP Ozturk, C Parlayan, H CANGÜL, ... | | |