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Fatma Busra Isik
Fatma Busra Isik
PhD candidate
Verified email at nottingham.ac.uk
Title
Cited by
Cited by
Year
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
322016
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
242017
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
132016
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
12023
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, ...
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