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Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|December 26, 2014
ALCAM is indirectly modulated by miR-125b in MCF7 cellsH Begum Akman, S Duygu Selcuklu, Mark T A Donoghue, et al.European Journal of Radiology|December 22, 2023
Identification of IDH and TERTp mutations using dynamic susceptibility contrast MRI with deep learning in 162 gliomasBuse Buz-Yalug, Gulce Turhan, Ayse Irem Cetin, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 26, 2015
Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31Yasar Bayri, Burcak Soylemez, Askin Seker, et al.BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.Proceedings of the National Academy of Sciences of the United States of America|February 8, 2006
Reprogramming of replicative senescence in hepatocellular carcinoma-derived cellsNuri Ozturk, Esra Erdal, Mine Mumcuoglu, et al.European Journal of Human Genetics : EJHG|May 7, 2015
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palateJeroen Breckpot, Britt-Marie Anderlid, Yasemin Alanay, et al.Neuromuscular Disorders : NMD|December 18, 2003
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycanPervin Dinçer, Burcu Balci, Yeliz Yuva, et al.Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.The Journal of Allergy and Clinical Immunology|November 21, 2017
Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiencyErsin Gul, Esra Hazar Sayar, Bilgi Gungor, et al.Pageof 3