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The Annals of Otology, Rhinology, and Laryngology|February 4, 1999
Carotid artery occlusion due to bacterial paranasal sinusitisM Z Ozüer, F N Ardiç, E Coskun, et al.Journal of Pediatric Hematology/Oncology|April 24, 2018
Respiratory Distress and Severe Anemia in a Child With Idiopathic Pulmonary HemosiderosisMünevver T Temel, Levent Temel, Mehmet E Coskun, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|January 1, 2019
Dynamic thiol/disulfide homeostasis in children with community-acquired pneumoniaMünevver Tugba Temel, Seniz Demiryürek, Levent Temel, et al.Biochimica Et Biophysica Acta|April 29, 2008
MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genesVaidya Subramaniam, Pawel Golik, Deborah G Murdock, et al.Cardiology in the Young|April 2, 2019
Determination of dynamic thiol/disulphide homeostasis in children with tetralogy of Fallot and ventricular septal defectMünevver T Temel, Seniz Demiryürek, Ahmet Saracaloglu, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 19, 2001
Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimeticsS Melov, S R Doctrow, J A Schneider, et al.Journal of Alzheimer'S Disease : JAD|May 14, 2010
Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementiaPinar E Coskun, Joanne Wyrembak, Olga Derbereva, et al.Science (New York, N.Y.)|February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutationsWeiwei Fan, Katrina G Waymire, Navneet Narula, et al.Clinical and Translational Science|October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndromePuya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.Neuroscience Letters|July 1, 2009
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndromeHailing Su, Weiwei Fan, Pinar E Coskun, et al.Pageof 6