Yazar "Aktan, Melih" için Rejeneratif ve Restoratif Tıp Araştırmaları Merkezi (REMER) listeleme
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Hereditary spherocytosis associated with defects of human red blood cell membrane
Albeniz, Işıl; Türker Şener, Leyla; Albeniz, Gürcan; Aktan, Melih; Üstek, Duran (Wiley-Blackwell, 2015)... -
Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Türker Şener, Leyla; Aktan, Melih; Albeniz, Gürcan; Şener, Aziz; Üstek, Duran; Albeniz, Işıl (Spandidos Publ Ltd, 2019)Hereditary spherocytosis (HS) is characterized by the morphological transformation of erythrocytes into a spherical shape due to a hereditary defect in cell membrane proteins (ghosts) associated with disruption of erythrocyte ...