𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis

✍ Scribed by Selen Peker; Nejat Akar; Duygu Ozel Demiralp


Publisher
Springer
Year
2011
Tongue
English
Weight
463 KB
Volume
39
Category
Article
ISSN
0301-4851

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Membrane cation and anion transport acti
✍ De Franceschi, Lucia; Olivieri, Oliviero; del Giudice, Emanuele Miraglia; Perrot πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 158 KB πŸ‘ 1 views

Hereditary spherocytosis (HS) is due to different membrane protein defects (i.e., deficiency of spectrin and ankyrin, band 3, or band 4.2). In order to gain new insight into the relationships between band 3 function and proteins associated with the cytoskeleton, we studied erythrocyte anion transpor

Increased adsorption of cytoplasmic prot
✍ David W. Allen; Jerome D. Groat; Barbara Finkel; Brian H. Rank; Patricia A. Wood πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 English βš– 893 KB

## Abstract How the metabolic defect of pyruvate kinase deficiency (PK(–)) accelerates red blood cell (RBC) destruction is not established, but may be related to RBC membrane abnormalities associated with altered cellular metabolism. Furthermore, it has been shown that PK(–) reticulocytes are espec