315 related articles for article (PubMed ID: 27247322)
1. Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.
Satchwell TJ; Bell AJ; Hawley BR; Pellegrin S; Mordue KE; van Deursen CT; Braak NH; Huls G; Leers MP; Overwater E; Tamminga RY; van der Zwaag B; Fermo E; Bianchi P; van Wijk R; Toye AM
Haematologica; 2016 Sep; 101(9):1018-27. PubMed ID: 27247322
[TBL] [Abstract][Full Text] [Related]
2. Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2).
van den Akker E; Satchwell TJ; Pellegrin S; Flatt JF; Maigre M; Daniels G; Delaunay J; Bruce LJ; Toye AM
Haematologica; 2010 Aug; 95(8):1278-86. PubMed ID: 20179084
[TBL] [Abstract][Full Text] [Related]
3. The cytoskeletal binding domain of band 3 is required for multiprotein complex formation and retention during erythropoiesis.
Satchwell TJ; Hawley BR; Bell AJ; Ribeiro ML; Toye AM
Haematologica; 2015 Jan; 100(1):133-42. PubMed ID: 25344524
[TBL] [Abstract][Full Text] [Related]
4. Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation.
Salomao M; Chen K; Villalobos J; Mohandas N; An X; Chasis JA
Blood; 2010 Jul; 116(2):267-9. PubMed ID: 20339087
[TBL] [Abstract][Full Text] [Related]
5. [Band 3 deficiency as a cause of hereditary spherocytosis].
Wada H; Suemori S; Nakanishi H; Sugihara T
Rinsho Ketsueki; 2015 Jul; 56(7):837-45. PubMed ID: 26251147
[TBL] [Abstract][Full Text] [Related]
6. Critical band 3 multiprotein complex interactions establish early during human erythropoiesis.
Satchwell TJ; Bell AJ; Pellegrin S; Kupzig S; Ridgwell K; Daniels G; Anstee DJ; van den Akker E; Toye AM
Blood; 2011 Jul; 118(1):182-191. PubMed ID: 21527529
[TBL] [Abstract][Full Text] [Related]
7. Ankyrin and band 3 differentially affect expression of membrane glycoproteins but are not required for erythroblast enucleation.
Ji P; Lodish HF
Biochem Biophys Res Commun; 2012 Jan; 417(4):1188-92. PubMed ID: 22226968
[TBL] [Abstract][Full Text] [Related]
8. Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation.
Nicolas V; Le Van Kim C; Gane P; Birkenmeier C; Cartron JP; Colin Y; Mouro-Chanteloup I
J Biol Chem; 2003 Jul; 278(28):25526-33. PubMed ID: 12719424
[TBL] [Abstract][Full Text] [Related]
9. Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47.
Mouro-Chanteloup I; Delaunay J; Gane P; Nicolas V; Johansen M; Brown EJ; Peters LL; Van Kim CL; Cartron JP; Colin Y
Blood; 2003 Jan; 101(1):338-44. PubMed ID: 12393467
[TBL] [Abstract][Full Text] [Related]
10. Architecture of the human erythrocyte ankyrin-1 complex.
Vallese F; Kim K; Yen LY; Johnston JD; Noble AJ; Calì T; Clarke OB
Nat Struct Mol Biol; 2022 Jul; 29(7):706-718. PubMed ID: 35835865
[TBL] [Abstract][Full Text] [Related]
11. Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.
Hassoun H; Vassiliadis JN; Murray J; Yi SJ; Hanspal M; Ware RE; Winter SS; Chiou SS; Palek J
J Clin Invest; 1995 Dec; 96(6):2623-9. PubMed ID: 8675627
[TBL] [Abstract][Full Text] [Related]
12. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis.
Reliene R; Mariani M; Zanella A; Reinhart WH; Ribeiro ML; del Giudice EM; Perrotta S; Iolascon A; Eber S; Lutz HU
Blood; 2002 Sep; 100(6):2208-15. PubMed ID: 12200387
[TBL] [Abstract][Full Text] [Related]
13. Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cells.
Nicolas V; Mouro-Chanteloup I; Lopez C; Gane P; Gimm A; Mohandas N; Cartron JP; Le Van Kim C; Colin Y
Transfus Clin Biol; 2006; 13(1-2):23-8. PubMed ID: 16580865
[TBL] [Abstract][Full Text] [Related]
14. Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts.
Hanspal M; Hanspal JS; Kalraiya R; Liu SC; Sahr KE; Howard D; Palek J
Blood; 1992 Jul; 80(2):530-9. PubMed ID: 1385736
[TBL] [Abstract][Full Text] [Related]
15. Regulation of band 3 rotational mobility by ankyrin in intact human red cells.
Cho MR; Eber SW; Liu SC; Lux SE; Golan DE
Biochemistry; 1998 Dec; 37(51):17828-35. PubMed ID: 9922149
[TBL] [Abstract][Full Text] [Related]
16. A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis.
Ideguchi H; Nishimura J; Nawata H; Hamasaki N
Br J Haematol; 1990 Mar; 74(3):347-53. PubMed ID: 2139792
[TBL] [Abstract][Full Text] [Related]
17. Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex.
Bruce LJ; Ghosh S; King MJ; Layton DM; Mawby WJ; Stewart GW; Oldenborg PA; Delaunay J; Tanner MJ
Blood; 2002 Sep; 100(5):1878-85. PubMed ID: 12176912
[TBL] [Abstract][Full Text] [Related]
18. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
Hanspal M; Yoon SH; Yu H; Hanspal JS; Lambert S; Palek J; Prchal JT
Blood; 1991 Jan; 77(1):165-73. PubMed ID: 1702027
[TBL] [Abstract][Full Text] [Related]
19. The erythroid niche: molecular processes occurring within erythroblastic islands.
Mohandas N; Chasis JA
Transfus Clin Biol; 2010 Sep; 17(3):110-1. PubMed ID: 20655267
[TBL] [Abstract][Full Text] [Related]
20. Fractional attachment of CD47 (IAP) to the erythrocyte cytoskeleton and visual colocalization with Rh protein complexes.
Dahl KN; Westhoff CM; Discher DE
Blood; 2003 Feb; 101(3):1194-9. PubMed ID: 12393442
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
