149 related articles for article (PubMed ID: 1487064)
1. Integral band 7 protein of the human erythrocyte membrane.
Stewart GW; Argent AC
Biochem Soc Trans; 1992 Nov; 20(4):785-90. PubMed ID: 1487064
[No Abstract] [Full Text] [Related]
2. Genetic disorders of the red cell membrane.
Delaunay J
Crit Rev Oncol Hematol; 1995 Jun; 19(2):79-110. PubMed ID: 7612181
[No Abstract] [Full Text] [Related]
3. Clinical expression and laboratory detection of red blood cell membrane protein mutations.
Palek J; Jarolim P
Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114
[No Abstract] [Full Text] [Related]
4. [Congenital stomatocytosis with hemolytic anemia--with abnormal cation permeability and defective membrane proteins].
Rix M; Bjerrum PJ; Wieth JO; Frandsen B
Ugeskr Laeger; 1991 Mar; 153(10):724-6. PubMed ID: 2008721
[TBL] [Abstract][Full Text] [Related]
5. Role of N-myristylation in targeting of band 4.2 (pallidin) in nonerythroid cells.
Risinger MA; Korsgren C; Cohen CM
Exp Cell Res; 1996 Dec; 229(2):421-31. PubMed ID: 8986625
[TBL] [Abstract][Full Text] [Related]
6. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane].
Boivin P
J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209
[No Abstract] [Full Text] [Related]
7. The membrane defect in hereditary stomatocytosis.
Stewart GW
Baillieres Clin Haematol; 1993 Jun; 6(2):371-99. PubMed ID: 8043931
[TBL] [Abstract][Full Text] [Related]
8. Cloning and nucleotide sequence of cDNA encoding human erythrocyte band 7 integral membrane protein.
Hiebl-Dirschmied CM; Entler B; Glotzmann C; Maurer-Fogy I; Stratowa C; Prohaska R
Biochim Biophys Acta; 1991 Aug; 1090(1):123-4. PubMed ID: 1883838
[TBL] [Abstract][Full Text] [Related]
9. Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects.
Mohandas N; Evans E
Annu Rev Biophys Biomol Struct; 1994; 23():787-818. PubMed ID: 7919799
[No Abstract] [Full Text] [Related]
10. Genetic disorders of the red cell membranes.
Delaunay J
FEBS Lett; 1995 Aug; 369(1):34-7. PubMed ID: 7641880
[TBL] [Abstract][Full Text] [Related]
11. ATP11C T418N, a gene mutation causing congenital hemolytic anemia, reduces flippase activity due to improper membrane trafficking.
Arashiki N; Niitsuma K; Seki M; Takakuwa Y; Nakamura F
Biochem Biophys Res Commun; 2019 Aug; 516(3):705-712. PubMed ID: 31253392
[TBL] [Abstract][Full Text] [Related]
12. Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells.
Genetet S; Ripoche P; Picot J; Bigot S; Delaunay J; Armari-Alla C; Colin Y; Mouro-Chanteloup I
Am J Physiol Cell Physiol; 2012 Jan; 302(2):C419-28. PubMed ID: 22012326
[TBL] [Abstract][Full Text] [Related]
13. Human erythrocyte membrane protein band 4.2 (pallidin).
Cohen CM; Dotimas E; Korsgren C
Semin Hematol; 1993 Apr; 30(2):119-37. PubMed ID: 8480187
[No Abstract] [Full Text] [Related]
14. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
Bruce LJ
Blood Cells Mol Dis; 2009; 42(3):216-22. PubMed ID: 19261491
[TBL] [Abstract][Full Text] [Related]
15. Stomatocytosis is absent in "stomatin"-deficient murine red blood cells.
Zhu Y; Paszty C; Turetsky T; Tsai S; Kuypers FA; Lee G; Cooper P; Gallagher PG; Stevens ME; Rubin E; Mohandas N; Mentzer WC
Blood; 1999 Apr; 93(7):2404-10. PubMed ID: 10090952
[TBL] [Abstract][Full Text] [Related]
16. [Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology].
Vettore L; De Mattels MC; Bonollo E; De Angelis V; Sorrentino F; Trevisan T; Guarini P; Girelli D; Olivieri O
Haematologica; 1991 Jun; 76 Suppl 3():213-9. PubMed ID: 1752516
[No Abstract] [Full Text] [Related]
17. [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia].
Schröter W; Eber SW
Monatsschr Kinderheilkd; 1989 Jul; 137(7):368-79. PubMed ID: 2677683
[TBL] [Abstract][Full Text] [Related]
18. [Physiopathology of erythrocyte membrane transport].
Brugnara C
Haematologica; 1991 Jun; 76 Suppl 3():191-8. PubMed ID: 1752514
[No Abstract] [Full Text] [Related]
19. Stomatin: a putative cation transport regulator in the red cell membrane.
Stewart GW; Argent AC; Dash BC
Biochim Biophys Acta; 1993 Nov; 1225(1):15-25. PubMed ID: 7694657
[No Abstract] [Full Text] [Related]
20. Identification of the phosphorylation site on human erythrocyte band 7 integral membrane protein: implications for a monotopic protein structure.
Salzer U; Ahorn H; Prohaska R
Biochim Biophys Acta; 1993 Sep; 1151(2):149-52. PubMed ID: 8373790
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]