226 related articles for article (PubMed ID: 6952254)
1. Defective spectrin dimer-dimer association with hereditary elliptocytosis.
Liu SC; Palek J; Prchal JT
Proc Natl Acad Sci U S A; 1982 Mar; 79(6):2072-6. PubMed ID: 6952254
[TBL] [Abstract][Full Text] [Related]
2. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
Eber SW; Morris SA; Schröter W; Gratzer WB
J Clin Invest; 1988 Feb; 81(2):523-30. PubMed ID: 3276733
[TBL] [Abstract][Full Text] [Related]
3. Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.
Liu SC; Palek J; Prchal J; Castleberry RP
J Clin Invest; 1981 Sep; 68(3):597-605. PubMed ID: 7276161
[TBL] [Abstract][Full Text] [Related]
4. Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
Tomaselli MB; John KM; Lux SE
Proc Natl Acad Sci U S A; 1981 Mar; 78(3):1911-5. PubMed ID: 6940197
[TBL] [Abstract][Full Text] [Related]
5. Defective membrane skeleton assembly in hereditary elliptocytosis.
Liu SC; Palek J; Prchal J
Prog Clin Biol Res; 1981; 56():157-69. PubMed ID: 7330008
[No Abstract] [Full Text] [Related]
6. Defective spectrin dimer-dimer association in a family with transfusion dependent homozygous hereditary elliptocytosis.
Evans JP; Baines AJ; Hann IM; Al-Hakim I; Knowles SM; Hoffbrand AV
Br J Haematol; 1983 Jun; 54(2):163-72. PubMed ID: 6849840
[TBL] [Abstract][Full Text] [Related]
7. Hemolytic anemias associated with deficient or dysfunctional spectrin.
Lux SE; Pease B; Tomaselli MB; John KM; Bernstein SE
Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037
[TBL] [Abstract][Full Text] [Related]
8. Spectrin tetramer-dimer equilibrium in hereditary elliptocytosis.
Coetzer T; Zail S
Blood; 1982 May; 59(5):900-5. PubMed ID: 7074218
[TBL] [Abstract][Full Text] [Related]
9. Spectrin beta-chain variant associated with hereditary elliptocytosis.
Dhermy D; Lecomte MC; Garbarz M; Bournier O; Galand C; Gautero H; Feo C; Alloisio N; Delaunay J; Boivin P
J Clin Invest; 1982 Oct; 70(4):707-15. PubMed ID: 7119110
[TBL] [Abstract][Full Text] [Related]
10. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
Liu SC; Derick LH; Agre P; Palek J
Blood; 1990 Jul; 76(1):198-205. PubMed ID: 2364170
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin.
Dhermy D; Feo C; Garbarz M; Lecomte MC; Bournier O; Chaveroche I; Gautero H; Boivin P; Daffos F; Forestier F
Prenat Diagn; 1987 Sep; 7(7):471-83. PubMed ID: 3671334
[TBL] [Abstract][Full Text] [Related]
12. Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
Zail SS; Coetzer TL
J Clin Invest; 1984 Sep; 74(3):753-62. PubMed ID: 6236232
[TBL] [Abstract][Full Text] [Related]
13. Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants.
Lecomte MC; Garbarz M; Gautero H; Bournier O; Galand C; Boivin P; Dhermy D
Br J Haematol; 1993 Nov; 85(3):584-95. PubMed ID: 8136282
[TBL] [Abstract][Full Text] [Related]
14. A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.
Lecomte MC; Dhermy D; Solis C; Ester A; Féo C; Gautero H; Bournier O; Boivin P
Blood; 1985 May; 65(5):1208-17. PubMed ID: 3922449
[TBL] [Abstract][Full Text] [Related]
15. The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.
Harper SL; Sriswasdi S; Tang HY; Gaetani M; Gallagher PG; Speicher DW
Blood; 2013 Oct; 122(17):3045-53. PubMed ID: 23974198
[TBL] [Abstract][Full Text] [Related]
16. A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
Lawler J; Liu SC; Palek J; Prchal J
J Clin Invest; 1984 Jun; 73(6):1688-95. PubMed ID: 6725555
[TBL] [Abstract][Full Text] [Related]
17. Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.
Dhermy D; Garbarz M; Lecomte MC; Féo C; Bournier O; Chaveroche I; Gautero H; Galand C; Boivin P
Nouv Rev Fr Hematol (1978); 1986; 28(3):129-40. PubMed ID: 3748797
[TBL] [Abstract][Full Text] [Related]
18. Sp alpha I/65 hereditary elliptocytosis in North Africa.
Alloisio N; Guetarni D; Morlé L; Pothier B; Ducluzeau MT; Soun A; Colonna P; Clerc M; Philippe N; Delaunay J
Am J Hematol; 1986 Oct; 23(2):113-22. PubMed ID: 3752066
[TBL] [Abstract][Full Text] [Related]
19. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW
Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.
Tchernia G; Mohandas N; Shohet SB
J Clin Invest; 1981 Aug; 68(2):454-60. PubMed ID: 6894932
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
