207 related articles for article (PubMed ID: 6725555)
1. 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]
2. 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]
3. 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]
4. Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
Marchesi SL; Letsinger JT; Speicher DW; Marchesi VT; Agre P; Hyun B; Gulati G
J Clin Invest; 1987 Jul; 80(1):191-8. PubMed ID: 3597773
[TBL] [Abstract][Full Text] [Related]
5. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G
Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784
[TBL] [Abstract][Full Text] [Related]
6. Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.
Lawler J; Liu SC; Palek J; Prchal J
J Clin Invest; 1982 Nov; 70(5):1019-30. PubMed ID: 7130392
[TBL] [Abstract][Full Text] [Related]
7. Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.
Palek J; Coetzer T
Blood Cells; 1987; 13(1-2):237-50. PubMed ID: 3311220
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variant.
Lecomte MC; Gautero H; Garbarz M; Boivin P; Dhermy D
Br J Haematol; 1990 Nov; 76(3):406-13. PubMed ID: 2261350
[TBL] [Abstract][Full Text] [Related]
10. Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis.
Lawler J; Coetzer TL; Mankad VN; Moore RB; Prchal JT; Palek J
Blood; 1988 Oct; 72(4):1412-5. PubMed ID: 3167214
[TBL] [Abstract][Full Text] [Related]
11. Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis.
Coetzer T; Lawler J; Prchal JT; Palek J
Blood; 1987 Sep; 70(3):766-72. PubMed ID: 3620700
[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. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.
Floyd PB; Gallagher PG; Valentino LA; Davis M; Marchesi SL; Forget BG
Blood; 1991 Sep; 78(5):1364-72. PubMed ID: 1878597
[TBL] [Abstract][Full Text] [Related]
14. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.
Garbarz M; Lecomte MC; Féo C; Devaux I; Picat C; Lefebvre C; Galibert F; Gautero H; Bournier O; Galand C
Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis.
Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Ester A; Galand C
Hum Genet; 1985; 71(4):351-7. PubMed ID: 4077050
[TBL] [Abstract][Full Text] [Related]
17. Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis.
Dhermy D; Garbarz M; Lecomte MC; Chaveroche I; Bournier O; Gautero H; Blot I; Boivin P
Hum Genet; 1986 Dec; 74(4):363-7. PubMed ID: 3793099
[TBL] [Abstract][Full Text] [Related]
18. Viscoelastic properties of red cell membrane in hereditary elliptocytosis.
Chabanel A; Sung KL; Rapiejko J; Prchal JT; Palek J; Liu SC; Chien S
Blood; 1989 Feb; 73(2):592-5. PubMed ID: 2917191
[TBL] [Abstract][Full Text] [Related]
19. Hereditary elliptocytosis with a spectrin molecular defect in a white patient.
Lecomte MC; Dhermy D; Garbarz M; Gautero H; Bournier O; Galand C; Boivin P
Acta Haematol; 1984; 71(4):235-40. PubMed ID: 6426236
[TBL] [Abstract][Full Text] [Related]
20. Abnormal spectrin in hereditary elliptocytosis.
Marchesi SL; Knowles WJ; Morrow JS; Bologna M; Marchesi VT
Blood; 1986 Jan; 67(1):141-51. PubMed ID: 3940543
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
