181 related articles for article (PubMed ID: 6863544)
1. Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis.
Knowles WJ; Morrow JS; Speicher DW; Zarkowsky HS; Mohandas N; Mentzer WC; Shohet SB; Marchesi VT
J Clin Invest; 1983 Jun; 71(6):1867-77. PubMed ID: 6863544
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit.
Lawler J; Palek J; Liu SC; Prchal J; Butler WM
Blood; 1983 Dec; 62(6):1182-9. PubMed ID: 6640107
[TBL] [Abstract][Full Text] [Related]
6. Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities.
Iarocci TA; Wagner GM; Mohandas N; Lane PA; Mentzer WC
Blood; 1988 May; 71(5):1390-6. PubMed ID: 3359047
[TBL] [Abstract][Full Text] [Related]
7. Altered spectrin association and membrane fragility without abnormal spectrin heat sensitivity in a case of congenital hemolytic anemia.
Ravindranath Y; Johnson RM
Am J Hematol; 1985 Sep; 20(1):53-65. PubMed ID: 4025321
[TBL] [Abstract][Full Text] [Related]
8. Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis.
Hanspal M; Hanspal JS; Sahr KE; Fibach E; Nachman J; Palek J
Blood; 1993 Sep; 82(5):1652-60. PubMed ID: 8364214
[TBL] [Abstract][Full Text] [Related]
9. Effect of heat on the circular dichroism of spectrin in hereditary pyropoikilocytosis.
Chang K; Williamson JR; Zarkowsky HS
J Clin Invest; 1979 Jul; 64(1):326-8. PubMed ID: 447859
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Severe recessive poikilocytic anaemia with a new spectrin alpha chain variant.
Lecomte MC; Feo C; Gautero H; Bournier O; Galand C; Garbarz M; Boivin P; Dhermy D
Br J Haematol; 1990 Apr; 74(4):497-507. PubMed ID: 2346729
[TBL] [Abstract][Full Text] [Related]
13. Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis.
Peterson LC; Dampier C; Coetzer T; Lawler J; White J; Palek J
Am J Clin Pathol; 1987 Jul; 88(1):58-65. PubMed ID: 3604989
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.
Gallagher PG; Tse WT; Coetzer T; Lecomte MC; Garbarz M; Zarkowsky HS; Baruchel A; Ballas SK; Dhermy D; Palek J
J Clin Invest; 1992 Mar; 89(3):892-8. PubMed ID: 1541680
[TBL] [Abstract][Full Text] [Related]
17. [Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry].
Dhermy D; Féo C; Garbarz M; Bournier O; Dommergues JP; Garcia J; Boivin P; Tchernia G
Nouv Rev Fr Hematol (1978); 1983; 25(1):7-16. PubMed ID: 6835836
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression.
Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Galand C; Boivin P
Hum Genet; 1987 Dec; 77(4):329-34. PubMed ID: 3692477
[TBL] [Abstract][Full Text] [Related]
20. Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis.
Palek J; Liu SC; Liu PY; Prchal J; Castleberry RP
Blood; 1981 Jan; 57(1):130-9. PubMed ID: 7448405
[No Abstract] [Full Text] [Related]
[Next] [New Search]