These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
157 related articles for article (PubMed ID: 8755921)
1. Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis. Gallagher PG; Kotula L; Wang Y; Marchesi SL; Curtis PJ; Speicher DW; Forget BG Am J Hum Genet; 1996 Aug; 59(2):351-9. PubMed ID: 8755921 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Genetic basis of the polymorphisms of the alphaI domain of spectrin. Gallagher PG; Romana M; Wong C; Forget BG Am J Hematol; 1997 Oct; 56(2):107-11. PubMed ID: 9326352 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes. Lecomte MC; Garbarz M; Grandchamp B; Féo C; Gautero H; Devaux I; Bournier O; Galand C; d'Auriol L; Galibert F Blood; 1989 Aug; 74(3):1126-33. PubMed ID: 2568862 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis. Gallagher PG; Forget BG Blood Cells Mol Dis; 1996; 22(3):254-8. PubMed ID: 9075575 [No Abstract] [Full Text] [Related]
11. 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]
12. Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants. Vives-Corrons JL; Krishnevskaya E; Hernández-Rodriguez I; Payán-Pernia S; Sevilla ÁFR; Badell I Ann Hematol; 2022 Mar; 101(3):549-555. PubMed ID: 34845540 [TBL] [Abstract][Full Text] [Related]
13. Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion. Gallagher PG; Roberts WE; Benoit L; Speicher DW; Marchesi SL; Forget BG Blood; 1993 Oct; 82(7):2210-5. PubMed ID: 8400271 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site. Parquet N; Devaux I; Boulanger L; Galand C; Boivin P; Lecomte MC; Dhermy D; Garbarz M Blood; 1994 Jul; 84(1):303-8. PubMed ID: 8018926 [TBL] [Abstract][Full Text] [Related]
17. An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphism. Dalla Venezia N; Wilmotte R; Morlé L; Forissier A; Parquet N; Garbarz M; Rousset T; Dhermy D; Alloisio N; Delaunay J Hum Genet; 1993 Feb; 90(6):641-4. PubMed ID: 8444470 [TBL] [Abstract][Full Text] [Related]
18. Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes. Shome DK; Das P; Akbar GA; Taha S; Radhi A; Al-Saad K; Helmy R Ann Hematol; 2023 Sep; 102(9):2343-2351. PubMed ID: 37400730 [TBL] [Abstract][Full Text] [Related]
19. Erythrocytes carrying mutations in spectrin and protein 4.1 show differing sensitivities to invasion by Plasmodium falciparum. Facer CA Parasitol Res; 1995; 81(1):52-7. PubMed ID: 7724514 [TBL] [Abstract][Full Text] [Related]
20. Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site. Gaetani M; Mootien S; Harper S; Gallagher PG; Speicher DW Blood; 2008 Jun; 111(12):5712-20. PubMed ID: 18218854 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]