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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

236 related articles for article (PubMed ID: 3604989)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia.
    Dhermy D; Lecomte MC; Garbarz M; Feo C; Gautero H; Bournier O; Galand C; Herrera A; Gretillat F; Boivin P
    Pediatr Res; 1984 Oct; 18(10):1005-12. PubMed ID: 6493844
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Partial spectrin deficiency in hereditary pyropoikilocytosis.
    Coetzer TL; Palek J
    Blood; 1986 Apr; 67(4):919-24. PubMed ID: 3955236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.