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 *

152 related articles for article (PubMed ID: 3752066)

  • 1. 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]  

  • 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. Sp alpha I/65: a new variant of the alpha subunit of spectrin in hereditary elliptocytosis.
    Lawler J; Coetzer TL; Palek J; Jacob HS; Luban N
    Blood; 1985 Sep; 66(3):706-9. PubMed ID: 4027386
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. A new variant of the alpha subunit of spectrin in hereditary elliptocytosis.
    Lambert S; Zail S
    Blood; 1987 Feb; 69(2):473-8. PubMed ID: 3801663
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A large erythroid spectrin beta-chain variant.
    Johnson RM; Ravindranath Y; Brohn F; Hussain M
    Br J Haematol; 1992 Jan; 80(1):6-14. PubMed ID: 1536811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
    Lane PA; Shew RL; Iarocci TA; Mohandas N; Hays T; Mentzer WC
    J Clin Invest; 1987 Mar; 79(3):989-96. PubMed ID: 3818958
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.