BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

38 related articles for article (PubMed ID: 3922449)

  • 1. Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis.
    Ma S; Qin J; Wei A; Li X; Qin Y; Liao L; Lin F
    Mol Med Rep; 2018 Apr; 17(4):5903-5911. PubMed ID: 29484404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Red cell membrane protein abnormalities as defined by sds-page among patients with anemia in a West African region hospital practice.
    Dosunmu A; Uche E; Osikomaiya B; Ismail A; Akinbami A; Akanmu A
    Caspian J Intern Med; 2020 May; 11(3):283-289. PubMed ID: 32874435
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity.
    Risinger M; Christakopoulos GE; Schultz CL; McGann PT; Zhang W; Kalfa TA
    Pediatr Blood Cancer; 2019 Feb; 66(2):e27531. PubMed ID: 30393954
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Impact of malaria on genetic polymorphism and genetic diseases in Africans and African Americans.
    Miller LH
    Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2415-9. PubMed ID: 8146132
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localization and abundance of fodrin during keratinocyte differentiation.
    Younes M; Paus R; Stenn KS; Braverman I; Keh-Yen A
    In Vitro Cell Dev Biol Anim; 1994 Feb; 30A(2):69-74. PubMed ID: 8012656
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
    Sahr KE; Tobe T; Scarpa A; Laughinghouse K; Marchesi SL; Agre P; Linnenbach AJ; Marchesi VT; Forget BG
    J Clin Invest; 1989 Oct; 84(4):1243-52. PubMed ID: 2794061
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormalities in the erythrocyte membrane in acute lymphoid leukaemia.
    Kundu M; Basu J; Chakrabarti P; Rakshit MM
    Biochem J; 1989 Mar; 258(3):903-6. PubMed ID: 2730573
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).
    Morlé L; Roux AF; Alloisio N; Pothier B; Starck J; Denoroy L; Morlé F; Rudigoz RC; Forget BG; Delaunay J
    J Clin Invest; 1990 Aug; 86(2):548-54. PubMed ID: 2384601
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.
    Guetarni D; Roux AF; Alloisio N; Morlé F; Ducluzeau MT; Forget BG; Colonna P; Delaunay J; Godet J
    Hum Genet; 1990 Oct; 85(6):627-30. PubMed ID: 2227954
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
    Tse WT; Lecomte MC; Costa FF; Garbarz M; Feo C; Boivin P; Dhermy D; Forget BG
    J Clin Invest; 1990 Sep; 86(3):909-16. PubMed ID: 1975598
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.
    del Giudice EM; Ducluzeau MT; Alloisio N; Wilmotte R; Delaunay J; Perrotta S; Cutillo S; Iolascon A
    Hum Genet; 1992 Jul; 89(5):553-6. PubMed ID: 1353056
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.