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Journal Abstract Search

195 related items for PubMed ID: 3186715

  • 1. Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.
    Birkenmeier CS, McFarland-Starr EC, Barker JE.
    Proc Natl Acad Sci U S A; 1988 Nov; 85(21):8121-5. PubMed ID: 3186715
    [Abstract] [Full Text] [Related]

  • 2. Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes.
    Bodine DM, Birkenmeier CS, Barker JE.
    Cell; 1984 Jul; 37(3):721-9. PubMed ID: 6234993
    [Abstract] [Full Text] [Related]

  • 3. Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.
    White RA, Birkenmeier CS, Lux SE, Barker JE.
    Proc Natl Acad Sci U S A; 1990 Apr; 87(8):3117-21. PubMed ID: 2139228
    [Abstract] [Full Text] [Related]

  • 4. The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.
    Bloom ML, Kaysser TM, Birkenmeier CS, Barker JE.
    Proc Natl Acad Sci U S A; 1994 Oct 11; 91(21):10099-103. PubMed ID: 7937844
    [Abstract] [Full Text] [Related]

  • 5. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
    Giorgi M, Cianci CD, Gallagher PG, Morrow JS.
    Exp Mol Pathol; 2001 Jun 11; 70(3):215-30. PubMed ID: 11418000
    [Abstract] [Full Text] [Related]

  • 6. [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 Jun 11; 203(4):284-95. PubMed ID: 1942935
    [Abstract] [Full Text] [Related]

  • 7. Hemolytic anemias due to abnormalities in red cell spectrin: a brief review.
    Lux SE, Wolfe LC, Pease B, Tomaselli MB, John KM, Bernstein SE.
    Prog Clin Biol Res; 1981 Jun 11; 45():159-68. PubMed ID: 7017750
    [No Abstract] [Full Text] [Related]

  • 8. Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene.
    Wandersee NJ, Birkenmeier CS, Gifford EJ, Mohandas N, Barker JE.
    Hematol J; 2000 Jun 11; 1(4):235-42. PubMed ID: 11920196
    [Abstract] [Full Text] [Related]

  • 9. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
    Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V.
    Nature; 1990 Jun 21; 345(6277):736-9. PubMed ID: 2141669
    [Abstract] [Full Text] [Related]

  • 10. Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene.
    Grimber G, Galand C, Garbarz M, Mattei MG, Cavard C, Zider A, Blanchet P, Boivin P, Briand P, Dhermy D.
    Transgenic Res; 1992 Nov 21; 1(6):268-74. PubMed ID: 1338695
    [Abstract] [Full Text] [Related]

  • 11. Complete nucleotide sequence of the murine erythroid beta-spectrin cDNA and tissue-specific expression in normal and jaundiced mice.
    Bloom ML, Birkenmeier CS, Barker JE.
    Blood; 1993 Nov 01; 82(9):2906-14. PubMed ID: 8219239
    [Abstract] [Full Text] [Related]

  • 12. Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis.
    Kaysser TM, Wandersee NJ, Bronson RT, Barker JE.
    Blood; 1997 Dec 01; 90(11):4610-9. PubMed ID: 9373273
    [Abstract] [Full Text] [Related]

  • 13. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.
    Bogardus H, Schulz VP, Maksimova Y, Miller BA, Li P, Forget BG, Gallagher PG.
    Haematologica; 2014 Sep 01; 99(9):e168-70. PubMed ID: 24895341
    [No Abstract] [Full Text] [Related]

  • 14. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M, Bibas D, Cynober T, Galand C, Bournier O, Devaux I, Tchernia G, Dhermy D.
    C R Acad Sci III; 1996 Oct 01; 319(10):913-9. PubMed ID: 8977772
    [Abstract] [Full Text] [Related]

  • 15. Normoblastosis, a murine model for ankyrin-deficient hemolytic anemia, is caused by a hypomorphic mutation in the erythroid ankyrin gene Ank1.
    Birkenmeier CS, Gifford EJ, Barker JE.
    Hematol J; 2003 Oct 01; 4(6):445-9. PubMed ID: 14671619
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.
    Hassoun H, Vassiliadis JN, Murray J, Yi SJ, Hanspal M, Ware RE, Winter SS, Chiou SS, Palek J.
    J Clin Invest; 1995 Dec 01; 96(6):2623-9. PubMed ID: 8675627
    [Abstract] [Full Text] [Related]

  • 17. Three Novel Spectrin Variants in Jaundiced Neonates.
    Christensen RD, Agarwal AM, Yaish HM, Reading NS, O'Brien EA, Prchal JT.
    Clin Pediatr (Phila); 2018 Jan 01; 57(1):19-26. PubMed ID: 28090778
    [Abstract] [Full Text] [Related]

  • 18. Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis.
    Nussenzveig RH, Christensen RD, Prchal JT, Yaish HM, Agarwal AM.
    Neonatology; 2014 Jan 01; 106(4):355-7. PubMed ID: 25277063
    [Abstract] [Full Text] [Related]

  • 19. Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.
    Hassoun H, Vassiliadis JN, Murray J, Yi SJ, Hanspal M, Johnson CA, Palek J.
    Blood; 1996 Mar 15; 87(6):2538-45. PubMed ID: 8630421
    [Abstract] [Full Text] [Related]

  • 20. Interferons as gene activators: a cluster of six interferon-activatable genes is linked to the erythroid alpha-spectrin locus on murine chromosome 1.
    Opdenakker G, Snoddy J, Choubey D, Toniato E, Pravtcheva DD, Seldin MF, Ruddle FH, Lengyel P.
    Virology; 1989 Aug 15; 171(2):568-78. PubMed ID: 2474894
    [Abstract] [Full Text] [Related]

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