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196 related items for PubMed ID: 2139228

  • 1. 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]

  • 2. Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
    Peters LL, Birkenmeier CS, Bronson RT, White RA, Lux SE, Otto E, Bennett V, Higgins A, Barker JE.
    J Cell Biol; 1991 Sep; 114(6):1233-41. PubMed ID: 1716634
    [Abstract] [Full Text] [Related]

  • 3. Distinct fetal Ank-1 and Ank-2 related proteins and mRNAs in normal and nb/nb mice.
    Peters LL, Turtzo LC, Birkenmeier CS, Barker JE.
    Blood; 1993 Apr 15; 81(8):2144-9. PubMed ID: 8471772
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 37(3):721-9. PubMed ID: 6234993
    [Abstract] [Full Text] [Related]

  • 5. Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient mice.
    Kordeli E, Bennett V.
    J Cell Biol; 1991 Sep 15; 114(6):1243-59. PubMed ID: 1832678
    [Abstract] [Full Text] [Related]

  • 6. 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 Sep 15; 4(6):445-9. PubMed ID: 14671619
    [Abstract] [Full Text] [Related]

  • 7. Fetal compensation of the hemolytic anemia in mice homozygous for the normoblastosis (nb) mutation.
    Peters LL, Birkenmeier CS, Barker JE.
    Blood; 1992 Oct 15; 80(8):2122-7. PubMed ID: 1391963
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 85(21):8121-5. PubMed ID: 3186715
    [Abstract] [Full Text] [Related]

  • 9. Decreased content of protein 4.2 in ankyrin-deficient normoblastosis (nb/nb) mouse red blood cells: evidence for ankyrin enhancement of protein 4.2 membrane binding.
    Rybicki AC, Musto S, Schwartz RS.
    Blood; 1995 Nov 01; 86(9):3583-9. PubMed ID: 7579467
    [Abstract] [Full Text] [Related]

  • 10. Resistance to malaria in ankyrin and spectrin deficient mice.
    Shear HL, Roth EF, Ng C, Nagel RL.
    Br J Haematol; 1991 Aug 01; 78(4):555-60. PubMed ID: 1832936
    [Abstract] [Full Text] [Related]

  • 11. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
    Hanspal M, Yoon SH, Yu H, Hanspal JS, Lambert S, Palek J, Prchal JT.
    Blood; 1991 Jan 01; 77(1):165-73. PubMed ID: 1702027
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Increased cation permeability in mutant mouse red blood cells with defective membrane skeletons.
    Joiner CH, Franco RS, Jiang M, Franco MS, Barker JE, Lux SE.
    Blood; 1995 Dec 01; 86(11):4307-14. PubMed ID: 7492791
    [Abstract] [Full Text] [Related]

  • 14. A deep intronic mutation in the ankyrin-1 gene causes diminished protein expression resulting in hemolytic anemia in mice.
    Huang H, Zhao P, Arimatsu K, Tabeta K, Yamazaki K, Krieg L, Fu E, Zhang T, Du X.
    G3 (Bethesda); 2013 Oct 03; 3(10):1687-95. PubMed ID: 23934996
    [Abstract] [Full Text] [Related]

  • 15. Isolation and characterization of cDNAs encoding human brain ankyrins reveal a family of alternatively spliced genes.
    Otto E, Kunimoto M, McLaughlin T, Bennett V.
    J Cell Biol; 1991 Jul 03; 114(2):241-53. PubMed ID: 1830053
    [Abstract] [Full Text] [Related]

  • 16. 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 03; 70(3):215-30. PubMed ID: 11418000
    [Abstract] [Full Text] [Related]

  • 17. Inherited hemolytic disease in mice: a review and update.
    Bernstein SE.
    Lab Anim Sci; 1980 Apr 03; 30(2 Pt 1):197-205. PubMed ID: 6763106
    [Abstract] [Full Text] [Related]

  • 18. Impaired echinocytic transformation of ankyrin- and spectrin-deficient erythrocytes in mice.
    Reinhart WH, Sung LP, Sung KL, Bernstein SE, Chien S.
    Am J Hematol; 1988 Dec 03; 29(4):195-200. PubMed ID: 2973228
    [Abstract] [Full Text] [Related]

  • 19. Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.
    Jarolim P, Palek J, Rubin HL, Prchal JT, Korsgren C, Cohen CM.
    Blood; 1992 Jul 15; 80(2):523-9. PubMed ID: 1378323
    [Abstract] [Full Text] [Related]

  • 20. Hematologic characterization and chromosomal localization of the novel dominantly inherited mouse hemolytic anemia, neonatal anemia (Nan).
    White RA, Sokolovsky IV, Britt MI, Nsumu NN, Logsdon DP, McNulty SG, Wilmes LA, Brewer BP, Wirtz E, Joyce HR, Fegley B, Smith A, Heruth DP.
    Blood Cells Mol Dis; 2009 Jul 15; 43(2):141-8. PubMed ID: 19409822
    [Abstract] [Full Text] [Related]

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