BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

480 related articles for article (PubMed ID: 10846232)

  • 21. Red cell membrane polypeptides under normal conditions and in genetic disorders.
    Delaunay J
    Transfus Clin Biol; 1995; 2(4):207-16. PubMed ID: 8542017
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context.
    Reithmeier RA; Casey JR; Kalli AC; Sansom MS; Alguel Y; Iwata S
    Biochim Biophys Acta; 2016 Jul; 1858(7 Pt A):1507-32. PubMed ID: 27058983
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Red cell membrane disorders.
    Gallagher PG
    Hematology Am Soc Hematol Educ Program; 2005; ():13-8. PubMed ID: 16304353
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The erythrocyte membrane skeleton: pathophysiology.
    Shohet SB; Lux SE
    Hosp Pract (Off Ed); 1984 Nov; 19(11):89-95, 99, 103 passim. PubMed ID: 6436279
    [No Abstract]   [Full Text] [Related]  

  • 25. [Normal and abnormal human erythrocyte membranes].
    Yahata Y
    Rinsho Ketsueki; 1976 Oct; 17(10):1049-70. PubMed ID: 187810
    [No Abstract]   [Full Text] [Related]  

  • 26. Red cell membrane disorders.
    Narla J; Mohandas N
    Int J Lab Hematol; 2017 May; 39 Suppl 1():47-52. PubMed ID: 28447420
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Erythroid band 3 variants and disease.
    Bruce LJ; Tanner MJ
    Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):637-54. PubMed ID: 10895257
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Recent progress in studies on red cell membrane disorders.
    Yawata Y
    Nihon Ketsueki Gakkai Zasshi; 1988 Dec; 51(8):1360-71. PubMed ID: 3073612
    [No Abstract]   [Full Text] [Related]  

  • 29. Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.
    Yawata Y; Kanzaki A; Inoue T; Ata K; Wada H; Okamoto N; Higo I; Yawata A; Sugihara T; Yamada O
    Int J Hematol; 1994 Jul; 60(1):23-38. PubMed ID: 7919236
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
    Bruce LJ
    Blood Cells Mol Dis; 2009; 42(3):216-22. PubMed ID: 19261491
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic disorders of the red cell membrane.
    Delaunay J
    Crit Rev Oncol Hematol; 1995 Jun; 19(2):79-110. PubMed ID: 7612181
    [No Abstract]   [Full Text] [Related]  

  • 32. 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; 70(3):215-30. PubMed ID: 11418000
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Red blood cell membrane defects.
    Iolascon A; Perrotta S; Stewart GW
    Rev Clin Exp Hematol; 2003 Mar; 7(1):22-56. PubMed ID: 14692233
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetics of the red cell membrane skeleton.
    Palek J; Lambert S
    Semin Hematol; 1990 Oct; 27(4):290-332. PubMed ID: 2255917
    [No Abstract]   [Full Text] [Related]  

  • 35. Clinical disorders of the erythrocyte membrane skeleton.
    McGuire M; Agre P
    Hematol Pathol; 1988; 2(1):1-14. PubMed ID: 3069829
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Inherited disorders of the red cell membrane skeleton.
    Lux SE; Wolfe LC
    Pediatr Clin North Am; 1980 May; 27(2):463-86. PubMed ID: 6992078
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Molecular mechanism of hereditary spherocytosis].
    Bogusławska DM; Heger E; Sikorski AF
    Pol Merkur Lekarski; 2006 Jan; 20(115):112-6. PubMed ID: 16617750
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Recent advances in the understanding of the erythrocyte membrane.
    Lam SK; Quah TC
    J Singapore Paediatr Soc; 1991; 33(3-4):140-8. PubMed ID: 1812330
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
    Rocha S; Costa E; Rocha-Pereira P; Ferreira F; Cleto E; Barbot J; Quintanilha A; Belo L; Santos-Silva A
    Br J Haematol; 2010 Jun; 149(5):785-94. PubMed ID: 20346007
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.
    Yawata Y; Kanzaki A; Yawata A; Nakanishi H; Kaku M
    Hematology; 2001; 6(6):399-422. PubMed ID: 27405697
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 24.