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 *

293 related articles for article (PubMed ID: 3755799)

  • 21. Update on the clinical spectrum and genetics of red blood cell membrane disorders.
    Gallagher PG
    Curr Hematol Rep; 2004 Mar; 3(2):85-91. PubMed ID: 14965483
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Clinical and biochemical study of 9 patients with hereditary elliptocytosis].
    Feldman L; Marick T; Cerone S; Sansinanea A; Lecomte MC; Dhermy D; Boivin P
    Medicina (B Aires); 1992; 52(2):109-15. PubMed ID: 1308902
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A shortened variant of red cell membrane protein 4.1.
    Alloisio N; Dorléac E; Delaunay J; Girot R; Galand C; Boivin P
    Blood; 1982 Jul; 60(1):265-7. PubMed ID: 7082842
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.
    Delaunay J; Alloisio N; Morle L; Baklouti F; Dalla Venezia N; Maillet P; Wilmotte R
    Ann Genet; 1996; 39(4):209-21. PubMed ID: 9037349
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis.
    Garbarz M; Dhermy D; Lecomte MC; Féo C; Chaveroche I; Galand C; Bournier O; Bertrand O; Boivin P
    Blood; 1984 Nov; 64(5):1006-15. PubMed ID: 6487803
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
    Kanzaki A; Wada H; Yawata Y
    Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The elliptocytoses, ovalocytosis and related disorders.
    Nurse GT; Coetzer TL; Palek J
    Baillieres Clin Haematol; 1992 Jan; 5(1):187-207. PubMed ID: 1534499
    [No Abstract]   [Full Text] [Related]  

  • 28. Homozygous deletion of EPB41 genuine AUG-containing exons results in mRNA splicing defects, NMD activation and protein 4.1R complete deficiency in hereditary elliptocytosis.
    Baklouti F; Morinière M; Haj-Khélil A; Fénéant-Thibault M; Gruffat H; Couté Y; Ninot A; Guitton C; Delaunay J
    Blood Cells Mol Dis; 2011 Oct; 47(3):158-65. PubMed ID: 21839655
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosis.
    Morinière M; Delhommeau F; Calender A; Ribeiro L; Delaunay J; Baklouti F
    Blood Cells Mol Dis; 2010 Dec; 45(4):284-8. PubMed ID: 20863723
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. [Hereditary elliptocytosis with detection of a membrane protein defect of erythrocytes].
    Hochhaus A; Wutke K; Meyer M
    Z Gesamte Inn Med; 1988 Mar; 43(5):128-9. PubMed ID: 3388917
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Disorders of red cell membrane.
    An X; Mohandas N
    Br J Haematol; 2008 May; 141(3):367-75. PubMed ID: 18341630
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon.
    Maillet P; Dalla Venezia N; Lorenzo F; Morinière M; Bozon M; Noël B; Delaunay J; Baklouti F
    Hum Mutat; 1999; 14(2):145-55. PubMed ID: 10425037
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A molecular study of heterozygous protein 4.1 deficiency in hereditary elliptocytosis.
    Lambert S; Conboy J; Zail S
    Blood; 1988 Dec; 72(6):1926-9. PubMed ID: 3058231
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Erythrocyte membrane skeletal protein 4.1: a brief review.
    Goodman SR; Shiffer K; Coleman DB; Whitfield CF
    Prog Clin Biol Res; 1984; 165():415-39. PubMed ID: 6390456
    [No Abstract]   [Full Text] [Related]  

  • 37. 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]  

  • 38. Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1.
    Conboy JG; Shitamoto R; Parra M; Winardi R; Kabra A; Smith J; Mohandas N
    Blood; 1991 Nov; 78(9):2438-43. PubMed ID: 1932756
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Red cell membrane disorders: historical perspectives from dawn to enlightenment (II)].
    Yawata Y
    Rinsho Ketsueki; 1999 Dec; 40(12):1223-35. PubMed ID: 10658475
    [No Abstract]   [Full Text] [Related]  

  • 40. Gerbich reactivity in 4.1 (-) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency.
    Sondag D; Alloisio N; Blanchard D; Ducluzeau MT; Colonna P; Bachir D; Bloy C; Cartron JP; Delaunay J
    Br J Haematol; 1987 Jan; 65(1):43-50. PubMed ID: 3814526
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.