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)

  • 1. Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency.
    Conboy J; Mohandas N; Tchernia G; Kan YW
    N Engl J Med; 1986 Sep; 315(11):680-5. PubMed ID: 3755799
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [1st instance of the absence of an erythrocyte membrane protein (band 4(1)) in a case of familial elliptocytic anemia].
    Feo CJ; Fischer S; Piau JP; Grange MJ; Tchernia G
    Nouv Rev Fr Hematol (1978); 1980; 22(4):315-25. PubMed ID: 7255153
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.
    Iolascon A; Miraglia del Giudice E; Camaschella C
    Haematologica; 1992; 77(1):60-72. PubMed ID: 1356891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Drug-induced severe hemolytic crisis in a patient with hemolytic hereditary elliptocytosis with complete deficiency of red cell membrane protein band 4.2].
    Fukuda M; Komatsu M; Inaba R; Kanzaki A; Hashimoto M; Ikeda A; Takahara M; Yawata Y
    Rinsho Ketsueki; 1988 Apr; 29(4):559-64. PubMed ID: 3404671
    [No Abstract]   [Full Text] [Related]  

  • 5. Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene.
    Dalla Venezia N; Gilsanz F; Alloisio N; Ducluzeau MT; Benz EJ; Delaunay J
    J Clin Invest; 1992 Nov; 90(5):1713-7. PubMed ID: 1430200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosis.
    Alloisio N; Dorleac E; Morle L; Girot R; Galant C; Boivin P; Delaunay J
    Biomed Biochim Acta; 1983; 42(11-12):S38-42. PubMed ID: 6675716
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
    Conboy JG; Chasis JA; Winardi R; Tchernia G; Kan YW; Mohandas N
    J Clin Invest; 1993 Jan; 91(1):77-82. PubMed ID: 8423235
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distinct variants of erythrocyte protein 4.1 inherited in linkage with elliptocytosis and Rh type in three white families.
    McGuire M; Smith BL; Agre P
    Blood; 1988 Jul; 72(1):287-93. PubMed ID: 3134067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane].
    Boivin P
    J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209
    [No Abstract]   [Full Text] [Related]  

  • 10. The genetic disorders of the red cell skeleton.
    Delaunay J; Alloisio N; Morle L; Baklouti F
    Nouv Rev Fr Hematol (1978); 1991; 33(2):63-70. PubMed ID: 1766857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The 4.1.(-) hereditary elliptocytosis.
    Delaunay J; Alloisio N; Morle L
    Acta Med Port; 1985; 6(7-8):S14-6. PubMed ID: 3832803
    [No Abstract]   [Full Text] [Related]  

  • 12. Homozygous hereditary elliptocytosis: implications for the function of membrane protein band 4.1.
    Shohet SB; Mohandas N; Tchernia G
    Prog Clin Biol Res; 1982; 97():45-52. PubMed ID: 7156170
    [No Abstract]   [Full Text] [Related]  

  • 13. Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.
    Tchernia G; Mohandas N; Shohet SB
    J Clin Invest; 1981 Aug; 68(2):454-60. PubMed ID: 6894932
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells.
    Conboy JG
    Semin Hematol; 1993 Jan; 30(1):58-73. PubMed ID: 8434260
    [No Abstract]   [Full Text] [Related]  

  • 15. Clinical expression and laboratory detection of red blood cell membrane protein mutations.
    Palek J; Jarolim P
    Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114
    [No Abstract]   [Full Text] [Related]  

  • 16. Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(-) hereditary elliptocytosis.
    Garbarz M; Devaux I; Bournier O; Grandchamp B; Dhermy D
    Hum Mutat; 1995; 5(4):339-40. PubMed ID: 7627190
    [No Abstract]   [Full Text] [Related]  

  • 17. Membrane proteins in hereditary spherocytosis, elliptocytosis and stomatocytosis.
    Sakal M; Chorváth B; Duraj J; Sakalová A
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1982; 109(5):787-91. PubMed ID: 6188665
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial deficiency of protein 4.1 in hereditary elliptocytosis.
    Lambert S; Zail S
    Am J Hematol; 1987 Nov; 26(3):263-72. PubMed ID: 3674005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rapid localization of membrane skeletal protein 4.1 (EL1) to human chromosome 1p33----p34.2 by nonradioactive in situ hybridization.
    Tang CJ; Tang TK
    Cytogenet Cell Genet; 1991; 57(2-3):119. PubMed ID: 1914519
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.
    Lorenzo F; Dalla Venezia N; Morlé L; Baklouti F; Alloisio N; Ducluzeau MT; Roda L; Lefrançois P; Delaunay J
    J Clin Invest; 1994 Oct; 94(4):1651-6. PubMed ID: 7929842
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.