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 *

127 related articles for article (PubMed ID: 8197407)

  • 1. Hereditary spherocytosis: diagnostic and anaemia-associated aberrations of ghost proteins.
    Orntoft TF; Clausen N
    Scand J Clin Lab Invest; 1994 Apr; 54(2):95-103. PubMed ID: 8197407
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
    Goodman SR; Shiffer KA; Casoria LA; Eyster ME
    Blood; 1982 Sep; 60(3):772-84. PubMed ID: 7104494
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
    Hill JS; Sawyer WH; Howlett GJ; Wiley JS
    Biochem J; 1982 Feb; 201(2):259-66. PubMed ID: 7082289
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Enhanced Mg(2+)-ATPase activity in ghosts from HS erythrocytes and in normal ghosts stripped of membrane skeletal proteins may reflect enhanced aminophospholipid translocase activity.
    Vermeulen WP; Briedé JJ; Bunt G; Op den Kamp JA; Kraaijenhagen RJ; Roelofsen B
    Br J Haematol; 1995 May; 90(1):56-64. PubMed ID: 7786796
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis.
    Burke BE; Shotton DM
    Br J Haematol; 1983 Jun; 54(2):173-87. PubMed ID: 6849841
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
    Kedar PS; Colah RB; Kulkarni S; Ghosh K; Mohanty D
    Clin Lab Haematol; 2003 Dec; 25(6):373-6. PubMed ID: 14641141
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
    King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D
    Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
    Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Study of a kindred with hereditary spherocytosis and glyceraldehyde-3-phosphate dehydrogenase deficiency.
    McCann SR; Finkel B; Cadman S; Allen DW
    Blood; 1976 Feb; 47(2):171-81. PubMed ID: 1244916
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
    Iolascon A; Miraglia del Giudice E; Perrotta S; Pinto L; Fiorelli G; Cappellini DM; Vasseur C; Bursaux E; Cutillo S
    Haematologica; 1992; 77(6):450-6. PubMed ID: 1289181
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
    Lee YK; Cho HI; Park SS; Lee YJ; Ra E; Chang YH; Hur M; Shin HY; Ahn HS
    J Korean Med Sci; 2000 Jun; 15(3):284-8. PubMed ID: 10895969
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.
    Cutillo S; Pinto L; Nobili B; Miraglia del Giudice E; Iolascon A
    Eur J Pediatr; 1992 Jan; 151(1):35-7. PubMed ID: 1728542
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.
    Wolfe LC; John KM; Falcone JC; Byrne AM; Lux SE
    N Engl J Med; 1982 Nov; 307(22):1367-74. PubMed ID: 6215583
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
    Saad ST; Costa FF; Vicentim DL; Salles TS; Pranke PH
    Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
    Ferrándiz F; Ródenas S; Villegas A
    Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin.
    Gauthier E; El Nemer W; Wautier MP; Renaud O; Tchernia G; Delaunay J; Le Van Kim C; Colin Y
    Br J Haematol; 2010 Feb; 148(3):456-65. PubMed ID: 20092464
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.
    Ayhan AC; Yildiz I; Yüzbaşıoğlu S; Celkan T; Apak H; Ozkan A; Karaman S
    Hematology; 2012 Jul; 17(4):232-6. PubMed ID: 22889517
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
    Choi HS; Choi Q; Kim JA; Im KO; Park SN; Park Y; Shin HY; Kang HJ; Kook H; Kim SY; Kim SJ; Kim I; Kim JY; Kim H; Park KD; Park KB; Park M; Park SK; Park ES; Park JA; Park JE; Park JK; Baek HJ; Seo JH; Shim YJ; Ahn HS; Yoo KH; Yoon HS; Won YW; Lee KS; Lee KC; Lee MJ; Lee SA; Lee JA; Lee JM; Lee JH; Lee JW; Lim YT; Jung HJ; Chueh HW; Choi EJ; Jung HL; Kim JH; Lee DS;
    Orphanet J Rare Dis; 2019 May; 14(1):114. PubMed ID: 31122244
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.