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 *

90 related articles for article (PubMed ID: 6492485)

  • 1. Hereditary spherocytosis associated with a variant of band 3 protein in the erythrocyte membrane.
    Imamura T; Matsuo T; Yanase T; Kagiyama S
    Jpn J Med; 1984 Aug; 23(3):216-9. PubMed ID: 6492485
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A de novo band 3 mutation in hereditary spherocytosis.
    Bogardus HH; Maksimova YD; Forget BG; Gallagher PG
    Pediatr Blood Cancer; 2012 Jun; 58(6):1004. PubMed ID: 22170767
    [No Abstract]   [Full Text] [Related]  

  • 3. Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred.
    Reinhart WH; Wyss EJ; Arnold D; Ott P
    Br J Haematol; 1994 Jan; 86(1):147-55. PubMed ID: 8011524
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis.
    Ideguchi H; Nishimura J; Nawata H; Hamasaki N
    Br J Haematol; 1990 Mar; 74(3):347-53. PubMed ID: 2139792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Band 3 Tokyo: Thr837-->Ala837 substitution in erythrocyte band 3 protein associated with spherocytic hemolysis.
    Iwase S; Ideguchi H; Takao M; Horiguchi-Yamada J; Iwasaki M; Takahara S; Sekikawa T; Mochizuki S; Yamada H
    Acta Haematol; 1998; 100(4):200-3. PubMed ID: 9973643
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The abnormal phosphorylation of spectrin in human hereditary spherocytosis.
    Thompson S; Maddy AH
    Biochim Biophys Acta; 1981 Nov; 649(1):31-7. PubMed ID: 6272858
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.
    Gallagher PG; Forget BG
    Blood Cells Mol Dis; 1997 Dec; 23(3):417-21. PubMed ID: 9446757
    [No Abstract]   [Full Text] [Related]  

  • 10. Band 3Tambaú: a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane.
    Lima PR; Baratti MO; Chiattone ML; Costa FF; Saad ST
    Eur J Haematol; 2005 May; 74(5):396-401. PubMed ID: 15813913
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Changes in proteolytic susceptibility of erythrocyte membrane proteins in hereditary spherocytosis.
    Gaczyńska M; Bartosz G; Judkiewicz L
    Clin Chim Acta; 1991 May; 198(3):267-70. PubMed ID: 1889126
    [No Abstract]   [Full Text] [Related]  

  • 13. Arginine 490 is a hot spot for mutation in the band 3 gene in hereditary spherocytosis.
    Lima PR; Sales TS; Costa FF; Saad ST
    Eur J Haematol; 1999 Nov; 63(5):360-1. PubMed ID: 10580570
    [No Abstract]   [Full Text] [Related]  

  • 14. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.
    Inaba M; Yawata A; Koshino I; Sato K; Takeuchi M; Takakuwa Y; Manno S; Yawata Y; Kanzaki A; Sakai J; Ban A; Ono K; Maede Y
    J Clin Invest; 1996 Apr; 97(8):1804-17. PubMed ID: 8621763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Combined ankyrin and spectrin deficiency in hereditary spherocytosis.
    Pekrun A; Eber SW; Kuhlmey A; Schröter W
    Ann Hematol; 1993 Aug; 67(2):89-93. PubMed ID: 8347735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The red blood cell band 3 variant (band 3Biceêtrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect.
    Dhermy D; Burnier O; Bourgeois M; Grandchamp B
    Mol Membr Biol; 1999; 16(4):305-12. PubMed ID: 10766130
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosis.
    Armbrust R; Eber SW; Schröter W
    Ann Hematol; 1992 Feb; 64(2):93-6. PubMed ID: 1554801
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency.
    Maciag M; Plochocka D; Mendek-Czajkowska E; Adamowicz-Salach A; Spychalska J; Zdebska E; Jablonska-Skwiecinska E; Koscielak J; Burzynska B
    Acta Haematol; 2006; 116(2):143-5. PubMed ID: 16914912
    [No Abstract]   [Full Text] [Related]  

  • 20. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
    Jenkins PB; Abou-Alfa GK; Dhermy D; Bursaux E; Féo C; Scarpa AL; Lux SE; Garbarz M; Forget BG; Gallagher PG
    J Clin Invest; 1996 Jan; 97(2):373-80. PubMed ID: 8567957
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.