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 *

97 related articles for article (PubMed ID: 16914912)

  • 1. 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]  

  • 2. [Hereditary spherocytosis -- prevalence of erythrocyte membrane protein deficiency].
    Granjo E; Manata P; Torres N; Rodrigues L; Ferreira F; Bauerle R; Quintanilha A
    Acta Med Port; 2003; 16(2):65-9. PubMed ID: 12828006
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
    Bogusławska DM; Heger E; Chorzalska A; Nierzwicka M; Hołojda J; Swiderska A; Straburzyńska A; Paździor G; Langner M; Sikorski AF
    Ann Hematol; 2004 Jan; 83(1):28-33. PubMed ID: 14517693
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
    Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
    Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
    Jarolim P; Rubin HL; Liu SC; Cho MR; Brabec V; Derick LH; Yi SJ; Saad ST; Alper S; Brugnara C
    J Clin Invest; 1994 Jan; 93(1):121-30. PubMed ID: 8282779
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Molecular aspects of erythrocyte membrane disorders].
    Saad ST; Costa FF
    Rev Assoc Med Bras (1992); 1994; 40(3):216-24. PubMed ID: 7787875
    [No Abstract]   [Full Text] [Related]  

  • 14. Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11.
    Maillet P; Vallier A; Reinhart WH; Wyss EJ; Ott P; Texier P; Baklouti F; Tanner MJ; Delaunay J; Alloisio N
    Br J Haematol; 1995 Dec; 91(4):804-10. PubMed ID: 8547122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK mallorca.
    Zarza R; Moscardó M; Alvarez R; García J; Morey M; Pujades A; Vives-Corrons JL
    Haematologica; 2000 Mar; 85(3):227-32. PubMed ID: 10702808
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis.
    Kanzaki A; Hayette S; Morlé L; Inoue F; Matsuyama R; Inoue T; Yawata A; Wada H; Vallier A; Alloisio N; Yawata Y; Delaunay J
    Br J Haematol; 1997 Dec; 99(3):522-30. PubMed ID: 9401060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
    Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE
    Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.
    Van Zwieten R; François JJ; Van Leeuwen K; Van Wesel AC; Van Bruggen R; Van Solinge WW; Roos D; Verhoeven AJ; Van Wijk R
    Am J Hematol; 2013 Feb; 88(2):159-60. PubMed ID: 23255290
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas).
    Alloisio N; Maillet P; Carré G; Texier P; Vallier A; Baklouti F; Philippe N; Delaunay J
    Blood; 1996 Aug; 88(3):1062-9. PubMed ID: 8704215
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.