BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 9299863)

  • 1. Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.
    Lanciotti M; Perutelli P; Valetto A; Di Martino D; Mori PG
    Haematologica; 1997; 82(4):460-2. PubMed ID: 9299863
    [No Abstract]   [Full Text] [Related]  

  • 2. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
    C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hematologically important mutations: ankyrin variants in hereditary spherocytosis.
    Gallagher PG
    Blood Cells Mol Dis; 2005; 35(3):345-7. PubMed ID: 16223590
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.
    Gundel F; Eber S; Heep A
    Ann Hematol; 2011 Feb; 90(2):231-2. PubMed ID: 20512576
    [No Abstract]   [Full Text] [Related]  

  • 6. Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutations.
    Leite RC; Basseres DS; Ferreira JS; Alberto FL; Costa FF; Saad ST
    Hum Mutat; 2000 Dec; 16(6):529. PubMed ID: 11102985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Band 3 deficiency as a cause of hereditary spherocytosis].
    Wada H; Suemori S; Nakanishi H; Sugihara T
    Rinsho Ketsueki; 2015 Jul; 56(7):837-45. PubMed ID: 26251147
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.
    Gallagher PG; Forget BG
    Blood Cells Mol Dis; 1998 Dec; 24(4):539-43. PubMed ID: 9887280
    [No Abstract]   [Full Text] [Related]  

  • 9. A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
    Bogusławska DM; Heger E; Listowski M; Wasiński D; Kuliczkowski K; Machnicka B; Sikorski AF
    Br J Haematol; 2014 Oct; 167(2):269-71. PubMed ID: 24903897
    [No Abstract]   [Full Text] [Related]  

  • 10. Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
    Tan AW; Leung P; Patil UP
    Fetal Pediatr Pathol; 2018 Aug; 37(4):296-300. PubMed ID: 30207817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
    Costa FF; Agre P; Watkins PC; Winkelmann JC; Tang TK; John KM; Lux SE; Forget BG
    N Engl J Med; 1990 Oct; 323(15):1046-50. PubMed ID: 1977081
    [No Abstract]   [Full Text] [Related]  

  • 12. [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]  

  • 13. [Identification of a novel ANK1 gene mutation in a newborn with hereditary spherocytosis].
    Jiang M; Lu J; Zhong Y; Wang Y; Yang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):44-7. PubMed ID: 26829732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Diagnosis and therapy of hemolytic anemia--genetic analysis and membrane protein deficiency in hereditary spherocytosis].
    Kanzaki A; Kaku M; Yawata Y
    Nihon Naika Gakkai Zasshi; 1999 Jun; 88(6):1003-9. PubMed ID: 10465942
    [No Abstract]   [Full Text] [Related]  

  • 15. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A
    Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.
    Miraglia del Giudice E; Francese M; Nobili B; Morlé L; Cutillo S; Delaunay J; Perrotta S
    J Pediatr; 1998 Jan; 132(1):117-20. PubMed ID: 9470011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.
    Gallagher PG; Nilson DG; Wong C; Weisbein JL; Garrett-Beal LJ; Eber SW; Bodine DM
    Hum Mol Genet; 2005 Sep; 14(17):2501-9. PubMed ID: 16037067
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
    Iolascon A; Miraglia del Giudice E; Camaschella C; Pinto L; Nobili B; Perrotta S; Cutillo S
    Br J Haematol; 1991 Aug; 78(4):551-4. PubMed ID: 1832935
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.
    Liu S; Jiang H; Huang LY; Li DZ
    Ann Hematol; 2017 Jun; 96(6):1067-1068. PubMed ID: 28280995
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.