BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 34672909)

  • 1. Efficacy of cytochemical tests in gene analysis of hereditary spherocytosis: a case study of six patients with different disease subtypes.
    Shibuya A; Kawashima H; Tanaka M
    Hematology; 2021 Dec; 26(1):827-834. PubMed ID: 34672909
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia.
    Shibuya A; Kawashima H; Tanaka M
    Hematology; 2018 Oct; 23(9):669-675. PubMed ID: 29623813
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A clinical and experimental study of adult hereditary spherocytosis in the Chinese population.
    Xue J; He Q; Xie XJ; Su AL; Cao SB
    Kaohsiung J Med Sci; 2020 Jul; 36(7):552-560. PubMed ID: 32133777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
    Park J; Jeong DC; Yoo J; Jang W; Chae H; Kim J; Kwon A; Choi H; Lee JW; Chung NG; Kim M; Kim Y
    Clin Genet; 2016 Jul; 90(1):69-78. PubMed ID: 26830532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.
    Miraglia del Giudice E; Iolascon A; Pinto L; Nobili B; Perrotta S
    Br J Haematol; 1994 Sep; 88(1):52-5. PubMed ID: 7803256
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina.
    Crisp RL; Solari L; Vota D; GarcĂ­a E; Miguez G; Chamorro ME; Schvartzman GA; Alfonso G; Gammella D; Caldarola S; Riccheri C; Vittori D; Venegas B; Nesse A; Donato H
    Ann Hematol; 2011 Jun; 90(6):625-34. PubMed ID: 21080168
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 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. 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]  

  • 12. Erythrocyte membrane protein analysis by sodium dodecyl sulphate-capillary gel electrophoresis in the diagnosis of hereditary spherocytosis.
    Debaugnies F; Cotton F; Boutique C; Gulbis B
    Clin Chem Lab Med; 2011 Mar; 49(3):485-92. PubMed ID: 21231903
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.
    Bianchi P; Fermo E; Vercellati C; Marcello AP; Porretti L; Cortelezzi A; Barcellini W; Zanella A
    Haematologica; 2012 Apr; 97(4):516-23. PubMed ID: 22058213
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.
    Peker S; Akar N; Demiralp DO
    Mol Biol Rep; 2012 Mar; 39(3):3161-7. PubMed ID: 21706353
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-phenotype correlation in children with hereditary spherocytosis.
    Tole S; Dhir P; Pugi J; Drury LJ; Butchart S; Fantauzzi M; Langer JC; Baker JM; Blanchette VS; Kirby-Allen M; Carcao MD
    Br J Haematol; 2020 Nov; 191(3):486-496. PubMed ID: 32436265
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study.
    Aggarwal A; Jamwal M; Sharma P; Sachdeva MUS; Bansal D; Malhotra P; Das R
    Br J Haematol; 2020 Mar; 188(5):784-795. PubMed ID: 31602632
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis.
    Wang R; Yang S; Xu M; Huang J; Liu H; Gu W; Zhang X
    Sci China Life Sci; 2018 Aug; 61(8):947-953. PubMed ID: 29572776
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.