BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 32133777)

  • 21. Regulation of band 3 rotational mobility by ankyrin in intact human red cells.
    Cho MR; Eber SW; Liu SC; Lux SE; Golan DE
    Biochemistry; 1998 Dec; 37(51):17828-35. PubMed ID: 9922149
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular mechanism of hereditary spherocytosis].
    Bogusławska DM; Heger E; Sikorski AF
    Pol Merkur Lekarski; 2006 Jan; 20(115):112-6. PubMed ID: 16617750
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [The characteristic of hereditary spherocytosis related gene mutation in 37 Chinese hereditary spherocytisis patients].
    Peng GX; Yang WR; Zhao X; Jin LP; Zhang L; Zhou K; Li Y; Ye L; Li Y; Li JP; Fan HH; Song L; Yang Y; Xiong YZ; Wu ZJ; Wang HJ; Zhang FK
    Zhonghua Xue Ye Xue Za Zhi; 2018 Nov; 39(11):898-903. PubMed ID: 30486584
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. [Characteristics of hereditary spherocytosis].
    Yawata Y
    Nihon Naika Gakkai Zasshi; 1999 Sep; 88(9):1825-33. PubMed ID: 10581770
    [No Abstract]   [Full Text] [Related]  

  • 27. Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia.
    King MJ; Behrens J; Rogers C; Flynn C; Greenwood D; Chambers K
    Br J Haematol; 2000 Dec; 111(3):924-33. PubMed ID: 11122157
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.
    Christensen RD; Agarwal AM; Nussenzveig RH; Heikal N; Liew MA; Yaish HM
    J Perinatol; 2015 May; 35(5):357-61. PubMed ID: 25357094
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Toward the harmonization of result presentation for the eosin-5'-maleimide binding test in the diagnosis of hereditary spherocytosis.
    Hunt L; Greenwood D; Heimpel H; Noel N; Whiteway A; King MJ
    Cytometry B Clin Cytom; 2015 Jan; 88(1):50-7. PubMed ID: 25227211
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A Novel
    Jang W; Kim SK; Nahm CH; Choi JW; Kim JJ; Moon Y
    Ann Clin Lab Sci; 2021 Jan; 51(1):136-139. PubMed ID: 33653793
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A previously unrecognized Ankyrin-1 mutation associated with Hereditary Spherocytosis in an Italian family.
    Lazzareschi I; Curatola A; Pedicelli C; Castiglia D; Buonsenso D; Gatto A; Attinà G; Valentini P
    Eur J Haematol; 2019 Nov; 103(5):523-526. PubMed ID: 31400153
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.
    Li J; Guo H; Zhu Z; Sun J
    Acta Haematol; 2022; 145(6):575-581. PubMed ID: 35817016
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.
    Li S; Guo P; Mi L; Chai X; Xi K; Liu T; Lu L; Li J
    Ann Hematol; 2022 Apr; 101(4):731-738. PubMed ID: 35099593
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis.
    Reliene R; Mariani M; Zanella A; Reinhart WH; Ribeiro ML; del Giudice EM; Perrotta S; Iolascon A; Eber S; Lutz HU
    Blood; 2002 Sep; 100(6):2208-15. PubMed ID: 12200387
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
    Jarolim P; Murray JL; Rubin HL; Taylor WM; Prchal JT; Ballas SK; Snyder LM; Chrobak L; Melrose WD; Brabec V; Palek J
    Blood; 1996 Dec; 88(11):4366-74. PubMed ID: 8943874
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The updated beta-spectrin mutations in patients with hereditary spherocytosis by targeted next-generation sequencing.
    Fan J; Yao L; Lu D; Yao Y; Sun Y; Tian Y; Mou L; Chen L; Zhao L; Qiao S; Hu S; Zhu Y
    J Hum Genet; 2021 Dec; 66(12):1153-1158. PubMed ID: 34140613
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis].
    Camacho-Torres AL; Sánchez-López JY; Mesa-Cornejo VM; Ibarra B; Perea-Díaz FJ
    Gac Med Mex; 2006; 142(5):435-7. PubMed ID: 17128827
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and molecular evaluation of non-dominant hereditary spherocytosis.
    Miraglia del Giudice E; Nobili B; Francese M; D'Urso L; Iolascon A; Eber S; Perrotta S
    Br J Haematol; 2001 Jan; 112(1):42-7. PubMed ID: 11167781
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing.
    Bogusławska DM; Skulski M; Machnicka B; Potoczek S; Kraszewski S; Kuliczkowski K; Sikorski AF
    Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681667
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.