BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

63 related articles for article (PubMed ID: 35099593)

  • 21. Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.
    Vives Corrons JL; Krishnevskaya E; Montllor L; Leguizamon V; Garcia Bernal M
    Cells; 2022 Mar; 11(7):. PubMed ID: 35406697
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry.
    Vives-Corrons JL; Krishnevskaya E; Rodriguez IH; Ancochea A
    Int J Hematol; 2021 Feb; 113(2):163-174. PubMed ID: 33074480
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. The impact of nonsense-mediated mRNA decay on genetic disease, gene editing and cancer immunotherapy.
    Lindeboom RGH; Vermeulen M; Lehner B; Supek F
    Nat Genet; 2019 Nov; 51(11):1645-1651. PubMed ID: 31659324
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Identification of pathways and genes associated with cerebral palsy.
    Zhu Q; Ni Y; Wang J; Yin H; Zhang Q; Zhang L; Bian W; Liang B; Kong L; Xuan L; Lu N
    Genes Genomics; 2018 Dec; 40(12):1339-1349. PubMed ID: 30109564
    [TBL] [Abstract][Full Text] [Related]  

  • 27. SWISS-MODEL: homology modelling of protein structures and complexes.
    Waterhouse A; Bertoni M; Bienert S; Studer G; Tauriello G; Gumienny R; Heer FT; de Beer TAP; Rempfer C; Bordoli L; Lepore R; Schwede T
    Nucleic Acids Res; 2018 Jul; 46(W1):W296-W303. PubMed ID: 29788355
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives.
    He BJ; Liao L; Deng ZF; Tao YF; Xu YC; Lin FQ
    Acta Haematol; 2018; 139(1):60-66. PubMed ID: 29402830
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.
    Yi Y; Dang X; Li Y; Zhao C; Tang H; Shi X
    Mol Med Rep; 2018 Jan; 17(1):382-387. PubMed ID: 29115431
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.
    Llaudet-Planas E; Vives-Corrons JL; Rizzuto V; Gómez-Ramírez P; Sevilla Navarro J; Coll Sibina MT; García-Bernal M; Ruiz Llobet A; Badell I; Velasco-Puyó P; Dapena JL; Mañú-Pereira MM
    Int J Lab Hematol; 2018 Feb; 40(1):94-102. PubMed ID: 29024480
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Red cell membrane disorders.
    Narla J; Mohandas N
    Int J Lab Hematol; 2017 May; 39 Suppl 1():47-52. PubMed ID: 28447420
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemias.
    Agarwal AM; Nussenzveig RH; Reading NS; Patel JL; Sangle N; Salama ME; Prchal JT; Perkins SL; Yaish HM; Christensen RD
    Br J Haematol; 2016 Sep; 174(5):806-14. PubMed ID: 27292444
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. IBS: an illustrator for the presentation and visualization of biological sequences.
    Liu W; Xie Y; Ma J; Luo X; Nie P; Zuo Z; Lahrmann U; Zhao Q; Zheng Y; Zhao Y; Xue Y; Ren J
    Bioinformatics; 2015 Oct; 31(20):3359-61. PubMed ID: 26069263
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.
    Wang C; Cui Y; Li Y; Liu X; Han J
    Intractable Rare Dis Res; 2015 May; 4(2):76-81. PubMed ID: 25984425
    [TBL] [Abstract][Full Text] [Related]  

  • 36. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
    King MJ; Garçon L; Hoyer JD; Iolascon A; Picard V; Stewart G; Bianchi P; Lee SH; Zanella A;
    Int J Lab Hematol; 2015 Jun; 37(3):304-25. PubMed ID: 25790109
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparison study of the eosin-5'-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis.
    Park SH; Park CJ; Lee BR; Cho YU; Jang S; Kim N; Koh KN; Im HJ; Seo JJ; Park ES; Lee JW; Yoo KH; Jung HL
    Am J Clin Pathol; 2014 Oct; 142(4):474-84. PubMed ID: 25239414
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MutationTaster2: mutation prediction for the deep-sequencing age.
    Schwarz JM; Cooper DN; Schuelke M; Seelow D
    Nat Methods; 2014 Apr; 11(4):361-2. PubMed ID: 24681721
    [No Abstract]   [Full Text] [Related]  

  • 39. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
    Da Costa L; Galimand J; Fenneteau O; Mohandas N
    Blood Rev; 2013 Jul; 27(4):167-78. PubMed ID: 23664421
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
    Bolton-Maggs PH; Langer JC; Iolascon A; Tittensor P; King MJ;
    Br J Haematol; 2012 Jan; 156(1):37-49. PubMed ID: 22055020
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.