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 *

222 related articles for article (PubMed ID: 31016877)

  • 21. Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
    Häuser F; Rossmann H; Adenaeuer A; Shrestha A; Marandiuc D; Paret C; Faber J; Lackner KJ; Lämmle B; Beck O
    Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069343
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing.
    Wang Y; Huang L; Zhu Y; An X; Li J; Zhen J; Yu J
    BMC Pediatr; 2023 Jan; 23(1):23. PubMed ID: 36647015
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report.
    Chai S; Jiao R; Sun X; Fu P; Zhao Q; Sang M
    BMC Med Genet; 2020 Nov; 21(1):223. PubMed ID: 33187473
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.
    Guan H; Liang X; Zhang R; Wang H; Liu W; Zhang R; Yang J; Liu S
    Hematology; 2018 Jul; 23(6):357-361. PubMed ID: 29099659
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.
    Han JH; Kim S; Jang H; Kim SW; Lee MG; Koh H; Lee JH
    PLoS One; 2015; 10(6):e0131251. PubMed ID: 26107955
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family.
    Xu L; Wei X; Liang G; Zhu D; Zhang Y; Zhang Y; Shang X
    Biochim Biophys Acta Mol Basis Dis; 2023 Jan; 1869(1):166595. PubMed ID: 36336297
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Analysis of ANK1 gene mutation in a family with hereditary spherocytosis type Ⅰ].
    Li D; Li B; Li S; Li W; Wang Y; Guo X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):999-1001. PubMed ID: 31598945
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.
    Hughes MR; Anderson N; Maltby S; Wong J; Berberovic Z; Birkenmeier CS; Haddon DJ; Garcha K; Flenniken A; Osborne LR; Adamson SL; Rossant J; Peters LL; Minden MD; Paulson RF; Wang C; Barber DL; McNagny KM; Stanford WL
    Exp Hematol; 2011 Mar; 39(3):305-20, 320.e1-2. PubMed ID: 21193012
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.
    Huang TL; Sang BH; Lei QL; Song CY; Lin YB; Lv Y; Yang CH; Li N; Yang YH; Zhang XW; Tian X
    BMC Pediatr; 2019 Feb; 19(1):62. PubMed ID: 30777044
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [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]  

  • 34. Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio.
    Randon J; Miraglia del Giudice E; Bozon M; Perrotta S; De Vivo M; Iolascon A; Delaunay J; Morle L
    Br J Haematol; 1997 Mar; 96(3):500-6. PubMed ID: 9054656
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Literature review on genotype-phenotype correlation in patients with hereditary spherocytosis.
    Yang L; Shu H; Zhou M; Gong Y
    Clin Genet; 2022 Dec; 102(6):474-482. PubMed ID: 36071563
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis.
    Bai L; Zheng L; Li B; Huang H; Shi X; Yi Y
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Apr; 48(4):565-574. PubMed ID: 37385619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China.
    Wang X; Zhang A; Huang M; Chen L; Hu Q; Lu Y; Cheng L
    Front Genet; 2020; 11():953. PubMed ID: 33014018
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 12.