BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

297 related articles for article (PubMed ID: 26830532)

  • 1. 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]  

  • 2. 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]  

  • 3. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.
    Qin L; Nie Y; Zhang H; Chen L; Zhang D; Lin Y; Ru K
    J Hum Genet; 2020 Apr; 65(4):427-434. PubMed ID: 31980736
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-degree of hemolysis correlation in hereditary spherocytosis.
    Shi Y; Li Y; Yang X; Li X; Peng G; Zhao X; Liu X; Zhao Y; Hu J; Hu X; Zhang B; Zhou K; Yang Y; Xiong Y; Li J; Fan H; Yang W; Ye L; Jing L; Zhang L; Zhang F
    BMC Genomics; 2023 Jun; 24(1):304. PubMed ID: 37280519
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
    More TA; Devendra R; Dongerdiye R; Warang P; Kedar P
    Mol Genet Genomics; 2023 Mar; 298(2):427-439. PubMed ID: 36598564
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.
    Wang D; Song L; Shen L; Zhang K; Lv Y; Gao M; Ma J; Wan Y; Gai Z; Liu Y
    Front Pharmacol; 2021; 12():644352. PubMed ID: 34335240
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Clinical characteristics and genetic analysis of hereditary spherocytosis caused by mutations of ANK1 and SPTB genes].
    Gong J; He XL; Zou RY; Chen KK; You YL; Zou H; Tian X; Zhu CG
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 Apr; 21(4):370-374. PubMed ID: 31014431
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
    Hao L; Li S; Ma D; Chen S; Zhang B; Xiao D; Zhang J; Jiang N; Jiang S; Ma J
    J Cell Mol Med; 2019 Jun; 23(6):4454-4463. PubMed ID: 31016877
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis.
    Shen H; Gao Z; Ye Q
    Genet Test Mol Biomarkers; 2024 Jan; 28(1):33-38. PubMed ID: 38294355
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.
    Xie F; Lei L; Cai B; Gan L; Gao Y; Liu X; Zhou L; Jiang J
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1577. PubMed ID: 33620149
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis.
    Fan LL; Liu JS; Huang H; Du R; Xiang R
    J Gene Med; 2019 Feb; 21(2-3):e3073. PubMed ID: 30690801
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature.
    Luo Y; Li Z; Huang L; Tian J; Xiong M; Yang Z
    Acta Haematol; 2018; 140(2):77-86. PubMed ID: 30227413
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.