BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 34335240)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. [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]  

  • 8. Identification of variants in 94 Chinese patients with hereditary spherocytosis by next-generation sequencing.
    Wang WJ; Xie JD; Yao H; Ding ZX; Jiang AR; Ma L; Shen HJ; Chen SN
    Clin Genet; 2023 Jan; 103(1):67-78. PubMed ID: 36203343
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. An
    Wang X; Mao L; Shen N; Peng J; Zhu Y; Hu Q; Lu Y
    Oncotarget; 2017 Dec; 8(68):113282-113286. PubMed ID: 29348906
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel
    Wang X; Yi B; Mu K; Shen N; Zhu Y; Hu Q; Lu Y
    Oncotarget; 2017 Nov; 8(57):96791-96797. PubMed ID: 29228571
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 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 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]  

  • 16. A novel
    Liu Y; Zheng J; Song L; Fang Y; Sun C; Li N; Liu G; Shu J
    Exp Ther Med; 2020 Oct; 20(4):3253-3259. PubMed ID: 32855695
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Novel SPTB frameshift mutation in a Chinese neonatal case of hereditary spherocytosis type 2: A case report.
    Xu C; Wu Y; Wang D; Zhang X; Wang N
    Exp Ther Med; 2022 Sep; 24(3):600. PubMed ID: 35949318
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of
    Tian Y; Wang Y; Yang J; Gao P; Xu H; Wu Y; Li M; Chen H; Lu D; Yan H
    Front Genet; 2023; 14():1221853. PubMed ID: 37795245
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.