BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 36035481)

  • 1. Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.
    Vercellati C; Marcello AP; Fattizzo B; Zaninoni A; Seresini A; Barcellini W; Bianchi P; Fermo E
    Front Physiol; 2022; 13():949044. PubMed ID: 36035481
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. The Spectrum of
    Chonat S; Risinger M; Sakthivel H; Niss O; Rothman JA; Hsieh L; Chou ST; Kwiatkowski JL; Khandros E; Gorman MF; Wells DT; Maghathe T; Dagaonkar N; Seu KG; Zhang K; Zhang W; Kalfa TA
    Front Physiol; 2019; 10():815. PubMed ID: 31333484
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis.
    Alshomar A; Ahmed AA; Rasheed Z; Alhumaydhi FA; Alsagaby S; Aljohani ASM; Alkhamiss AS; Alghsham R; Althwab SA; Khan MI; Fernández N; Al Abdulmonem W
    Nucleosides Nucleotides Nucleic Acids; 2024 Feb; ():1-20. PubMed ID: 38319988
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience.
    Agarwal AM; McMurty V; Clayton AL; Bolia A; Reading NS; Mani C; Patel JL; Rets A
    Eur J Haematol; 2023 Jun; 110(6):688-695. PubMed ID: 36825813
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Effects of
    Herrera-Tirado IM; Espinoza-Mata LL; Rizo-delaTorre LDC; Becerra-Solano LE; Ibarra-Cortés B; Perea-Díaz FJ
    Genet Test Mol Biomarkers; 2022 May; 26(5):270-276. PubMed ID: 35638908
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. [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]  

  • 19. 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]  

  • 20. Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil.
    Svidnicki MCCM; Zanetta GK; Congrains-Castillo A; Costa FF; Saad STO
    Ann Hematol; 2020 May; 99(5):955-962. PubMed ID: 32266426
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.