BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 28575107)

  • 1. Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling.
    Tomar S; Sethi R; Sundar G; Quah TC; Quah BL; Lai PS
    PLoS One; 2017; 12(6):e0178776. PubMed ID: 28575107
    [TBL] [Abstract][Full Text] [Related]  

  • 2. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
    Parma D; Ferrer M; Luce L; Giliberto F; Szijan I
    PLoS One; 2017; 12(12):e0189736. PubMed ID: 29261756
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of mutations in the
    Kiet NC; Khuong LT; Minh DD; ; Quan NHM; Xinh PT; Trang NNC; Luan NT; Khai NM; Vu HA
    Mol Vis; 2019; 25():215-221. PubMed ID: 30996590
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectrum of germline
    Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
    Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational screening of germline
    Nguyen HH; Nguyen HTT; Vu NP; Le QT; Pham CM; Huyen TT; Manh H; Pham HLB; Nguyen TD; Le HTT; Van Nong H
    Mol Vis; 2018; 24():231-238. PubMed ID: 29568217
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients.
    Dommering CJ; Mol BM; Moll AC; Burton M; Cloos J; Dorsman JC; Meijers-Heijboer H; van der Hout AH
    J Med Genet; 2014 Jun; 51(6):366-74. PubMed ID: 24688104
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic screening in patients with Retinoblastoma in Israel.
    Sagi M; Frenkel A; Eilat A; Weinberg N; Frenkel S; Pe'er J; Abeliovich D; Lerer I
    Fam Cancer; 2015 Sep; 14(3):471-80. PubMed ID: 25754945
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
    Kalsoom S; Wasim M; Afzal S; Shahzad MS; Ramzan S; Awan AR; Anjum AA; Ramzan K
    Mol Vis; 2015; 21():1085-92. PubMed ID: 26396485
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.
    Mohd Khalid MK; Yakob Y; Md Yasin R; Wee Teik K; Siew CG; Rahmat J; Ramasamy S; Alagaratnam J
    Mol Vis; 2015; 21():1185-90. PubMed ID: 26539030
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing.
    Zou Y; Li J; Hua P; Liang T; Ji X; Zhao P
    Mol Vis; 2021; 27():1-16. PubMed ID: 33456302
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
    Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
    Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.
    Abidi O; Knari S; Sefri H; Charif M; Senechal A; Hamel C; Rouba H; Zaghloul K; El Kettani A; Lenaers G; Barakat A
    Mol Vis; 2011; 17():3541-7. PubMed ID: 22219649
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening of RB1 gene mutations in Chinese patients with retinoblastoma and preliminary exploration of genotype-phenotype correlations.
    He MY; An Y; Gao YJ; Qian XW; Li G; Qian J
    Mol Vis; 2014; 20():545-52. PubMed ID: 24791139
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
    Chai P; Luo Y; Yu J; Li Y; Yang J; Zhuang A; Fan J; Han M; Jia R
    Exp Eye Res; 2021 Apr; 205():108456. PubMed ID: 33493472
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.
    Parsam VL; Kannabiran C; Honavar S; Vemuganti GK; Ali MJ
    J Genet; 2009 Dec; 88(4):517-27. PubMed ID: 20090211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
    Quiñonez-Silva G; Dávalos-Salas M; Recillas-Targa F; Ostrosky-Wegman P; Aranda DA; Benítez-Bribiesca L
    Clin Epigenetics; 2016; 8():1. PubMed ID: 26753011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma.
    Grotta S; D'Elia G; Scavelli R; Genovese S; Surace C; Sirleto P; Cozza R; Romanzo A; De Ioris MA; Valente P; Tomaiuolo AC; Lepri FR; Franchin T; Ciocca L; Russo S; Locatelli F; Angioni A
    BMC Cancer; 2015 Nov; 15():841. PubMed ID: 26530098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
    Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
    Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults.
    Ayari Jeridi H; Bouguila H; Ansperger-Rescher B; Baroudi O; Mdimegh I; Omran I; Charradi K; Bouzayene H; Benammar-Elgaaïed A; Lohmann DR
    Exp Eye Res; 2014 Jul; 124():48-55. PubMed ID: 24810223
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.