BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 26962827)

  • 1. Clinical and Molecular Characterization of NF1 Patients: Single-Center Experience of 32 Patients From China.
    Zhu L; Zhang Y; Tong H; Shao M; Gu Y; Du X; Wang P; Shi L; Zhang L; Bi M; Wang X; Zhang G
    Medicine (Baltimore); 2016 Mar; 95(10):e3043. PubMed ID: 26962827
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A highly sensitive genetic protocol to detect NF1 mutations.
    Valero MC; Martín Y; Hernández-Imaz E; Marina Hernández A; Meleán G; Valero AM; Javier Rodríguez-Álvarez F; Tellería D; Hernández-Chico C
    J Mol Diagn; 2011 Mar; 13(2):113-22. PubMed ID: 21354044
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.
    Ko JM; Sohn YB; Jeong SY; Kim HJ; Messiaen LM
    Pediatr Neurol; 2013 Jun; 48(6):447-53. PubMed ID: 23668869
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.
    Palma Milla C; Lezana Rosales JM; López Montiel J; Andrés Garrido LD; Sánchez Linares C; Carmona Tamajón S; Torres Fernández C; Sánchez González P; Franco Freire S; Benito López C; López Siles J
    Ann Hum Genet; 2018 Nov; 82(6):425-436. PubMed ID: 30014477
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1.
    Mao B; Chen S; Chen X; Yu X; Zhai X; Yang T; Li L; Wang Z; Zhao X; Zhang X
    BMC Med Genet; 2018 Jun; 19(1):101. PubMed ID: 29914388
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Analysis of NF1 gene mutations in two sporadic patients with neurofibromatosis type 1].
    Zhao X; Zhou Q; Cai L; Zhao Z; Zhang L; Wang P; Zhang G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):489-492. PubMed ID: 30098240
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular diagnosis of neurofibromatosis type 1: 2 years experience.
    Griffiths S; Thompson P; Frayling I; Upadhyaya M
    Fam Cancer; 2007; 6(1):21-34. PubMed ID: 16944272
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.
    N Abdel-Aziz N; Y El-Kamah G; A Khairat R; R Mohamed H; Z Gad Y; El-Ghor AM; Amr KS
    Mol Genet Genomic Med; 2021 Dec; 9(12):e1631. PubMed ID: 34080803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1.
    Esposito T; Piluso G; Saracino D; Uccello R; Schettino C; Dato C; Capaldo G; Giugliano T; Varriale B; Paolisso G; Di Iorio G; Melone MA
    J Neurochem; 2015 Dec; 135(6):1123-8. PubMed ID: 26478990
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.
    Jeong SY; Park SJ; Kim HJ
    J Korean Med Sci; 2006 Feb; 21(1):107-12. PubMed ID: 16479075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotype categorization of neurofibromatosis type I and correlation to NF1 mutation types.
    Kang E; Kim YM; Seo GH; Oh A; Yoon HM; Ra YS; Kim EK; Kim H; Heo SH; Kim GH; Osborn MJ; Tolar J; Yoo HW; Lee BH
    J Hum Genet; 2020 Jan; 65(2):79-89. PubMed ID: 31776437
    [TBL] [Abstract][Full Text] [Related]  

  • 12. NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience.
    Sabbagh A; Pasmant E; Imbard A; Luscan A; Soares M; Blanché H; Laurendeau I; Ferkal S; Vidaud M; Pinson S; Bellanné-Chantelot C; Vidaud D; Parfait B; Wolkenstein P
    Hum Mutat; 2013 Nov; 34(11):1510-8. PubMed ID: 23913538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel and recurrent mutations in the NF1 gene in Italian patients with neurofibromatosis type 1.
    De Luca A; Schirinzi A; Buccino A; Bottillo I; Sinibaldi L; Torrente I; Ciavarella A; Dottorini T; Porciello R; Giustini S; Calvieri S; Dallapiccola B
    Hum Mutat; 2004 Jun; 23(6):629. PubMed ID: 15146469
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population.
    Zhang J; Tong H; Fu X; Zhang Y; Liu J; Cheng R; Liang J; Peng J; Sun Z; Liu H; Zhang F; Lu W; Li M; Yao Z
    Sci Rep; 2015 Jun; 5():11291. PubMed ID: 26056819
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype.
    Terzi YK; Sirin B; Hosgor G; Serdaroglu E; Anlar B; Aysun S; Ayter S
    Childs Nerv Syst; 2012 Jun; 28(6):943-6. PubMed ID: 22159552
    [No Abstract]   [Full Text] [Related]  

  • 16. Breast cancer in women with neurofibromatosis type 1 (NF1): a comprehensive case series with molecular insights into its aggressive phenotype.
    Yap YS; Munusamy P; Lim C; Chan CHT; Prawira A; Loke SY; Lim SH; Ong KW; Yong WS; Ng SBH; Tan IBH; Callen DF; Lim JCT; Thike AA; Tan PH; Lee ASG
    Breast Cancer Res Treat; 2018 Oct; 171(3):719-735. PubMed ID: 29926297
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical characteristics and NF1 gene mutation analysis of three successive generations in three different Indian families with neurofibromatosis type 1 and peripheral nerve sheath tumours.
    Prasad BCM; Chandra VVR; Sudarsan A; Kumar PS; Sarma PVGK
    J Clin Neurosci; 2018 Jul; 53():62-68. PubMed ID: 29680440
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.
    Terzi YK; Oguzkan-Balci S; Anlar B; Aysun S; Guran S; Ayter S
    Genet Couns; 2009; 20(2):195-202. PubMed ID: 19650418
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients.
    Wimmer K; Yao S; Claes K; Kehrer-Sawatzki H; Tinschert S; De Raedt T; Legius E; Callens T; Beiglböck H; Maertens O; Messiaen L
    Genes Chromosomes Cancer; 2006 Mar; 45(3):265-76. PubMed ID: 16283621
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of novel NF1 mutations and rapid mutation prescreening with Pyrosequencing.
    Brinckmann A; Mischung C; Bässmann I; Kühnisch J; Schuelke M; Tinschert S; Nürnberg P
    Electrophoresis; 2007 Dec; 28(23):4295-301. PubMed ID: 18041031
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.