BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 25935441)

  • 21. Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours.
    Aury-Landas J; Bougeard G; Castel H; Hernandez-Vargas H; Drouet A; Latouche JB; Schouft MT; Férec C; Leroux D; Lasset C; Coupier I; Caron O; Herceg Z; Frebourg T; Flaman JM
    Eur J Hum Genet; 2013 Dec; 21(12):1369-76. PubMed ID: 23612572
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Tumor protein 53 mutations and inherited cancer: beyond Li-Fraumeni syndrome.
    Palmero EI; Achatz MI; Ashton-Prolla P; Olivier M; Hainaut P
    Curr Opin Oncol; 2010 Jan; 22(1):64-9. PubMed ID: 19952748
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Next generation sequencing is informing phenotype: a TP53 example.
    O'Shea R; Clarke R; Berkley E; Giffney C; Farrell M; O'Donovan E; Gallagher DJ
    Fam Cancer; 2018 Jan; 17(1):123-128. PubMed ID: 28509937
    [TBL] [Abstract][Full Text] [Related]  

  • 24. p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers.
    Macedo GS; Vieira IA; Vianna FSL; Alemar B; Giacomazzi J; Brandalize APC; Caleffi M; Volc SM; de Campos Reis Galvão H; Palmero EI; Achatz MI; Ashton-Prolla P
    Fam Cancer; 2018 Apr; 17(2):269-274. PubMed ID: 28756477
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.
    Silva AG; Ewald IP; Sapienza M; Pinheiro M; Peixoto A; de Nóbrega AF; Carraro DM; Teixeira MR; Ashton-Prolla P; Achatz MI; Rosenberg C; Krepischi AC
    BMC Cancer; 2012 Jun; 12():237. PubMed ID: 22691290
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiple primary tumors in a family with Li-Fraumeni syndrome with a TP53 germline mutation identified by next-generation sequencing.
    Zampiga V; Danesi R; Tedaldi G; Tebaldi M; Cangini I; Pirini F; Pittureri C; Amaducci E; Guidi L; Faedi M; Amadori D; Falcini F; Calistri D
    Int J Biol Markers; 2016 Dec; 31(4):e461-e465. PubMed ID: 27516001
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.
    Valdez JM; Nichols KE; Kesserwan C
    Br J Haematol; 2017 Feb; 176(4):539-552. PubMed ID: 27984644
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Tissue-specific expression of SV40 in tumors associated with the Li-Fraumeni syndrome.
    Malkin D; Chilton-MacNeill S; Meister LA; Sexsmith E; Diller L; Garcea RL
    Oncogene; 2001 Jul; 20(33):4441-9. PubMed ID: 11494139
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype.
    Olivier M; Goldgar DE; Sodha N; Ohgaki H; Kleihues P; Hainaut P; Eeles RA
    Cancer Res; 2003 Oct; 63(20):6643-50. PubMed ID: 14583457
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li-Fraumeni syndrome).
    Petry V; Bonadio RC; Cagnacci AQC; Senna LAL; Campos RDNG; Cotti GC; Hoff PM; Fragoso MCBV; Estevez-Diz MDP
    Fam Cancer; 2020 Jan; 19(1):47-53. PubMed ID: 31748977
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome.
    Castronovo C; Rossetti R; Rusconi D; Recalcati MP; Cacciatore C; Beccaria E; Calcaterra V; Invernizzi P; Larizza D; Finelli P; Persani L
    Hum Reprod; 2014 Feb; 29(2):368-79. PubMed ID: 24324027
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Whole-exome analysis of a Li-Fraumeni family trio with a novel TP53 PRD mutation and anticipation profile.
    Franceschi S; Spugnesi L; Aretini P; Lessi F; Scarpitta R; Galli A; Congregati C; Caligo MA; Mazzanti CM
    Carcinogenesis; 2017 Sep; 38(9):938-943. PubMed ID: 28911001
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Functional studies of a novel germline p53 splicing mutation identified in a patient with Li-Fraumeni-like syndrome.
    Piao J; Sakurai N; Iwamoto S; Nishioka J; Nakatani K; Komada Y; Mizutani S; Takagi M
    Mol Carcinog; 2013 Oct; 52(10):770-6. PubMed ID: 22495821
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evaluation of TP53 Pro72Arg and MDM2 SNP285-SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations.
    Ponti F; Corsini S; Gnoli M; Pedrini E; Mordenti M; Sangiorgi L
    Fam Cancer; 2016 Oct; 15(4):635-43. PubMed ID: 26956143
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A child with Li-Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies.
    Schlegelberger B; Kreipe H; Lehmann U; Steinemann D; Ripperger T; Göhring G; Thomay K; Rump A; Di Donato N; Suttorp M
    Pediatr Blood Cancer; 2015 Aug; 62(8):1481-4. PubMed ID: 25787918
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Atypical fibroxanthoma arising in a young patient with Li-Fraumeni syndrome.
    Lee SM; Zhang W; Fernandez MP
    J Cutan Pathol; 2014 Mar; 41(3):303-7. PubMed ID: 24299451
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Number of rare germline CNVs and TP53 mutation types.
    Silva AG; Achatz IM; Krepischi AC; Pearson PL; Rosenberg C
    Orphanet J Rare Dis; 2012 Dec; 7():101. PubMed ID: 23259501
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rectal leiomyosarcoma as the initial phenotypic manifestation of Li-Fraumeni-like syndrome: a case report and review of the literature.
    Severino NP; Waisberg J; Fragoso MCBV; de Lima LGCA; Balsamo F; Henriques AC; Bianco B; de Sousa Gehrke F
    J Med Case Rep; 2022 Dec; 16(1):468. PubMed ID: 36529791
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis.
    Light N; Layeghifard M; Attery A; Subasri V; Zatzman M; Anderson ND; Hatkar R; Blay S; Chen D; Novokmet A; Fuligni F; Tran J; de Borja R; Agarwal H; Waldman L; Abegglen LM; Albertson D; Finlay JL; Hansford JR; Behjati S; Villani A; Gerstung M; Alexandrov LB; Somers GR; Schiffman JD; Rotter V; Malkin D; Shlien A
    Nat Commun; 2023 Jan; 14(1):77. PubMed ID: 36604421
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High frequency of de novo mutations in Li-Fraumeni syndrome.
    Gonzalez KD; Buzin CH; Noltner KA; Gu D; Li W; Malkin D; Sommer SS
    J Med Genet; 2009 Oct; 46(10):689-93. PubMed ID: 19556618
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.