BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 8157761)

  • 1. p53 expression in three separate tumours from a patient with Li-Fraumeni's syndrome.
    King P; Craft AW; Malcolm AJ
    J Clin Pathol; 1993 Jul; 46(7):676-7. PubMed ID: 8157761
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multiple synchronous lung cancers and atypical adenomatous hyperplasia in Li-Fraumeni syndrome.
    Nadav Y; Pastorino U; Nicholson AG
    Histopathology; 1998 Jul; 33(1):52-4. PubMed ID: 9726049
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Detection of both mutant and wild-type p53 protein in normal skin fibroblasts and demonstration of a shared 'second hit' on p53 in diverse tumors from a cancer-prone family with Li-Fraumeni syndrome.
    Srivastava S; Tong YA; Devadas K; Zou ZQ; Sykes VW; Chen Y; Blattner WA; Pirollo K; Chang EH
    Oncogene; 1992 May; 7(5):987-91. PubMed ID: 1373881
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Li-Fraumeni syndrome: a p53 family affair.
    Iwakuma T; Lozano G; Flores ER
    Cell Cycle; 2005 Jul; 4(7):865-7. PubMed ID: 15917654
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein.
    Frebourg T; Kassel J; Lam KT; Gryka MA; Barbier N; Andersen TI; Børresen AL; Friend SH
    Proc Natl Acad Sci U S A; 1992 Jul; 89(14):6413-7. PubMed ID: 1631137
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple primary cutaneous melanomas in Li-Fraumeni syndrome.
    Curiel-Lewandrowski C; Speetzen LS; Cranmer L; Warneke JA; Loescher LJ
    Arch Dermatol; 2011 Feb; 147(2):248-50. PubMed ID: 21339461
    [No Abstract]   [Full Text] [Related]  

  • 9. RNA polymerase III transcription can be derepressed by oncogenes or mutations that compromise p53 function in tumours and Li-Fraumeni syndrome.
    Stein T; Crighton D; Boyle JM; Varley JM; White RJ
    Oncogene; 2002 May; 21(19):2961-70. PubMed ID: 12082526
    [TBL] [Abstract][Full Text] [Related]  

  • 10. p53+/mdm2- atypical lipomatous tumor/well-differentiated liposarcoma in young children: an early expression of Li-Fraumeni syndrome.
    Debelenko LV; Perez-Atayde AR; Dubois SG; Grier HE; Pai SY; Shamberger RC; Kozakewich HP
    Pediatr Dev Pathol; 2010; 13(3):218-24. PubMed ID: 20028212
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Li-Fraumeni syndrome].
    Frebourg T
    Bull Cancer; 1997 Jul; 84(7):735-40. PubMed ID: 9339200
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of the oligomerization defects of two p53 mutants found in families with Li-Fraumeni and Li-Fraumeni-like syndrome.
    Davison TS; Yin P; Nie E; Kay C; Arrowsmith CH
    Oncogene; 1998 Aug; 17(5):651-6. PubMed ID: 9704931
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complex replication error causes p53 mutation in a Li-Fraumeni family.
    Strauss EA; Hosler MR; Herzog P; Salhany K; Louie R; Felix CA
    Cancer Res; 1995 Aug; 55(15):3237-41. PubMed ID: 7614454
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Divergent control of Cav-1 expression in non-cancerous Li-Fraumeni syndrome and human cancer cell lines.
    Sherif ZA; Sultan AS
    Cancer Biol Ther; 2013 Jan; 14(1):29-38. PubMed ID: 23114650
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of p53 oligomerization domain mutations isolated from Li-Fraumeni and Li-Fraumeni like family members.
    Lomax ME; Barnes DM; Hupp TR; Picksley SM; Camplejohn RS
    Oncogene; 1998 Aug; 17(5):643-9. PubMed ID: 9704930
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Potential of Advexin: a p53 gene-replacement therapy in Li-Fraumeni syndrome.
    Nemunaitis JM; Nemunaitis J
    Future Oncol; 2008 Dec; 4(6):759-68. PubMed ID: 19086841
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Li-Fraumeni syndrome: multiple distinct brain tumours in two brothers.
    Lechien JR; Brotchi J; Van Maldergem L; Costa de Araujo P; Bruninx G; Hilbert P; Nubourgh Y
    Neurochirurgie; 2014; 60(1-2):51-4. PubMed ID: 24636404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The first case of Li-Fraumeni syndrome in Bosnia and Herzegovina: case report.
    Vranic S; Kapur L; Foco F; Bilalovic N; Hainaut P
    Pathologica; 2006 Apr; 98(2):156-9. PubMed ID: 16929790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Li-Fraumeni syndrome and germ-line mutations of the p53 gene].
    Leblanc T; Soussi T
    Arch Pediatr; 1994 Jan; 1(1):61-70. PubMed ID: 8087224
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.