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Journal Abstract Search

266 related items for PubMed ID: 10435620

  • 1. p53 compound heterozygosity in a severely affected child with Li-Fraumeni syndrome.
    Quesnel S, Verselis S, Portwine C, Garber J, White M, Feunteun J, Malkin D, Li FP.
    Oncogene; 1999 Jul 08; 18(27):3970-8. PubMed ID: 10435620
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  • 2. [Li-Fraumeni syndrome].
    Frebourg T.
    Bull Cancer; 1997 Jul 08; 84(7):735-40. PubMed ID: 9339200
    [Abstract] [Full Text] [Related]

  • 3. [Germline mutations of the p53 gene].
    Frebourg T.
    Pathol Biol (Paris); 1997 Dec 08; 45(10):845-51. PubMed ID: 9769948
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  • 4. A germline 2.35 kb deletion of p53 genomic DNA creating a specific loss of the oligomerization domain inherited in a Li-Fraumeni syndrome family.
    Plummer SJ, Santibáñez-Koref M, Kurosaki T, Liao S, Noble B, Fain PR, Anton-Culver H, Casey G.
    Oncogene; 1994 Nov 08; 9(11):3273-80. PubMed ID: 7936651
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  • 5. Cancer risks from germ line tumor suppressor gene mutations.
    Frebourg T, Malkin D, Friend S.
    Princess Takamatsu Symp; 1991 Nov 08; 22():61-70. PubMed ID: 1844252
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  • 6. Germ-line exclusion of a single p53 allele by premature termination of translation in a Li-Fraumeni syndrome family.
    Stolzenberg MC, Brugières L, Gardes M, Dessarps-Freichey F, Chompret A, Bressac B, Lenoir G, Bonaïti-Pellié C, Lemerle J, Feunteun J.
    Oncogene; 1994 Oct 08; 9(10):2799-804. PubMed ID: 8084585
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  • 7. 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 27; 20(33):4441-9. PubMed ID: 11494139
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  • 8. [Li-Fraumeni syndrome and germ-line mutations of the p53 gene].
    Leblanc T, Soussi T.
    Arch Pediatr; 1994 Jan 27; 1(1):61-70. PubMed ID: 8087224
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  • 10. p53 Germline mutation in a patient with Li-Fraumeni Syndrome and three metachronous malignancies.
    Pötzsch C, Voigtländer T, Lübbert M.
    J Cancer Res Clin Oncol; 2002 Aug 27; 128(8):456-60. PubMed ID: 12200603
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  • 14. 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 15; 63(20):6643-50. PubMed ID: 14583457
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  • 16. Early detection of adrenocortical carcinoma in a child with Li-Fraumeni syndrome.
    Lin MT, Shieh JJ, Chang JH, Chang SW, Chen TC, Hsu WH.
    Pediatr Blood Cancer; 2009 Apr 15; 52(4):541-4. PubMed ID: 19101993
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  • 18. Germline mutations of the p53 tumor-suppressor gene in cancer-prone families: a review.
    Soussi T, Leblanc T, Baruchel A, Schaison G.
    Nouv Rev Fr Hematol (1978); 1993 Feb 15; 35(1):33-6. PubMed ID: 8511038
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  • 19. The Li-Fraumeni syndrome: an inherited susceptibility to cancer.
    Evans SC, Lozano G.
    Mol Med Today; 1997 Sep 15; 3(9):390-5. PubMed ID: 9302689
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  • 20. The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.
    Achatz MI, Olivier M, Le Calvez F, Martel-Planche G, Lopes A, Rossi BM, Ashton-Prolla P, Giugliani R, Palmero EI, Vargas FR, Da Rocha JC, Vettore AL, Hainaut P.
    Cancer Lett; 2007 Jan 08; 245(1-2):96-102. PubMed ID: 16494995
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