229 related articles for article (PubMed ID: 7676234)
21. Molecular genetic studies of sporadic and familial renal cell carcinoma.
Gnarra JR; Glenn GM; Latif F; Anglard P; Lerman MI; Zbar B; Linehan WM
Urol Clin North Am; 1993 May; 20(2):207-16. PubMed ID: 8098558
[TBL] [Abstract][Full Text] [Related]
22. [Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma].
Menko FH; Nooy MA; Vasen HF
Ned Tijdschr Geneeskd; 1996 Jun; 140(26):1347-50. PubMed ID: 8710022
[No Abstract] [Full Text] [Related]
23. Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.
Bahuau M; Vidaud D; Jenkins RB; Bièche I; Kimmel DW; Assouline B; Smith JS; Alderete B; Cayuela JM; Harpey JP; Caille B; Vidaud M
Cancer Res; 1998 Jun; 58(11):2298-303. PubMed ID: 9622062
[TBL] [Abstract][Full Text] [Related]
24. Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?
Kehrer-Sawatzki H; Cooper DN
J Med Genet; 2008 Oct; 45(10):622-31. PubMed ID: 18511569
[TBL] [Abstract][Full Text] [Related]
25. Genetic basis of tumour development.
Ponz de Leon M
Ital J Gastroenterol; 1996 May; 28(4):232-45. PubMed ID: 8842841
[TBL] [Abstract][Full Text] [Related]
26. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.
Balogh K; Hunyady L; Patocs A; Gergics P; Valkusz Z; Toth M; Racz K
Clin Endocrinol (Oxf); 2007 Nov; 67(5):727-34. PubMed ID: 17953629
[TBL] [Abstract][Full Text] [Related]
27. Phaeochromocytoma in children.
Armstrong R; Sridhar M; Greenhalgh KL; Howell L; Jones C; Landes C; McPartland JL; Moores C; Losty PD; Didi M
Arch Dis Child; 2008 Oct; 93(10):899-904. PubMed ID: 18499773
[TBL] [Abstract][Full Text] [Related]
28. Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas.
Kanno H; Kondo K; Ito S; Yamamoto I; Fujii S; Torigoe S; Sakai N; Hosaka M; Shuin T; Yao M
Cancer Res; 1994 Sep; 54(18):4845-7. PubMed ID: 8069849
[TBL] [Abstract][Full Text] [Related]
29. The cell-type-specificity of inherited predispositions to tumours: review and hypothesis.
Bignold LP
Cancer Lett; 2004 Dec; 216(2):127-46. PubMed ID: 15533589
[TBL] [Abstract][Full Text] [Related]
30. Inherited predisposition to cancer: a historical overview.
Lynch HT; Shaw TG; Lynch JF
Am J Med Genet C Semin Med Genet; 2004 Aug; 129C(1):5-22. PubMed ID: 15264268
[TBL] [Abstract][Full Text] [Related]
31. Tumor suppressor genes and their alterations in breast cancer.
Lee EY
Semin Cancer Biol; 1995 Jun; 6(3):119-25. PubMed ID: 7495979
[TBL] [Abstract][Full Text] [Related]
32. Lack of mutations in the TP53 tumor suppressor gene exons 5 to 8 in Fanconi's anemia.
Jonveaux P; Le Coniat M; Grausz D; Berger R
Nouv Rev Fr Hematol (1978); 1991; 33(5):343-5. PubMed ID: 1803324
[TBL] [Abstract][Full Text] [Related]
33. [Tumor suppressor genes: occurrence, significance and function].
Scheurlen W; Kreth HW
Monatsschr Kinderheilkd; 1991 Oct; 139(10):650-4. PubMed ID: 1660097
[TBL] [Abstract][Full Text] [Related]
34. Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.
Marsh DJ; Theodosopoulos G; Howell V; Richardson AL; Benn DE; Proos AL; Eng C; Robinson BG
Neoplasia; 2001; 3(3):236-44. PubMed ID: 11494117
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [Cancer genetics of TSC2 gene mutant(Eker) rat model].
Hino O
Nihon Rinsho; 2000 Jun; 58(6):1255-61. PubMed ID: 10879050
[TBL] [Abstract][Full Text] [Related]
37. [Basic science and clinical aspects of familial brain tumors].
Kanno H
Brain Nerve; 2012 May; 64(5):557-64. PubMed ID: 22570069
[TBL] [Abstract][Full Text] [Related]
38. Tumor suppressor genes and inherited predisposition to malignancy.
Skuse GR; Rowley PT
Semin Oncol; 1989 Apr; 16(2):128-37. PubMed ID: 2565603
[No Abstract] [Full Text] [Related]
39. Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
Whelan AJ; Bartsch D; Goodfellow PJ
N Engl J Med; 1995 Oct; 333(15):975-7. PubMed ID: 7666917
[No Abstract] [Full Text] [Related]
40. Imaging of cancer predisposition syndromes in children.
Monsalve J; Kapur J; Malkin D; Babyn PS
Radiographics; 2011; 31(1):263-80. PubMed ID: 21257945
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
