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2. Investigation of germline PTEN, p53, p16(INK4A)/p14(ARF), and CDK4 alterations in familial glioma. Tachibana I; Smith JS; Sato K; Hosek SM; Kimmel DW; Jenkins RB Am J Med Genet; 2000 May; 92(2):136-41. PubMed ID: 10797439 [TBL] [Abstract][Full Text] [Related]
3. Analysis of p53 tumor suppressor gene in families with multiple glioma patients. Paunu N; Syrjäkoski K; Sankila R; Simola KO; Helén P; Niemelä M; Matikainen M; Isola J; Haapasalo H J Neurooncol; 2001 Dec; 55(3):159-65. PubMed ID: 11859970 [TBL] [Abstract][Full Text] [Related]
4. Distinct PTEN mutational spectra in hereditary non-polyposis colon cancer syndrome-related endometrial carcinomas compared to sporadic microsatellite unstable tumors. Zhou XP; Kuismanen S; Nystrom-Lahti M; Peltomaki P; Eng C Hum Mol Genet; 2002 Feb; 11(4):445-50. PubMed ID: 11854177 [TBL] [Abstract][Full Text] [Related]
5. Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome. Burt EC; McGown G; Thorncroft M; James LA; Birch JM; Varley JM Br J Cancer; 1999 Apr; 80(1-2):9-10. PubMed ID: 10389970 [TBL] [Abstract][Full Text] [Related]
6. Turcot's syndrome of glioma and polyposis occurs in the absence of germ line mutations of exons 5 to 9 of the p53 gene. Kikuchi T; Rempel SA; Rutz HP; de Tribolet N; Mulligan L; Cavenee WK; Jothy S; Leduy L; Van Meir EG Cancer Res; 1993 Mar; 53(5):957-61. PubMed ID: 8439970 [TBL] [Abstract][Full Text] [Related]
7. Chromosomal instability and p53 inactivation are required for genesis of glioblastoma but not for colorectal cancer in patients with germline mismatch repair gene mutation. Leung SY; Yuen ST; Chan TL; Chan AS; Ho JW; Kwan K; Fan YW; Hung KN; Chung LP; Wyllie AH Oncogene; 2000 Aug; 19(35):4079-83. PubMed ID: 10962567 [TBL] [Abstract][Full Text] [Related]
8. Germline mutations of p53 but not p16/CDKN2 or PTEN/MMAC1 tumor suppressor genes predispose to gliomas. The ANOCEF Group. Association des NeuroOncologues d'Expression Française. Zhou XP; Sanson M; Hoang-Xuan K; Robin E; Taillandier L; He J; Mokhtari K; Cornu P; Delattre JY; Thomas G; Hamelin R Ann Neurol; 1999 Dec; 46(6):913-6. PubMed ID: 10589545 [TBL] [Abstract][Full Text] [Related]
9. PTEN mutational spectra, expression levels, and subcellular localization in microsatellite stable and unstable colorectal cancers. Zhou XP; Loukola A; Salovaara R; Nystrom-Lahti M; Peltomäki P; de la Chapelle A; Aaltonen LA; Eng C Am J Pathol; 2002 Aug; 161(2):439-47. PubMed ID: 12163369 [TBL] [Abstract][Full Text] [Related]
10. Germline mutations in the PTEN gene in Israeli patients with Bannayan-Riley-Ruvalcaba syndrome and women with familial breast cancer. Figer A; Kaplan A; Frydman M; Lev D; Paswell J; Papa MZ; Goldman B; Friedman E Clin Genet; 2002 Oct; 62(4):298-302. PubMed ID: 12372056 [TBL] [Abstract][Full Text] [Related]
11. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer. Carethers JM; Stoffel EM World J Gastroenterol; 2015 Aug; 21(31):9253-61. PubMed ID: 26309352 [TBL] [Abstract][Full Text] [Related]
13. Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients. Kim IJ; Ku JL; Kang HC; Park JH; Yoon KA; Shin Y; Park HW; Jang SG; Lim SK; Han SY; Shin YK; Lee MR; Jeong SY; Shin HR; Lee JS; Kim WH; Park JG Hum Genet; 2004 Nov; 115(6):498-503. PubMed ID: 15449173 [TBL] [Abstract][Full Text] [Related]
14. Identification and characterization of families with aggregation of lung cancer. Tomizawa Y; Adachi J; Kohno T; Yamaguchi N; Saito R; Yokota J Jpn J Clin Oncol; 1998 Mar; 28(3):192-5. PubMed ID: 9614442 [TBL] [Abstract][Full Text] [Related]
15. Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene. De Rosa M; Fasano C; Panariello L; Scarano MI; Belli G; Iannelli A; Ciciliano F; Izzo P Oncogene; 2000 Mar; 19(13):1719-23. PubMed ID: 10763829 [TBL] [Abstract][Full Text] [Related]
16. Presence of allelic loss and PTEN mutations in malignant gliomas from Malay patients. Zainuddin N; Jaafar H; Isa MN; Abdullah JM Med J Malaysia; 2004 Oct; 59(4):468-79. PubMed ID: 15779579 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel PTEN intronic deletion in Li-Fraumeni syndrome and its effect on RNA processing. Brown LT; Sexsmith E; Malkin D Cancer Genet Cytogenet; 2000 Nov; 123(1):65-8. PubMed ID: 11120338 [TBL] [Abstract][Full Text] [Related]
19. Absence of hereditary mutations in exons 5 through 9 of the p53 gene and exon 24 of the neurofibromin gene in families with glioma. van Meyel DJ; Ramsay DA; Chambers AF; Macdonald DR; Cairncross JG Ann Neurol; 1994 Jan; 35(1):120-2. PubMed ID: 8285583 [TBL] [Abstract][Full Text] [Related]
20. Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability. Kuismanen SA; Moisio AL; Schweizer P; Truninger K; Salovaara R; Arola J; Butzow R; Jiricny J; Nyström-Lahti M; Peltomäki P Am J Pathol; 2002 Jun; 160(6):1953-8. PubMed ID: 12057899 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]