119 related articles for article (PubMed ID: 11975096)
1. [Glioblastoma multiforme as a manifestation of Turcot syndrome].
Grips E; Wentzensen N; Sutter C; Sedlaczek O; Gebert J; Weigel R; Schwartz A; von Knebel-Doeberitz M; Hennerici M
Nervenarzt; 2002 Feb; 73(2):177-82. PubMed ID: 11975096
[TBL] [Abstract][Full Text] [Related]
2. [The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation].
Czakó L; Tiszlavicz L; Takács R; Baradnay G; Lonovics J; Cserni G; Závodná K; Bartosova Z
Orv Hetil; 2005 May; 146(20):1009-16. PubMed ID: 15945244
[TBL] [Abstract][Full Text] [Related]
3. The molecular basis of Turcot's syndrome.
Hamilton SR; Liu B; Parsons RE; Papadopoulos N; Jen J; Powell SM; Krush AJ; Berk T; Cohen Z; Tetu B
N Engl J Med; 1995 Mar; 332(13):839-47. PubMed ID: 7661930
[TBL] [Abstract][Full Text] [Related]
4. Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.
Schiemann U; Müller-Koch Y; Gross M; Daum J; Lohse P; Baretton G; Muders M; Mussack T; Kopp R; Holinski-Feder E
Digestion; 2004; 69(3):166-76. PubMed ID: 15118395
[TBL] [Abstract][Full Text] [Related]
5. Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer.
Raevaara TE; Timoharju T; Lönnqvist KE; Kariola R; Steinhoff M; Hofstra RM; Mangold E; Vos YJ; Nyström-Lahti M
J Med Genet; 2002 Oct; 39(10):747-50. PubMed ID: 12362032
[No Abstract] [Full Text] [Related]
6. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
Lindor NM; Rabe K; Petersen GM; Haile R; Casey G; Baron J; Gallinger S; Bapat B; Aronson M; Hopper J; Jass J; LeMarchand L; Grove J; Potter J; Newcomb P; Terdiman JP; Conrad P; Moslein G; Goldberg R; Ziogas A; Anton-Culver H; de Andrade M; Siegmund K; Thibodeau SN; Boardman LA; Seminara D
JAMA; 2005 Apr; 293(16):1979-85. PubMed ID: 15855431
[TBL] [Abstract][Full Text] [Related]
7. Genetic testing for hereditary nonpolyposis colorectal cancer.
Hoedema R; Monroe T; Bos C; Palmer S; Kim D; Marvin M; Luchtefeld M
Am Surg; 2003 May; 69(5):387-91; discussion 391-2. PubMed ID: 12769209
[TBL] [Abstract][Full Text] [Related]
8. Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.
Millar AL; Pal T; Madlensky L; Sherman C; Temple L; Mitri A; Cheng H; Marcus V; Gallinger S; Redston M; Bapat B; Narod S
Hum Mol Genet; 1999 May; 8(5):823-9. PubMed ID: 10196371
[TBL] [Abstract][Full Text] [Related]
9. Clinical significance of early-onset "sporadic" colorectal cancer with microsatellite instability.
Jass JR
Dis Colon Rectum; 2003 Oct; 46(10):1305-9. PubMed ID: 14530666
[No Abstract] [Full Text] [Related]
10. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene.
Shin KH; Shin JH; Kim JH; Park JG
Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355
[TBL] [Abstract][Full Text] [Related]
11. Hereditary non-polyposis colorectal cancer (HNPCC): new germline mutation (190-191 del AA) in the human MLH1 gene and review of clinical guidelines for surveillance of affected families.
Schiemann U; Papatheodorou L; Glasl S; Gross M
Eur J Med Res; 2001 Mar; 6(3):93-100. PubMed ID: 11309221
[TBL] [Abstract][Full Text] [Related]
12. Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening.
Potocnik U; Glavac D; Golouh R; Ravnik-Glavac M
Cancer Genet Cytogenet; 2001 Apr; 126(2):85-96. PubMed ID: 11376800
[TBL] [Abstract][Full Text] [Related]
13. A novel Q562X mutation identified in the hMLH1 gene in a Slovenian patient with hereditary nonpolyposis colorectal cancer.
Potocnik U; Glavac D; Golouh R; Ravnik-Glavac M
Hum Hered; 2000; 50(2):140-1. PubMed ID: 10799973
[No Abstract] [Full Text] [Related]
14. The novel germline mutation of the hMLH1 gene in a case of suspected hereditary non-polyposis colorectal cancer (HNPCC) in a patient with no family history of cancer.
Tomita N; Fukunaga M; Okamura S; Nakata K; Ohzato H; Tamura S; Sugimoto K; Aihara T; Miki H; Takatsuka Y; Matsuura N; Ishikawa H; Iwanaga T; Fukayama N; Sugano K
Jpn J Clin Oncol; 2004 Sep; 34(9):556-60. PubMed ID: 15466831
[TBL] [Abstract][Full Text] [Related]
15. Genomic structure of the human DNA mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC).
Olipitz W; Sill H
Hum Mol Genet; 2000 Jan; 9(2):321. PubMed ID: 11769276
[No Abstract] [Full Text] [Related]
16. Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome.
Risinger JI; Barrett JC; Watson P; Lynch HT; Boyd J
Cancer; 1996 May; 77(9):1836-43. PubMed ID: 8646682
[TBL] [Abstract][Full Text] [Related]
17. Diagnosis and management of hereditary non-polyposis colon cancer.
DeFrancisco J; Grady WM
Gastrointest Endosc; 2003 Sep; 58(3):390-408. PubMed ID: 14528214
[No Abstract] [Full Text] [Related]
18. Early-age-at-onset colorectal cancer and microsatellite instability as markers of hereditary nonpolyposis colorectal cancer.
Pucciarelli S; Agostini M; Viel A; Bertorelle R; Russo V; Toppan P; Lise M
Dis Colon Rectum; 2003 Mar; 46(3):305-12. PubMed ID: 12626904
[TBL] [Abstract][Full Text] [Related]
19. The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer.
Samowitz WS; Curtin K; Lin HH; Robertson MA; Schaffer D; Nichols M; Gruenthal K; Leppert MF; Slattery ML
Gastroenterology; 2001 Oct; 121(4):830-8. PubMed ID: 11606497
[TBL] [Abstract][Full Text] [Related]
20. Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer.
Rey JM; Noruzinia M; Brouillet JP; Sarda P; Maudelonde T; Pujol P
Cancer Genet Cytogenet; 2004 Dec; 155(2):149-51. PubMed ID: 15571801
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]