93 related articles for article (PubMed ID: 17139886)
61. Elevated microsatellite alterations at selected tetranucleotides (EMAST) and mismatch repair gene expression in prostate cancer.
Burger M; Denzinger S; Hammerschmied CG; Tannapfel A; Obermann EC; Wieland WF; Hartmann A; Stoehr R
J Mol Med (Berl); 2006 Oct; 84(10):833-41. PubMed ID: 16924473
[TBL] [Abstract][Full Text] [Related]
62. Immunohistochemical pattern of hMSH2/hMLH1 in familial and sporadic colorectal, gastric, endometrial and ovarian carcinomas with instability in microsatellite sequences.
Chiaravalli AM; Furlan D; Facco C; Tibiletti MG; Dionigi A; Casati B; Albarello L; Riva C; Capella C
Virchows Arch; 2001 Jan; 438(1):39-48. PubMed ID: 11213834
[TBL] [Abstract][Full Text] [Related]
63. Mutational analysis of transforming growth factor beta receptor type II and DNA mismatch repair genes in sporadic endometrial carcinomas with microsatellite instability.
Ohwada M; Suzuki M; Saga Y; Suzuki T; Ikeda M; Yamada M; Sato I
Oncol Rep; 2000; 7(4):789-92. PubMed ID: 10854545
[TBL] [Abstract][Full Text] [Related]
64. Microsatellite instability differences between familial and sporadic ovarian cancers.
Arzimanoglou II; Lallas T; Osborne M; Barber H; Gilbert F
Carcinogenesis; 1996 Sep; 17(9):1799-804. PubMed ID: 8824498
[TBL] [Abstract][Full Text] [Related]
65. Mutations in DNA mismatch repair genes are not responsible for microsatellite instability in most sporadic endometrial carcinomas.
Katabuchi H; van Rees B; Lambers AR; Ronnett BM; Blazes MS; Leach FS; Cho KR; Hedrick L
Cancer Res; 1995 Dec; 55(23):5556-60. PubMed ID: 7585634
[TBL] [Abstract][Full Text] [Related]
66. Clinical and genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer families.
Wang XL; Yuan Y; Zhang SZ; Cai SR; Huang YQ; Jiang Q; Zheng S
World J Gastroenterol; 2006 Jul; 12(25):4074-7. PubMed ID: 16810763
[TBL] [Abstract][Full Text] [Related]
67. Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.
Plaschke J; Krüger S; Pistorius S; Theissig F; Saeger HD; Schackert HK
Int J Cancer; 2002 Feb; 97(5):643-8. PubMed ID: 11807791
[TBL] [Abstract][Full Text] [Related]
68. Methylation of the hMLH1 promoter but no hMLH1 mutations in sporadic gastric carcinomas with high-level microsatellite instability.
Bevilacqua RA; Simpson AJ
Int J Cancer; 2000 Jul; 87(2):200-3. PubMed ID: 10861474
[TBL] [Abstract][Full Text] [Related]
69. Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.
Skeldon SC; Semotiuk K; Aronson M; Holter S; Gallinger S; Pollett A; Kuk C; van Rhijn B; Bostrom P; Cohen Z; Fleshner NE; Jewett MA; Hanna S; Shariat SF; Van Der Kwast TH; Evans A; Catto J; Bapat B; Zlotta AR
Eur Urol; 2013 Feb; 63(2):379-85. PubMed ID: 22883484
[TBL] [Abstract][Full Text] [Related]
70. Mismatch repair deficiency in sporadic synchronous colorectal cancer.
Brueckl WM; Limmert T; Brabletz T; Guenther K; Jung A; Hermann K; Wiest GH; Kirchner T; Hohenberger W; Hahn EG; Wein A
Anticancer Res; 2000; 20(6C):4727-32. PubMed ID: 11205208
[TBL] [Abstract][Full Text] [Related]
71. Molecular genetics of hereditary nonpolyposis colorectal cancer.
Boland CR
Ann N Y Acad Sci; 2000 Jun; 910():50-9; discussion 59-61. PubMed ID: 10911905
[TBL] [Abstract][Full Text] [Related]
72. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
Lagerstedt Robinson K; Liu T; Vandrovcova J; Halvarsson B; Clendenning M; Frebourg T; Papadopoulos N; Kinzler KW; Vogelstein B; Peltomäki P; Kolodner RD; Nilbert M; Lindblom A
J Natl Cancer Inst; 2007 Feb; 99(4):291-9. PubMed ID: 17312306
[TBL] [Abstract][Full Text] [Related]
73. Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.
Pistorius S; Görgens H; Plaschke J; Hoehl R; Krüger S; Engel C; Saeger HD; Schackert HK
Cancer Lett; 2007 Apr; 248(1):89-95. PubMed ID: 16837128
[TBL] [Abstract][Full Text] [Related]
74. 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]
75. Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women.
Smolarz B; Makowska M; Samulak D; Michalska MM; Romanowicz H
Fam Cancer; 2015 Mar; 14(1):81-8. PubMed ID: 25134804
[TBL] [Abstract][Full Text] [Related]
76. [DNA mismatch repair enzyme hMSH2 genetic polymorphism in southern Chinese Han population].
He Y; Zhuang ZX; He CH; Liu RQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):256-8. PubMed ID: 12778459
[TBL] [Abstract][Full Text] [Related]
77. [Association of IVS10+12G>A polymorphism in hMSH2 gene with colorectal cancer in Chinese].
Zhou JN; Wang DQ; Song L; Li SP; Ding JH; Ma GJ; Chen SQ; Zhang XM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):579-83. PubMed ID: 20931542
[TBL] [Abstract][Full Text] [Related]
78. Loss of hMSH2 gene expression correlates with improved survival in patients with sporadic colorectal cancer.
Langner E; Przybylowska K; Trzcinski R; Mik M; Galbfach P; Smolarz B; Romanowicz-Makowska H; Smigileski J; Kulig A; Dziki A
J Genet; 2010 Apr; 89(1):101-4. PubMed ID: 20505253
[No Abstract] [Full Text] [Related]
79. The T/G mutation in exon 8 of hMSH2 gene in the sporadic colon cancer patients.
Langner E; Przybyłowska K; Przemysław G; Kunierz J; Smolarz B; Romanowicz-Makowska H; Migileski J; Kulig A; Dziki A
Acta Chir Iugosl; 2006; 53(2):57-60. PubMed ID: 17139886
[TBL] [Abstract][Full Text] [Related]
80. Novel hMSH2, hMSH6 and hMLH1 gene mutations and microsatellite instability in sporadic colorectal cancer.
Chaksangchaichot P; Punyarit P; Petmitr S
J Cancer Res Clin Oncol; 2007 Jan; 133(1):65-70. PubMed ID: 16902769
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]