219 related articles for article (PubMed ID: 16086322)
1. The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences.
Charbonnier F; Baert-Desurmont S; Liang P; Di Fiore F; Martin C; Frerot S; Olschwang S; Wang Q; Buisine MP; Gilbert B; Nilbert M; Lindblom A; Frebourg T
Hum Mutat; 2005 Sep; 26(3):255-61. PubMed ID: 16086322
[TBL] [Abstract][Full Text] [Related]
2. Characterization of new founder Alu-mediated rearrangements in MSH2 gene associated with a Lynch syndrome phenotype.
Pérez-Cabornero L; Borrás Flores E; Infante Sanz M; Velasco Sampedro E; Acedo Becares A; Lastra Aras E; Cuevas González J; Pineda Riu M; Ramón y Cajal Asensio T; Capellá Munar G; Miner Pino C; Durán Domínguez M
Cancer Prev Res (Phila); 2011 Oct; 4(10):1546-55. PubMed ID: 21778331
[TBL] [Abstract][Full Text] [Related]
3. Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC.
Stella A; Surdo NC; Lastella P; Barana D; Oliani C; Tibiletti MG; Viel A; Natale C; Piepoli A; Marra G; Guanti G
Clin Genet; 2007 Feb; 71(2):130-9. PubMed ID: 17250661
[TBL] [Abstract][Full Text] [Related]
4. Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
Wehner M; Mangold E; Sengteller M; Friedrichs N; Aretz S; Friedl W; Propping P; Pagenstecher C
Eur J Hum Genet; 2005 Aug; 13(8):983-6. PubMed ID: 15870828
[TBL] [Abstract][Full Text] [Related]
5. Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC).
Li L; McVety S; Younan R; Liang P; Du Sart D; Gordon PH; Hutter P; Hogervorst FB; Chong G; Foulkes WD
Hum Mutat; 2006 Apr; 27(4):388. PubMed ID: 16541406
[TBL] [Abstract][Full Text] [Related]
6. Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer.
Baert-Desurmont S; Buisine MP; Bessenay E; Frerot S; Lovecchio T; Martin C; Olschwang S; Wang Q; Frebourg T
Eur J Hum Genet; 2007 Mar; 15(3):383-6. PubMed ID: 17228328
[TBL] [Abstract][Full Text] [Related]
7. Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion.
Pastrello C; Baglioni S; Tibiletti MG; Papi L; Fornasarig M; Morabito A; Agostini M; Genuardi M; Viel A
Eur J Hum Genet; 2006 Jan; 14(1):63-8. PubMed ID: 16251890
[TBL] [Abstract][Full Text] [Related]
8. [Detection of MSH2 gene mutation by PCR].
Zheng D; Liu XP; Li TG; Li J; Tang LJ; Hu WX
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Apr; 31(2):200-3. PubMed ID: 16706114
[TBL] [Abstract][Full Text] [Related]
9. A large MSH2 Alu insertion mutation causes HNPCC in a German kindred.
Kloor M; Sutter C; Wentzensen N; Cremer FW; Buckowitz A; Keller M; von Knebel Doeberitz M; Gebert J
Hum Genet; 2004 Oct; 115(5):432-8. PubMed ID: 15340835
[TBL] [Abstract][Full Text] [Related]
10. A novel germline mutation of MSH2 in a hereditary nonpolyposis colorectal cancer patient with liposarcoma.
Hirata K; Kanemitsu S; Nakayama Y; Nagata N; Itoh H; Ohnishi H; Ishikawa H; Furukawa Y;
Am J Gastroenterol; 2006 Jan; 101(1):193-6. PubMed ID: 16405554
[TBL] [Abstract][Full Text] [Related]
11. Homeologous recombination between AluSx-sequences as a cause of hemophilia.
Rossetti LC; Goodeve A; Larripa IB; De Brasi CD
Hum Mutat; 2004 Nov; 24(5):440. PubMed ID: 15459970
[TBL] [Abstract][Full Text] [Related]
12. Functional analysis of HNPCC-related missense mutations in MSH2.
Lützen A; de Wind N; Georgijevic D; Nielsen FC; Rasmussen LJ
Mutat Res; 2008 Oct; 645(1-2):44-55. PubMed ID: 18822302
[TBL] [Abstract][Full Text] [Related]
13. Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.
Viel A; Petronzelli F; Della Puppa L; Lucci-Cordisco E; Fornasarig M; Pucciarelli S; Rovella V; Quaia M; Ponz de Leon M; Boiocchi M; Genuardi M
Hum Mutat; 2002 Nov; 20(5):368-74. PubMed ID: 12402334
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?
Hiltunen M; Helisalmi S; Mannermaa A; Alafuzoff I; Koivisto AM; Lehtovirta M; Pirskanen M; Sulkava R; Verkkoniemi A; Soininen H
Eur J Hum Genet; 2000 Apr; 8(4):259-66. PubMed ID: 10854108
[TBL] [Abstract][Full Text] [Related]
15. Novel germline and somatic mutations of the MSH2 gene in hereditary non-polyposis colorectal cancer.
Ding DC; Huang RL; Chen CH; Chao CF; Chu TY
Clin Genet; 2007 Feb; 71(2):190-2. PubMed ID: 17250671
[No Abstract] [Full Text] [Related]
16. Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancer.
Morak M; Laner A; Scholz M; Madorf T; Holinski-Feder E
Eur J Gastroenterol Hepatol; 2008 Nov; 20(11):1101-5. PubMed ID: 19047842
[TBL] [Abstract][Full Text] [Related]
17. New founding mutation in MSH2 associated with hereditary nonpolyposis colorectal cancer syndrome on the Island of Tenerife.
Medina-Arana V; Barrios Y; Fernández-Peralta A; Herrera M; Chinea N; Lorenzo N; Jiménez A; Martín-López JV; González-Hermoso F; Salido E; González-Aguilera JJ
Cancer Lett; 2006 Dec; 244(2):268-73. PubMed ID: 16500024
[TBL] [Abstract][Full Text] [Related]
18. The 10-Mb paracentric inversion of chromosome arm 2p in activating MSH2 and causing hereditary nonpolyposis colorectal cancer: re-annotation and mutational mechanisms.
Chen JM
Genes Chromosomes Cancer; 2008 Jun; 47(6):543-5. PubMed ID: 18335504
[No Abstract] [Full Text] [Related]
19. A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.
Park SJ; Lee KA; Park TS; Kim NK; Song J; Kim BY; Choi JR
Cancer Genet Cytogenet; 2008 Apr; 182(2):136-9. PubMed ID: 18406877
[TBL] [Abstract][Full Text] [Related]
20. A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Liu Q; Hesson LB; Nunez AC; Packham D; Williams R; Ward RL; Sloane MA
Carcinogenesis; 2016 Jan; 37(1):10-17. PubMed ID: 26498247
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]