291 related articles for article (PubMed ID: 32814491)
1.
Lou H; Zhai C; Gong L; Pan H; Pan H; Zhang Y; Yang M; Hu Z
J Int Med Res; 2020 Aug; 48(8):300060519896435. PubMed ID: 32814491
[TBL] [Abstract][Full Text] [Related]
2. A de novo germline mutation of APC for inheritable colon cancer in a Chinese family using multigene next generation sequencing.
Zhang Y; Lu G; Hu Q; Wang X; Li C; Mao Y; Cui M
Biochem Biophys Res Commun; 2014 May; 447(3):503-7. PubMed ID: 24735542
[TBL] [Abstract][Full Text] [Related]
3. Detection of mismatch repair gene germline mutation carrier among Chinese population with colorectal cancer.
Jin HY; Liu X; Li VK; Ding Y; Yang B; Geng J; Lai R; Ding S; Ni M; Zhao R
BMC Cancer; 2008 Feb; 8():44. PubMed ID: 18257912
[TBL] [Abstract][Full Text] [Related]
4. BRIP-1 germline mutation and its role in colon cancer: presentation of two case reports and review of literature.
Ali M; Delozier CD; Chaudhary U
BMC Med Genet; 2019 May; 20(1):75. PubMed ID: 31064327
[TBL] [Abstract][Full Text] [Related]
5. [KRAS and BRAF gene mutations in correlation with clinicopathologic features of colorectal carcinoma in Chinese].
Zhu XL; Cai X; Zhang L; Yang F; Sheng WQ; Lu YM; Du X; Zhou XY
Zhonghua Bing Li Xue Za Zhi; 2012 Sep; 41(9):584-9. PubMed ID: 23157824
[TBL] [Abstract][Full Text] [Related]
6. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.
Wang D; Liang S; Zhang Z; Zhao G; Hu Y; Liang S; Zhang X; Banerjee S
Oncotarget; 2017 Mar; 8(13):21327-21335. PubMed ID: 28423518
[TBL] [Abstract][Full Text] [Related]
7. A Chinese family affected by lynch syndrome caused by MLH1 mutation.
Jia S; Zhang M; Sun Y; Yan H; Zhao F; Li Z; Ji J
BMC Med Genet; 2018 Jun; 19(1):106. PubMed ID: 29929473
[TBL] [Abstract][Full Text] [Related]
8. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
[TBL] [Abstract][Full Text] [Related]
9. Germline mutations in patients with multiple colorectal polyps in China.
Li CG; Jin P; Yang L; Zang WC; Kang Q; Li N; He Y; Xu J; Zhang C; Wang X; Sheng JQ
J Gastroenterol Hepatol; 2017 Oct; 32(10):1723-1729. PubMed ID: 28251689
[TBL] [Abstract][Full Text] [Related]
10. Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study.
Yi D; Xu L; Luo J; You X; Huang T; Zi Y; Li X; Wang R; Zhong Z; Tang X; Li A; Shi Y; Rao J; Zhang Y; Sang J
Hum Genomics; 2019 Jan; 13(1):4. PubMed ID: 30630526
[TBL] [Abstract][Full Text] [Related]
11. NRAS germline variant G138R and multiple rare somatic mutations on APC in colorectal cancer patients in Taiwan by next generation sequencing.
Chang PY; Chen JS; Chang NC; Chang SC; Wang MC; Tsai SH; Wen YH; Tsai WS; Chan EC; Lu JJ
Oncotarget; 2016 Jun; 7(25):37566-37580. PubMed ID: 27121310
[TBL] [Abstract][Full Text] [Related]
12. KRAS mutation and primary tumor location do not affect efficacy of bevacizumab-containing chemotherapy in stagae IV colorectal cancer patients.
Sun DC; Shi Y; Wang YR; Lv Y; Yan H; Mao H; Wang ZK; Wu ZY; Shi WW; Dai GH
Sci Rep; 2017 Oct; 7(1):14368. PubMed ID: 29085005
[TBL] [Abstract][Full Text] [Related]
13. Genomic Signature of Driver Genes Identified by Target Next-Generation Sequencing in Chinese Non-Small Cell Lung Cancer.
Wen S; Dai L; Wang L; Wang W; Wu D; Wang K; He Z; Wang A; Chen H; Zhang P; Dong X; Dong YA; Wang K; Yao M; Wang M
Oncologist; 2019 Nov; 24(11):e1070-e1081. PubMed ID: 30902917
[TBL] [Abstract][Full Text] [Related]
14. A novel heterozygous large deletion of MSH6 gene in a Chinese family with Lynch syndrome.
Liu Y; Wang M; Chen Q; Zheng Q; Li G; Cheng Q; Liu S; Ye S
Gene; 2019 Jul; 704():103-112. PubMed ID: 30974197
[TBL] [Abstract][Full Text] [Related]
15. [Study on the germline mutation of MSH6 gene in Chinese hereditary nonpolyposis colorectal cancer pedigrees using PCR based sequencing].
Yan SY; Zhou XY; Cai SJ; Yu BH; Zhang TM; Li XM; Lu YM; Zhou HH; Mo SJ; Du X; Shi DR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):640-5. PubMed ID: 18067074
[TBL] [Abstract][Full Text] [Related]
16. Case report of ascending colon cancer and multiple jejunal GISTs in a patient with neurofibromatosis type 1 (NF1).
Shang L; Fang Z; Liu J; Du F; Jing H; Xu Y; Dong K; Zhang X; Wu H; Jing C; Li L
BMC Cancer; 2019 Dec; 19(1):1196. PubMed ID: 31805970
[TBL] [Abstract][Full Text] [Related]
17. A germline mutation in Rab43 gene identified from a cancer family predisposes to a hereditary liver-colon cancer syndrome.
Jiang Y; Sun Y; Hu J; Yu N; Liu H; Fan J; Ning X; Li Y; Liu B; Sun Y; Zhang J; Qiu X; Fu S; Zhou C; Xu H
BMC Cancer; 2019 Jun; 19(1):613. PubMed ID: 31226964
[TBL] [Abstract][Full Text] [Related]
18. Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer.
Chan TL; Yuen ST; Chung LP; Ho JW; Kwan KY; Chan AS; Ho JC; Leung SY; Wyllie AH
J Natl Cancer Inst; 1999 Jul; 91(14):1221-6. PubMed ID: 10413423
[TBL] [Abstract][Full Text] [Related]
19. Somatic mutation profiling and HER2 status in KRAS-positive Chinese colorectal cancer patients.
Dong Z; Kong L; Wan Z; Zhu F; Zhong M; Lv Y; Zhao P; Shi H
Sci Rep; 2019 Nov; 9(1):16894. PubMed ID: 31729406
[TBL] [Abstract][Full Text] [Related]
20. Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1.
Mao B; Chen S; Chen X; Yu X; Zhai X; Yang T; Li L; Wang Z; Zhao X; Zhang X
BMC Med Genet; 2018 Jun; 19(1):101. PubMed ID: 29914388
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]