190 related articles for article (PubMed ID: 27721366)
1. Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome.
Chen C; Zhang X; Wang D; Wang F; Pan J; Wang Z; Liu C; Wu L; Lu H; Li N; Wei J; Shi H; Wan H; Zhu M; Chen S; Zhou Y; Zhou X; Yang L; Liu J
Med Sci Monit; 2016 Oct; 22():3628-3640. PubMed ID: 27721366
[TBL] [Abstract][Full Text] [Related]
2. One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.
Chen C; Zhang X; Wang F; Liu C; Lu H; Wan H; Wei J; Liu J
DNA Cell Biol; 2012 Oct; 31(10):1535-40. PubMed ID: 22928647
[TBL] [Abstract][Full Text] [Related]
3. LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.
Volikos E; Robinson J; Aittomäki K; Mecklin JP; Järvinen H; Westerman AM; de Rooji FW; Vogel T; Moeslein G; Launonen V; Tomlinson IP; Silver AR; Aaltonen LA
J Med Genet; 2006 May; 43(5):e18. PubMed ID: 16648371
[TBL] [Abstract][Full Text] [Related]
4. Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
Ylikorkala A; Avizienyte E; Tomlinson IP; Tiainen M; Roth S; Loukola A; Hemminki A; Johansson M; Sistonen P; Markie D; Neale K; Phillips R; Zauber P; Twama T; Sampson J; Järvinen H; Mäkelä TP; Aaltonen LA
Hum Mol Genet; 1999 Jan; 8(1):45-51. PubMed ID: 9887330
[TBL] [Abstract][Full Text] [Related]
5. [Mutation screening of LKB1 gene in familial Peutz-Jeghers syndrome patients].
Chen CY; Zhang XM; Wang FY; Wang ZK; Zhu M; Ma GJ; Zhang YY; Jin XX; Shi H; Liu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):121-5. PubMed ID: 22487816
[TBL] [Abstract][Full Text] [Related]
6. High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
Papp J; Kovacs ME; Solyom S; Kasler M; Børresen-Dale AL; Olah E
BMC Med Genet; 2010 Nov; 11():169. PubMed ID: 21118512
[TBL] [Abstract][Full Text] [Related]
7. Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome.
Gu GL; Zhang Z; Zhang YH; Yu PF; Dong ZW; Yang HR; Yuan Y
World J Gastroenterol; 2021 Oct; 27(39):6631-6646. PubMed ID: 34754157
[TBL] [Abstract][Full Text] [Related]
8. Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
de Leng WW; Jansen M; Carvalho R; Polak M; Musler AR; Milne AN; Keller JJ; Menko FH; de Rooij FW; Iacobuzio-Donahue CA; Giardiello FM; Weterman MA; Offerhaus GJ
Clin Genet; 2007 Dec; 72(6):568-73. PubMed ID: 17924967
[TBL] [Abstract][Full Text] [Related]
9. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients.
Yoon KA; Ku JL; Choi HS; Heo SC; Jeong SY; Park YJ; Kim NK; Kim JC; Jung PM; Park JG
Br J Cancer; 2000 Apr; 82(8):1403-6. PubMed ID: 10780518
[TBL] [Abstract][Full Text] [Related]
10. [Clinical characteristics and mutation analysis of the LKB1 gene in a Peutz-Jeghers syndrome pedigree].
Pan J; Li M; Jin Y; Zhang XM; Zhu M; Chen SQ
Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):145-9. PubMed ID: 23527983
[TBL] [Abstract][Full Text] [Related]
11. [Germline LKB1 gene mutation screening in 4 Chinese Peutz-Jeghers syndrome pedigrees].
Wang Z; Yan Z; Bi G; Xu W; Huang T
Zhonghua Wai Ke Za Zhi; 2000 Feb; 38(2):104-5. PubMed ID: 11832000
[TBL] [Abstract][Full Text] [Related]
12. Peutz-Jeghers syndrome without
Jiang LX; Chen YR; Xu ZX; Zhang YH; Zhang Z; Yu PF; Dong ZW; Yang HR; Gu GL
World J Gastroenterol; 2023 Jun; 29(21):3302-3317. PubMed ID: 37377590
[TBL] [Abstract][Full Text] [Related]
13. Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.
Zheng B; Pan J; Wang Y; Li M; Lian M; Zheng Y; Jin Y
Dig Dis Sci; 2013 Oct; 58(10):2868-72. PubMed ID: 23892522
[TBL] [Abstract][Full Text] [Related]
14. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.
Su GH; Hruban RH; Bansal RK; Bova GS; Tang DJ; Shekher MC; Westerman AM; Entius MM; Goggins M; Yeo CJ; Kern SE
Am J Pathol; 1999 Jun; 154(6):1835-40. PubMed ID: 10362809
[TBL] [Abstract][Full Text] [Related]
15. A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.
Zheng B; Wang C; Jia Z; Liu Z; Li M; Jin Y; Pan J
J Pediatr Gastroenterol Nutr; 2017 Apr; 64(4):559-564. PubMed ID: 27467201
[TBL] [Abstract][Full Text] [Related]
16. Distinct promoter methylation patterns of LKB1 in the hamartomatous polyps of Peutz-Jeghers syndrome and its potential in gastrointestinal malignancy prediction.
Li T; Lin W; Zhao Y; Zhu J; Sun T; Ren L
Orphanet J Rare Dis; 2020 Aug; 15(1):208. PubMed ID: 32799895
[TBL] [Abstract][Full Text] [Related]
17. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
[TBL] [Abstract][Full Text] [Related]
18. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
Mehenni H; Gehrig C; Nezu J; Oku A; Shimane M; Rossier C; Guex N; Blouin JL; Scott HS; Antonarakis SE
Am J Hum Genet; 1998 Dec; 63(6):1641-50. PubMed ID: 9837816
[TBL] [Abstract][Full Text] [Related]
19. A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
Liu L; Du X; Nie J
Clin Res Hepatol Gastroenterol; 2011 Mar; 35(3):221-6. PubMed ID: 21411391
[TBL] [Abstract][Full Text] [Related]
20. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
BMC Med Genet; 2017 Nov; 18(1):130. PubMed ID: 29141581
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
