201 related articles for article (PubMed ID: 29141581)
1. 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]
2. A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.
Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
Dig Dis Sci; 2017 Nov; 62(11):3014-3020. PubMed ID: 28986664
[TBL] [Abstract][Full Text] [Related]
3. A novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.
Wang Z; Chen Y; Wu B; Zheng H; He J; Jiang B
BMC Med Genet; 2011 Dec; 12():161. PubMed ID: 22168747
[TBL] [Abstract][Full Text] [Related]
4. A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.
Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Sun SH; Ning SB
Medicine (Baltimore); 2017 Dec; 96(49):e8591. PubMed ID: 29245219
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome.
Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR
BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044
[TBL] [Abstract][Full Text] [Related]
7. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
Huang Z; Miao S; Wang L; Zhang P; Wu B; Wu J; Huang Y
BMC Gastroenterol; 2015 Nov; 15():166. PubMed ID: 26607058
[TBL] [Abstract][Full Text] [Related]
8. [Mutation analysis of STK11 gene coding region for 20 Chinese patients with Peutz-Jeghers syndrome].
Zhao X; Li Y; Ling Y; Chen H; Zhang B; Xia T; Zhou P
Nan Fang Yi Ke Da Xue Xue Bao; 2012 Apr; 32(4):511-4. PubMed ID: 22543132
[TBL] [Abstract][Full Text] [Related]
9. [Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].
Zhao X; Huang Y; Yang B; Zhao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):294-7. PubMed ID: 24928005
[TBL] [Abstract][Full Text] [Related]
10. A De Novo mutation of STK11 gene in a Chinese patient with Peutz-Jeghers syndrome.
Gao Y; Zhang FM; Huang S; Wang X; Zhang P; Huang XD; Ji GZ; Fan ZN
Dig Dis Sci; 2010 Apr; 55(4):1032-6. PubMed ID: 19507030
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Identification of a novel de novo STK11 mutation in a Chinese child with Peutz-Jeghers syndrome.
Liu WL; Li F; He ZX; Jiang HY; Ai R; Zhu XP; Chen XX; Ma HW
J Int Med Res; 2011; 39(5):2033-8. PubMed ID: 22118009
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.
Thakur N; Reddy DN; Rao GV; Mohankrishna P; Singh L; Chandak GR
BMC Med Genet; 2006 Sep; 7():73. PubMed ID: 17010210
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report.
Chen JH; Zheng JJ; Guo Q; Liu C; Luo B; Tang SB; Cheng JD; Huang EW
BMC Med Genet; 2017 Feb; 18(1):19. PubMed ID: 28231849
[TBL] [Abstract][Full Text] [Related]
16. Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.
Tan H; Mei L; Huang Y; Yang P; Li H; Peng Y; Chen C; Wei X; Pan Q; Liang D; Wu L
BMC Med Genet; 2016 Nov; 17(1):77. PubMed ID: 27821076
[TBL] [Abstract][Full Text] [Related]
17. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome.
Lipsa A; Kowtal P; Sarin R
Hum Mol Genet; 2019 Jun; 28(11):1885-1893. PubMed ID: 30689838
[TBL] [Abstract][Full Text] [Related]
18. Clinical manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome.
Chiang JM; Chen TC
Asian J Surg; 2018 Sep; 41(5):480-485. PubMed ID: 28869103
[TBL] [Abstract][Full Text] [Related]
19. Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.
Zhao ZY; Jiang YL; Li BR; Li J; Jin XW; Yu ED; Ning SB
BMC Surg; 2018 Apr; 18(1):24. PubMed ID: 29685139
[TBL] [Abstract][Full Text] [Related]
20. Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.
Dai L; Fu L; Liu D; Zhang K; Wu Y; Meng H; Zhang B; Guan X; Guo H; Bai Y
Dig Dis Sci; 2014 Aug; 59(8):1856-61. PubMed ID: 24604241
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
