169 related articles for article (PubMed ID: 23892522)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.
Wu BD; Wang YJ; Fan LL; Huang H; Zhou P; Yang M; Shi XL
Biomed Res Int; 2020; 2020():9159315. PubMed ID: 32462036
[TBL] [Abstract][Full Text] [Related]
7. Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.
Ausavarat S; Leoyklang P; Vejchapipat P; Chongsrisawat V; Suphapeetiporn K; Shotelersuk V
World J Gastroenterol; 2009 Nov; 15(42):5364-7. PubMed ID: 19908348
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
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. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome.
Yang HR; Ko JS; Seo JK
Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878
[TBL] [Abstract][Full Text] [Related]
19. De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.
Hernan I; Roig I; Martin B; Gamundi MJ; Martinez-Gimeno M; Carballo M
Clin Genet; 2004 Jul; 66(1):58-62. PubMed ID: 15200509
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
