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Items: 1 to 20 of 116

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. doi: 10.1007/s10620-013-2737-3. Epub 2013 Jul 27.

PMID:
23892522
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 25;15:166. doi: 10.1186/s12876-015-0397-9.

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.

4.

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. doi: 10.1007/s10620-009-0837-x. Epub 2009 Jun 9.

PMID:
19507030
5.
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 30;11:169. doi: 10.1186/1471-2350-11-169.

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 14;15(42):5364-7.

8.

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 10;22:3628-3640.

9.
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 8;17(1):77.

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. doi: 10.1007/s10620-017-4741-5. Epub 2017 Oct 6.

PMID:
28986664
12.

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. doi: 10.1007/s10620-014-3077-7. Epub 2014 Mar 7.

PMID:
24604241
13.

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. Epub 2012 Aug 28.

PMID:
22928647
14.

Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.

Zuo YG, Xu KJ, Su B, Ho MG, Liu YH.

Chin Med J (Engl). 2007 Jul 5;120(13):1183-6.

PMID:
17637250
15.

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. doi: 10.1097/MD.0000000000008591.

16.

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.

PMID:
22118009
17.

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.

PMID:
15200509
18.

Mutations in STK11 gene in Czech Peutz-Jeghers patients.

Vasovcák P, Puchmajerová A, Roubalík J, Krepelová A.

BMC Med Genet. 2009 Jul 19;10:69. doi: 10.1186/1471-2350-10-69.

19.

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 22;9:44. doi: 10.1186/1471-2350-9-44.

20.

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 23;18(1):19. doi: 10.1186/s12881-017-0373-z.

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