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Items: 1 to 20 of 178

1.

[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. doi: 10.3760/cma.j.issn.1003-9406.2014.03.008. Chinese.

PMID:
24928005
2.

[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. Chinese.

PMID:
22543132
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 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
5.

[Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].

Mao X, Zhang Y, Wang H, Mao G, Ning S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):186-90. doi: 10.3760/cma.j.issn.1003-9406.2016.02.013. Chinese.

PMID:
27060312
6.

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
7.
8.

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 14;12:161. doi: 10.1186/1471-2350-12-161.

9.

[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. Chinese.

PMID:
11832000
11.

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.

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. Epub 2012 Aug 28.

PMID:
22928647
13.

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

Borun P, Bartkowiak A, Banasiewicz T, Nedoszytko B, Nowakowska D, Teisseyre M, Limon J, Lubinski J, Kubaszewski L, Walkowiak J, Czkwianianc E, Siolek M, Kedzia A, Krokowicz P, Cichy W, Plawski A.

BMC Med Genet. 2013 May 30;14:58. doi: 10.1186/1471-2350-14-58.

14.

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.

15.

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.

PMID:
16287113
16.

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.

17.

Two variants in STK11 gene in Chinese patients with Peutz-Jeghers syndrome.

Liu D, Guo H, Xu X, Yu Y, Bai Y.

J Genet. 2012 Aug;91(2):205-8. No abstract available.

18.

Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.

Trojan J, Brieger A, Raedle J, Roth WK, Zeuzem S.

Am J Gastroenterol. 1999 Jan;94(1):257-61.

PMID:
9934767
19.

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
20.

A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer.

Shinmura K, Goto M, Tao H, Shimizu S, Otsuki Y, Kobayashi H, Ushida S, Suzuki K, Tsuneyoshi T, Sugimura H.

Clin Genet. 2005 Jan;67(1):81-6.

PMID:
15617552

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