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Items: 1 to 20 of 179

1.

[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.

2.

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.

3.

[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
4.

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
5.

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.

6.

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
7.

Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.

Kruse R, Uhlhaas S, Lamberti C, Keller KM, Jackisch C, Steinhard J, Knöpfle G, Loff S, Back W, Stolte M, Jungck M, Propping P, Friedl W, Jenne DE.

Hum Mutat. 1999;13(3):257-8.

PMID:
10090485
8.

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
10.

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.

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. Chinese.

PMID:
11832000
12.

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 30;7:73.

13.

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome.

Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Matsuura N, Monden M, Nakamura Y.

Hum Genet. 1998 Aug;103(2):168-72.

PMID:
9760200
14.

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.

Wang ZJ, Churchman M, Avizienyte E, McKeown C, Davies S, Evans DG, Ferguson A, Ellis I, Xu WH, Yan ZY, Aaltonen LA, Tomlinson IP.

J Med Genet. 1999 May;36(5):365-8.

15.

[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
16.
17.

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.

18.

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
19.

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.

20.

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.

Jiang CY, Esufali S, Berk T, Gallinger S, Cohen Z, Tobi M, Redston M, Bapat B.

Clin Genet. 1999 Aug;56(2):136-41.

PMID:
10517250

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