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Items: 1 to 20 of 153

1.

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
2.

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
3.

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.

4.

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.

5.

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
6.
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.

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.

9.

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
10.

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.

11.

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.

12.

STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.

Wang Z, Wu B, Mosig RA, Chen Y, Ye F, Zhang Y, Gong W, Gong L, Huang F, Wang X, Nie B, Zheng H, Cui M, Wang Y, Wang J, Chen C, Polydorides AD, Zhang DY, Martignetti JA, Jiang B.

Hum Mutat. 2014 Jul;35(7):851-8. doi: 10.1002/humu.22549. Epub 2014 Jun 3.

PMID:
24652667
13.

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
14.

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.

15.

A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.

Zheng B, Wang C, Jia Z, Liu Z, Li M, Jin Y, Pan J.

J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):559-564. doi: 10.1097/MPG.0000000000001316.

PMID:
27467201
16.

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
17.

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
18.

First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.

McKay V, Cairns D, Gokhale D, Mountford R, Greenhalgh L.

Fam Cancer. 2016 Jan;15(1):57-61. doi: 10.1007/s10689-015-9839-3.

PMID:
26386697
19.

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.

20.

Genotype-phenotype correlations in Peutz-Jeghers syndrome.

Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML.

J Med Genet. 2004 May;41(5):327-33.

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