358 related articles for article (PubMed ID: 26386697)
1. 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. PubMed ID: 26386697
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 16287113
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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. PubMed ID: 27467201
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
Westerman AM; Entius MM; Boor PP; Koole R; de Baar E; Offerhaus GJ; Lubinski J; Lindhout D; Halley DJ; de Rooij FW; Wilson JH
Hum Mutat; 1999; 13(6):476-81. PubMed ID: 10408777
[TBL] [Abstract][Full Text] [Related]
7. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
Hearle NC; Rudd MF; Lim W; Murday V; Lim AG; Phillips RK; Lee PW; O'donohue J; Morrison PJ; Norman A; Hodgson SV; Lucassen A; Houlston RS
J Med Genet; 2006 Apr; 43(4):e15. PubMed ID: 16582077
[TBL] [Abstract][Full Text] [Related]
8. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
[TBL] [Abstract][Full Text] [Related]
9. Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.
Orellana P; López-Köstner F; Heine C; Suazo C; Pinto E; Church J; Carvallo P; Alvarez K
Clin Genet; 2013 Apr; 83(4):365-9. PubMed ID: 22775437
[TBL] [Abstract][Full Text] [Related]
10. 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; 120(13):1183-6. PubMed ID: 17637250
[TBL] [Abstract][Full Text] [Related]
11. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.
Su GH; Hruban RH; Bansal RK; Bova GS; Tang DJ; Shekher MC; Westerman AM; Entius MM; Goggins M; Yeo CJ; Kern SE
Am J Pathol; 1999 Jun; 154(6):1835-40. PubMed ID: 10362809
[TBL] [Abstract][Full Text] [Related]
12. Two cases of somatic STK11 mosaicism in Danish patients with Peutz-Jeghers syndrome.
Jelsig AM; Bertelsen B; Forss I; Karstensen JG
Fam Cancer; 2021 Jan; 20(1):55-59. PubMed ID: 32504210
[TBL] [Abstract][Full Text] [Related]
13. Mutations in STK11 gene in Czech Peutz-Jeghers patients.
Vasovcák P; Puchmajerová A; Roubalík J; Krepelová A
BMC Med Genet; 2009 Jul; 10():69. PubMed ID: 19615099
[TBL] [Abstract][Full Text] [Related]
14. Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.
Zhao HM; Yang YJ; Duan JQ; Ouyang HJ; Liu L; Yi LC; Xiao ZH; Zheng Y; Peng L; Attard TM; Li DY; You JY
J Pediatr Gastroenterol Nutr; 2019 Feb; 68(2):199-206. PubMed ID: 30334930
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
Mehenni H; Resta N; Guanti G; Mota-Vieira L; Lerner A; Peyman M; Chong KA; Aissa L; Ince A; Cosme A; Costanza MC; Rossier C; Radhakrishna U; Burt RW; Picard D
Dig Dis Sci; 2007 Aug; 52(8):1924-33. PubMed ID: 17404884
[TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.
Scott RJ; Crooks R; Meldrum CJ; Thomas L; Smith CJ; Mowat D; McPhillips M; Spigelman AD
Clin Genet; 2002 Oct; 62(4):282-7. PubMed ID: 12372054
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.
Volikos E; Robinson J; Aittomäki K; Mecklin JP; Järvinen H; Westerman AM; de Rooji FW; Vogel T; Moeslein G; Launonen V; Tomlinson IP; Silver AR; Aaltonen LA
J Med Genet; 2006 May; 43(5):e18. PubMed ID: 16648371
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 22118009
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
