170 related articles for article (PubMed ID: 14726968)
1. A new mutation of LKB1 gene in a Japanese patient with Peutz-Jeghers syndrome.
Tate G; Suzuki T; Mitsuya T
Acta Med Okayama; 2003 Dec; 57(6):305-8. PubMed ID: 14726968
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 15200509
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 10780518
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Clinical characteristics and mutation analysis of the LKB1 gene in a Peutz-Jeghers syndrome pedigree].
Pan J; Li M; Jin Y; Zhang XM; Zhu M; Chen SQ
Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):145-9. PubMed ID: 23527983
[TBL] [Abstract][Full Text] [Related]
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; 120(13):1183-6. PubMed ID: 17637250
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 10353780
[TBL] [Abstract][Full Text] [Related]
8. Molecular insights into Peutz-Jeghers syndrome: two probands with a germline mutation of LKB1.
Hosogi H; Nagayama S; Kawamura J; Koshiba Y; Nomura A; Itami A; Okabe H; Satoh S; Watanabe G; Sakai Y
J Gastroenterol; 2008; 43(6):492-7. PubMed ID: 18600394
[TBL] [Abstract][Full Text] [Related]
9. Ganglioglioma arising in a Peutz-Jeghers patient: a case report with molecular implications.
Resta N; Lauriola L; Puca A; Susca FC; Albanese A; Sabatino G; Di Giacomo MC; Gessi M; Guanti G
Acta Neuropathol; 2006 Jul; 112(1):106-11. PubMed ID: 16733653
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer.
Takahashi M; Sakayori M; Takahashi S; Kato T; Kaji M; Kawahara M; Suzuki T; Kato S; Kato S; Shibata H; Murakawa Y; Yoshioka T; Ishioka C
J Gastroenterol; 2004 Dec; 39(12):1210-4. PubMed ID: 15622488
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. LKB1 mutations frequently detected in mucinous bronchioloalveolar carcinoma.
Osoegawa A; Kometani T; Nosaki K; Ondo K; Hamatake M; Hirai F; Seto T; Sugio K; Ichinose Y
Jpn J Clin Oncol; 2011 Sep; 41(9):1132-7. PubMed ID: 21816872
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
Liu L; Du X; Nie J
Clin Res Hepatol Gastroenterol; 2011 Mar; 35(3):221-6. PubMed ID: 21411391
[TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome.
Zhang Z; Duan FX; Gu GL; Yu PF
World J Gastroenterol; 2020 Apr; 26(16):1926-1937. PubMed ID: 32390703
[TBL] [Abstract][Full Text] [Related]
18. [Peutz-Jeghers syndrome].
Miyaki M
Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
[TBL] [Abstract][Full Text] [Related]
19. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
Mehenni H; Gehrig C; Nezu J; Oku A; Shimane M; Rossier C; Guex N; Blouin JL; Scott HS; Antonarakis SE
Am J Hum Genet; 1998 Dec; 63(6):1641-50. PubMed ID: 9837816
[TBL] [Abstract][Full Text] [Related]
20. 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; 7():73. PubMed ID: 17010210
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
