236 related articles for article (PubMed ID: 9887330)
1. Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
Ylikorkala A; Avizienyte E; Tomlinson IP; Tiainen M; Roth S; Loukola A; Hemminki A; Johansson M; Sistonen P; Markie D; Neale K; Phillips R; Zauber P; Twama T; Sampson J; Järvinen H; Mäkelä TP; Aaltonen LA
Hum Mol Genet; 1999 Jan; 8(1):45-51. PubMed ID: 9887330
[TBL] [Abstract][Full Text] [Related]
2. Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome.
Chen C; Zhang X; Wang D; Wang F; Pan J; Wang Z; Liu C; Wu L; Lu H; Li N; Wei J; Shi H; Wan H; Zhu M; Chen S; Zhou Y; Zhou X; Yang L; Liu J
Med Sci Monit; 2016 Oct; 22():3628-3640. PubMed ID: 27721366
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Stability of the Peutz-Jeghers syndrome kinase LKB1 requires its binding to the molecular chaperones Hsp90/Cdc37.
Nony P; Gaude H; Rossel M; Fournier L; Rouault JP; Billaud M
Oncogene; 2003 Dec; 22(57):9165-75. PubMed ID: 14668798
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
de Leng WW; Jansen M; Carvalho R; Polak M; Musler AR; Milne AN; Keller JJ; Menko FH; de Rooij FW; Iacobuzio-Donahue CA; Giardiello FM; Weterman MA; Offerhaus GJ
Clin Genet; 2007 Dec; 72(6):568-73. PubMed ID: 17924967
[TBL] [Abstract][Full Text] [Related]
11. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
[TBL] [Abstract][Full Text] [Related]
12. [Mutation screening of LKB1 gene in familial Peutz-Jeghers syndrome patients].
Chen CY; Zhang XM; Wang FY; Wang ZK; Zhu M; Ma GJ; Zhang YY; Jin XX; Shi H; Liu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):121-5. PubMed ID: 22487816
[TBL] [Abstract][Full Text] [Related]
13. [Peutz-Jeghers syndrome].
Miyaki M
Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
[TBL] [Abstract][Full Text] [Related]
14. Genetic heterogeneity in Peutz-Jeghers syndrome.
Boardman LA; Couch FJ; Burgart LJ; Schwartz D; Berry R; McDonnell SK; Schaid DJ; Hartmann LC; Schroeder JJ; Stratakis CA; Thibodeau SN
Hum Mutat; 2000; 16(1):23-30. PubMed ID: 10874301
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity.
de Leng WW; Westerman AM; Weterman MA; Jansen M; van Dekken H; Giardiello FM; de Rooij FW; Paul Wilson JH; Offerhaus GJ; Keller JJ
J Clin Pathol; 2007 Apr; 60(4):392-6. PubMed ID: 16775120
[TBL] [Abstract][Full Text] [Related]
17. Functional analysis of Peutz-Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity.
Forcet C; Etienne-Manneville S; Gaude H; Fournier L; Debilly S; Salmi M; Baas A; Olschwang S; Clevers H; Billaud M
Hum Mol Genet; 2005 May; 14(10):1283-92. PubMed ID: 15800014
[TBL] [Abstract][Full Text] [Related]
18. Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.
Wang ZJ; Ellis I; Zauber P; Iwama T; Marchese C; Talbot I; Xue WH; Yan ZY; Tomlinson I
J Pathol; 1999 May; 188(1):9-13. PubMed ID: 10398133
[TBL] [Abstract][Full Text] [Related]
19. Distinct promoter methylation patterns of LKB1 in the hamartomatous polyps of Peutz-Jeghers syndrome and its potential in gastrointestinal malignancy prediction.
Li T; Lin W; Zhao Y; Zhu J; Sun T; Ren L
Orphanet J Rare Dis; 2020 Aug; 15(1):208. PubMed ID: 32799895
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
