414 related articles for article (PubMed ID: 28900777)
1. An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.
Daniell J; Plazzer JP; Perera A; Macrae F
Fam Cancer; 2018 Jul; 17(3):421-427. PubMed ID: 28900777
[TBL] [Abstract][Full Text] [Related]
2. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome.
Lipsa A; Kowtal P; Sarin R
Hum Mol Genet; 2019 Jun; 28(11):1885-1893. PubMed ID: 30689838
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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. PubMed ID: 15121768
[TBL] [Abstract][Full Text] [Related]
5. Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.
Tan H; Mei L; Huang Y; Yang P; Li H; Peng Y; Chen C; Wei X; Pan Q; Liang D; Wu L
BMC Med Genet; 2016 Nov; 17(1):77. PubMed ID: 27821076
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Role of the Serine/Threonine Kinase 11 (STK11) or Liver Kinase B1 (LKB1) Gene in Peutz-Jeghers Syndrome.
Altamish M; Dahiya R; Singh AK; Mishra A; Aljabali AAA; Satija S; Mehta M; Dureja H; Prasher P; Negi P; Kapoor DN; Goyal R; Tambuwala MM; Chellappan DK; Dua K; Gupta G
Crit Rev Eukaryot Gene Expr; 2020; 30(3):245-252. PubMed ID: 32749111
[TBL] [Abstract][Full Text] [Related]
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; 18(1):19. PubMed ID: 28231849
[TBL] [Abstract][Full Text] [Related]
9. Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
Lim W; Hearle N; Shah B; Murday V; Hodgson SV; Lucassen A; Eccles D; Talbot I; Neale K; Lim AG; O'Donohue J; Donaldson A; Macdonald RC; Young ID; Robinson MH; Lee PW; Stoodley BJ; Tomlinson I; Alderson D; Holbrook AG; Vyas S; Swarbrick ET; Lewis AA; Phillips RK; Houlston RS
Br J Cancer; 2003 Jul; 89(2):308-13. PubMed ID: 12865922
[TBL] [Abstract][Full Text] [Related]
10. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.
Olschwang S; Boisson C; Thomas G
J Med Genet; 2001 Jun; 38(6):356-60. PubMed ID: 11389158
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Peutz-Jeghers syndrome: risks of a hereditary condition.
Westerman AM; Wilson JH
Scand J Gastroenterol Suppl; 1999; 230():64-70. PubMed ID: 10499464
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Resta N; Pierannunzio D; Lenato GM; Stella A; Capocaccia R; Bagnulo R; Lastella P; Susca FC; Bozzao C; Loconte DC; SabbĂ C; Urso E; Sala P; Fornasarig M; Grammatico P; Piepoli A; Host C; Turchetti D; Viel A; Memo L; Giunti L; Stigliano V; Varesco L; Bertario L; Genuardi M; Lucci Cordisco E; Tibiletti MG; Di Gregorio C; Andriulli A; Ponz de Leon M;
Dig Liver Dis; 2013 Jul; 45(7):606-11. PubMed ID: 23415580
[TBL] [Abstract][Full Text] [Related]
17. Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant.
Huang ZH; Song Z; Zhang P; Wu J; Huang Y
World J Gastroenterol; 2016 Mar; 22(11):3261-7. PubMed ID: 27004004
[TBL] [Abstract][Full Text] [Related]
18. Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.
Wu BD; Wang YJ; Fan LL; Huang H; Zhou P; Yang M; Shi XL
Biomed Res Int; 2020; 2020():9159315. PubMed ID: 32462036
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 24652667
[TBL] [Abstract][Full Text] [Related]
20. Peutz-Jeghers syndrome without
Jiang LX; Chen YR; Xu ZX; Zhang YH; Zhang Z; Yu PF; Dong ZW; Yang HR; Gu GL
World J Gastroenterol; 2023 Jun; 29(21):3302-3317. PubMed ID: 37377590
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]