220 related articles for article (PubMed ID: 34754157)
1. 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]
2. 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]
3. 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]
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. PubMed ID: 10780518
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
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. 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]
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. 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]
15. Clinical manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome.
Chiang JM; Chen TC
Asian J Surg; 2018 Sep; 41(5):480-485. PubMed ID: 28869103
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas.
Rowan A; Bataille V; MacKie R; Healy E; Bicknell D; Bodmer W; Tomlinson I
J Invest Dermatol; 1999 Apr; 112(4):509-11. PubMed ID: 10201537
[TBL] [Abstract][Full Text] [Related]
19. STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.
Jiang CY; Esufali S; Berk T; Gallinger S; Cohen Z; Tobi M; Redston M; Bapat B
Clin Genet; 1999 Aug; 56(2):136-41. PubMed ID: 10517250
[TBL] [Abstract][Full Text] [Related]
20. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
BMC Med Genet; 2017 Nov; 18(1):130. PubMed ID: 29141581
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
