205 related articles for article (PubMed ID: 17924967)
1. 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]
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. 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]
4. 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]
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. 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]
7. 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]
8. 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]
9. 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]
10. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4).
Abed AA; Günther K; Kraus C; Hohenberger W; Ballhausen WG
Hum Mutat; 2001 Nov; 18(5):397-410. PubMed ID: 11668633
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.
Chen C; Zhang X; Wang F; Liu C; Lu H; Wan H; Wei J; Liu J
DNA Cell Biol; 2012 Oct; 31(10):1535-40. PubMed ID: 22928647
[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. 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]
19. [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]
20. 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]
[Next] [New Search]
