These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 16648371)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
    Hearle NC; Rudd MF; Lim W; Murday V; Lim AG; Phillips RK; Lee PW; O'donohue J; Morrison PJ; Norman A; Hodgson SV; Lucassen A; Houlston RS
    J Med Genet; 2006 Apr; 43(4):e15. PubMed ID: 16582077
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome.
    Yang HR; Ko JS; Seo JK
    Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
    Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
    Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
    Hearle NC; Tomlinson I; Lim W; Murday V; Swarbrick E; Lim G; Phillips R; Lee P; O'Donohue J; Trembath RC; Morrison PJ; Norman A; Taylor R; Hodgson S; Lucassen A; Houlston RS
    BMC Genomics; 2005 Mar; 6():38. PubMed ID: 15774015
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. 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]  

  • 19. Mutations in STK11 gene in Czech Peutz-Jeghers patients.
    Vasovcák P; Puchmajerová A; Roubalík J; Krepelová A
    BMC Med Genet; 2009 Jul; 10():69. PubMed ID: 19615099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 12.