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 *

250 related articles for article (PubMed ID: 17026623)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.
    Le Meur N; Martin C; Saugier-Veber P; Joly G; Lemoine F; Moirot H; Rossi A; Bachy B; Cabot A; Joly P; Frébourg T
    Eur J Hum Genet; 2004 May; 12(5):415-8. PubMed ID: 14970844
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
    Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
    Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer.
    Shinmura K; Goto M; Tao H; Shimizu S; Otsuki Y; Kobayashi H; Ushida S; Suzuki K; Tsuneyoshi T; Sugimura H
    Clin Genet; 2005 Jan; 67(1):81-6. PubMed ID: 15617552
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.
    Resta N; Stella A; Susca FC; Di Giacomo M; Forleo G; Miccolis I; Rossini FP; Genuardi M; Piepoli A; Grammatico P; Guanti G
    Hum Mutat; 2002 Jul; 20(1):78-9. PubMed ID: 12112668
    [TBL] [Abstract][Full Text] [Related]  

  • 11. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.
    Resta N; Simone C; Mareni C; Montera M; Gentile M; Susca F; Gristina R; Pozzi S; Bertario L; Bufo P; Carlomagno N; Ingrosso M; Rossini FP; Tenconi R; Guanti G
    Cancer Res; 1998 Nov; 58(21):4799-801. PubMed ID: 9809980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.
    Orellana P; López-Köstner F; Heine C; Suazo C; Pinto E; Church J; Carvallo P; Alvarez K
    Clin Genet; 2013 Apr; 83(4):365-9. PubMed ID: 22775437
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Mutations in the human LKB1/STK11 gene.
    Launonen V
    Hum Mutat; 2005 Oct; 26(4):291-7. PubMed ID: 16110486
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
    Jenne DE; Reimann H; Nezu J; Friedel W; Loff S; Jeschke R; Müller O; Back W; Zimmer M
    Nat Genet; 1998 Jan; 18(1):38-43. PubMed ID: 9425897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of STK11 gene expression in homozygous twins with Peutz-Jeghers syndrome.
    Tseng CJ; Chen SF; Liou SI; Lu SC; Chen JM; Sun CF; Chang SD; Cheng PJ; Liou JD; Chu DC
    Ann Clin Lab Sci; 2004; 34(2):154-8. PubMed ID: 15228227
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.