257 related articles for article (PubMed ID: 15774015)
1. 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]
2. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.
Wang ZJ; Churchman M; Avizienyte E; McKeown C; Davies S; Evans DG; Ferguson A; Ellis I; Xu WH; Yan ZY; Aaltonen LA; Tomlinson IP
J Med Genet; 1999 May; 36(5):365-8. PubMed ID: 10353780
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
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 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. [Sequence polymorphism of the promoter region of gene STK11 in patients with Peutz-Jeghers syndrome].
Yi X; Yao MJ; Wang YJ; Tang JG; Ning WF; Wang XP; Zhou SQ; Li CJ; Wang F; Xia K; Shi XL
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Feb; 32(1):74-7. PubMed ID: 17344591
[TBL] [Abstract][Full Text] [Related]
12. STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia.
Bartosova Z; Zavodna K; Krivulcik T; Usak J; Mlkva I; Kruzliak T; Hromec J; Usakova V; Kopecka I; Veres P; Bartosova Z; Bujalkova M
Neoplasma; 2007; 54(2):101-7. PubMed ID: 17319781
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer.
Takahashi M; Sakayori M; Takahashi S; Kato T; Kaji M; Kawahara M; Suzuki T; Kato S; Kato S; Shibata H; Murakawa Y; Yoshioka T; Ishioka C
J Gastroenterol; 2004 Dec; 39(12):1210-4. PubMed ID: 15622488
[TBL] [Abstract][Full Text] [Related]
16. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE
Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485
[TBL] [Abstract][Full Text] [Related]
17. Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma.
Guldberg P; thor Straten P; Ahrenkiel V; Seremet T; Kirkin AF; Zeuthen J
Oncogene; 1999 Mar; 18(9):1777-80. PubMed ID: 10208439
[TBL] [Abstract][Full Text] [Related]
18. Genetic heterogeneity in Peutz-Jeghers syndrome.
Boardman LA; Couch FJ; Burgart LJ; Schwartz D; Berry R; McDonnell SK; Schaid DJ; Hartmann LC; Schroeder JJ; Stratakis CA; Thibodeau SN
Hum Mutat; 2000; 16(1):23-30. PubMed ID: 10874301
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]