197 related articles for article (PubMed ID: 10379360)
21. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3.
Nakagawa H; Koyama K; Tanaka T; Miyoshi Y; Ando H; Baba S; Watatani M; Yasutomi M; Monden M; Nakamura Y
Hum Genet; 1998 Feb; 102(2):203-6. PubMed ID: 9521590
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity.
de Leng WW; Westerman AM; Weterman MA; Jansen M; van Dekken H; Giardiello FM; de Rooij FW; Paul Wilson JH; Offerhaus GJ; Keller JJ
J Clin Pathol; 2007 Apr; 60(4):392-6. PubMed ID: 16775120
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
Hemminki A; Markie D; Tomlinson I; Avizienyte E; Roth S; Loukola A; Bignell G; Warren W; Aminoff M; Höglund P; Järvinen H; Kristo P; Pelin K; Ridanpää M; Salovaara R; Toro T; Bodmer W; Olschwang S; Olsen AS; Stratton MR; de la Chapelle A; Aaltonen LA
Nature; 1998 Jan; 391(6663):184-7. PubMed ID: 9428765
[TBL] [Abstract][Full Text] [Related]
28. Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis.
Jishage K; Nezu J; Kawase Y; Iwata T; Watanabe M; Miyoshi A; Ose A; Habu K; Kake T; Kamada N; Ueda O; Kinoshita M; Jenne DE; Shimane M; Suzuki H
Proc Natl Acad Sci U S A; 2002 Jun; 99(13):8903-8. PubMed ID: 12060709
[TBL] [Abstract][Full Text] [Related]
29. Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.
Olschwang S; Markie D; Seal S; Neale K; Phillips R; Cottrell S; Ellis I; Hodgson S; Zauber P; Spigelman A; Iwama T; Loff S; McKeown C; Marchese C; Sampson J; Davies S; Talbot I; Wyke J; Thomas G; Bodmer W; Hemminki A; Avizienyte E; de la Chapelle A; Aaltonen L; Tomlinson I
J Med Genet; 1998 Jan; 35(1):42-4. PubMed ID: 9475093
[TBL] [Abstract][Full Text] [Related]
30. Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain.
Sobottka SB; Haase M; Fitze G; Hahn M; Schackert HK; Schackert G
J Neurooncol; 2000 Sep; 49(3):187-95. PubMed ID: 11212897
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.
Stratakis CA; Kirschner LS; Taymans SE; Tomlinson IP; Marsh DJ; Torpy DJ; Giatzakis C; Eccles DM; Theaker J; Houlston RS; Blouin JL; Antonarakis SE; Basson CT; Eng C; Carney JA
J Clin Endocrinol Metab; 1998 Aug; 83(8):2972-6. PubMed ID: 9709978
[TBL] [Abstract][Full Text] [Related]
33. Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer.
Bignell GR; Barfoot R; Seal S; Collins N; Warren W; Stratton MR
Cancer Res; 1998 Apr; 58(7):1384-6. PubMed ID: 9537235
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Peutz-Jeghers syndrome: risks of a hereditary condition.
Westerman AM; Wilson JH
Scand J Gastroenterol Suppl; 1999; 230():64-70. PubMed ID: 10499464
[TBL] [Abstract][Full Text] [Related]
36. The STK11/LKB1 Peutz-Jegher gene is not involved in the pathogenesis of sporadic sex cord-stromal tumors, although loss of heterozygosity at 19p13.3 indicates other gene alteration in these tumors.
Kato N; Romero M; Catasus L; Prat J
Hum Pathol; 2004 Sep; 35(9):1101-4. PubMed ID: 15343512
[TBL] [Abstract][Full Text] [Related]
37. 5'-CpG island methylation of the LKB1/STK11 promoter and allelic loss at chromosome 19p13.3 in sporadic colorectal cancer.
Trojan J; Brieger A; Raedle J; Esteller M; Zeuzem S
Gut; 2000 Aug; 47(2):272-6. PubMed ID: 10896921
[TBL] [Abstract][Full Text] [Related]
38. Germline mutation of the LKB1/STK11 gene with loss of the normal allele in an aggressive breast cancer of Peutz-Jeghers syndrome.
Nakanishi C; Yamaguchi T; Iijima T; Saji S; Toi M; Mori T; Miyaki M
Oncology; 2004; 67(5-6):476-9. PubMed ID: 15714005
[TBL] [Abstract][Full Text] [Related]
39. Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Resta N; Pierannunzio D; Lenato GM; Stella A; Capocaccia R; Bagnulo R; Lastella P; Susca FC; Bozzao C; Loconte DC; Sabbà C; Urso E; Sala P; Fornasarig M; Grammatico P; Piepoli A; Host C; Turchetti D; Viel A; Memo L; Giunti L; Stigliano V; Varesco L; Bertario L; Genuardi M; Lucci Cordisco E; Tibiletti MG; Di Gregorio C; Andriulli A; Ponz de Leon M;
Dig Liver Dis; 2013 Jul; 45(7):606-11. PubMed ID: 23415580
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
