208 related articles for article (PubMed ID: 9399902)
1. Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
Mehenni H; Blouin JL; Radhakrishna U; Bhardwaj SS; Bhardwaj K; Dixit VB; Richards KF; Bermejo-Fenoll A; Leal AS; Raval RC; Antonarakis SE
Am J Hum Genet; 1997 Dec; 61(6):1327-34. PubMed ID: 9399902
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p.
Amos CI; Bali D; Thiel TJ; Anderson JP; Gourley I; Frazier ML; Lynch PM; Luchtefeld MA; Young A; McGarrity TJ; Seldin MF
Cancer Res; 1997 Sep; 57(17):3653-6. PubMed ID: 9288765
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.
Tomlinson IP; Olschwang S; Abelovitch D; Nakamura Y; Bodmer WF; Thomas G; Markie D
Ann Hum Genet; 1996 Sep; 60(5):377-84. PubMed ID: 8912790
[TBL] [Abstract][Full Text] [Related]
9. Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome.
Marneros AG; Mehenni H; Reichenberger E; Antonarakis SE; Krieg T; Olsen BR
Cytogenet Cell Genet; 2001; 92(3-4):213-6. PubMed ID: 11435690
[TBL] [Abstract][Full Text] [Related]
10. STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.
Jiang CY; Esufali S; Berk T; Gallinger S; Cohen Z; Tobi M; Redston M; Bapat B
Clin Genet; 1999 Aug; 56(2):136-41. PubMed ID: 10517250
[TBL] [Abstract][Full Text] [Related]
11. Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2.
Buchet-Poyau K; Mehenni H; Radhakrishna U; Antonarakis SE
Cytogenet Genome Res; 2002; 97(3-4):171-8. PubMed ID: 12438709
[TBL] [Abstract][Full Text] [Related]
12. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
Gruber SB; Entius MM; Petersen GM; Laken SJ; Longo PA; Boyer R; Levin AM; Mujumdar UJ; Trent JM; Kinzler KW; Vogelstein B; Hamilton SR; Polymeropoulos MH; Offerhaus GJ; Giardiello FM
Cancer Res; 1998 Dec; 58(23):5267-70. PubMed ID: 9850045
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.
Hemminki A; Tomlinson I; Markie D; Järvinen H; Sistonen P; Björkqvist AM; Knuutila S; Salovaara R; Bodmer W; Shibata D; de la Chapelle A; Aaltonen LA
Nat Genet; 1997 Jan; 15(1):87-90. PubMed ID: 8988175
[TBL] [Abstract][Full Text] [Related]
15. Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome.
Connolly DC; Katabuchi H; Cliby WA; Cho KR
Am J Pathol; 2000 Jan; 156(1):339-45. PubMed ID: 10623683
[TBL] [Abstract][Full Text] [Related]
16. The molecular basis and clinical aspects of Peutz-Jeghers syndrome.
Hemminki A
Cell Mol Life Sci; 1999 May; 55(5):735-50. PubMed ID: 10379360
[TBL] [Abstract][Full Text] [Related]
17. [Peutz-Jeghers syndrome].
Miyaki M
Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
[TBL] [Abstract][Full Text] [Related]
18. [Peutz-Jeghers syndrome: case report and update on diagnosis and treatment].
Capasso L; Lombari P; Scarano MI; Izzo P; D'Ambrosio R; Iannucci A; Formisano V; Lombari C
Minerva Chir; 2001 Dec; 56(6):643-7. PubMed ID: 11721206
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome.
Kortschak RD; Reimann H; Zimmer M; Eyre HJ; Saint R; Jenne DE
Genomics; 1998 Jul; 51(2):288-92. PubMed ID: 9722953
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
