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Results: 1 to 20 of 114

1.

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.

PMID:
9709978
[PubMed - indexed for MEDLINE]
2.

Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses.

Stratakis CA.

Horm Res. 2000;54(5-6):334-43. Review.

PMID:
11595829
[PubMed - indexed for MEDLINE]
3.

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).

Stratakis CA, Jenkins RB, Pras E, Mitsiadis CS, Raff SB, Stalboerger PG, Tsigos C, Carney JA, Chrousos GP.

J Clin Endocrinol Metab. 1996 Oct;81(10):3607-14.

PMID:
8855810
[PubMed - indexed for MEDLINE]
4.

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 1;58(23):5267-70.

PMID:
9850045
[PubMed - indexed for MEDLINE]
Free Article
5.

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.

Marsh DJ, Roth S, Lunetta KL, Hemminki A, Dahia PL, Sistonen P, Zheng Z, Caron S, van Orsouw NJ, Bodmer WF, Cottrell SE, Dunlop MG, Eccles D, Hodgson SV, Järvinen H, Kellokumpu I, Markie D, Neale K, Phillips R, Rozen P, Syngal S, Vijg J, Tomlinson IP, Aaltonen LA, Eng C.

Cancer Res. 1997 Nov 15;57(22):5017-21.

PMID:
9371495
[PubMed - indexed for MEDLINE]
Free Article
6.

Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes.

Stratakis CA.

Front Biosci. 2000 Mar 1;5:D353-66. Review.

PMID:
10704431
[PubMed - indexed for MEDLINE]
7.

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.

Marsh DJ, Coulon V, Lunetta KL, Rocca-Serra P, Dahia PL, Zheng Z, Liaw D, Caron S, Duboué B, Lin AY, Richardson AL, Bonnetblanc JM, Bressieux JM, Cabarrot-Moreau A, Chompret A, Demange L, Eeles RA, Yahanda AM, Fearon ER, Fricker JP, Gorlin RJ, Hodgson SV, Huson S, Lacombe D, Eng C, et al.

Hum Mol Genet. 1998 Mar;7(3):507-15.

PMID:
9467011
[PubMed - indexed for MEDLINE]
Free Article
8.

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.

PMID:
9399902
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

Stratakis CA, Carney JA, Lin JP, Papanicolaou DA, Karl M, Kastner DL, Pras E, Chrousos GP.

J Clin Invest. 1996 Feb 1;97(3):699-705.

PMID:
8609225
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome.

Entius MM, Keller JJ, Westerman AM, van Rees BP, van Velthuysen ML, de Goeij AF, Wilson JH, Giardiello FM, Offerhaus GJ.

J Clin Pathol. 2001 Feb;54(2):126-31.

PMID:
11215281
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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.

PMID:
10623683
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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.

PMID:
9521590
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
9837816
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.

Marsh DJ, Dahia PL, Coulon V, Zheng Z, Dorion-Bonnet F, Call KM, Little R, Lin AY, Eeles RA, Goldstein AM, Hodgson SV, Richardson AL, Robinson BG, Weber HC, Longy M, Eng C.

Genes Chromosomes Cancer. 1998 Jan;21(1):61-9.

PMID:
9443042
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
10517250
[PubMed - indexed for MEDLINE]
16.

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, et al.

J Med Genet. 1998 Jan;35(1):42-4.

PMID:
9475093
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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.

PMID:
15287029
[PubMed - indexed for MEDLINE]
19.

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(Pt 5):377-84.

PMID:
8912790
[PubMed - indexed for MEDLINE]
20.

Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.

Olschwang S, Boisson C, Thomas G.

J Med Genet. 2001 Jun;38(6):356-60.

PMID:
11389158
[PubMed - indexed for MEDLINE]
Free PMC Article

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