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Items: 1 to 20 of 142

1.

Overexpression of aromatase associated with loss of heterozygosity of the STK11 gene accounts for prepubertal gynecomastia in boys with Peutz-Jeghers syndrome.

Ham S, Meachem SJ, Choong CS, Charles AK, Baynam GS, Jones TW, Samarajeewa NU, Simpson ER, Brown KA.

J Clin Endocrinol Metab. 2013 Dec;98(12):E1979-87. doi: 10.1210/jc.2013-2291. Epub 2013 Sep 13.

PMID:
24037887
2.

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. Epub 2006 Jun 14.

3.

Aromatase expression in the human male.

Brodie A, Inkster S, Yue W.

Mol Cell Endocrinol. 2001 Jun 10;178(1-2):23-8.

PMID:
11403890
4.

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.

PMID:
15714005
5.

Prepubertal gynecomastia in two monozygotic twins with Peutz-Jeghers syndrome: two years' treatment with anastrozole and genetic study.

Grandone A, del Giudice EM, Cirillo G, Santarpia M, Coppola F, Perrone L.

Horm Res Paediatr. 2011;75(5):374-9. doi: 10.1159/000324178. Epub 2011 Feb 19.

PMID:
21335955
6.
7.

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
8.
9.

Prepubertal gynecomastia in Peutz-Jeghers syndrome: incomplete penetrance in a familial case and management with an aromatase inhibitor.

Lefevre H, Bouvattier C, Lahlou N, Adamsbaum C, Bougnères P, Carel JC.

Eur J Endocrinol. 2006 Feb;154(2):221-7.

10.

Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.

Su GH, Hruban RH, Bansal RK, Bova GS, Tang DJ, Shekher MC, Westerman AM, Entius MM, Goggins M, Yeo CJ, Kern SE.

Am J Pathol. 1999 Jun;154(6):1835-40.

11.

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 Spring;34(2):154-8.

PMID:
15228227
12.

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.

13.

Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas.

Rowan A, Bataille V, MacKie R, Healy E, Bicknell D, Bodmer W, Tomlinson I.

J Invest Dermatol. 1999 Apr;112(4):509-11.

14.

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.

PMID:
15200509
15.

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 1;58(21):4799-801.

16.

Large-cell calcifying Sertoli cell tumors of the testes in pediatrics.

Gourgari E, Saloustros E, Stratakis CA.

Curr Opin Pediatr. 2012 Aug;24(4):518-22. doi: 10.1097/MOP.0b013e328355a279. Review.

17.

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 21;89(2):308-13.

18.

Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age.

Crocker MK, Gourgari E, Lodish M, Stratakis CA.

J Clin Endocrinol Metab. 2014 Dec;99(12):E2673-80. doi: 10.1210/jc.2014-2530.

19.

Altered LKB1/AMPK/TSC1/TSC2/mTOR signaling causes disruption of Sertoli cell polarity and spermatogenesis.

Tanwar PS, Kaneko-Tarui T, Zhang L, Teixeira JM.

Hum Mol Genet. 2012 Oct 15;21(20):4394-405. Epub 2012 Jul 12.

20.

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.

PMID:
12112668

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