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Items: 1 to 20 of 164

1.

Clinicopathologic and molecular features of pancreatic adenocarcinoma associated with Peutz-Jeghers syndrome.

Yee NS, Furth EE, Pack M.

Cancer Biol Ther. 2003 Jan-Feb;2(1):38-47. Review.

PMID:
12673116
2.
3.

Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.

Mehenni H, Resta N, Guanti G, Mota-Vieira L, Lerner A, Peyman M, Chong KA, Aissa L, Ince A, Cosme A, Costanza MC, Rossier C, Radhakrishna U, Burt RW, Picard D.

Dig Dis Sci. 2007 Aug;52(8):1924-33.

PMID:
17404884
4.

Genetic screening for Peutz-Jeghers syndrome.

Ballhausen WG, Günther K.

Expert Rev Mol Diagn. 2003 Jul;3(4):471-9. Review.

PMID:
12877386
5.

Duodenal cancer in a patient with Peutz-Jeghers syndrome: molecular analysis.

Nakamura T, Suzuki S, Yokoi Y, Kashiwabara H, Maruyama K, Baba S, Nakagawa H, Nakamura S.

J Gastroenterol. 2002;37(5):376-80.

PMID:
12051537
6.

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.

Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, de Rooij FW, Wilson JH, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RK, Spigelman AD, Houlston RS.

Clin Cancer Res. 2006 May 15;12(10):3209-15.

7.

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.

PMID:
15622488
8.

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.

9.

No evidence for germline mutations of the LKB1/STK11 gene in familial pancreatic carcinoma.

Grützmann R, McFaul C, Bartsch DK, Sina-Frey M, Rieder H, Koch R, McCarthy E, Greenhalf W, Neoptolemos JP, Saeger HD, Pilarsky C.

Cancer Lett. 2004 Oct 8;214(1):63-8.

PMID:
15331174
10.

A role for LKB1 gene in human cancer beyond the Peutz-Jeghers syndrome.

Sanchez-Cespedes M.

Oncogene. 2007 Dec 13;26(57):7825-32. Review.

PMID:
17599048
11.

STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreas.

Sato N, Rosty C, Jansen M, Fukushima N, Ueki T, Yeo CJ, Cameron JL, Iacobuzio-Donahue CA, Hruban RH, Goggins M.

Am J Pathol. 2001 Dec;159(6):2017-22.

12.

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 5;120(13):1183-6.

PMID:
17637250
13.

Association of Peutz-Jeghers-like mucocutaneous pigmentation with breast and gynecologic carcinomas in women.

Boardman LA, Pittelkow MR, Couch FJ, Schaid DJ, McDonnell SK, Burgart LJ, Ahlquist DA, Carney JA, Schwartz DI, Thibodeau SN, Hartmann LC.

Medicine (Baltimore). 2000 Sep;79(5):293-8.

14.

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.

Scott RJ, Crooks R, Meldrum CJ, Thomas L, Smith CJ, Mowat D, McPhillips M, Spigelman AD.

Clin Genet. 2002 Oct;62(4):282-7.

PMID:
12372054
15.

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
16.

A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome.

Yoo JH, Yoo JH, Choi YJ, Kang JG, Sun YK, Ki CS, Lee KA, Choi JR.

BMC Med Genet. 2008 May 22;9:44. doi: 10.1186/1471-2350-9-44.

17.

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
18.

Peutz-Jeghers syndrome: clinicopathology and molecular alterations.

McGarrity TJ, Amos C.

Cell Mol Life Sci. 2006 Sep;63(18):2135-44. Review.

PMID:
16952058
19.

Mutations in STK11 gene in Czech Peutz-Jeghers patients.

Vasovcák P, Puchmajerová A, Roubalík J, Krepelová A.

BMC Med Genet. 2009 Jul 19;10:69. doi: 10.1186/1471-2350-10-69.

20.

Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 gene.

Heinritz W, Strenge S, Kujat A, Hockel M, Froster UG.

Onkologie. 2008 Nov;31(11):625-8. doi: 10.1159/000162284.

PMID:
19145097
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