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Items: 1 to 20 of 36

1.

Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits; a syndrome of diagnostic significance.

JEGHERS H, McKUSICK VA, KATZ KH.

N Engl J Med. 1949 Dec 29;241(26):1031-6. No abstract available.

PMID:
15398245
2.

Immunohistochemical labeling for dpc4 mirrors genetic status in pancreatic adenocarcinomas : a new marker of DPC4 inactivation.

Wilentz RE, Su GH, Dai JL, Sparks AB, Argani P, Sohn TA, Yeo CJ, Kern SE, Hruban RH.

Am J Pathol. 2000 Jan;156(1):37-43.

3.

Growth suppression by Lkb1 is mediated by a G(1) cell cycle arrest.

Tiainen M, Ylikorkala A, Mäkelä TP.

Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9248-51.

4.

Optimizing the APC gene mutation analysis in archival colorectal tumor tissue.

Poncin J, Mulkens J, Arends JW, de Goeij A.

Diagn Mol Pathol. 1999 Mar;8(1):11-9.

PMID:
10408788
5.

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.

PMID:
10408777
6.

The molecular basis and clinical aspects of Peutz-Jeghers syndrome.

Hemminki A.

Cell Mol Life Sci. 1999 May;55(5):735-50. Review.

PMID:
10379360
7.

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.

8.

Peutz-Jeghers syndrome: 78-year follow-up of the original family.

Westerman AM, Entius MM, de Baar E, Boor PP, Koole R, van Velthuysen ML, Offerhaus GJ, Lindhout D, de Rooij FW, Wilson JH.

Lancet. 1999 Apr 10;353(9160):1211-5.

PMID:
10217080
9.

LKB1 somatic mutations in sporadic tumors.

Avizienyte E, Loukola A, Roth S, Hemminki A, Tarkkanen M, Salovaara R, Arola J, Bützow R, Husgafvel-Pursiainen K, Kokkola A, Järvinen H, Aaltonen LA.

Am J Pathol. 1999 Mar;154(3):677-81.

10.

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.

11.

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.

12.

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.

13.
14.

Mutations of the STK11 gene in sporadic gastric carcinoma.

Park WS, Moon YW, Yang YM, Kim YS, Kim YD, Fuller BG, Vortmeyer AO, Fogt F, Lubensky IA, Zhuang Z.

Int J Oncol. 1998 Sep;13(3):601-4.

PMID:
9683800
15.

Increased risk for cancer in patients with the Peutz-Jeghers syndrome.

Boardman LA, Thibodeau SN, Schaid DJ, Lindor NM, McDonnell SK, Burgart LJ, Ahlquist DA, Podratz KC, Pittelkow M, Hartmann LC.

Ann Intern Med. 1998 Jun 1;128(11):896-9.

PMID:
9634427
16.

Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors.

Avizienyte E, Roth S, Loukola A, Hemminki A, Lothe RA, Stenwig AE, Fosså SD, Salovaara R, Aaltonen LA.

Cancer Res. 1998 May 15;58(10):2087-90.

17.

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 1;58(7):1384-6.

18.

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.

19.

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 8;391(6663):184-7.

PMID:
9428765
20.

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.

Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Müller O, Back W, Zimmer M.

Nat Genet. 1998 Jan;18(1):38-43.

PMID:
9425897

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