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Items: 1 to 20 of 113

1.

Sporadic medulloblastomas contain PTCH mutations.

Raffel C, Jenkins RB, Frederick L, Hebrink D, Alderete B, Fults DW, James CD.

Cancer Res. 1997 Mar 1;57(5):842-5.

2.

Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.

Vorechovský I, Tingby O, Hartman M, Strömberg B, Nister M, Collins VP, Toftgård R.

Oncogene. 1997 Jul 17;15(3):361-6.

3.

Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.

Vortmeyer AO, Stavrou T, Selby D, Li G, Weil RJ, Park WS, Moon YW, Chandra R, Goldstein AM, Zhuang Z.

Cancer. 1999 Jun 15;85(12):2662-7.

PMID:
10375116
4.

Identification of PATCHED mutations in medulloblastomas by direct sequencing.

Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE.

Hum Mutat. 2000 Jul;16(1):89-90.

PMID:
10874314
5.

Analysis of PTCH/SMO/SHH pathway genes in medulloblastoma.

Zurawel RH, Allen C, Chiappa S, Cato W, Biegel J, Cogen P, de Sauvage F, Raffel C.

Genes Chromosomes Cancer. 2000 Jan;27(1):44-51.

PMID:
10564585
6.

Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.

Unden AB, Holmberg E, Lundh-Rozell B, Stähle-Bäckdahl M, Zaphiropoulos PG, Toftgård R, Vorechovsky I.

Cancer Res. 1996 Oct 15;56(20):4562-5.

7.

Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.

Reifenberger J, Wolter M, Knobbe CB, Köhler B, Schönicke A, Scharwächter C, Kumar K, Blaschke B, Ruzicka T, Reifenberger G.

Br J Dermatol. 2005 Jan;152(1):43-51.

PMID:
15656799
8.

Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas.

Schofield D, West DC, Anthony DC, Marshal R, Sklar J.

Am J Pathol. 1995 Feb;146(2):472-80.

9.

Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched.

Pietsch T, Waha A, Koch A, Kraus J, Albrecht S, Tonn J, Sörensen N, Berthold F, Henk B, Schmandt N, Wolf HK, von Deimling A, Wainwright B, Chenevix-Trench G, Wiestler OD, Wicking C.

Cancer Res. 1997 Jun 1;57(11):2085-8.

10.

Evidence that haploinsufficiency of Ptch leads to medulloblastoma in mice.

Zurawel RH, Allen C, Wechsler-Reya R, Scott MP, Raffel C.

Genes Chromosomes Cancer. 2000 May;28(1):77-81.

PMID:
10738305
12.

Mutations in SUFU predispose to medulloblastoma.

Taylor MD, Liu L, Raffel C, Hui CC, Mainprize TG, Zhang X, Agatep R, Chiappa S, Gao L, Lowrance A, Hao A, Goldstein AM, Stavrou T, Scherer SW, Dura WT, Wainwright B, Squire JA, Rutka JT, Hogg D.

Nat Genet. 2002 Jul;31(3):306-10. Epub 2002 Jun 17.

PMID:
12068298
13.

PTCH gene mutations in odontogenic keratocysts.

Barreto DC, Gomez RS, Bale AE, Boson WL, De Marco L.

J Dent Res. 2000 Jun;79(6):1418-22.

PMID:
10890722
14.

Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors.

Xie J, Johnson RL, Zhang X, Bare JW, Waldman FM, Cogen PH, Menon AG, Warren RS, Chen LC, Scott MP, Epstein EH Jr.

Cancer Res. 1997 Jun 15;57(12):2369-72.

15.

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C, Wainwright BJ.

Hum Mol Genet. 1999 Feb;8(2):291-7.

16.

Analysis of the PTCH coding region in human rhabdomyosarcoma.

Calzada-Wack J, Schnitzbauer U, Walch A, Wurster KH, Kappler R, Nathrath M, Hahn H.

Hum Mutat. 2002 Sep;20(3):233-4.

PMID:
12204003
17.

Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients.

Fujii K, Kohno Y, Sugita K, Nakamura M, Moroi Y, Urabe K, Furue M, Yamada M, Miyashita T.

Hum Mutat. 2003 Apr;21(4):451-2.

PMID:
12655573
18.

Unbalanced overexpression of the mutant allele in murine Patched mutants.

Calzada-Wack J, Kappler R, Schnitzbauer U, Richter T, Nathrath M, Rosemann M, Wagner SN, Hein R, Hahn H.

Carcinogenesis. 2002 May;23(5):727-33.

19.

Deletions of AXIN1, a component of the WNT/wingless pathway, in sporadic medulloblastomas.

Dahmen RP, Koch A, Denkhaus D, Tonn JC, Sörensen N, Berthold F, Behrens J, Birchmeier W, Wiestler OD, Pietsch T.

Cancer Res. 2001 Oct 1;61(19):7039-43.

20.

Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases.

Situm M, Levanat S, Crnic I, Pavelic B, Macan D, Grgurević J, Mubrin-Koncar M, Lipozencić J.

Croat Med J. 1999 Dec;40(4):533-8.

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