-
1
-
-
0003713446
-
-
2nd ed. Philadelphia: WB Saunders
-
Neville BW, Damm DD, Allen CM, Bouquot JE. Oral and Maxillofacial Pathology, 2nd ed. Philadelphia: WB Saunders, 2002:674-7.
-
(2002)
Oral and Maxillofacial Pathology
, pp. 674-677
-
-
Neville, B.W.1
Damm, D.D.2
Allen, C.M.3
Bouquot, J.E.4
-
3
-
-
33746718114
-
DHPLC analysis of patients with nevoid basal cell carcinoma syndrome reveals novel PTCH missense mutations in the sterol-sensing domain
-
Marsh A, Wicking C, Wainwright B, Chenevix-Trench G. DHPLC analysis of patients with nevoid basal cell carcinoma syndrome reveals novel PTCH missense mutations in the sterol-sensing domain. Hum Mutat 2005;26:283.
-
(2005)
Hum Mutat
, vol.26
, pp. 283
-
-
Marsh, A.1
Wicking, C.2
Wainwright, B.3
Chenevix-Trench, G.4
-
4
-
-
28744437736
-
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles
-
Savino M, d'Apolito M, Formica V, et al. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles. Hum Mutat 2004;24:441.
-
(2004)
Hum Mutat
, vol.24
, pp. 441
-
-
Savino, M.1
D'Apolito, M.2
Formica, V.3
-
5
-
-
0033137316
-
Nevoid basal cell carcinoma syndrome: Molecular biology and new hypotheses
-
Cohen MM Jr. Nevoid basal cell carcinoma syndrome: Molecular biology and new hypotheses. Int J Oral Maxillofac Surg 1999;28:216-23.
-
(1999)
Int J Oral Maxillofac Surg
, vol.28
, pp. 216-223
-
-
Cohen Jr., M.M.1
-
6
-
-
33846372262
-
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation
-
Scott A, Strouthidis NG, Robson AG, et al. Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation. Am J Ophthalmol 2007;143:346-8.
-
(2007)
Am J Ophthalmol
, vol.143
, pp. 346-348
-
-
Scott, A.1
Strouthidis, N.G.2
Robson, A.G.3
-
7
-
-
33748772228
-
PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts
-
Gu XM, Zhao HS, Sun LS, Li TJ. PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts. J Dent Res 2006;85:859-63.
-
(2006)
J Dent Res
, vol.85
, pp. 859-863
-
-
Gu, X.M.1
Zhao, H.S.2
Sun, L.S.3
Li, T.J.4
-
8
-
-
33646734450
-
Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome
-
Song YL, Zhang WF, Peng B, Wang CN, Wang Q, Bian Z. Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome. Tumour Biol 2006;27:175-80.
-
(2006)
Tumour Biol
, vol.27
, pp. 175-180
-
-
Song, Y.L.1
Zhang, W.F.2
Peng, B.3
Wang, C.N.4
Wang, Q.5
Bian, Z.6
-
9
-
-
27944431759
-
Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays
-
Nagao K, Togawa N, Fujii K, et al. Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays. Hum Mol Genet 2005;14:3379-88.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3379-3388
-
-
Nagao, K.1
Togawa, N.2
Fujii, K.3
-
10
-
-
4344689818
-
PTC gene mutations and expression of SHH, PTC, SMO, and GLI-1 in odontogenic keratocysts
-
Ohki K, Kumamoto H, Ichinohasama R, Sato T, Takahashi N, Ooya K. PTC gene mutations and expression of SHH, PTC, SMO, and GLI-1 in odontogenic keratocysts. Int J Oral Maxillofac Surg 2004;33:584-92.
-
(2004)
Int J Oral Maxillofac Surg
, vol.33
, pp. 584-592
-
-
Ohki, K.1
Kumamoto, H.2
Ichinohasama, R.3
Sato, T.4
Takahashi, N.5
Ooya, K.6
-
11
-
-
0037387938
-
Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients
-
Fujii K, Kohno Y, Sugita K, et al. Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients. Hum Mutat 2003;21: 451-2.
-
(2003)
Hum Mutat
, vol.21
, pp. 451-452
-
-
Fujii, K.1
Kohno, Y.2
Sugita, K.3
-
12
-
-
0036724944
-
Analysis of the PTCH coding region in human rhabdomyosarcoma
-
Calzada-Wack J, Schnitzbauer U, Walch A, et al. Analysis of the PTCH coding region in human rhabdomyosarcoma. Hum Mutat 2002;20:233-4.
-
(2002)
Hum Mutat
, vol.20
, pp. 233-234
-
-
Calzada-Wack, J.1
Schnitzbauer, U.2
Walch, A.3
-
13
-
-
0034221629
-
Identification of PATCHED mutations in medulloblastomas by direct sequencing
-
Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE. Identification of PATCHED mutations in medulloblastomas by direct sequencing. Hum Mutat 2000;16:89-90.
-
(2000)
Hum Mutat
, vol.16
, pp. 89-90
-
-
Dong, J.1
Gailani, M.R.2
Pomeroy, S.L.3
Reardon, D.4
Bale, A.E.5
-
14
-
-
0034688339
-
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
-
D'Errico M, Calcagnile A, Canzona F, et al. UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients. Oncogene 2000;19:463-7.
-
(2000)
Oncogene
, vol.19
, pp. 463-467
-
-
D'Errico, M.1
Calcagnile, A.2
Canzona, F.3
-
15
-
-
0031937726
-
Mutation analysis of the human homologue of Drosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin
-
Eklund LK, Lindstrom E, Unden AB, et al. Mutation analysis of the human homologue of Drosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin. Mol Carcinog 1998;21:87-92.
-
(1998)
Mol Carcinog
, vol.21
, pp. 87-92
-
-
Eklund, L.K.1
Lindstrom, E.2
Unden, A.B.3
-
16
-
-
0033923974
-
The spectrum of patched mutations in a collection of Australian basal cell carcinomas
-
Evans T, Boonchai W, Shanley S, et al. The spectrum of patched mutations in a collection of Australian basal cell carcinomas. Hum Mutat 2000;16:43-8.
-
(2000)
Hum Mutat
, vol.16
, pp. 43-48
-
-
Evans, T.1
Boonchai, W.2
Shanley, S.3
-
17
-
-
18544371994
-
Novel mutations in the PATCHED gene in basal cell nevus syndrome
-
Lam CW, Leung CY, Lee KC, et al. Novel mutations in the PATCHED gene in basal cell nevus syndrome. Mol Genet Metab 2002;76:57-61.
-
(2002)
Mol Genet Metab
, vol.76
, pp. 57-61
-
-
Lam, C.W.1
Leung, C.Y.2
Lee, K.C.3
-
18
-
-
0031744766
-
The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome
-
Smyth I, Wicking C, Wainwright B, Chenevix-Trench G. The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome. Hum Genet 1998;102: 598-601.
-
(1998)
Hum Genet
, vol.102
, pp. 598-601
-
-
Smyth, I.1
Wicking, C.2
Wainwright, B.3
Chenevix-Trench, G.4
-
19
-
-
45849150375
-
PTCH1 and SMO gene alterations in keratocystic odontogenic tumors
-
Sun LS, Li XF, Li TJ. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors. J Dent Res 2008;87: 575-9.
-
(2008)
J Dent Res
, vol.87
, pp. 575-579
-
-
Sun, L.S.1
Li, X.F.2
Li, T.J.3
-
20
-
-
0041333165
-
Spectrum of PTCH1 mutations in French patients with Gorlin syndrome
-
Boutet N, Bignon Y, Drouin-Garraud V, et al. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome. J Invest Dermatol 2003;121:478-81.
-
(2003)
J Invest Dermatol
, vol.121
, pp. 478-481
-
-
Boutet, N.1
Bignon, Y.2
Drouin-Garraud, V.3
-
21
-
-
0029793064
-
Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients
-
Chidambaram A, Goldstein AM, Gailani MR, et al. Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients. Cancer Res 1996;56:4599-601.
-
(1996)
Cancer Res
, vol.56
, pp. 4599-4601
-
-
Chidambaram, A.1
Goldstein, A.M.2
Gailani, M.R.3
-
22
-
-
1342327596
-
Nevoid basal cell carcinoma syndrome-clinical manifestations and mutation analysis of a Taiwanese family
-
Chung CH, Wong TY, Shieh TY, Shieh DB, Chao SC. Nevoid basal cell carcinoma syndrome-clinical manifestations and mutation analysis of a Taiwanese family. J Formos Med Assoc 2003;102:793-7.
-
(2003)
J Formos Med Assoc
, vol.102
, pp. 793-797
-
-
Chung, C.H.1
Wong, T.Y.2
Shieh, T.Y.3
Shieh, D.B.4
Chao, S.C.5
-
23
-
-
0031447980
-
Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes
-
Richards FM, Goudie DR, Cooper WN, et al. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes. Hum Genet 1997;101:317-22.
-
(1997)
Hum Genet
, vol.101
, pp. 317-322
-
-
Richards, F.M.1
Goudie, D.R.2
Cooper, W.N.3
-
24
-
-
0032241173
-
Gorlin syndrome: Identification of 4 novel germ-line mutations of the human patched (PTCH) gene
-
Hasenpusch-Theil K, Bataille V, Laehdetie J, Obermayr F, Sampson JR, Frischauf AM. Gorlin syndrome: Identification of 4 novel germ-line mutations of the human patched (PTCH) gene. Hum Mutat 1998;11:480.
-
(1998)
Hum Mutat
, vol.11
, pp. 480
-
-
Hasenpusch-Theil, K.1
Bataille, V.2
Laehdetie, J.3
Obermayr, F.4
Sampson, J.R.5
Frischauf, A.M.6
-
25
-
-
0030738693
-
Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system
-
Wolter M, Reifenberger J, Sommer C, Ruzicka T, Reifenberger G. Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. Cancer Res 1997;57:2581-5.
-
(1997)
Cancer Res
, vol.57
, pp. 2581-2585
-
-
Wolter, M.1
Reifenberger, J.2
Sommer, C.3
Ruzicka, T.4
Reifenberger, G.5
-
26
-
-
0030874617
-
Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours
-
Vorechovsky I, Tingby O, Hartman M, et al. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours. Oncogene 1997;15:361-1.
-
(1997)
Oncogene
, vol.15
, pp. 361-361
-
-
Vorechovsky, I.1
Tingby, O.2
Hartman, M.3
-
28
-
-
15644373337
-
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors
-
Xie J, Johnson RL, Zhang X, et al. Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors. Cancer Res 1997;57:2369-72.
-
(1997)
Cancer Res
, vol.57
, pp. 2369-2372
-
-
Xie, J.1
Johnson, R.L.2
Zhang, X.3
-
29
-
-
33745208440
-
MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas
-
Liboutet M, Portela M, Delestaing G, et al. MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas. J Invest Dermatol 2006;126:1510-7.
-
(2006)
J Invest Dermatol
, vol.126
, pp. 1510-1517
-
-
Liboutet, M.1
Portela, M.2
Delestaing, G.3
-
30
-
-
36248987761
-
UV fingerprints predominate in the PTCH mutation spectra of basal cell carcinomas independent of clinical phenotype
-
Heitzer E, Lassacher A, Quehenberger F, Kerl H, Wolf P. UV fingerprints predominate in the PTCH mutation spectra of basal cell carcinomas independent of clinical phenotype. J Invest Dermatol 2007;127:2872-81.
-
(2007)
J Invest Dermatol
, vol.127
, pp. 2872-2881
-
-
Heitzer, E.1
Lassacher, A.2
Quehenberger, F.3
Kerl, H.4
Wolf, P.5
-
31
-
-
0035135744
-
Role of PTCH and p53 genes in early-onset basal cell carcinoma
-
Zhang H, Ping XL, Lee PK, et al. Role of PTCH and p53 genes in early-onset basal cell carcinoma. Am J Pathol 2001;158: 381-5.
-
(2001)
Am J Pathol
, vol.158
, pp. 381-385
-
-
Zhang, H.1
Ping, X.L.2
Lee, P.K.3
-
32
-
-
16044363842
-
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
-
Gailani MR, Stahle-Backdahl M, Leffell DJ, et al. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet 1996;14:78-81.
-
(1996)
Nat Genet
, vol.14
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
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