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Archives of Dermatological Research

Volumn 292, Issue 9, 2000, Pages 475-476

Allelic loss at the PTCH gene locus in jaw cysts but not in palmar pits in patients with basal cell nevus syndrome

(4) Matsumura, Y a Nishigori, C a Murakami, K a Miyachi, Y a

a KYOTO UNIVERSITY (Japan)

Author keywords

Allelic loss; Basal cell nevus syndrome; Jaw cyst; Palmar pit; PTCH gene

Indexed keywords

MICROSATELLITE DNA;

ALLELE; ARTICLE; AUTORADIOGRAPHY; AUTOSOMAL DOMINANT DISORDER; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; GENE LOCUS; GENE REPRESSION; GENE SEQUENCE; JAW CYST; PRIORITY JOURNAL;

EID: 0033793507 PISSN: 03403696 EISSN: None Source Type: Journal
DOI: 10.1007/s004030000154 Document Type: Article

Times cited : (11)

References (13)

1
- 0028878117
- Nevoid basal cell carcinoma syndrome
- (1995) Dermatol Clin , vol.13 , pp. 113-125
- Gorlin, R.J.¹

2
- 15844386165
- Mutations of the human homologue of Drosophila patched in the nevoid basal cell carcinoma syndrome
- (1996) Cell , vol.85 , pp. 841-851
- Hahn, H.¹ Wicking, C.² Zaphiropoulos, P.G.³ Gailami, M.R.⁴ Shanley, S.⁵ Chidambaram, A.⁶ Vorechovsky, I.⁷ Holmberg, E.⁸ Unden, A.B.⁹ Gillies, S.¹⁰ Negus, K.¹¹ Smyth, I.¹² Pressman, C.¹³ Leffell, D.J.¹⁴ Gerrard, B.¹⁵ Goldstein, A.M.¹⁶ Dean, M.¹⁷ Toftgard, R.¹⁸ Chenevix-Trench, G.¹⁹ Wainwright, B.²⁰ Bale, A.E.²¹ more..

3
- 15844381336
- Human homologue of patched, a candidate gene for the basal cell nevus syndrome
- (1996) Science , vol.272 , pp. 1668-1671
- Johnson, R.L.¹ Rothman, A.L.² Xie, J.³ Goodrich, L.V.⁴ Bare, J.W.⁵ Bonifas, J.M.⁶ Quinn, A.G.⁷ Myers, R.M.⁸ Cox, D.R.⁹ Epstein, E.H.¹⁰ Scott, M.P.¹¹

4
- 0029841366
- Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: Different in vivo mechanisms of PTCH inactivation
- (1996) Cancer Res , vol.56 , pp. 562-4565
- Unden, A.B.¹ Holmberg, E.² Lundh-Rozell, B.³ Stahle-Backdahl, M.⁴ Zaphiropoulos, P.G.⁵ Toftgard, R.⁶ Vorechovsky, I.⁷

5
- 12844276949
- Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident
- (1997) Am J Hum Genet , vol.60 , pp. 21-26
- Wicking, C.¹ Shanley, S.² Smyth, I.³ Gillies, S.⁴ Negus, K.⁵ Graham, S.⁶ Suthers, G.⁷ Haites, N.⁸ Edwards, M.⁹ Wainwright, B.¹⁰ Chenevix-Trench, G.¹¹

6
- 0031837549
- Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome
- (1998) J Invest Dermatol , vol.110 , pp. 885-888
- Aszterbaum, M.¹ Rothman, A.² Johnson, R.L.³ Fisher, M.⁴ Xie, J.⁵ Bonifas, J.M.⁶ Zhang, X.⁷ Scott, M.P.⁸ Epstein, E.H.⁹

7
- 0030034250
- A two-hit model for development defects in Gorlin syndrome
- (1996) Nat Genet , vol.12 , pp. 85-87
- Levanat, S.¹ Gorlin, R.J.² Fallet, S.³ Johnson, D.R.⁴ Fantasia, J.E.⁵ Bale, A.E.⁶

8
- 0027231001
- Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study
- (1993) J Med Genet , vol.30 , pp. 460-464
- Evans, D.G.R.¹ Ladusans, E.² Rimmer, S.³ Burnell, L.D.⁴ Thakker, N.⁵ Farndon, P.A.⁶

9
- 0028978357
- Direct molecular analysis of archival tumor tissue for loss of heterozygosity
- (1995) Biotechniques , vol.19 , pp. 190-192
- Johnson, D.R.¹ Levanat, S.² Bale, A.E.³

10
- 0026627965
- Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
- (1992) Cell , vol.69 , pp. 111-117
- Gailani, M.R.¹ Bale, S.J.² Leffell, D.J.³ DiGiovanna, J.J.⁴ Peck, G.L.⁵ Poliak, S.⁶ Drum, M.A.⁷ Pastakia, B.⁸ McBride, O.W.⁹ Kase, R.¹⁰ Greene, M.¹¹ Mulvihill, J.J.¹² Bale, A.E.¹³

11
- 0026094584
- Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
- (1991) Cell , vol.67 , pp. 437-447
- Pelletier, J.¹ Bruening, W.² Kashtan, C.E.³ Mauer, S.M.⁴ Manivel, J.C.⁵ Stiegel, J.E.⁶ Houghton, D.C.⁷ Junien, C.⁸ Habib, R.⁹ Fouser, L.¹⁰ Fine, R.N.¹¹ Silverman, B.L.¹² Haber, D.A.¹³ Housman, D.¹⁴

12
- 0028058986
- Human haploinsufficiency - One for sorrow, two for joy
- (1994) Nat Genet , vol.7 , pp. 5-7
- Fisher, E.¹ Scambler, P.²

13
- 0034123010
- Evidence that haploinsufficiency of Ptch leads to medulloblastoma in mice
- (2000) Genes Chromosome Cancer , vol.28 , pp. 77-81
- Zurawel, R.H.¹ Allen, C.² Wechsler-Reya, R.³ Scott, M.P.⁴ Raffel, C.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.