174 related articles for article (PubMed ID: 16024850)
1. Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation.
Ragge NK; Salt A; Collin JR; Michalski A; Farndon PA
Br J Ophthalmol; 2005 Aug; 89(8):988-91. PubMed ID: 16024850
[TBL] [Abstract][Full Text] [Related]
2. Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.
Gloude NJ; Yoon JM; Crawford JR
Pediatr Blood Cancer; 2016 Jun; 63(6):1128-9. PubMed ID: 26840755
[No Abstract] [Full Text] [Related]
3. Medulloblastoma associated with novel PTCH mutation as primary manifestation of Gorlin syndrome.
Crawford JR; Rood BR; Rossi CT; Vezina G
Neurology; 2009 May; 72(18):1618. PubMed ID: 19414732
[No Abstract] [Full Text] [Related]
4. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
[TBL] [Abstract][Full Text] [Related]
5. Gorlin syndrome and desmoplastic medulloblastoma: Report of 3 cases with unfavorable clinical course and novel mutations.
Gururangan S; Robinson G; Ellison DW; Wu G; He X; Lu QR; McLendon R; Grant G; Driscoll T; Neuberg R
Pediatr Blood Cancer; 2015 Oct; 62(10):1855-8. PubMed ID: 25940061
[TBL] [Abstract][Full Text] [Related]
6. 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; 15(3):361-6. PubMed ID: 9233770
[TBL] [Abstract][Full Text] [Related]
7. A mouse model for medulloblastoma and basal cell nevus syndrome.
Corcoran RB; Scott MP
J Neurooncol; 2001 Jul; 53(3):307-18. PubMed ID: 11718263
[TBL] [Abstract][Full Text] [Related]
8. Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene.
Kitsiou-Tzeli S; Willems P; Kosmadaki M; Leze E; Vrettou C; Kanavakis E; Katsarou A
J Dermatol; 2011 Dec; 38(12):1205-8. PubMed ID: 21950490
[No Abstract] [Full Text] [Related]
9. PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts.
Gu XM; Zhao HS; Sun LS; Li TJ
J Dent Res; 2006 Sep; 85(9):859-63. PubMed ID: 16931872
[TBL] [Abstract][Full Text] [Related]
10. Mutation in exon 7 of PTCH deregulates SHH/PTCH/SMO signaling: possible linkage to WNT.
Musani V; Gorry P; Basta-Juzbasic A; Stipic T; Miklic P; Levanat S
Int J Mol Med; 2006 May; 17(5):755-9. PubMed ID: 16596257
[TBL] [Abstract][Full Text] [Related]
11. Multifocal desmoplastic medulloblastoma in an african-american child with nevoid basal cell carcinoma (gorlin) syndrome. Case report.
Smucker PS; Smith JL
J Neurosurg; 2006 Oct; 105(4 Suppl):315-20. PubMed ID: 17328283
[TBL] [Abstract][Full Text] [Related]
12. Patched mutations and hairy skin patches: a new sign in Gorlin syndrome.
Wilson LC; Ajayi-Obe E; Bernhard B; Maas SM
Am J Med Genet A; 2006 Dec; 140(23):2625-30. PubMed ID: 16906569
[TBL] [Abstract][Full Text] [Related]
13. Analysis of mutation in exon 17 of PTCH in patients with nevoid basal cell carcinoma syndrome.
Li J; Wang J; Liu Y; Wang W
Mol Biol Rep; 2010 Jan; 37(1):359-62. PubMed ID: 19728145
[TBL] [Abstract][Full Text] [Related]
14. Nonsense-associated altered splicing of the Patched gene fails to suppress carcinogenesis in Gorlin syndrome.
Laimer M; Onder K; Schlager P; Lanschuetzer CM; Emberger M; Selhofer S; Hintner H; Bauer JW
Br J Dermatol; 2008 Jul; 159(1):222-7. PubMed ID: 18476955
[TBL] [Abstract][Full Text] [Related]
15. Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in
Ikemoto Y; Miyashita T; Nasu M; Hatsuse H; Kajiwara K; Fujii K; Motojima T; Kokido I; Toyoda M; Umezawa A
Aging (Albany NY); 2020 May; 12(10):9935-9947. PubMed ID: 32436863
[TBL] [Abstract][Full Text] [Related]
16. Nevoid basal cell carcinoma syndrome.
Leger M; Quintana A; Tzu J; Yee H; Kamino H; Sanchez M
Dermatol Online J; 2011 Oct; 17(10):23. PubMed ID: 22031649
[TBL] [Abstract][Full Text] [Related]
17. 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
Cancer Res; 1997 Jul; 57(13):2581-5. PubMed ID: 9205058
[TBL] [Abstract][Full Text] [Related]
18. Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients: two familial and three sporadic cases including the first Japanese patient with medulloblastoma.
Fujii M; Noguchi K; Urade M; Muraki Y; Moridera K; Kishimoto H; Hashimoto-Tamaoki T; Nakano Y
J Hum Genet; 2011 Apr; 56(4):277-83. PubMed ID: 21368767
[TBL] [Abstract][Full Text] [Related]
19. Identification of a SUFU germline mutation in a family with Gorlin syndrome.
Pastorino L; Ghiorzo P; Nasti S; Battistuzzi L; Cusano R; Marzocchi C; Garrè ML; Clementi M; Scarrà GB
Am J Med Genet A; 2009 Jul; 149A(7):1539-43. PubMed ID: 19533801
[TBL] [Abstract][Full Text] [Related]
20. Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays.
Nagao K; Togawa N; Fujii K; Uchikawa H; Kohno Y; Yamada M; Miyashita T
Hum Mol Genet; 2005 Nov; 14(22):3379-88. PubMed ID: 16203740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
