| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1035610829 |
| P356 | DOI | 10.1038/NG0196-85 |
| P698 | PubMed publication ID | 8528259 |
| P50 | author | John E Fantasia | Q98936044 |
| P2093 | author name string | Gorlin RJ | |
| Johnson DR | |||
| Bale AE | |||
| Fallet S | |||
| Levanat S | |||
| P2860 | cites work | Mutation and cancer: statistical study of retinoblastoma | Q24618185 |
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 85-87 | |
| P577 | publication date | 1996-01-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | A two-hit model for developmental defects in Gorlin syndrome | |
| P478 | volume | 12 |
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| Q52132499 | Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome. |
| Q33677701 | Gorlin syndrome associated with midline nasal dermoid cyst |
| Q42465346 | Gorlin syndrome with bilateral polydactyly: a rare case report |
| Q35593440 | Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation |
| Q36265088 | Gorlin's syndrome - Report of a case and management of cystic lesions |
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| Q50066385 | Hh-Gli signaling pathway activity in oral and oropharyngeal squamous cell carcinoma. |
| Q37181138 | Identifying candidate genes involved in brain tumor formation |
| Q42486304 | Impaired removal of 8-hydroxydeoxyguanosine induced by UVB radiation in naevoid basal cell carcinoma syndrome cells |
| Q36519478 | Impaired skin and hair follicle development in Runx2 deficient mice |
| Q34948316 | Integrated genotypic analysis of hedgehog-related genes identifies subgroups of keratocystic odontogenic tumor with distinct clinicopathological features |
| Q40736871 | Introduction of wild-type patched gene suppresses the oncogenic potential of human squamous cell carcinoma cell lines including A431. |
| Q42489597 | Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report |
| Q33699908 | Loss of heterozygosity in human skin |
| Q98177862 | Maspin, Syndecan-1, and Ki-67 in the Odontogenic Keratocyst: An Immunohistochemical Analysis |
| Q39295594 | Molecular alterations in odontogenic keratocysts as potential therapeutic targets. |
| Q35881960 | Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients |
| Q34577342 | Molecular and genetic aspects of odontogenic lesions. |
| Q42439631 | Molecular evidence of type 2 mosaicism in Gorlin syndrome |
| Q42474915 | Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report |
| Q42509637 | Multisystem Involvement in a Patient with a PTCH1 Mutation: Clinical and Imaging Findings |
| Q24336457 | Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome |
| Q49045477 | Neuropilin-2 contributes to tumorigenicity in a mouse model of Hedgehog pathway medulloblastoma |
| Q60843775 | Nevoid Basal Cell Carcinoma (Gorlin) Syndrome |
| Q36819990 | Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome) |
| Q38511941 | Nevoid Basal Cell Carcinoma Syndrome: A Long-Term Study in a Family |
| Q64245651 | Nevoid Basal Cell Carcinoma Syndrome: Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients |
| Q35951367 | Nevoid basal cell carcinoma (Gorlin) syndrome |
| Q42481036 | Nevoid basal cell carcinoma (Gorlin) syndrome: unanswered issues |
| Q21202903 | Nevoid basal cell carcinoma syndrome (Gorlin syndrome) |
| Q42436687 | Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction |
| Q40822428 | Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals |
| Q39595462 | Nevoid basal cell carcinoma syndrome: a 40-year study in the South African population |
| Q34405646 | Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome |
| Q35190387 | Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report |
| Q90166275 | Ocular manifestations in Gorlin-Goltz syndrome |
| Q38148139 | Odontogenic keratocyst: What is in the name? |
| Q35222019 | Odontogenic keratocysts arise from quiescent epithelial rests and are associated with deregulated hedgehog signaling in mice and humans |
| Q80221833 | Odontogenic keratocysts: natural history and immunohistochemistry |
| Q54588181 | Opposite modifying effects of HR and NHEJ deficiency on cancer risk in Ptc1 heterozygous mouse cerebellum. |
| Q42490431 | PTCH gene mutations in odontogenic keratocysts |
| Q42525130 | PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients |
| Q42500354 | PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts |
| Q42436593 | PTCH1 and SMO gene alterations in keratocystic odontogenic tumors |
| Q34640943 | Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report |
| Q90044947 | Patched1 haploinsufficiency severely impacts intermediary metabolism in the skin of Ptch1+/-/ODC transgenic mice |
| Q52551234 | Polarity, proliferation and the hedgehog pathway. |
| Q36189626 | Regulation of human PTCH1b expression by different 5' untranslated region cis-regulatory elements |
| Q42455110 | Rhabdomyosarcomas and radiation hypersensitivity in a mouse model of Gorlin syndrome |
| Q42506769 | Surgery for cystic lymphangioma in Gorlin-Goltz syndrome |
| Q34699463 | The aggressive nature of the odontogenic keratocyst: is it a benign cystic neoplasm? Part 2. Proliferation and genetic studies |
| Q55067670 | The concise handbook of family cancer syndromes. Mayo Familial Cancer Program. |
| Q36422767 | The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma |
| Q37832612 | The odontogenic keratocyst: a cyst, or a cystic neoplasm? |
| Q38092920 | The role of microRNAs in medulloblastoma. |
| Q41462850 | Towards a unified model of tumor suppression: lessons learned from the human patched gene |
| Q80221850 | Treatment options for the recurrent odontogenic keratocyst |
| Q46084741 | Two modifications in the treatment of keratocystic odontogenic tumors (KCOT) and the use of Carnoy's solution (CS)--a retrospective study lasting between 2 and 10 years |
| Q42519757 | Two-hit model for tumorigenesis of nevoid basal cell carcinoma (Gorlin) syndrome-associated hepatic mesenchymal tumor |
| Q42528554 | Variable expressivity of patched mutations in flies and humans. |
| Q24310216 | Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2 |
| Q26782853 | Vismodegib hedgehog-signaling inhibition and treatment of basal cell carcinomas as well as keratocystic odontogenic tumors in Gorlin syndrome |
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