Basal cell carcinomas in gorlin syndrome: a review of 202 patients

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Basal cell carcinomas in gorlin syndrome: a review of 202 patients is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1155/2011/217378
P932PMC publication ID2998699
P698PubMed publication ID21152126
P5875ResearchGate publication ID49677818

P50authorGareth EvansQ29642643
P2093author name stringElizabeth A Jones
Andrew Shenton
Mohammed Imran Sajid
P2860cites workBirth incidence and prevalence of tumor-prone syndromes: Estimates from a UK family genetic register serviceQ57266646
The hedgehog pathway and basal cell carcinomasQ95721032
Nevoid basal cell carcinoma syndrome (Gorlin syndrome)Q21202903
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 evidentQ24310445
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndromeQ24336457
Human homolog of patched, a candidate gene for the basal cell nevus syndromeQ28281033
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomasQ28288407
Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patientsQ28292205
PTCH mutations: distribution and analysesQ28292366
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndromeQ28307305
Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutationsQ30495361
Complications of the naevoid basal cell carcinoma syndrome: results of a population based studyQ33595421
Nevoid basal cell carcinoma (Gorlin) syndromeQ35951367
The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastomaQ35993240
The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastomaQ36422767
Predictors of the risk of mortality in neurofibromatosis 2Q37202827
Time-point and dosage of gene inactivation determine the tumor spectrum in conditional Ptch knockoutsQ38510595
Nevoid basal cell carcinoma syndrome: review of 118 affected individualsQ40678901
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French studyQ42208514
Spectrum of PTCH1 mutations in French patients with Gorlin syndromeQ42446262
Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.Q42719337
P275copyright licenseCreative Commons Attribution 3.0 UnportedQ14947546
P6216copyright statuscopyrightedQ50423863
P304page(s)217378
P577publication date2010-09-28
P1433published inJournal of Skin CancerQ26842488
P1476titleBasal cell carcinomas in gorlin syndrome: a review of 202 patients
P478volume2011

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cites work (P2860)
Q36406904Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome
Q42511712Clinical and radiological features in young individuals with nevoid basal cell carcinoma syndrome
Q42511026Clinical manifestations and treatment for keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome: a study in 25 Japanese patients
Q35477995Common variants modify the age of onset for basal cell carcinomas in Gorlin syndrome
Q38013102Congenital hypotrichosis, eruptive milia, and palmoplantar pits: a case report with review of literature
Q53148301Consensus statement from the first international colloquium on basal cell nevus syndrome (BCNS).
Q38672696Delayed diagnosis of Gorlin syndrome: Learning from mistakes!
Q64110314Developments in Transduction, Connectivity and AI/Machine Learning for Point-of-Care Testing
Q38807597Diagnosis and Management of Hereditary Basal Cell Skin Cancer
Q42459126Early-onset acral basal cell carcinomas in Gorlin syndrome
Q49548506Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk and prognosis.
Q64240239Global gene expression of histologically normal primary skin cells from BCNS subjects reveals "single-hit" effects that are influenced by rapamycin
Q41615625Gorlin-Goltz Syndrome: A Rare Case Report of a 11-Year-Old Child
Q37136993Hereditary nonmelanoma skin cancer
Q37856435Hereditary tumour syndromes featuring basal cell carcinomas
Q40175707Imaging findings in a case of Gorlin-Goltz syndrome: a survey using advanced modalities
Q41857270Incidental finding of lamellar calcification of the falx cerebri leading to the diagnosis of gorlin-goltz syndrome
Q58795605Infantile-onset palmo-plantar basal cell carcinomas and pits in Gorlin syndrome
Q42456221Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
Q38194590Locally advanced and metastatic basal cell carcinoma: molecular pathways, treatment options and new targeted therapies
Q42483872Mesenteric cysts in naevoid basal cell carcinoma syndrome: a mimic of metastatic disease.
Q42176413Multiple orthokeratinized odontogenic cysts: a case report
Q54764863Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
Q35487317New basal cell carcinoma susceptibility loci
Q35190387Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report
Q89181527PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome
Q37166764Perigestational dietary folic acid deficiency protects against medulloblastoma formation in a mouse model of nevoid basal cell carcinoma syndrome
Q41963939Radiological features of familial Gorlin-Goltz syndrome.
Q36923522Targeted therapy for advanced Basal-cell carcinoma: vismodegib and beyond
Q55282893The relevance of a suppressor of fused (SUFU) mutation in the diagnosis and treatment of Gorlin syndrome.
Q26782853Vismodegib hedgehog-signaling inhibition and treatment of basal cell carcinomas as well as keratocystic odontogenic tumors in Gorlin syndrome
Q90266281Wnt, Notch, and TGF-β Pathways Impinge on Hedgehog Signaling Complexity: An Open Window on Cancer

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