Associated Papers
Clinical vs. molecular diagnosis of Gorlin syndrome: relevance of diagnostic criteria depends on the age of the patients.
Hercent A et al.
Clinical and Experimental Dermatology, 2025
Osmolytes and crowders regulate aggregation of the cancer-related L106R mutant of the Axin protein.
Garfagnini T et al.
Biophysical Journal, 2021
Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research.
Onodera S et al.
International Journal of Molecular Sciences, 2020
33066274 (PubMed )
Supplement: ijms-21-07559-s001.pdf
Biallelic PTCH1 Inactivation Is a Dominant Genomic Change in Sporadic Keratocystic Odontogenic Tumors.
Stojanov IJ et al.
The American Journal of Surgical Pathology, 2020
PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review.
Guo YY et al.
Plos One, 2013
24204797 (PubMed )
Supplement: pone.0077305.s001.docx
Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis.
Pan S et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2010
PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients.
Li TJ et al.
Oral Diseases, 2008
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