Back to search

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Somatic Mutations in the PTCH, SMOH, SUFUH, and TP53 Genes in Sporadic Basal Cell CarcinomasDOI 10.1016/s0093-3619(08)70201-6
Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.Semantic proximity
High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencingSemantic proximity
PTCH mutations: distribution and analyses.Semantic proximity
Biallelic PTCH1 Inactivation Is a Dominant Genomic Change in Sporadic Keratocystic Odontogenic Tumors.Semantic proximity
Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients.Semantic proximity
PTCH1 mutation is a frequent event in oesophageal basaloid squamous cell carcinoma.Semantic proximity
Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndromeSemantic proximity
Activating Smoothened mutations in sporadic basal-cell carcinoma.Semantic proximity
Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma.Semantic proximity
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.Semantic proximity
PTCH mutations are not mainly involved in the pathogenesis of sporadic trichoblastomas.Semantic proximity
Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis.Semantic proximity
Select a neighboring publication to make it the new centre.