Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.

Journal of dermatological science - 1 Apr 2008

Honma Masaru, Ohishi Yasushi, Uehara Jiro, Ibe Masaki, Kinouchi Motoshi, Ishida-Yamamoto Akemi, Iizuka Hajime

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Basal Cell Nevus Syndrome
Share to Child, Preschool
Share to Patched-1 Receptor
Share to Patched Receptors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Polymorphism, Single-Stranded Conformational

Share to Receptors, Cell Surface

Share to Skin Neoplasms

Source

Identifiers

PMID: 18068337
DOI: 10.1016/j.jdermsci.2007.10.009

Genes

PTCH1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.PMID 18068337Read ↗

Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis.Semantic proximity Read ↗

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndromeSemantic proximity Read ↗

Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma Syndrome.Semantic proximity Read ↗

Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations.Semantic proximity Read ↗

Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing.Semantic proximity Read ↗

Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation dataSemantic proximity Read ↗

Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

New mutations and an updated database for the patched-1 (PTCH1) gene.Semantic proximity Read ↗

Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.Semantic proximity Read ↗

Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.Semantic proximity Read ↗

A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.