Nevoid Basal Cell Carcinoma Syndrome Latest Advances

Genetic Insight into Gorlin-Goltz Syndrome.

Journal: Indian journal of dermatology

Published: March 26, 2026

A Novel Mutation of PTCHD3 Identified in a Chinese Family with Basal Cell Nevus Syndrome-associated Odontogenic Keratocysts.

Journal: The Chinese journal of dental research

Published: March 18, 2026

Report of Concomitant Intracranial Cysts in Unrelated Patients With Heterozygous Germline NF1 Pathogenic Variants.

Journal: Annals of internal medicine. Clinical cases

Published: February 16, 2026

Building consensus in pediatric dermatology research.

Journal: The Journal of investigative dermatology

Published: January 26, 2026

AlphaFold3 predictions of novel GLI-SUFU interfaces identify binding-defective SUFU missense variants from medulloblastoma and Gorlin Syndrome patients.

Journal: bioRxiv : the preprint server for biology

Published: January 16, 2026

Resection of intracardiac tumors in infants.

Journal: Acta chirurgica Belgica

Published: January 12, 2026

Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study.

Journal: Frontiers in medicine

Published: December 31, 2025

Basaloid Proliferations in Palmar Lesions of Gorlin Syndrome: A Distinct Entity or Precursor Lesion?

Journal: The American Journal of dermatopathology

Published: December 11, 2025

Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature.

Journal: Hereditary cancer in clinical practice

Published: December 06, 2025

Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.

Journal: Advances in experimental medicine and biology

Published: November 22, 2025

Nevoid Basal Cell Carcinoma Syndrome: Three Cases from the Same Family.

Journal: Indian journal of dermatology

Published: November 20, 2025

Dual PI3K/AKT and CDK4/6 inhibition reveals selective sensitivity in an SHH medulloblastoma stem cell model.

Journal: Molecular oncology

Published: November 12, 2025

Nevoid Basal Cell Carcinoma Syndrome Latest Advances

Find the Latest Research About Nevoid Basal Cell Carcinoma Syndrome

Genetic Insight into Gorlin-Goltz Syndrome.

Genetic Insight into Gorlin-Goltz Syndrome.

A Novel Mutation of PTCHD3 Identified in a Chinese Family with Basal Cell Nevus Syndrome-associated Odontogenic Keratocysts.

A Novel Mutation of PTCHD3 Identified in a Chinese Family with Basal Cell Nevus Syndrome-associated Odontogenic Keratocysts.

Report of Concomitant Intracranial Cysts in Unrelated Patients With Heterozygous Germline NF1 Pathogenic Variants.

Report of Concomitant Intracranial Cysts in Unrelated Patients With Heterozygous Germline NF1 Pathogenic Variants.

Building consensus in pediatric dermatology research.

Building consensus in pediatric dermatology research.

AlphaFold3 predictions of novel GLI-SUFU interfaces identify binding-defective SUFU missense variants from medulloblastoma and Gorlin Syndrome patients.

AlphaFold3 predictions of novel GLI-SUFU interfaces identify binding-defective SUFU missense variants from medulloblastoma and Gorlin Syndrome patients.

Resection of intracardiac tumors in infants.

Resection of intracardiac tumors in infants.

Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study.

Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study.

Basaloid Proliferations in Palmar Lesions of Gorlin Syndrome: A Distinct Entity or Precursor Lesion?

Basaloid Proliferations in Palmar Lesions of Gorlin Syndrome: A Distinct Entity or Precursor Lesion?

Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature.

Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature.

Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.

Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.

Nevoid Basal Cell Carcinoma Syndrome: Three Cases from the Same Family.

Nevoid Basal Cell Carcinoma Syndrome: Three Cases from the Same Family.

Dual PI3K/AKT and CDK4/6 inhibition reveals selective sensitivity in an SHH medulloblastoma stem cell model.

Dual PI3K/AKT and CDK4/6 inhibition reveals selective sensitivity in an SHH medulloblastoma stem cell model.