Results 101 to 110 of about 7,017,185 (188)

Frameshift mutation in exon 17 of PTCH1 gene in Nevoid basal cell carcinoma syndrome: A case report. [PDF]

J Oral Maxillofac Pathol, 2023
Aravind T, Savithri V, Suresh R, Subash P.   +3 more
europepmc   +1 more source

Establishment of induced pluripotent stem cells derived from patients and healthy siblings of a nevoid basal cell carcinoma syndrome family. [PDF]

In Vitro Cell Dev Biol Anim, 2023
Nakase Y, Hamada A, Obayashi F, Kitamura N, Hata T, Yamamoto T, Okamoto T.   +6 more
europepmc   +1 more source

Analysis of Sonic Hedgehog signalling pathway gene expression in Basal Cell Carcinoma and in GLII induced systems [PDF]

, 2007
PhDEmbryonic development is regulated by a number of signalling pathways, Which are critical for normal growth. Many of these genes then continue to play an important role in the regulation of cell growth and differentiation in adult.
Ikram, Mohammed S, Ikram, Mohammed. S.
core   +1 more source

Management of multiple odontogenic keratocysts associated with nevoid basal cell carcinoma syndrome: a case report of 11-year follow-up. [PDF]

J Korean Assoc Oral Maxillofac Surg, 2022
Kim HM, Lim SJ, Cho YC, Sung IY, Son JH.
europepmc   +1 more source

Electrophysiological Study of Visual Pathways in Nevoid Basal Cell Carcinoma Syndrome Patients. [PDF]

Eye Brain, 2021
Moramarco A, Alisi L, Lambiase A, Giustini S, Lucchino L, Miraglia E, Roberti V, Nebbioso M.   +7 more
europepmc   +1 more source

Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization. [PDF]

Sci Rep, 2021
Gold NB, Campbell IM, Sheppard SE, Tan WH.   +3 more
europepmc   +1 more source

Standard Poster Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions

Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
wiley   +1 more source

Nevoid basal cell carcinoma syndrome with anophthalmia: a case report. [PDF]

Hua Xi Kou Qiang Yi Xue Za Zhi, 2022
Chen M, Tao S, Chen G, Tang Y, Mai H.
europepmc   +1 more source

Medulloblastoma with Extensive Nodularity in a Child with Gorlin Syndrome - Case Report from Regional Cancer Centre

Clinical Pediatric Hematology-Oncology
Gorlin syndrome, also known as Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome (NBCCS), or basal cell nevus syndrome, is a rare autosomal dominant cancer predisposition disorder characterized by high penetrance and variable expressivity.
M. Vijay Krishnan, Appaji Lingegowda, Arun Kumar, Prakruthi S. Kaushik, Meena Haldorai, R. Nikila, Avinash Thummalapalli, T. M. Surekha   +7 more
doaj   +1 more source

Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing. [PDF]

Sci Rep, 2021
Kim B, Kim MJ, Hur K, Jo SJ, Ko JM, Park SS, Seong MW, Mun JH.   +7 more
europepmc   +1 more source