Associated Papers
CYLD mutation characterizes a subset of HPV-positive head and neck squamous cell carcinomas with distinctive genomics and frequent cylindroma-like histologic features.
Williams EA et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2021
Genetic Testing in CYLD Cutaneous Syndrome: An Update.
Nagy N et al.
The Application of Clinical Genetics, 2021
Epigenetic modifiers DNMT3A and BCOR are recurrently mutated in CYLD cutaneous syndrome.
Davies HR et al.
Nature Communications, 2019
31624251 (PubMed )
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p63 and smooth muscle actin expression in low-grade spiradenocarcinomas in a case of CYLD cutaneous syndrome.
Hoyle A et al.
Journal of Cutaneous Pathology, 2018
Phenotype variability in tumor disorders of the skin appendages associated with mutations in the CYLD gene.
Parren LJMT et al.
Archives of Dermatological Research, 2018
Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation.
Tantcheva-Poór I et al.
Dermatology (basel, Switzerland), 2016
The cylindromatosis (CYLD) gene and head and neck tumorigenesis.
Verhoeft KR et al.
Cancers of the Head & Neck, 2016
Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke-Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens.
Grossmann P et al.
The American Journal of Dermatopathology, 2013
Update of cylindromatosis gene (CYLD) mutations in Brooke-Spiegler syndrome: novel insights into the role of deubiquitination in cell signaling.
Blake PW et al.
Human Mutation, 2009
Diverse phenotype of Brooke-Spiegler syndrome associated with a nonsense mutation in the CYLD tumor suppressor gene.
Zhang G et al.
Experimental Dermatology, 2006
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