• A case of Brooke-Spiegler syndrome with a novel mutation in the CYLD gene in a patient with aggressive non-Hodgkin's lymphoma
• A case of multiple familial trichoepitheliomas responding to treatment with the Hedgehog signaling pathway inhibitor vismodegib
• A de novo missense mutation of the CYLD gene with multiple familial trichoepithelioma
• A large family with CYLD cutaneous syndrome: medical genetics at the community level
• A novel large deletion of the CYLD gene causes CYLD cutaneous syndrome in a Chinese family
• A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma
• A novel splicing CYLD variant associated with trichoepithelioma papulosum multiplex demonstrating intrafamilial severity variability
• A Simple and Effective Method for Treating Cylindromas in Brooke-Spiegler Syndrome
• An extremely rare association of multiple familial trichoepitheliomas and hereditary multiple osteochondromas
• Autosomal dominant genodermatoses in adults being heralded by superimposed skin lesions in children
• Basal Cell Carcinoma in a Patient With Brooke-Spiegler Syndrome
• Breast Neoplasms with Dermal Analogue Differentiation (Mammary Cylindroma): Report of 3 Cases and a Proposal for a New Terminology
• Brooke-Spiegler syndrome
• Brooke-Spiegler syndrome
• Brooke-Spiegler Syndrome and Phenotypic Variants: An Update
• Brooke-Spiegler syndrome with chronic obstructive pulmonary disease and chronic sinusitis
• Brooke-Spiegler Syndrome with Parotid Gland Involvement
• Brooke-Spiegler Syndrome: Familial Cylindromatosis, a Rare Variant of a Rare Familial Syndrome
• Brooke-Spiegler syndrome: focus on reflectance confocal microscopy findings of trichoepithelioma and flat cylindroma
• Brooke-Spiegler syndrome: radiotherapy as the last resort?
• Brooke-Spiegler syndrome: report of a case
• Brooke-Spiegler Syndrome: Two Patients From a Turkish Family With Multiple Familial Trichoepithelioma
• CALML6 Controls TAK1 Ubiquitination and Confers Protection against Acute Inflammation
• Can we clinically identify patients at risk of malignant transformation of skin tumors in Brooke-Spiegler syndrome?
• Catalytic domain mutation in CYLD inactivates its enzyme function by structural perturbation and induces cell migration and proliferation
• CENPV Is a CYLD-Interacting Molecule Regulating Ciliary Acetylated α-Tubulin
• Clinical, genetic and experimental studies of the Brooke-Spiegler (CYLD) skin tumor syndrome
• Clustered unilateral trichoepitheliomas indicate Type 1 segmental manifestation of multiple familial trichoepithelioma
• Conductive hearing loss caused by ear canal stenosis
• CYLD destabilizes NoxO1 protein by promoting ubiquitination and regulates prostate cancer progression
• CYLD mutations differentially affect splicing and mRNA decay in Brooke-Spiegler syndrome
• Cylindroma spine metastasis: Long-term follow-up is required
• Cylindromas-rare but striking
• Cylindromatosis (Cyld) gene mutation in T cells promotes the development of an IL-9-dependent allergic phenotype in experimental asthma
• Cylindromatosis drives synapse pruning and weakening by promoting macroautophagy through Akt-mTOR signaling
• Dermoscopy of Adnexal Tumors
• Diverse assays from a single skin punch biopsy to assess topical drug intervention
• Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission
• Downregulation of m⁶A Reader YTHDC2 Promotes the Proliferation and Migration of Malignant Lung Cells via CYLD/NF-κB Pathway
• Eccrine cylindroma of the face and scalp
• Effect of Topical Rapamycin 1% on Multiple Trichoepitheliomas
• Epigenetic modifiers DNMT3A and BCOR are recurrently mutated in CYLD cutaneous syndrome
• Fibroblast Growth Factor Receptor 2 Overexpression in Multiple Familial Trichoepithelioma
• First Japanese case of trichoepithelioma papulosum multiplex successfully treated with sirolimus gel
• Free latissimus dorsi flap lacing and local care in two-stage scalp reconstruction
• Genetic Testing in CYLD Cutaneous Syndrome: An Update
• Heterozygous Cylindromatosis Gene Mutation c.1628_1629delCT in a Family with Brook-Spiegler Syndrome
• Hypermethylation of protocadherin γ subfamily A12 and solute carrier family 19 A 1 promoters contributes to the occurrence and metastasis of colorectal cancer
• Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome
• In Vivo Reflectance Confocal Microscopy of Adnexal Tumors: Evaluation of Trichoepithelioma, Sebaceoma, and Fibrofolliculoma
• Inherited pulmonary cylindromas: extending the phenotype of CYLD mutation carriers
• Laser-assisted delivery of imiquimod in Brooke-Spiegler syndrome
• Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family
• Metastatic cylindrocarcinoma in Brooke-Spiegler Syndrome - Report of a case and review of the literature
• Multiple Facial Trichoepitheliomas and Vulval Cysts: Extending the Phenotypic Spectrum in CYLD Cutaneous Syndrome
• Multiple Familial Trichoepithelioma
• Multiple Familial Trichoepithelioma Successfully Treated With CO₂ Laser and Imiquimod
• Multiple familial trichoepithelioma with a novel mutation of the CYLD gene
• Multiple familial trichoepithelioma: 9 cases from a family
• Multiple familial trichoepithelioma: report of a disfiguring case
• Multiple familial trichoepitheliomas: Ultrasonographic findings
• Multiple nodular papules and tumors of the head and face
• Multiple papulonodular lesions on central area of the face: what is your diagnosis?
• Overexpression of MYB drives proliferation of CYLD-defective cylindroma cells
• p63 and smooth muscle actin expression in low-grade spiradenocarcinomas in a case of CYLD cutaneous syndrome
• Phenotype variability in tumor disorders of the skin appendages associated with mutations in the CYLD gene
• Primary cutaneous adenoid cystic carcinoma mimicking dermal cylindroma: histology of the complete surgical excision as the key to diagnosis
• Reduced expression of CYLD promotes cell survival and inflammation in gefitinib-treated NSCLC PC-9 cells: Targeting CYLD may be beneficial for acquired resistance to gefitinib therapy
• Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation
• Research progress of deubiquitinating enzyme CYLD to regulate liver-related diseases
• Solitary trichoepithelioma: clinical, dermatoscopic and histopathological findings
• Sporadic Trichoblastomas and Those Occurring in the Setting of Multiple Familial Trichoepithelioma/Brooke-Spiegler Syndrome Show No BAP1 Loss
• Squamous Cell Carcinoma and Multiple Familial Trichoepitheliomas: A Recurrent Association
• Successful treatment of trichoepithelioma with a novel insulated, monopolar, radiofrequency microneedle device
• Surgical Treatment of Brooke-Spiegler Syndrome
• Targeting Tropomyosin Receptor Kinase in Cutaneous CYLD Defective Tumors With Pegcantratinib: The TRAC Randomized Clinical Trial
• The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
• The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene
• The cylindromatosis (<em>CYLD</em>) gene and head and neck tumorigenesis
• The deubiquitinase CYLD controls protective immunity against helminth infection by regulation of Treg cell plasticity
• The Potential of Cylindromatosis (CYLD) as a Therapeutic Target in Oxidative Stress-Associated Pathologies: A Comprehensive Evaluation
• The role of MARCH9 in colorectal cancer progression
• The role of vesicular overexpressed in cancer pro-survival protein 1 in hepatocellular carcinoma proliferation
• The SPATA2/CYLD pathway contributes to doxorubicin-induced cardiomyocyte ferroptosis via enhancing ferritinophagy
• The surgical treatment of familial cylindromatosis through subgaleal scalp excision
• TRAF3 and NBR1 both influence the effect of the disease-causing CYLD(Arg936X) mutation on NF-κB activity
• Trichoblastic carcinoma arising in trichoepithelioma in Brooke-Spiegler syndrome
• Trichoepithelioma: A Comprehensive Review
• Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours: study protocol for a randomised controlled trial
• Tumor suppressor protein CYLD regulates morphogenesis of dendrites and spines
• Turban Tumor Syndrome: In Search of a Gold Standard - A Case Report
• Turban tumour with intracranial invasion
• Ulcerating Tumor of the Scalp: Answer
• Ulcerating Tumor of the Scalp: Challenge
• Understanding Inherited Cylindromas: Clinical Implications of Gene Discovery
• Unilateral facial papules and plaques
• Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes
• Use of topical sirolimus in the management of multiple familial trichoepitheliomas
• UVB radiation represses CYLD expression in melanocytes
• YTHDC2 Retards Cell Proliferation and Triggers Apoptosis in Papillary Thyroid Cancer by Regulating CYLD-Mediated Inactivation of Akt Signaling