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Research 241–270 of 1000+
- Cases Report the Cronkhite-Canada Syndrome
- Ernährungsstörungen des Haares und deren Management
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Alopecia in Children
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- TONGUE, RED
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- E-Poster
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- The molecular basis of human keratin disorders
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Antihypertensive Agents in Dermatology
- Author Index
- Subject Index
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Cronkhite-Canada syndrome: A case report and literature review
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Comparative Spatial Transcriptomic and Single-Cell Analyses of Human Nail Units and Hair Follicles Show Transcriptional Similarities between the Onychodermis and Follicular Dermal Papilla
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches