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Research 61–90 of 1000+
- Molecular Genetics of Human Hair Diseases
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- TONGUE, RED
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- The Genetics of Human Skin Disease
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Molecular Mechanisms Regulating Hair Follicle Development
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- NF-κB Activity Is Required for Anagen Maintenance in Human Hair Follicles In Vitro
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Madarosis: A marker of many Maladies
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Alopecia in Children
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Ichthyosis with confetti: clinics, molecular genetics and management
- Immunological control of skin development: from homeostasis to developmental pathologies
- Steatocystoma Multiplex
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Atrichia with papular lesions
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V