Search
for
Sort by
Research 61–90 of 1000+
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- The Basic Science of Hair Biology
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- An Overview of Alopecias
- Label Retaining Cells (LRCs) with Myoepithelial Characteristic from the Proximal Acinar Region Define Stem Cells in the Sweat Gland
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Darier Sign: A Historical Note
- Regeneration of skin appendages and nerves: current status and further challenges
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Hair follicles and their role in skin health
- Hair Loss in Children
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Diseases of Periocular Hair
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Expression of mineralized tissue associated proteins: Dentin sialoprotein and phosphophoryn in rodent hair follicles
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Molecular Genetics of Human Hair Diseases
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Cell death in the skin
- The Genetics of Human Skin Disease
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Genetic Hair Disorders: A Review
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis