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Research 661–690 of 1000+
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Molecular Genetics of Human Hair Diseases
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- A guide to diagnosis and management of hypertrichosis
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Telogen Effluvium
- Diseases of Hair
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Diseases of Hair
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Topical minoxidil for nail growth: A conventional medication with a novel indication
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Table of Contents
- Hyperactivation of sympathetic nerves drives depletion of melanocyte stem cells
- Identification of Anabolic Selective Androgen Receptor Modulators with Reduced Activities in Reproductive Tissues and Sebaceous Glands
- Neurological post‐acute sequelae of SARS‐CoV‐2 infection
- Dicer- and Bulge Stem Cell-Dependent MicroRNAs During Induced Anagen Hair Follicle Development
- Hair restoration in the age of MRSA
- Commonly encountered symptoms and their management in patients with cirrhosis
- Männlicher Haarausfall – was uns unsere Gene verraten
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- MicroRNA-149-Mediated MAPK1/ERK2 Suppression Attenuates Hair Follicle Stem Cell Differentiation
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Intercellular junctions in normal epidermis
- Oral isotretinoin for acne
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Androgen sensitivity gateway to COVID‐19 disease severity