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Research 271–300 of 834
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- WNT10B (wingless-type MMTV integration site family)
- Genetic Defects of Female Sexual Differentiation
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Genetics of Structural Hair Disorders
- Biotinidase deficiency characterized by skin and hair findings
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Characteristics of Men Who Report Persistent Sexual Symptoms After Finasteride Use for Hair Loss
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Molecular pathology of skin adnexal tumours
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Molecular Genetics of Alopecias
- AIMP1-Derived Peptide Secreted from Hair Follicle Stem Cells Promotes Hair Growth by Activating Dermal Papilla Cells
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- The human keratins: biology and pathology
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Biology and Genetics of Hair