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Research 661–690 of 1000+
- Third International Research Workshop on Alopecia Areata
- Update on Melasma—Part I: Pathogenesis
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- A missense mutation in Lama3 causes androgen alopecia
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hairy tale of signaling in hair follicle development and cycling
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- Human epidermal neural crest stem cells as a source of Schwann cells
- Turner's syndrome associated with psoriasis and alopecia areata
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Hair and Nail Relationship
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Polymorphism of keratin-associated protein (KAP) 7 gene and its association with wool traits in Rambouillet sheep
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- Gray Hair: From Preventive to Treatment
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Finasteride and Dutasteride in the Treatment of Androgenetic Alopecia: Risk or Benefit?