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Research 781–810 of 803
- Comparative immunohistochemical analysis suggests a conserved role of EPS8L1 in epidermal and hair follicle barriers of mammals
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- In Vitro and Ex Vivo Hair Follicle Models to Explore Therapeutic Options for Hair Regeneration
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Acne-Associated Syndromes
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- Ernährungsstörungen des Haares und deren Management
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Lrig1-expressing epidermal progenitors require SCD1 to maintain the dermal papilla niche
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Author response: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Decision letter: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Clouston’s syndrome: a rare case report
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Monilethrix – Case report of a rare disease
- Molecular Genetics of Human Hair Diseases
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Hordenine Activated Dermal Papilla Cells and Promoted Hair Regrowth by Activating Wnt Signaling Pathway
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant