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Research 511–540 of 1000+
- Animal models and culture methods in the study of hair growth
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- A missense mutation in Lama3 causes androgen alopecia
- La voie de la PGI2 pour améliorer la cicatrisation des plaies du pied diabétique
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Update on Melasma—Part I: Pathogenesis
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Treatment of Hair Loss in the Trichorhinophalangeal Syndrome
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Constitutive activation of Stat3 in mouse epidermis is linked to hair deficiency and cytoskeletal network damage
- Ehlers-Danlos syndrome: From bedside to bench
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- An integrative analysis of the lncRNA-miRNA-mRNA competitive endogenous RNA network reveals potential mechanisms in the murine hair follicle cycle
- Iron deficient toxic milk leads to the mask phenotype in hephaestin knockout mice (907.4)
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Molecular basis of androgen insensitivity
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Epidermal Vascular Endothelial Growth Factor Production Is Required for Permeability Barrier Homeostasis, Dermal Angiogenesis, and the Development of Epidermal Hyperplasia
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Genetics of Inherited Ichthyoses and Related Diseases
- Cylindroma as Tumor of Hair Follicle Origin
- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children