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Research 121–150 of 1000+
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- 46,XY DSD due to impaired androgen production
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Therapeutic strategies for treating hair loss
- Hydrogen peroxide and monoethanolamine are the key causative ingredients for hair dye-induced dermatitis and hair loss
- Hair physiology and its disorders
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Immune cell regulation of the hair cycle
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- The Genetics of Human Skin Disease
- Natural Scalp Hair Regression in Preclinical Stages of Male Androgenetic Alopecia and Its Reversal by Finasteride
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Electron paramagnetic resonance (EPR) spectroscopy for investigating murine telogen skin after spontaneous or depilation-induced hair growth
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Prevalence of telogen effluvium hair loss in COVID-19 patients and its relationship with disease severity
- Natural Hair Supplement: Friend or Foe? Saw Palmetto, a Systematic Review in Alopecia
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Spironolactone May Reduce the Risk of Incident Rosacea
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- Clinical, trichoscopic, and folliscopic identification of the impact of metabolic syndrome on the response to intradermal dutasteride 0.02% injection in patients with female pattern hair loss: a prospective cohort study
- Short communication: Clinical evaluation of pea sprout extract in the treatment of hair loss
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia