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Research 631–660 of 806
- Skin Development and Disease: A Molecular Perspective
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Growth Hormone and the Human Hair Follicle
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Differences between ultrastructure and protein composition in straight hair fibres
- Hair shaft disorders in children – An update
- Scalp Biophysical Characteristics in Males with Androgenetic Alopecia: A Comparative Study with Healthy Controls
- Exploring the Potential of Mesenchymal Stem Cell–Derived Exosomes for the Treatment of Alopecia
- Contemporary Management of Alopecia: A Systematic Review and Meta-analysis for Surgeons
- Alopecia areata – Current understanding and management
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Protease activity, localization and inhibition in the human hair follicle
- Iron Metabolism of the Skin: Recycling versus Release
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Clinicopathologic Characteristics and Response to Treatment of Persistent Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Measuring Patient Quality of Life Following Treatment for Alopecia
- 308-nm Excimer Lamp vs. Combination of 308-nm Excimer Lamp and 10% Liquor Carbonis Detergens in Patients With Scalp Psoriasis: A Randomized, Single-Blinded, Controlled Trial
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation