Search
for
Sort by
Research 211–240 of 1000+
- A comparative proteomic-based study identifies essential factors involved in hair follicle growth in inner Mongolia cashmere goats
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Effects of oxytocin on the hair growth ability of dermal papilla cells
- Pathologic Quiz Case: A Nodule on the Back
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Widespread and eruptive comedonal lesions with alopecia
- Acne Vulgaris
- Zinc and Zinc Transporters in Dermatology
- Acne Syndromes and Mosaicism
- Pentacyclic Triterpenoid Maslinic Acid Promotes Hair Growth Comparable to Minoxidil: A New Insight on the Potential Involvement of Cilia Activity
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Significance of stress keratin expression in normal and diseased epithelia
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- Unveiling the Effect of Age and IgE Level on Alopecia Areata: Insights from Comparative RNAseq Analysis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Current Genetics in Hair Diseases
- Molecular Mechanisms Regulating Hair Follicle Development
- Towards Defining the Pathogenesis of the Hairless Phenotype
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Transcriptomic landscape of early hair follicle and epidermal development
- New developments in the molecular treatment of ichthyosis: review of the literature
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus