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Research 361–390 of 735
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Single-cell RNA-seq highlights heterogeneity in human primary Wharton’s jelly mesenchymal stem/stromal cells cultured in vitro
- The Skin Microbiome: Current Landscape and Future Opportunities
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Androgenetic Alopecia: An Update of Treatment Options
- Advances in the human skin microbiota and its roles in cutaneous diseases
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Wnt/β‐catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- Characterization of the in vitro, ex vivo, and in vivo Efficacy of the Antimicrobial Peptide DPK-060 Used for Topical Treatment
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Exosomal Micro RNAs Derived from Dermal Papilla Cells Mediate Hair Follicle Stem Cell Proliferation and Differentiation
- Exploring the new horizons of drug repurposing: A vital tool for turning hard work into smart work
- Aldo-Keto Reductase (AKR) 1C3 inhibitors: a patent review
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development
- Therapeutic, Prophylactic, and Functional Use of Probiotics: A Current Perspective
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Who do we invent for? Patents by women focus more on women’s health, but few women get to invent
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Leveraging nature’s nanocarriers: Translating insights from extracellular vesicles to biomimetic synthetic vesicles for biomedical applications
- Lysophospholipid Mediators in Health and Disease
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Scalp bacterial shift in Alopecia areata
- Significance of stress keratin expression in normal and diseased epithelia
- Plant-derived exosome-like nanovesicles: a novel therapeutic perspective for skin diseases
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury