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Research 301–330 of 587
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Targeting integrin pathways: mechanisms and advances in therapy
- The PDE4 inhibitor, apremilast, suppresses experimentally induced alopecia areata in human skin in vivo
- Alarmin Cytokines as Central Regulators of Cutaneous Immunity
- S100A6: molecular function and biomarker role
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- Lysophospholipid Mediators in Health and Disease
- Topical drug delivery strategies for enhancing drug effectiveness by skin barriers, drug delivery systems and individualized dosing
- Effects of Curcumin and Its Different Formulations in Preclinical and Clinical Studies of Peripheral Neuropathic and Postoperative Pain: A Comprehensive Review
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Transcriptomic analyses of regenerating adult feathers in chicken
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Endocrine controls of primary adult human stem cell biology: Thyroid hormones stimulate keratin 15 expression, apoptosis, and differentiation in human hair follicle epithelial stem cells in situ and in vitro
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Scalp Pruritus: Review of the Pathogenesis, Diagnosis, and Management
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- CXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17
- The functions of ocu-miR-205 in regulating hair follicle development in Rex rabbits
- Photobiomodulation therapy in management of cancer therapy-induced side effects: WALT position paper 2022
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Emerging Roles for Ion Channels in Ovarian Cancer: Pathomechanisms and Pharmacological Treatment
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole