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Research 391–420 of 1000+
- Prolactin—a novel neuroendocrine regulator of human keratin expression<i>in situ</i>
- Selective delivery of adapalene to the human hair follicle under finite dose conditions using polymeric micelle nanocarriers
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- Simultaneous determination of androgens and prostaglandins in human urine using ultra-high-performance liquid chromatography–tandem mass spectrometry
- Finasteride Enhances the Generation of Human Myeloid-Derived Suppressor Cells by Up-Regulating the COX2/PGE2 Pathway
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Low fucosylation defines the glycocalyx of progenitor cells and melanocytes in the human limbal stem cell niche
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Simultaneous determination of androgens and prostaglandins in human urine using ultra-high-performance liquid chromatography–tandem mass spectrometry
- Visualizing Integrative Functioning in the Human Brainstem and Spinal Cord With Spinal Functional Magnetic Resonance Imaging
- Model systems for the study of dermatophyte and non-dermatophyte invasion of human keratin.
- 237 Unveiling Skin Cancers Pathophysiology via the Modeling of Xeroderma Pigmentosum Disease Modeling Using CRISPR-Cas9 Technology
- Preclinical Evidence and Underlying Mechanisms of <i>Polygonum multiflorum</i> and Its Chemical Constituents Against Cognitive Impairments and Alzheimer’s Disease
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Exosomes derived from uMSCs promote hair regrowth in alopecia areata through accelerating human hair follicular keratinocyte proliferation and migration
- LB708 ILC1-like innate lymphocytes in human autoimmunity: Lessons from Alopecia Areata
- Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in mice
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Editor's evaluation: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Impact of Stat3 activation upon skin biology: A dichotomy of its role between homeostasis and diseases
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- The many faces of interleukin-17 in inflammatory skin diseases
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Thyrotropin-releasing hormone and oestrogen differentially regulate prolactin and prolactin receptor expression in female human skin and hair follicles <i>in vitro</i>
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- New hopes and strategies for the treatment of severe ocular surface disease
- Regulatory T cells in autoimmune skin diseases