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Research 421–450 of 649
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Implication of Human Bacterial Gut Microbiota on Immune-Mediated and Autoimmune Dermatological Diseases and Their Comorbidities: A Narrative Review
- N6-methyladenosine RNA Methylation Correlates with Immune Microenvironment and Immunotherapy Response of Melanoma
- Skin Microbiome, Metabolome and Skin Phenome, from the Perspectives of Skin as an Ecosystem
- Identification of functional circRNAs regulating ovarian follicle development in goats
- The secondary role of UV light in swimmers melanoma genesis
- Proteolysis‐targeting chimeras in cancer therapy: Targeted protein degradation for next‐generation treatment
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- SOX18 Promotes the Proliferation of Dermal Papilla Cells via the Wnt/β-Catenin Signaling Pathway
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Hyaluronic Acid Hydrogel Incorporating Dexpanthenol-Engineered Extracellular Vesicles for Accelerated Wound Closure and Mitigated Secondary Infection Risk
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- Hair follicle targeting via gelatin coated transferosomes loaded with tofacitinib citrate for enhanced treatment of alopecia areata: Clinical evaluation of alopecia areata patients
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- Hair follicle stem cells and mitochondria
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- The TOR–Auxin Connection Upstream of Root Hair Growth