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Research 751–780 of 1000+
- 671 Impaired follicular Nrf2 signaling: Potential early therapeutic target in hidradenitis suppurativa
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- The ophthalmological complications of targeted agents in cancer therapy: what do we need to know as ophthalmologists?
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- In This Issue
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Alopezien und Hypotrichosen im Kindesalter
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Phenyl Propanoid 1’s-1′-Acetoxychavicol Acetate Protects Against Testosterone-Induced Alopecia by Inhibiting Nadph Oxidase
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Monilethrix
- Expression of Three Adipokines (Adiponectin, Leptin and Resistin) in Normal Canine Skin: a Pilot Study
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- Role of Cytotoxic T Cells in Chronic Alopecia Areata
- Melatonin induces a stimulatory action on the scrotal skin components of Soay ram in the non-breeding season
- Mapping Human Skin: One Sequenced Cell at a Time
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Immunolocalization of 5α-Reductase Isozymes in Acne Lesions and Normal Skin
- NG2 Proteoglycan Expression in Mouse Skin: Altered Postnatal Skin Development in the NG2 Null Mouse
- Expression patterns of programmed cell death 4 protein in normal human skin and some representative skin lesions
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Scientific opinion on the tolerable upper intake level for selenium
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Nanostructured lipid carriers loaded with an association of minoxidil and latanoprost for targeted topical therapy of alopecia
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Overexpression of hypoxia-inducible factor-1α in hidradenitis suppurativa: the link between deviated immunity and metabolism