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Research 751–780 of 1000+
- PCSK9: From Nature’s Loss to Patient’s Gain
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- Genetic Disorders and Defects in Vitamin D Action
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Endogenous retinoids in the hair follicle and sebaceous gland
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Pathomechanisms of immune-mediated alopecia
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- A simple method using ex vivo culture of hair follicle tissue to investigate intrinsic circadian characteristics in humans
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Comparative Analysis of the Cutaneous Microbiome in Psoriasis Patients and Healthy Individuals—Insights into Microbial Dysbiosis: Final Results
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Chrysanthemum species used as food and medicine: Understanding quality differences on the global market
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- Medical Dermatology
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse