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Research 691–720 of 1000+
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Alopezien und Hypotrichosen im Kindesalter
- “Structural imprinting” of the cutaneous immune effector function
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- A Comprehensive Review of GWASs of Human Hair Traits
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- First Symposium of Ichthyosis Experts
- 0932 Spatiotemporal gradient of mesenchymal stiffness controls sweat gland morphogenesis
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Unravelling the threads of central centrifugal cicatricial alopecia
- 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Assessment of Trial to Use Exosomes and Salmon DNA with Minoxidil as Multisource Mixture for Hair Follicle Activation an In Vivo Study
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Synergistic treatment of androgenetic alopecia with follicular co-delivery of minoxidil and cedrol in metal-organic frameworks stabilized by covalently cross-linked cyclodextrins
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- 918 Tissue engineered human hair follicles from genetically, environmentally and extrinsically reprogrammed dermal papilla cells
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Identification and profiling of microRNA between back and belly Skin in Rex rabbits (Oryctolagus cuniculus)
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Wound repair at a glance