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Research 361–390 of 1000+
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Generalized atrophic benign epidermolysis bullosa.
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Hair follicles’ transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- cDermo-1 misexpression induces dense dermis, feathers, and scales
- Influence of Recombinant Codon-Optimized Plasmid DNA Encoding VEGF and FGF2 on Co-Induction of Angiogenesis
- Growth Hormone and the Human Hair Follicle
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Unravelling the threads of central centrifugal cicatricial alopecia
- Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Hair Follicle Stem Cell SLC3A2 Regulates Epithelial Regenerative Properties
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Molecular Mechanisms Regulating Hair Follicle Development
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Lysophospholipid Mediators in Health and Disease
- Gsdma3 is required for hair follicle differentiation in mice
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules