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Research 331–360 of 1000+
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- E-Poster
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Cutaneous wound healing: recruiting developmental pathways for regeneration
- Reversible Activation of c-Myc in Skin
- Biotin and biotinidase deficiency
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Macrophages induce AKT/β-catenin-dependent Lgr5+ stem cell activation and hair follicle regeneration through TNF
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Visualising Androgen Receptor Activity in Male and Female Mice
- Pathology of Mouse Models of Accelerated Aging
- Adipocytes in Skin Health and Disease
- Improved health-span and lifespan in mtDNA mutator mice treated with the mitochondrially targeted antioxidant SkQ1
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- The Safety and Efficacy of Tofacitinib in 24 Cases of Pediatric Rheumatic Diseases: Single Centre Experience
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Genetic Hair Disorders: A Review
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- New developments in the molecular treatment of ichthyosis: review of the literature
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Developmental genetics of color pattern establishment in cats
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1