Search
for
Sort by
Research 121–150 of 1000+
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A newborn presenting with congenital blistering
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Defining the identity of mouse embryonic dermal fibroblasts
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- 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
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Human basal cell carcinoma: the induction of anagen hair follicle differentiation
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Establishment of a culture model for the prolonged maintenance of chicken feather follicles structure in vitro
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- M2 Macrophage and Extracellular Matrix Genes Are Enriched in High‐Activity Lichen Planopilaris
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Establishment of SV40T-transformed human dermal papilla cells and identification of dihydrotestosterone-regulated genes by cDNA microarray
- Decision letter: Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
- Evaluation of noninvasive biospecimens for transcriptome studies