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Research 541–570 of 1000+
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Hair-Cycle-Associated Remodeling of the Peptidergic Innervation of Murine Skin, and Hair Growth Modulation by Neuropeptides
- Congenital Adrenal Hyperplasia
- Hair follicles’ transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Expression of bioactive recombinant human fibroblast growth factor 9 in oil bodies of Arabidopsis thaliana
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Skin tissue engineering
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
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- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Acne Syndromes and Mosaicism
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Comparative Analysis of Bacteriome in Hair Follicle Layers of Patients with Female Pattern Androgenic Alopecia
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Bachmann–Bupp syndrome and treatment
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- Microbiome in the hair follicle of androgenetic alopecia patients
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function