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Research 91–120 of 1000+
- Regulatory T cells in dominant immunologic tolerance
- Advances in clinical applications of microneedle
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- New developments in the molecular treatment of ichthyosis: review of the literature
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Melanocytes: The new Black
- An Update of Congenital Adrenal Hyperplasia
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Learning from nudity: lessons from the nude phenotype
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- Regenerative Medicine of Epidermal Structures
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Identification of the cell lineage at the origin of basal cell carcinoma
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation