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Research 451–480 of 1000+
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Highlights from the Literature
- Characterization and isolation of stem cell-enriched human hair follicle bulge cells
- Keratin 15 Promoter Targets Putative Epithelial Stem Cells in the Hair Follicle Bulge
- Activating an adaptive immune response from a hydrogel scaffold imparts regenerative wound healing
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Chitin and Chitosans: Characteristics, Eco-Friendly Processes, and Applications in Cosmetic Science
- A Novel Marker of Tissue Junctions, Collagen XXII
- Single-Cell Transcriptomics of Traced Epidermal and Hair Follicle Stem Cells Reveals Rapid Adaptations during Wound Healing
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Intracrine androgen biosynthesis, metabolism and action revisited
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- The Pathobiology of Skin Aging
- Proteome Analysis of Human Hair Shaft
- Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease
- The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth
- The structure of people’s hair
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Advances in Chitosan-Based Nanoparticles for Drug Delivery
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- TRPV3 as a Therapeutic Target for Itch
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Trichoscopy in genetic hair shaft abnormalities