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Research 31–60 of 1000+
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Tinea capitis mimicking alopecia areata
- The distributions of type IV collagen .ALPHA. chains in basement membranes of human epidermis and skin appendages
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Insulin Promotes Corneal Nerve Repair and Wound Healing in Type 1 Diabetic Mice by Enhancing Wnt/β-Catenin Signaling
- Molecular functional analyses revealed essential roles of HSP90 and lamin A/C in growth, migration, and self-aggregation of dermal papilla cells
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Emulgel Considered as Anovel Type of Dosage Form for Topical Application
- A umbilical cord blood-derived exosome product simulates hair growth through laminin V and collagen XVII: an ex vivo study
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Lack of Evidence for Sprouting of Aβ Afferents into the Superficial Laminas of the Spinal Cord Dorsal Horn after Nerve Section
- Production of 5α-Reduced Neurosteroids Is Developmentally Regulated and Shapes GABA<sub>A</sub>Miniature IPSCs in Lamina II of the Spinal Cord
- Equine Hoof Stem Progenitor Cells (HPC) CD29 + /Nestin + /K15 + – a Novel Dermal/epidermal Stem Cell Population With a Potential Critical Role for Laminitis Treatment
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- BMP4 and nuclear laminC orchestrate a expression of AHF/Trichohyalin molecule, a key modulator of keratin intermediate filaments in the hair follicle
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Transforming Growth Factor-??, Smad, and Collagen Expression Patterns in Fetal and Adult Keratinocytes
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Repairing the lungs one breath at a time: How dedicated or facultative are you?
- Basement Membrane Zone Remodeling During Appendageal Development in Human Fetal Skin. The Absence of Type VII Collagen is Associated with Gelatinase-A (MMP2) Activity
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Induction of Skin-Derived Precursor Cells from Human Induced Pluripotent Stem Cells
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Dermal-epidermal interactions—follicle-derived cell populations in the study of hair-growth mechanisms
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Droplet-Based Microfluidics as a Platform to Design Food-Grade Delivery Systems Based on the Entrapped Compound Type