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Research 661–690 of 1000+
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- S100A6: molecular function and biomarker role
- Endogenous retinoids in the hair follicle and sebaceous gland
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Identification of hair shaft progenitors that create a niche for hair pigmentation
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- PROTACs: A novel strategy for cancer drug discovery and development
- Heparan Sulfate Regulates Hair Follicle and Sebaceous Gland Morphogenesis and Homeostasis
- Control by a hair’s breadth: the role of microRNAs in the skin
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands
- Regeneration Genetics
- Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Glutamate transporter Slc1a3 mediates inter‐niche stem cell activation during skin growth
- Runx3 is involved in hair shape determination
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Miz1 is required for hair follicle structure and hair morphogenesis
- IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice