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Research 331–360 of 665
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Long-Term Differential Changes in Mouse Intestinal Metabolomics after γ and Heavy Ion Radiation Exposure
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- The Pharmacology of Regenerative Medicine
- 5α-Reduced glucocorticoids: a story of natural selection
- Animal and in vitro Models for the Study of Hair Follicles
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Identification of hair shaft progenitors that create a niche for hair pigmentation
- Mechanisms and cell lineages in lymphatic vascular development
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- Down-regulation of Melanocortin Receptor Signaling Mediated by the Amino Terminus of Agouti Protein in XenopusMelanophores
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- Regulation of melanocyte stem cells in the pigmentation of skin and its appendages: Biological patterning and therapeutic potentials
- The nude gene and the skin
- Selective Ablation of Ctip2/Bcl11b in Epidermal Keratinocytes Triggers Atopic Dermatitis-Like Skin Inflammatory Responses in Adult Mice
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Regeneration Genetics
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- Teriflunomide: A Once-daily Oral Medication for the Treatment of Relapsing Forms of Multiple Sclerosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells
- The cDNA-deduced amino acid sequence for trichohyalin, a differentiation marker in the hair follicle, contains a 23 amino acid repeat.
- SIRT 7 activates quiescent hair follicle stem cells to ensure hair growth in mice
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss