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Research 931–960 of 1000+
- Flavonoids as Potential Wound-Healing Molecules: Emphasis on Pathways Perspective
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Dihydrotestosterone-Inducible IL-6 Inhibits Elongation of Human Hair Shafts by Suppressing Matrix Cell Proliferation and Promotes Regression of Hair Follicles in Mice
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- Pharmacologic inhibition of JAK-STAT signaling promotes hair growth
- Wnt signaling induces epithelial differentiation during cutaneous wound healing
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Localization, Age- and Site-Dependent Expression, and Regulation of 11β-Hydroxysteroid Dehydrogenase Type 1 in Skin
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Expression of μ-Opiate Receptor in Human Epidermis and Keratinocytes
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Phospholipase C 1 is required for skin stem cell lineage commitment
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Age-Related Loss of Innate Immune Antimicrobial Function of Dermal Fat Is Mediated by Transforming Growth Factor Beta
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- LGR5 is a Marker of Poor Prognosis in Glioblastoma and is Required for Survival of Brain Cancer Stem‐Like Cells
- <i>Arabidopsis</i> VILLIN4 is involved in root hair growth through regulating actin organization in a Ca<sup>2+</sup>‐dependent manner
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71