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Research 961–990 of 1000+
- Two distinct signaling pathways in hair cycle induction: Stat3-dependent and -independent pathways
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- The protease corin regulates electrolyte homeostasis in eccrine sweat glands
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- 2063-LB: Transgenic Erythropoietin Overexpression Inhibits Dermal Fat Formation and HIF1a in the Skin and Causes Telogen Effluvium in Mouse Pups during the First Hair Cycle
- Glycerol Regulates Stratum Corneum Hydration in Sebaceous Gland Deficient (Asebia) Mice
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Decreased GATA3 levels cause changed mouse cutaneous innate lymphoid cell fate, facilitating hair follicle recycling
- Defining the impact of β-catenin/Tcf transactivation on epithelial stem cells
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Epigenetics of Colorectal Cancer
- The stem cell niche
- Pharmacologic inhibition of JAK-STAT signaling promotes hair growth
- Transdifferentiation of corneal epithelium into epidermis occurs by means of a multistep process triggered by dermal developmental signals
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Constitutive Internalization of the Leucine-rich G Protein-coupled Receptor-5 (LGR5) to the Trans-Golgi Network
- Lef1 Contributes to the Differentiation of Bulge Stem Cells by Nuclear Translocation and Cross-Talk with the Notch Signaling Pathway
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Endogenous Retinoids in the Pathogenesis of Alopecia Areata