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Research 421–450 of 703
- Considering the risk of a coloring shampoo with the function of gray hair cover cosmetology and skin barrier: A systematic review
- Therapeutic Approach for Hair Growth and Regeneration Using Bioactive Formulation Containing Mesenchymal Stromal Cell-Derived Conditioned Medium
- Medicinal and cosmetic products used in treatment of hair loss
- Seborrheic dermatitis and pityriasis sicca: A review
- Comparitive Study of Various Brands of Synthetic Hair Gels and Herbal Hair Gels
- NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Glycerol Regulates Stratum Corneum Hydration in Sebaceous Gland Deficient (Asebia) Mice
- Epithelial-Mesenchymal Micro-niches Govern Stem Cell Lineage Choices
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- Biotin and biotinidase deficiency
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1