Search
for
Sort by
Research 211–240 of 1000+
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Role of peptide growth factors in the rhythm of change hair
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Skin Graft Harvesting and Donor Site Selection
- The Hair Transplant Megasession Technique: A Review
- Scarring Alopecia
- Transforming growth factor-β in stem cells and tissue homeostasis
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Mesenchymal Stem Cells from Adipose Tissue in Clinical Applications for Dermatological Indications and Skin Aging
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Aged differentiated cells reverse into native stemness-like state by niche cytokines to sustain lifelong homeostasis and tissue repair
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera.
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Molecular Genetics of Human Hair Diseases
- Myotonic Dystrophy—A Progeroid Disease?
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Corticotropin releasing hormone and the skin
- Edar Signaling in the Control of Hair Follicle Development
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Epithelial–mesenchymal transition in keloid tissues and TGF‐β1–induced hair follicle outer root sheath keratinocytes
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization