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Research 61–90 of 1000+
- Molecular biology of hair morphogenesis: Development and cycling
- Learning from nudity: lessons from the nude phenotype
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- Aging, alopecia, and stem cells
- The nude gene and the skin
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Gsdma3 is required for hair follicle differentiation in mice
- Survivin as a Novel Biomarker in the Pathogenesis of Acne Vulgaris and Its Correlation to Insulin-Like Growth Factor-I
- Formation of regulator/target gene relationships during evolution
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Structure and expression of the ovine Hoxc-13 gene
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Protein kinase Akt2/PKBβ is involved in blastomere proliferation of preimplantation mouse embryos
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Skin aging and barrier dysfunction: bridging current therapies with future genetic and nanotechnological interventions
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Transcriptional Governance of Hair Follicle Stem Cell Quiescence and Niche Maintenance in Long-Term Tissue Regeneration
- Integrative transcriptomic and metabolomic analyses reveal the role of melatonin in promoting secondary hair follicle development in cashmere goats
- Melatonin-Mediated Circadian Rhythm Signaling Exhibits Bidirectional Regulatory Effects on the State of Hair Follicle Stem Cells
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region