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Research 751–780 of 1000+
- Systematic Analysis of Non-coding RNAs Involved in the Angora Rabbit (Oryctolagus cuniculus) Hair Follicle Cycle by RNA Sequencing
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- LncRNA H19 Overexpression Activates Wnt Signaling to Maintain the Hair Follicle Regeneration Potential of Dermal Papilla Cells
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Syndecan-1 Is Required to Maintain Intradermal Fat and Prevent Cold Stress
- The molecular basis of human keratin disorders
- Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Preliminary study on microR-148a and microR-10a in dermal papilla cells of Hu sheep
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Stem cells supporting other stem cells
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Quorum sensing and other collective regenerative behavior in organ populations
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Profiling of hair proteome revealed individual demographics
- Editors' Picks
- Evidence for Masculinization of Adipokine Gene Expression in Visceral and Subcutaneous Adipose Tissue of Obese Women With Polycystic Ovary Syndrome (PCOS)
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Trichoscopy
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- <i>Hoxc13</i> mutant mice lack external hair