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Research 721–750 of 1000+
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Constitutive Internalization of the Leucine-rich G Protein-coupled Receptor-5 (LGR5) to the Trans-Golgi Network
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Lineage Analysis of Epidermal Stem Cells
- Cylindroma as Tumor of Hair Follicle Origin
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- 17β-estradiol Inhibits the Production of RANTES in Human Keratinocytes
- The Vitamin D Receptor as Tumor Suppressor in Skin
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Regulation of stem cell function by protein ubiquitylation
- TGFβ and cancer metastasis: an inflammation link
- Clock genes, hair growth and aging
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- SARS-CoV-2 Non-Structural Proteins and Their Roles in Host Immune Evasion
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Sprouty/FGF signaling regulates the proximal–distal feather morphology and the size of dermal papillae
- Do Changes in Chromosomes Cause Aging?
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- 1α,25(OH)2-Dihydroxyvitamin D3/VDR protects the skin from UVB-induced tumor formation by interacting with the β-catenin pathway
- Animal and in vitro Models for the Study of Hair Follicles