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Research 931–960 of 1000+
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- PROTACs: A novel strategy for cancer drug discovery and development
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Different Ligands of the TRPV3 Cation Channel Cause Distinct Conformational Changes as Revealed by Intrinsic Tryptophan Fluorescence Quenching
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- Advancing Design Strategy of PROTACs for Cancer Therapy
- Skin regional specification and higher-order <i>HoxC</i> regulation
- TRPV3 Ion Channel: From Gene to Pharmacology
- Identification of A p300–SP1–BRD4 Transcriptional Axis as a Key Driver of AR Hyperactivation in Polycystic Ovarian Syndrome
- Implication of microRNA regulation in para-phenylenediamine-induced cell death and senescence in normal human hair dermal papilla cells
- Mathematical Modeling and Inference of Epidermal Growth Factor-Induced Mitogen-Activated Protein Kinase Cell Signaling Pathways
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- The triacylglycerol synthesis enzyme DGAT1 also catalyzes the synthesis of diacylglycerols, waxes, and retinyl esters
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- A Review of the Evidence for and against a Role for Mast Cells in Cutaneous Scarring and Fibrosis
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Vitamin D and the Parenteral Nutrition Patient
- Adaptive Balance in Posterior Cerebellum
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Phosphatidylinositol 3-Kinase/Akt-Dependent and -Independent Protection Against Apoptosis in Normal Human Melanocytes
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle