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Research 121–150 of 1000+
- Food and medicine homology: a potential nutritional intervention strategy for post-acute COVID-19 syndrome
- Exosomes: A Promising Strategy for Repair, Regeneration and Treatment of Skin Disorders
- Mesenchymal stem cell exosomes enhance the development of hair follicle to ameliorate androgenetic alopecia
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Exploring the Complexities of TGF-beta Signaling in Keloids: Beyond the Classical Smad Pathway
- Poly-D,L-Lactic Acid Filler Restores Hair Thickness and Shine by Ameliorating Age-Associated Follicular Decline
- The Role of LncRNAs in Radio- and Chemoresistance of Glioblastoma: Prognostic or Therapeutic?
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Saponins of Paris polyphylla for the Improvement of Acne: Anti-Inflammatory, Antibacterial, Antioxidant and Immunomodulatory Effects
- Efficacy of derinat as a treatment for murine and androgenetic alopecia (AGA) patients
- Therapeutic Potential of Brassinosteroids in Biomedical and Clinical Research
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Gender Differences in Response to COVID-19 Infection and Vaccination
- SARS-CoV-2 Infection and Alpha-Synucleinopathies: Potential Links and Underlying Mechanisms
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Skin expression of mammalian target of rapamycin and forkhead box transcription factor O1, and serum insulin‐like growth factor‐1 in patients with acne vulgaris and their relationship with diet
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Transcriptional Governance of Hair Follicle Stem Cell Quiescence and Niche Maintenance in Long-Term Tissue Regeneration
- Elastogenesis Stimulation by Minoxidil or Nebivolol Reduces Premature Aging of the Aortic Wall in Diabetic Mice
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Leave the Fat, Skip the Bolster: Thinking outside the Box in Lower Third Nasal Reconstruction
- Incidence of trichostasis spinulosa at a single institution in Yemen
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses