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Research 601–630 of 1000+
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Caloric Restriction Promotes Structural and Metabolic Changes in the Skin
- Adenosine Stimulates Fibroblast Growth Factor-7 Gene Expression Via Adenosine A2b Receptor Signaling in Dermal Papilla Cells
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Going below and beyond the surface: Microneedle structure, materials, drugs, fabrication, and applications for wound healing and tissue regeneration
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Advances and Innovations of 3D Bioprinting Skin
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- 5α-Reduced glucocorticoids: a story of natural selection
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Down-regulation of Melanocortin Receptor Signaling Mediated by the Amino Terminus of Agouti Protein in XenopusMelanophores
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Advances in Digital Light Processing (DLP) Bioprinting: A Review of Biomaterials and Its Applications, Innovations, Challenges, and Future Perspectives
- Pre-Clinical Cell-Based Therapy for Limbal Stem Cell Deficiency
- A Successfully Treated Case of Criminal Thallium Poisoning
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Current Biomedical Applications of 3D-Printed Hydrogels
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- New and Consolidated Therapeutic Options for Pubertal Induction in Hypogonadism: In-depth Review of the Literature
- Unlocking the Potential of Oleanolic Acid: Integrating Pharmacological Insights and Advancements in Delivery Systems
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor