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Research 661–690 of 1000+
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
- The Role of the Mammalian Target of Rapamycin (mTOR) in Pulmonary Fibrosis
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Nanoparticle-Based Targeting of Vaccine Compounds to Skin Antigen-Presenting Cells By Hair Follicles and their Transport in Mice
- Comparative Anatomy of Mouse and Human Nail Units
- SIRT 7 activates quiescent hair follicle stem cells to ensure hair growth in mice
- Betacellulin Regulates Hair Follicle Development and Hair Cycle Induction and Enhances Angiogenesis in Wounded Skin
- The 3D Bioprinted Scaffolds for Wound Healing
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Expression of Kruppel-Like Factor KLF4 in Mouse Hair Follicle Stem Cells Contributes to Cutaneous Wound Healing
- sPLA2-IIA Overexpression in Mice Epidermis Depletes Hair Follicle Stem Cells and Induces Differentiation Mediated Through Enhanced JNK/c-Jun Activation
- Biomimetic Cell Membrane‐Coated Scaffolds for Enhanced Tissue Regeneration
- Yangyin Qingre Huoxue Method in Traditional Chinese Medicine Ameliorates Atherosclerosis in ApoE<sup>−/−</sup> Mice Suffering from High-Fat Diet and HSP65 Aggression
- Tissue Repair Mechanisms of Dental Pulp Stem Cells: A Comprehensive Review from Cutaneous Regeneration to Mucosal Healing
- Differential transcriptome study on the damage of testicular tissues caused by chronic infection of T. gondii in mice
- Canagliflozin alleviates progestin resistance by suppressing RARβ/CRABP2 signaling in THRB knockout endometrial cancer cells
- Cisd2 deficiency impairs neutrophil function by regulating calcium homeostasis via Calnexin and SERCA
- Ten years of injectable platelet‐rich fibrin
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- Homozygous K5Cre transgenic mice have wavy hair and accelerated malignant progression in a murine model of skin carcinogenesis
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Comparison of the Efficacy of Homologous and Autologous Platelet-Rich Plasma (PRP) for Treating Androgenic Alopecia
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes