Search
for
Sort by
Research 901–930 of 1000+
- Molecular Mechanisms Regulating Hair Follicle Development
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Reversible Activation of c-Myc in Skin
- Transgenic mice provide new insights into the role of TGF-alpha during epidermal development and differentiation.
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Tissue engineering of skin and regenerative medicine for wound care
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- Matriptase: Potent Proteolysis on the Cell Surface
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Post-COVID-19 Syndrome: The Persistent Symptoms at the Post-viral Stage of the Disease. A Systematic Review of the Current Data
- Inactivation of the Vitamin D Receptor Enhances Susceptibility of Murine Skin to UV-Induced Tumorigenesis
- WNT Signaling in Disease
- Pathophysiological mechanisms implicated in postpartum depression
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The Role of Vitamins and Minerals in Hair Loss: A Review
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Cell death in the skin
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- Small extracellular vesicles from menstrual blood-derived mesenchymal stem cells (MenSCs) as a novel therapeutic impetus in regenerative medicine
- More than 50 Long-term effects of COVID-19: a systematic review and meta-analysis
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- FGF Family: From Drug Development to Clinical Application