Search
for
Sort by
Research 871–900 of 884
- Baldness: Comprehensive aspects and its reassuring remedies
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- The Potential Utility of Tirzepatide for the Management of Polycystic Ovary Syndrome
- Effect of injectable calcium alginate-amelogenin hydrogel on macrophage polarization and promotion of jaw bone osteogenesis
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- How to treat acne in women with polycystic ovary syndrome (PCOS)? Review of the available literature
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Table_1_Bioinformatics and Network Pharmacology Identify the Therapeutic Role and Potential Mechanism of Melatonin in AD and Rosacea.xlsx
- A single arm, exploratory and pilot study to evaluate the efficacy of a multi-component water-based herbal supplement in hair growth, density, follicle strength and hair fall in healthy male and female subjects
- The Acne-treatment Potential of Cinnamomum Camphora Chvar. Borneol Essential Oil in Vitro and in Vivo
- Hair Follicle Stem Cells and Hair Regeneration
- Hair & Cutaneous Development
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- FOXN1 deficient nude severe combined immunodeficiency
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Foxn1 promotes keratinocyte differentiation by regulating the activity of protein kinase C
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice