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Research 241–270 of 1000+
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- TMT-Based Quantitative Proteomic Analysis Reveals the Effect of Bone Marrow Derived Mesenchymal Stem Cell on Hair Follicle Regeneration
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Free Testosterone: Pumping up the Tires or Ending the Free Ride?
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- The role of WNT10B in physiology and disease: A 10-year update
- Genetic Hair Disorders: A Review
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits