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Research 181–210 of 1000+
- Expression patterns of TRα and CRABPII genes in Chinese cashmere goat skin during prenatal development
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Competitive balance of intrabulge BMP/Wnt signaling reveals a robust gene network ruling stem cell homeostasis and cyclic activation
- Elucidation of the Potential Hair Growth-Promoting Effect of Botryococcus terribilis, Its Novel Compound Methylated-Meijicoccene, and C32 Botryococcene on Cultured Hair Follicle Dermal Papilla Cells Using DNA Microarray Gene Expression Analysis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- The impact of AP collagen peptides (APCPs) on hair shaft elasticity and gloss: A comprehensive analysis
- Clinical Snippets
- Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Current Genetics in Hair Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Monilethrix
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Semidominant Inheritance in Epidermolytic Ichthyosis
- A newborn presenting with congenital blistering
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Revealing biological mechanisms of skin pigment recovery during treatment in vitiligo patients: A proteomic analysis
- Alopezien und Hypotrichosen im Kindesalter
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium