Search
for
Sort by
Research 91–120 of 1000+
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- MicroRNA in skin diseases
- Disease causing homozygous variants in the human hairless gene
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Congenital Atrichia: A Case Report
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Mouse notch: expression in hair follicles correlates with cell fate determination.
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Sex-limited chromosomes and non-reproductive traits
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Dermal lymphatic dilation in a mouse model of alopecia areata
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Characterization of a new, inducible transgenic mouse model with GFP expression in melanocytes and their precursors
- Nutritional roles of selenium in cellular and mouse aging
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Pathology of Mouse Models of Accelerated Aging
- Matrix Metalloproteinase-19 Expression in Normal and Diseased Skin: Dysregulation by Epidermal Proliferation