Search
for
Sort by
Research 61–90 of 1000+
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Mechanical stretch induces hair regeneration through the alternative activation of macrophages
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Ottawa, Ontario, Canada, February 13–16, 2013
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Gut–ovary axis and multiomic insights into PCOS in a DHEA-induced rat model
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Weathering the Storm: Harnessing the Resolution of Inflammation to Limit COVID-19 Pathogenesis
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Transdifferentiation of corneal epithelium into epidermis occurs by means of a multistep process triggered by dermal developmental signals
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Modulation of Macrophage Function by Bioactive Wound Dressings with an Emphasis on Extracellular Matrix-Based Scaffolds and Nanofibrous Composites
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development