Search
for
Sort by
Research 541–570 of 1000+
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Visualising Androgen Receptor Activity in Male and Female Mice
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- In vivo monitoring of hair cycle stages via bioluminescence imaging of hair follicle NG2 cells
- Re-investigating the Basement Membrane Zone of Psoriatic Epidermal Lesions: Is Laminin-511 a New Player in Psoriasis Pathogenesis?
- Skin microbiota and diabetic foot ulcers
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Multifunctional Bioactivity of Saccharomyces cerevisiae Extracellular Vesicle in Hair Follicle-Related Cellular Models
- Molecular pathology of skin adnexal tumours
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- <i>Sept4/</i> ARTS Regulates Stem Cell Apoptosis and Skin Regeneration
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- <i>Pten</i> loss in Lgr5<sup>+</sup> hair follicle stem cells promotes SCC development
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- MICROBIOMA DO COURO CABELUDO E SUA INFLUÊNCIA NAS ALOPECIAS: EVIDÊNCIAS ATUAIS E PERSPECTIVAS TERAPÊUTICAS
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population