Search
for
Sort by
Research 391–420 of 1000+
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- Cutaneous signs in COVID ‐19 patients: A review
- Dermal Adipocyte Lipolysis and Myofibroblast Conversion Are Required for Efficient Skin Repair
- Skin Adipocyte Stem Cell Self-Renewal Is Regulated by a PDGFA/AKT-Signaling Axis
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Central hair loss in African American women: Incidence and potential risk factors
- Androgen receptors and their biology
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Roles of tumor suppressors in regulating tumor-associated inflammation
- De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle
- Fluoroquinolone-induced serious, persistent, multisymptom adverse effects
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion
- Lichen planus and other cutaneous manifestations in chronic hepatitis C: pre- and post-interferon-based treatment prevalence vary in a cohort of patients from low hepatitis C virus endemic area
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- What does acne genetics teach us about disease pathogenesis?
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Congenital adrenal hyperplasia
- Apoptotic cells represent a dynamic stem cell niche governing proliferation and tissue regeneration
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- Congenital adrenal hyperplasia