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Research 601–630 of 1000+
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Protein Microarrays
- Exploring Acne Treatments: From Pathophysiological Mechanisms to Emerging Therapies
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Frontiers in alopecia areata pathobiology research
- Regulation of stem cell function by protein ubiquitylation
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Functional characterization of soybean strigolactone biosynthesis and signaling genes in Arabidopsis MAX mutants and GmMAX3 in soybean nodulation
- Myotonic Dystrophy—A Progeroid Disease?
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Ichthyosis with confetti: clinics, molecular genetics and management
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Changing Incidence Trends of Cutaneous B-Cell Lymphoma