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Research 361–390 of 450
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Making the head: Caspases in life and death
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Mechanisms of autophagy and their implications in dermatological disorders
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Store-operated calcium channels in skin
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- The beneficial effects of chick embryo extract preconditioning on hair follicle stem cells: A promising strategy to generate Schwann cells
- Increased Expression of Zyxin and Its Potential Function in Androgenetic Alopecia
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- The Role of Natural Hydrogels in Enhancing Wound Healing: From Biomaterials to Bioactive Therapies
- Inhibition of T-cell activity in alopecia areata: recent developments and new directions
- Exosomes based advancements for application in medical aesthetics
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Scoparone Induces Expression of Pluripotency Transcription Factors SOX2 and NANOG in Dermal Papilla Cells
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- The post-finasteride syndrome: possible etiological mechanisms and symptoms
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Parental Uveitis Influences Offspring With an Increased Susceptibility to the Experimental Autoimmune Uveitis
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Multi-omics and AI-driven advances in miRNA-mediated hair follicle regulation in cashmere goats
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)