Search
for
Sort by
Research 391–420 of 831
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- PCSK9: From Nature’s Loss to Patient’s Gain
- Genetics
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Multi-omics analyses, cell experiments, and network pharmacology tools identified key proteins and candidate drugs for alopecia areata treatment
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The molecular basis of human keratin disorders
- Trichoscopy in genetic hair shaft abnormalities
- p63: a crucial player in epithelial stemness regulation
- Clinical biochemistry of dihydrotestosterone
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- New developments in the molecular treatment of ichthyosis: review of the literature
- Platelet-Rich Plasma and Acellular Dermal Matrix in the Surgical Treatment of Hidradenitis Suppurativa: A Comparative Retrospective Study
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep