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Research 931–960 of 1000+
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Non-viral delivery of the CRISPR/Cas system: DNA<i>versus</i>RNA<i>versus</i>RNP
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Identification of microRNAs involved in growth arrest and cell death in hydrogen peroxide-treated human dermal papilla cells
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Expression profile analysis of microRNAs during hair follicle development in the sheep foetus
- Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Differential distribution and genetic determination of eccrine sweat glands and hair follicles in the volar skin of C57BL/6 mice and SD rats
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Role of regeneration in tissue repairing and therapies
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Global Trends in Research of Androgen Receptor Associated With Breast Cancer From 2011 to 2020: A Scientometric Analysis
- Single-cell analysis of temporal immune cell dynamics in alopecia areata reveals a causal role for clonally expanded CD8+ T cells in disease
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction