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Research 781–810 of 1000+
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Regulatory T cells in dominant immunologic tolerance
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- The Genetic Architecture of Alopecia Areata
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Non-viral delivery of the CRISPR/Cas system: DNA<i>versus</i>RNA<i>versus</i>RNP
- Developmental genetics of color pattern establishment in cats
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Advances in clinical applications of microneedle
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Dynamic Transcriptome Profile Analysis of Mechanisms Related to Melanin Deposition in Chicken Muscle Development
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders