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Research 391–420 of 1000+
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Biotin and biotinidase deficiency
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Gene therapy to enhance angiogenesis in chronic wounds
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Safety and Efficacy of Tofacitinib in 24 Cases of Pediatric Rheumatic Diseases: Single Centre Experience
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Genetic Hair Disorders: A Review
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- The Genetics of Human Skin Disease
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Palatogenesis and cutaneous repair: A two‐headed coin
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene