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Research 31–60 of 1000+
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Noncoding dsRNA induces retinoic acid synthesis to stimulate hair follicle regeneration via TLR3
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Generation of iPS-derived model cells for analyses of hair shaft differentiation
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- TTNPB Promotes Human Pluripotent Stem Cell‐to‐Neural Stem Cell Transition via Modulation of Chromatin Accessibility and the S‐(5′‐adenosyl)‐L‐homocysteine/Choline Metabolic Network
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Sterol Intermediates of Cholesterol Biosynthesis Inhibit Hair Growth and Trigger an Innate Immune Response in Cicatricial Alopecia
- Epidemiologic Study of Gene Distribution in Romanian and Brazilian Patients with Non-Cicatricial Alopecia
- Expression Profiles of Reproduction- and Thyroid Hormone-Related Transcripts in the Brains of Chemically-Induced Intersex Frogs
- The Retinoic-Acid-Related Orphan Receptor Alpha May Be Highly Involved in the Regulation of Seasonal Hair Molting
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- The Genetics of Human Skin Disease
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Different gene expression profile observed in dermal papilla cells related to androgenic alopecia by DNA macroarray analysis
- Low Humidity Alters Epidermal Gene Expression in vivo
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Effect of Topical Gel Administration of Secretome Hypoxia Mesenchymal Stem Cells (SH-MSCs) on IL-10 and TNF- α Gene Expression (In Vivo Experimental Study in Male Rats of Wistar Strains Model of Fluconazole-Induced Alopecia)
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia
- Differential expression of retinoic acid-synthesizing (RALDH) enzymes during fetal development and organ differentiation in the mouse
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- Regulation of Involucrin Gene Expression
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes