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Research 961–990 of 1000+
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Coming of Age of Melanogenesis-Related Proteins
- An Autophagy-Related Kinase Is Essential for the Symbiotic Relationship between <i>Phaseolus vulgaris</i> and Both Rhizobia and Arbuscular Mycorrhizal Fungi
- Ichthyosis with confetti: clinics, molecular genetics and management
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Granzyme B in Autoimmune Skin Disease
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Miz1 is required for hair follicle structure and hair morphogenesis
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- Oncogenic senescence: a multi-functional perspective
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Developing stratified epithelia: lessons from the epidermis and thymus
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- A role for the Tgf-β/Bmp co-receptor Endoglin in the molecular oscillator that regulates the hair follicle cycle
- Expression and function of nuclear receptor co-activator 4: evidence of a potential role independent of co-activator activity
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The impact of VDR expression and regulation in vivo
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)