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Research 451–480 of 1000+
- The role of WNT10B in physiology and disease: A 10-year update
- Pathology of Mouse Models of Accelerated Aging
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Trichothiodystrophy
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Cellular heterogeneity and microenvironmental control of skin cancer
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Regulation of stem cell function by protein ubiquitylation
- Toll-like receptor-targeted anti-tumor therapies: Advances and challenges
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Do Changes in Chromosomes Cause Aging?
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits