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Research 481–510 of 720
- Hair Keratin: Composition, Structure and Biogenesis
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Myotonic Dystrophy—A Progeroid Disease?
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- The nude gene and the skin
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Prostanoid receptors in anagen human hair follicles
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- SIRT 7 activates quiescent hair follicle stem cells to ensure hair growth in mice
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Human Follicular Papilla Cells Carry Out Nonadipose Tissue Production of Leptin
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Multipotent Nestin-Positive Stem Cells Reside in the Stroma of Human Eccrine and Apocrine Sweat Glands and Can Be Propagated Robustly In Vitro
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Disentangling the Coronavirus Disease 2019 Health Disparities in African Americans: Biological, Environmental, and Social Factors
- Potassium Channel Openers Increase Aortic Elastic Fiber Formation and Reverse the Genetically Determined Elastin Deficit in the BN Rat
- Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
- 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