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Research 451–480 of 1000+
- Atypical Pediatric Presentation of Pilomatricoma
- Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Androgen receptor gene polymorphism and biological age markers in men
- EDA Fibronectin Microarchitecture and YAP Translocation During Wound Closure
- ARHGEF3 Regulates Hair Follicle Morphogenesis
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- WNT10B (wingless-type MMTV integration site family)
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- How to diagnose a lipodystrophy syndrome
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Skin manifestations among<i>GATA2</i>-deficient patients
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Pro-Insulin-Like Growth Factor-II Ameliorates Age-Related Inefficient Regenerative Response by Orchestrating Self-Reinforcement Mechanism of Muscle Regeneration
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Stem Cells and their Niches
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Registrars’ Symposium: Summaries of Papers
- National scientific medical meeting 1996 abstracts
- Molecular genetics of androgen insensitivity
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs