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Research 91–120 of 95
- Diseases of the Canine Prostate Gland
- Cyclin‐dependent kinase 4 expression alters the number of keratinocyte stem cells in the mouse hair follicle
- Mendelian randomization analysis of the causal relationship between low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and androgenic alopecia
- Transcriptomic Analysis of Skin Tissue Reveals Molecular Mechanisms of Thermal Adaptation in Cold-Exposed Lambs
- Safety First: A Comprehensive Review of Nutritional Supplements for Hair Loss in Breast Cancer Patients
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Hair follicles modulate skin barrier function
- Genome scan for signatures of adaptive evolution in wild African goat (capra nubiana)
- The pattern recognition receptor toll-like receptor 3 regulates skin barrier homeostasis
- 371 Hair follicles are critical modulators of skin barrier function
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Jieduquyuziyin prescription alleviates SLE complicated by atherosclerosis via promoting cholesterol efflux and suppressing TLR9/MyD88 activation
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Microarray analysis reveals distinct RNA expression profiles in endothelial progenitor cells exposed to pro-inflammatory environment or oxidized LDL
- Vitamin D metabolism and function in the skin
- Extraskeletal actions of vitamin D
- Management of congenital ichthyoses: European guidelines of care, part two
- The Genetics of Human Skin Disease
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ
- ИСПОЛЬЗОВАНИЕ ПОЛИНУКЛЕОТИДОВ В АНТИВОЗРАСТНОЙ ИНЪЕКЦИОННОЙ КОСМЕТОЛОГИИ С ПОЗИЦИИ ДОКАЗАТЕЛЬНОЙ МЕДИЦИНЫ
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Immunological control of skin development: from homeostasis to developmental pathologies
- LATE-ONSET NEVUS COMEDONICUS IN AN ADULT PATIENT WITH DIABETES MELLITUS