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Research 91–120 of 96
- Phytochemicals of Alpinia zerumbet: A Review
- Xinyang tablet ameliorates sepsis-induced myocardial dysfunction by regulating Beclin-1 to mediate macrophage autophagy and M2 polarization through LncSICRNT1 targeting E3 ubiquitin ligase TRAF6
- Recent Insights in Multi‐Target Drugs in Pharmacology and Medicinal Chemistry
- A bibliometric analysis of endoplasmic reticulum stress and atherosclerosis
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Drug Survival and Long-term Outcome of Tofacitinib in Patients with Alopecia Areata: A Retrospective Study
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Hair follicles modulate skin barrier function
- 371 Hair follicles are critical modulators of skin barrier function
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Jieduquyuziyin prescription alleviates SLE complicated by atherosclerosis via promoting cholesterol efflux and suppressing TLR9/MyD88 activation
- 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
- The Genetics of Human Skin Disease
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Genetics of Inherited Ichthyoses and Related Diseases
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- New clinico‐genetic classification of trichothiodystrophy
- Management of congenital ichthyoses: European guidelines of care, part two
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- The Rotterdam Study: 2016 objectives and design update