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Research 301–330 of 1000+
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells
- Analysis of lncRNAs Expression Profiles in Hair Follicle of Hu Sheep Lambskin
- Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- Role of vitamin D and calcium signaling in epidermal wound healing
- The intragenic mRNA-microRNA regulatory network during telogen-anagen hair follicle transition in the cashmere goat
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Controlled Release of the α-Tocopherol-Derived Metabolite α-13′-Carboxychromanol from Bacterial Nanocellulose Wound Cover Improves Wound Healing
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Biotinidase deficiency characterized by skin and hair findings
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Alopecia: Association with Resistance to Thyroid Hormones
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Disease causing homozygous variants in the human hairless gene
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- The seasonal development dynamics of the yak hair cycle transcriptome
- Significance of iron status in hair loss in women
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Le gène<i>hairless</i>de la souris
- Epigenetic orchestration of RNA m<sup>6</sup>A methylation in wound healing and post-wound events
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population