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Research 421–450 of 1000+
- Proteomics Reveals the Role of PLIN2 in Regulating the Secondary Hair Follicle Cycle in Cashmere Goats
- Keratin disorders: from gene to therapy
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Beyond Expectations
- LncRNA-PCAT1 maintains characteristics of dermal papilla cells and promotes hair follicle regeneration by regulating miR-329/Wnt10b axis
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Screening of microRNA and mRNA related to secondary hair follicle morphogenesis and development and functional analysis in cashmere goats
- LncRNA H19 Overexpression Activates Wnt Signaling to Maintain the Hair Follicle Regeneration Potential of Dermal Papilla Cells
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Low Humidity Alters Epidermal Gene Expression in vivo
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Androgen receptors and their biology
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- The ITGB6 gene: its role in experimental and clinical biology
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Disease causing homozygous variants in the human hairless gene
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- ATP-dependent chromatin remodeling during mammalian development
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Genetic Fate Mapping Using Site-Specific Recombinases
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis