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Research 751–780 of 1000+
- Lysophospholipid Mediators in Health and Disease
- Spatiotemporal Expression, Distribution, and Processing of POMC and POMC-derived Peptides in Murine Skin
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Dynamic expression of Runx1 in skin affects hair structure
- Alleviation of Multidrug Resistance by Flavonoid and Non-Flavonoid Compounds in Breast, Lung, Colorectal and Prostate Cancer
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- 1α,25(OH)2-Dihydroxyvitamin D3/VDR protects the skin from UVB-induced tumor formation by interacting with the β-catenin pathway
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Ornithine decarboxylase is upregulated by the androgen receptor in skeletal muscle and regulates myoblast proliferation
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- The nude gene and the skin
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Genetic Basis of Alopecia Areata
- Against the Rules: Human Keratin K80
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Recently Identified Forms of Epidermolysis Bullosa
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Persistent hair growth during treatment with the EGFR inhibitor erlotinib
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings