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Research 811–840 of 1000+
- 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
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Ornithine decarboxylase is upregulated by the androgen receptor in skeletal muscle and regulates myoblast proliferation
- Genetic Basis of Alopecia Areata
- Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands
- Against the Rules: Human Keratin K80
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Inflammatory and Anti-Inflammatory Parameters in PCOS Patients Depending on Body Mass Index: A Case-Control Study
- Comparison of CD146 +/− mesenchymal stem cells in improving premature ovarian failure
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- EGFR Inhibitors and Cutaneous Complications: A Practical Approach to Management
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Current evidence for the involvement of sex steroid receptors and sex hormones in benign prostatic hyperplasia
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Activation of TRPV4 Induces Exocytosis and Ferroptosis in Human Melanoma Cells
- Genetic and molecular aspects of androgenetic alopecia
- Transcriptome-based selection and validation of optimal house-keeping genes for skin research in goats (Capra hircus)