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Research 61–90 of 1000+
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Inhibition of T-cell activity in alopecia areata: recent developments and new directions
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Abstracts
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Essential Oil and Important Activities of<i>Thuja orientalis</i>and<i>Thuja occidentalis</i>
- Functional characterization of soybean strigolactone biosynthesis and signaling genes in Arabidopsis MAX mutants and GmMAX3 in soybean nodulation
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- 332 OTULIN maintains skin homeostasis by controlling keratinocyte death and stem cell identity
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- The Association of Gene Expression and Single Nucleotide Polymorphism (rs 6152 SNP) in Androgen Receptor Gene with Recurrent Spontaneous Abortion (RSA) in Iraqi Women
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Hair follicle immune privilege and its collapse in alopecia areata