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Research 211–240 of 1000+
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- Critical Factors in Sample Collection and Preparation for Clinical Metabolomics of Underexplored Biological Specimens
- Are STK11 polymorphisms a predictor of the response to metformin in polycystic ovarian syndrome?
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Activated Polyamine Catabolism Depletes Acetyl-CoA Pools and Suppresses Prostate Tumor Growth in TRAMP Mice
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Current evidence for the involvement of sex steroid receptors and sex hormones in benign prostatic hyperplasia
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Converging physiological roles of the anthrax toxin receptors
- Sorafenib-Associated Facial Acneiform Eruption
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Understanding Type 3 Innate Lymphoid Cells and Crosstalk with the Microbiota: A Skin Connection
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Atypical Protein Kinase C Isoform, aPKCλ, Is Essential for Maintaining Hair Follicle Stem Cell Quiescence