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Research 31–60 of 82
- The antiandrogen enzalutamide downregulates TMPRSS2 and reduces cellular entry of SARS-CoV-2 in human lung cells
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Melatonin promotes Cashmere goat (<i>Capra hircus</i>) secondary hair follicle growth: a view from integrated analysis of long non-coding and coding RNAs
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Defining the identity of mouse embryonic dermal fibroblasts
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- TMPRSS2: A Key Host Factor in SARS-CoV-2 Infection and Potential Therapeutic Target
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Evolutionary Divergence of Fibroblast Growth Factors Across Species: Insight into Functional Diversification
- Priorities for efficacy trials of gender-affirming hormone therapy with estrogen: collaborative design and results of a community survey
- Nanoemulsion Vehicles as Carriers for Follicular Delivery of Luteolin
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- 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
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- The molecular pathogenesis of Trichilemmal carcinoma
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Janus kinase inhibition in Down syndrome: 2 cases of therapeutic benefit for alopecia areata
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle