Search
for
Sort by
Research 331–360 of 1000+
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Are there temporal subtypes of premenstrual dysphoric disorder?: using group-based trajectory modeling to identify individual differences in symptom change
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Epidermal Notch1 recruits RORγ+ group 3 innate lymphoid cells to orchestrate normal skin repair
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Hydrogen peroxide and monoethanolamine are the key causative ingredients for hair dye-induced dermatitis and hair loss
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- SOX2 in the Skin
- Chitosan stimulates root hair callose deposition and inhibits root hair growth
- Male pattern baldness: current treatments, future prospects
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- HSP90 Inhibition and Cellular Stress Elicits Phenotypic Plasticity in Hematopoietic Differentiation