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Research 301–330 of 1000+
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Hyperinnervation inhibits organ-level regeneration in mammalian skin
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Prolactin delays hair regrowth in mice
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- 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
- 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
- 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
- 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
- Plasma Zinc Levels in Males with Androgenetic Alopecia as Possible Predictors of the Subsequent Conservative Therapy’s Effectiveness
- 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
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations