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Research 511–540 of 765
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Genetic hair and nail disorders
- The extraction and characterization of human nail keratin
- Granzyme B in Autoimmune Skin Disease
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Disentangling the Coronavirus Disease 2019 Health Disparities in African Americans: Biological, Environmental, and Social Factors
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Expression and function of nuclear receptor co-activator 4: evidence of a potential role independent of co-activator activity
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Genetic and molecular aspects of androgenetic alopecia
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- The Genetic Architecture of Alopecia Areata
- Advances in single-cell transcriptomics in animal research
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Endocrinology of the Aging Prostate: Current Concepts
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Altered FGF expression profile in human scalp-derived fibroblasts upon WNT activation: implication of their role to provide folliculogenetic microenvironment
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat