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Research 331–360 of 1000+
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Transcriptomic inspection revealed a possible pathway regulating the formation of the high-quality brush hair in Chinese Haimen goat ( <i>Capra hircus</i> )
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Biology of Human Hair: Know Your Hair to Control It
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Woolly Antics between the Sheaths
- Polycystic ovary syndrome
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Discovery of differentially expressed genes in cashmere goat (Capra hircus) hair follicles by RNA sequencing
- Ectodermal Dysplasia: Variable Expressions
- Keratin disorders: from gene to therapy
- Analysis of LncRNA-mRNA Co-Expression Profiles in Patients With Polycystic Ovary Syndrome: A Pilot Study
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Chronic overlapping pain conditions and nociplastic pain
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza