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Research 331–360 of 1000+
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Human and animal cells under influence of different lighting and stimulus
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Pathway enrichment and network analysis of differentially expressed genes in pashmina goat
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Tfap2b specifies an embryonic melanocyte stem cell that retains adult multi-fate potential
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- FGF5 is a crucial regulator of hair length in humans
- Transcriptome Sequencing Reveals Differences between Primary and Secondary Hair Follicle-derived Dermal Papilla Cells of the Cashmere Goat (Capra hircus)
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Transcriptomic analyses of regenerating adult feathers in chicken
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber