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Research 31–60 of 1000+
- Abstract 5020: Characterization of epidermal stem cells in SKH1 hairless mice, a widely used mouse model to investigate ultraviolet radiation carcinogenesis.
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- rPanglaoDB: an R package to download and merge labeled single-cell RNA-seq data from the PanglaoDB database
- Author response: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Pathophysiology of the Behçet's Disease
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Biochemical and trichological characterization of diffuse alopecia in women
- Learning from nudity: lessons from the nude phenotype
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Deep phenotyping of skin tissue remodeling in patients with systemic sclerosis treated with CD19-CAR T cells
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Generation and characterization of rat liver stem cell lines and their engraftment in a rat model of liver failure
- Exogen hair characterization in human scalp
- Characterisation of cell cycle arrest and terminal differentiation in a maximally proliferative human epithelial tissue: Lessons from the human hair follicle matrix
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Enrichment and Characterization of Human Dermal Stem/Progenitor Cells by Intracellular Granularity
- Isolation and Characterization of Cutaneous Epithelial Stem Cells
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Observation of phenotypic variation among Indian women with polycystic ovary syndrome (PCOS) from Delhi and Srinagar
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Evaluation of the phenotypic, proliferative and secretory profile of mesenchymal stem cells from adipose tissue captured by laser-assisted liposuction