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Research 511–540 of 1000+
- Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin
- Potential Use of Human Periapical Cyst-Mesenchymal Stem Cells (hPCy-MSCs) as a Novel Stem Cell Source for Regenerative Medicine Applications
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Isolation of Mouse Hair Follicle Bulge Stem Cells and Their Functional Analysis in a Reconstitution Assay
- CD201+ fascia progenitors choreograph injury repair
- Molecular and spatial design of early skin development
- Adipose-Derived Stem/Stromal Cells
- Keratinocyte Stem Cells: Role in Aging
- Dermal Adnexal Neoplasms: Exploring Rare Variants and Their Clinical Behavior
- Single-Cell Transcriptomics to Map Cellular Heterogeneity in Tissue Regeneration Models
- Regulation of adipocyte dedifferentiation at the skin wound edge
- 1032 Characterization of the human scalp hair follicle microbiome reveals differential spatial distribution, abundance and viability of intrafollicular microbiota and modulation of hair growth and metabolism by staphylococcus epidermidis
- Equine adipose tissue derived stem cells and their multilineage differentiation
- Defining compartmentalized stem and progenitor populations with distinct cell division frequency in the ocular surface epithelium
- Single-cell sequencing reveals the intermediate cell state and function of dermal papilla cells in the hair follicle cycle of cashmere goats
- Decision letter: Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
- The post-terminal differentiation fate of RNAs revealed by next-generation sequencing
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Long-term renewal of hair follicles from clonogenic multipotent stem cells
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Abnormal neuronal differentiation and mitochondrial dysfunction in hair follicle-derived induced pluripotent stem cells of schizophrenia patients
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Hopx expression defines a subset of multipotent hair follicle stem cells and a progenitor population primed to give rise to K6+ niche cells
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Disease causing homozygous variants in the human hairless gene