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Research 751–780 of 1000+
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- <i>ZmSPL10</i>, <i>ZmSPL14</i> and <i>ZmSPL26</i> act together to promote stigmatic papilla formation in maize through regulating auxin signaling and <i>ZmWOX3A</i> expression
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and<i>UBTF</i>Genes
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Skin and hair: models for exploring organ regeneration
- LncRNA H19 Overexpression Activates Wnt Signaling to Maintain the Hair Follicle Regeneration Potential of Dermal Papilla Cells
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Epidermal patterning and induction of different hair types during mouse embryonic development
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Polycomb repressive complex 2 in adult hair follicle stem cells is dispensable for hair regeneration
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Human epidermal neural crest stem cells as candidates for cell-based therapies, disease modeling, and drug discovery
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Stem cells supporting other stem cells
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer