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Research 661–690 of 1000+
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- FOXN1 deficient nude severe combined immunodeficiency
- Sex‐dependent responsiveness of hippocampal neurons to sex neurosteroids: A role of Arc/Arg3.1
- Structural basis for the catalysis and inhibition of human steroid 5α‐reductase 2
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- Wnt activator CHIR99021-stimulated human dermal papilla spheroids contribute to hair follicle formation and production of reconstituted follicle-enriched human skin
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- 14-3-3σ Is Required for Club Hair Retention
- Motoneuron-Specific PTEN Deletion in Mice Induces Neuronal Hypertrophy and Also Regeneration after Facial Nerve Injury
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Review of Women with Vision: The Presentation Sisters of South Dakota, 1880-1985
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Upregulation of the truncated basic hair keratin 1(hHb1‐ΔN) in carcinoma cells by Epstein‐Barr virus (EBV)
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Glycome profiling by lectin microarray reveals dynamic glycan alterations during epidermal stem cell aging
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- The transcription elongation factors Spt4 and Spt6 promote dermal adipocyte differentiation
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Role of alkaline ceramidase 1 (Acer1) in regulating epidermal homeostasis and tumorigenesis
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Downregulation of mRNAs Encoding Keratin-Associated Proteins in the Tongue of Mice Fed a High-Fat Diet
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Circadian clocks: from stem cells to tissue homeostasis and regeneration