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Research 61–90 of 1000+
- Clinically relevant aberrant Filip1l DNA methylation detected in a murine model of cutaneous squamous cell carcinoma
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- eLife assessment: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Single-Cell RNA Sequencing Reveals Cellular and Transcriptional Changes Associated With M1 Macrophage Polarization in Hidradenitis Suppurativa
- Class IIa HDAC4 and HDAC7 cooperatively regulate gene transcription in Th17 cell differentiation
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Molecular stratification of the human fetal vaginal epithelium by spatial transcriptome analysis
- Single-cell transcriptomics reveals hair growth retardation mediated by aberrant connective tissue sheath contraction in male androgenetic alopecia
- Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- In Ovo Injection of CHIR-99021 Promotes Feather Follicle Development via Modulating the Wnt Signaling Pathway and Transcriptome in Goose Embryos (Anser cygnoides)
- 766 H3K9me3 methyltransferase SETDB1 controls retrotransposon silencing, DNA methylation, constitutive heterochromatin maintenance and 3D-chromatin structure in epidermal keratinocytes
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- 1431 Skin aging and hair follicle stem cell dysfunction caused by T cells with defective mitochondrial metabolism
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Keratin 17 in disease pathogenesis: from cancer to dermatoses
- Cellular plasticity in reprogramming, rejuvenation and tumorigenesis: a pioneer TF perspective
- Genetically separable determinants of hair keratin gene expression
- Isotretinoin treatment upregulates the expression of p53 in the skin and sebaceous glands of patients with acne vulgaris
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- DNA Methylation Mediates lncRNA2919 Regulation of Hair Follicle Regeneration
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- A transcriptomic map of murine and human alopecia areata
- MitoQ enhances CYP19A1 expression to stimulate WNT/β-catenin signaling pathway for promoting hair growth in androgenetic alopecia