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Research 811–840 of 1000+
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- GPRC6A-Duox1 Axis Regulates the Hair Cycle Through H2O2 Generation
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Knockout of the ING5 epigenetic regulator confirms roles in stem cell maintenance and tumor suppression in vivo
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics
- Spatiotemporal Expression Characterization of KRTAP6 Family Genes and Its Effect on Wool Traits
- Dicer- and Bulge Stem Cell-Dependent MicroRNAs During Induced Anagen Hair Follicle Development
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Local circadian clock gates cell cycle progression of transient amplifying cells during regenerative hair cycling
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- The molecular basis of human keratin disorders
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Tcf3 promotes cell migration and wound repair through regulation of lipocalin 2
- Regulation of stem cell function by protein ubiquitylation
- Clock genes, hair growth and aging