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Research 421–450 of 1000+
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Quantitative Analysis of Hair Luster in a Novel Ultraviolet-Irradiated Mouse Model
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Keratin 75 Is a Component of the LINC Complex and Has an Essential Role in Mediating the SOX2 Rapid Healing Response during Wound Repair
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Downregulation of mRNAs Encoding Keratin-Associated Proteins in the Tongue of Mice Fed a High-Fat Diet
- Keratin Gel as Conduit Filler for Peripheral Nerve Regeneration on a Rat Sciatic Nerve Injury Model
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Clinical Snippets
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- An Updated Nomenclature for Keratin-Associated Proteins (KAPs)
- Differential expression of type I IRS keratin genes in three breeds of sheep
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Regulatory pathway analysis of coat color genes in Mongolian horses
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Genetically Induced Cell Death in Bulge Stem Cells Reveals Their Redundancy for Hair and Epidermal Regeneration
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Characters of KRT80 and its roles in neoplasms diseases
- Bioinformatics analysis of genes associated with the patchy-type alopecia areata: CD2 may be a new therapeutic target
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia