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Research 31–60 of 1000+
- Human Hair Keratin‐Associated Proteins (KAPs)
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- Types I and II Keratin Intermediate Filaments
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Expression of keratin K14 in the epidermis and hair follicle: insights into complex programs of differentiation.
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Keratin gene mutations in disorders of human skin and its appendages
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Delayed Wound Healing in Keratin 6a Knockout Mice
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Keratin expression in basal cell carcinomas
- Chapter 2 The Human Keratin Genes and Their Differential Expression
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- Keratin expression in the normal nail unit: markers of regional differentiation
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Keratin disorders: from gene to therapy
- The effect of human hair keratin hydrogel on early cellular response to sciatic nerve injury in a rat model
- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Keratin hydrogels support the sustained release of bioactive ciprofloxacin
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Regulation of Keratin Gene Expression in Hair Follicle Differentiation<sup>a</sup>
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture