Annexin A2 and S100A10 regulate human papillomavirus type 16 entry and intracellular trafficking
in human keratinocytes.
Induction of GITRL expression
in human keratinocytes by Th2 cytokines and TNF - α: implications for atopic dermatitis.
AV119, a Natural Sugar from Avocado gratissima, Modulates the LPS - Induced Proinflammatory Response
in Human Keratinocytes.
Not exact matches
A comparison of epidermal equivalents generated from iPSC, hESC and primary
human keratinocytes (skin cells) from skin biopsies showed no significant difference
in their structural or functional properties compared with the outermost layer of normal
human skin.
«We culture typical skin cell of the epidermis, such as
human keratinocytes,
in our dishes to form an artificial epidermis with all of its natural layers,» explained Sibylle Thude, the biologist who led the investigation into the accreditation.
Wei Long Ng explained: «The two - step bioprinting strategy involves the fabrication of hierarchical porous collagen - based structures (that closely resembles the skin's dermal region), and deposition of epidermal cells such as
keratinocytes and melanocytes at pre-defined positions on top of the biomimetic dermal skin constructs, to create 3D
in - vitro pigmented
human skin constructs.
In humans, iRhoms have been implicated in EGFR - mediated keratinocyte proliferation and cancer growth, but the molecular mechanisms underlying these biological functions have not been well defined.&raqu
In humans, iRhoms have been implicated
in EGFR - mediated keratinocyte proliferation and cancer growth, but the molecular mechanisms underlying these biological functions have not been well defined.&raqu
in EGFR - mediated
keratinocyte proliferation and cancer growth, but the molecular mechanisms underlying these biological functions have not been well defined.»
Papillomaviruses are a diverse group of DNA - based viruses that infect the skin and mucous membranes of
humans and a variety of animals (replicating exclusively
in keratinocytes).
In human skin, keratinocytes, the cells found in the outer layer of our skin known as the epidermis, soak up our naturally occurring melanosome
In human skin,
keratinocytes, the cells found
in the outer layer of our skin known as the epidermis, soak up our naturally occurring melanosome
in the outer layer of our skin known as the epidermis, soak up our naturally occurring melanosomes.
Gianneschi and his team found that the synthetic melanin nanoparticles
in their experiments were not only absorbed and distributed normally by the
keratinocytes in the epidermis, but they also protected
human skin cells from UV radiation damage.
For the expansion and differentiation of
human keratinocyte stem cells for permanent skin restoration
in victims of extensive burns.
Ng explains, «The two - step bioprinting strategy involves the fabrication of hierarchical porous collagen - based structures (that closely resembles the skin's dermal region), and deposition of epidermal cells such as
keratinocytes and melanocytes at pre-defined positions on top of the biomimetic dermal skin constructs, to create 3D
in - vitro pigmented
human skin constructs.
Functional and phenotypic characterization of
human keratinocytes expanded
in microcarrier culture.
In fact, they repeatedly generated iPS cells from the tiny number of
keratinocytes attached to a single hair plucked from a
human scalp.
The researchers then successfully prodded what they call
keratinocyte - derived iPS cells or KiPS cells to distinguish them from fibroblast - derived iPS cells into becoming all the cell types
in the
human body, including heart muscle cells and dopamine - producing neurons, which are affected by Parkinson's disease.
For the first set of experiments, first author Trond Aasen, Ph.D., a postdoctoral researcher at the Center of Regenerative Medicine
in Barcelona, used viral vectors to slip the genes for the master regulators Oct4, Sox2, as well as Klf4 and c - Myc into
keratinocytes cultured from
human skin explants.
In a study published in Molecular & Cellular Proteomics, researchers at the University of Freiburg led by Jorn Dengjel performed a global transcriptome and proteome profiling comparing primary DEB keratinocytes to normal human keratinocyte
In a study published
in Molecular & Cellular Proteomics, researchers at the University of Freiburg led by Jorn Dengjel performed a global transcriptome and proteome profiling comparing primary DEB keratinocytes to normal human keratinocyte
in Molecular & Cellular Proteomics, researchers at the University of Freiburg led by Jorn Dengjel performed a global transcriptome and proteome profiling comparing primary DEB
keratinocytes to normal
human keratinocytes.
The research, described
in the journal Stem Cells under the title «Reprogramming Postnatal
Human Epidermal
Keratinocytes Toward Functional Neural Crest Fates,» was supported by grants from the National Institutes of Health.
Pioneering work by Barrandon and Green more than 20 years ago (2) showed that when primary
human keratinocytes were put
in culture, their abilities to establish a clone were related to the heterogeneity
in cell size — only cells ≤ 11 μm
in diameter could form a clone whereas cells ≥ 12 μm were irreversibly committed to terminal differentiation.
Parsa R, Yang A, McKeon F, Green H. Association of p63 with proliferative potential
in normal and neoplastic
human keratinocytes.