glial fibrillary acidic protein , GFAP (Abkürzung)

Their components include glial fibrillary acidic protein.

The cause of Alexander disease is a mutation in the gene encoding glial fibrillary acidic protein.

These cell types can develop into a normal oligodendrocyte or a glial fibrillary acidic protein positive astrocyte depending on environmental factors.

GFAP (glial fibrillary acidic protein) is found in astrocytes and other glia.

The sustentacular cells are S-100 positive and focally positive for Glial fibrillary acidic protein.

Glial fibrillary acidic protein has been shown to interact with MEN1 and PSEN1.

The primitive neuroectodermal cells variably express neurofilament protein, glial fibrillary acidic protein, keratin, or desmin.

It is caused by mutations in the gene for glial fibrillary acidic protein (GFAP) that maps to chromosome 17q21.

After injury, astrocytes undergo morphological changes, extend their processes, and increase synthesis of glial fibrillary acidic protein (GFAP).

Substrate histology was visualized using phase-contrast optics or by immunohistochemically labelling glial fibrillary acidic protein (GFAP).

Astrocytes are classically identified using histological analysis; many of these cells express the intermediate filament glial fibrillary acidic protein (GFAP).

Lack of glial differentiation, as demonstrated by negative staining for glial fibrillary acidic protein (GFAP), may confer a favourable prognosis.

Glial fibrillary acidic protein (GFAP) was named and first isolated and characterized by Lawrence F. Eng in 1969.

Class III contains the proteins vimentin, desmin, peripherin and glial fibrillary acidic protein (GFAP).

The glial tissue is highlighted with S100 protein and with glial fibrillary acidic protein, although the latter is much more sensitive for glial tissue.

After 10 days of exposure, astroglial cells can be detected using glial fibrillary acidic protein (GFAP), which is a specific marker of glial cells.

NFI-X3, a splice variant of NFIX, regulates Glial fibrillary acidic protein and YKL-40 in astrocytes.

The cells were not immunoreactive for neurofilament, neuron-specific enolase (NSE), and glial fibrillary acidic protein (GFAP).

In histology, the GFAP stain is done to determine whether cells contain glial fibrillary acidic protein, a protein found in glial cells.

During neuro- and gliogenesis, nestin is replaced by cell type-specific intermediate filaments, e.g. neurofilaments and glial fibrillary acidic protein (GFAP).

Glial fibrillary acidic protein (GFAP) is a protein that is encoded by the GFAP gene in humans .

However, the tumor cells are almost always negative with glial fibrillary acidic protein, S100 protein, cytokeratin, epithelial membrane antigen, CD68, FLI1, CD99 and CD56.

GFAP immunohistochemistry Glial Fibrillary Acidic Protein (GFAP) was labelled in the same spinal cord sections on which neurons had been cultured.

They have been determined to be astrocytes based on the typical expression of GFAP (glial fibrillary acidic protein) and more specifically as protoplasmic astrocytes based on their morphology.

Glial fibrillary acidic protein is an intermediate filament (IF) protein that is expressed by numerous cell types of the central nervous system (CNS) including astrocytes, and ependymal cells.