- hyperphosphorylated
-
phosphorylated to a more than normal extent, or fully saturated with phosphate groups
Wikipedia foundation.
Wikipedia foundation.
Neurofibrillary tangle — Microscopy image of a neurofibrillary tangle, conformed by hyperphosphorylated tau protein Neurofibrillary Tangles (NFTs) are aggregates of hyperphosphorylated tau protein that are most commonly known as a primary marker of Alzheimer s Disease.… … Wikipedia
Alzheimer's disease — Alzheimer redirects here. For other uses, see Alzheimer (disambiguation). Alzheimer s disease Classification and external resources … Wikipedia
Hyperphosphorylation — occurs when a biochemical with multiple phosphorylation sites is fully saturated. Hyperphosphorylation is one of the signalling mechanisms used by the cell to regulate mitosis. When these mechanisms fail, developmental problems or cancer are a… … Wikipedia
Biochemistry of Alzheimer's disease — The biochemistry of Alzheimer s disease (AD), one of the most common causes of adult dementia, is as yet not well understood at the molecular level. It has been identified as a protein misfolding disease due to the accumulation of abnormally… … Wikipedia
Transcription elongation regulator 1 — Transcription elongation regulator 1, also known as TCERG1, is a human gene.cite web | title = Entrez Gene: TCERG1 transcription elongation regulator 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=10915| … Wikipedia
Cell cycle — For the separation of chromosomes that occurs as part of the cell cycle, see mitosis. For the Academic journal, see Cell Cycle. Each turn of the cell cycle divides the chromosomes in a cell nucleus. The cell cycle, or cell division cycle, is the… … Wikipedia
Tau protein — Tau proteins are microtubule associated proteins that are abundant in neurons in the central nervous system and are less common elsewhere. They were discovered in 1975 in Marc Kirschner s laboratory at Princeton University… … Wikipedia
Pick's disease — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 10034 ICD10 = ICD10|G|31|0|g|30, ICD10|F|02|0|f|00 ICD9 = ICD9|331.11 ICDO = OMIM = 172700 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 311 MeshID = D020774 Pick’s disease, also known … Wikipedia
RNA polymerase II — (also called RNAP II and Pol II) is an enzyme found in eukaryotic cells. It catalyzes the transcription of DNA to synthesize precursors of mRNA and most snRNA and microRNA. [cite journal | author = Kronberg, R.D. | title = Eukaryotic… … Wikipedia
Hereditary inclusion body myopathy — Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary… … Wikipedia