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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02610] Proteases and signal transduction (Hirano et

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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02610] Proteases and signal transduction (Hirano etdisease: Defects in F8 are the cause of hemophilia A (HEMA)

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Description

and signal transduction (Hirano et al

MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease| Pick's disease| frontotemporal dementia| cortico-basal degeneration and progressive supranuclear palsy

One pseudogene is known to exist

This gene is expressed in the inner ear of vertebrates with the highest level of expression seen at the embryonic stage and lowest in adult

The encoded type II transmembrane protein is a downstream target of CCAAT/enhancer binding protein (C/EBP)| beta (CEBPB) and may play a role in inflammation

FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02610] Proteases and signal transduction (Hirano etdisease: Defects in F8 are the cause of hemophilia A (HEMA)

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