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CTE, a progressive neurodegenerative disease caused by repetitive trauma to the brain, is characterized by the build-up of a toxic protein called tau in the form of neurofibrillary tangles (NFTs) and neuropil threads (NTs) throughout the brain.
The brain is characterized by an enormous degree of complexity and diversity of neural networks, making it one of the most complicated organs.
Indeed, the teleost fish brain is characterized by an important aromatase activity due to the expression of a brain-specific aromatase-B gene (aro-B) [59].
Further, the teleost brain is characterized by remarkable sexual plasticity [ 110].
The mammalian brain is characterized by distinct classes of cells that differ in morphology, structure, signaling, and function.
The early postnatal period (from P1 to P10) in the rat brain is characterized by dramatic changes contributing to synaptic formation, growth, regression and stabilization of connections [41].
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Many regions of the mammalian brain are characterized by iterated ensembles of nerve cells which can be distinguished anatomically and physiologically.
Dopamine neurons in the substantia nigra region of PD brain are characterized by intracellular amyloid deposits of α-synuclein known as Lewy bodies [19].
The developmental lesions in the brain were characterized by the apparent absence of well defined mesencephalic vesicles and lateral ventricles, resulting in a wide range of defects in the formation of the telencephalon, mesencephalon and metencephalon.
Transcripts expressed in the PFC, and more generally in the brain, are characterized by extended 3′UTR regions [ 12].
Aged c-rel−/− mouse brain were characterized by increased microglial reactivity in the basal ganglia, but no astrocytic reaction.
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