Browsing Molekulare Medizin by Referee "Bayer, Thomas A. Prof. Dr."
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Comparative analysis of the mitochondrial proteome in a mouse model of Rett syndrome
(2023-10-12)Rett syndrome is a neural development disorder. The gene, for culprit protein, MeCP2 (methylated CpG binding protein) is located on chromosome X and the majority of patients are young girls. Rett syndrome patients do not ... -
Impact of N-terminally truncated Aß4-42 on memory and synaptic plasticity - Tg4-42 a new mouse model of Alzheimer's disease
(2015-01-14)A heterogeneous mixture of amyloid beta (Aβ) variants exists in Alzheimer’s disease (AD) brains. So far, little is known how individual Aβ species contribute to development and progression of this neurodegenerative disorder. ... -
The role of amyloid beta 4-42 in the etiology of Alzheimer's disease
(2015-01-06)N-truncated Aβ4-42 has been identified as a particular abundant Aβ species in the hippocampus and cortex of Alzheimer's patients. However, relatively little is known about the contribution of Aβ4-42 to the development and ...