Apo E and apo E receptor gene expression in the brain of Alzheimer's disease subjects with different apoE genotype

2000 ◽  
Vol 21 ◽  
pp. 115
Author(s):  
Doris Dea ◽  
Nicole Aumont ◽  
Judes Poirier
2020 ◽  
Vol 81 (3) ◽  
pp. e33-e34 ◽  
Author(s):  
Key-Hwan Lim ◽  
Sumin Yang ◽  
Sung-Hyun Kim ◽  
Jae-Yeol Joo

1993 ◽  
Vol 18 (3) ◽  
pp. 239-245 ◽  
Author(s):  
Jonathan R. Seckl ◽  
Karen L. French ◽  
Dajan O'Donnell ◽  
Michael J. Meaney ◽  
N.P.V. Nair ◽  
...  

2016 ◽  
Vol 55 (3) ◽  
pp. 1273-1283 ◽  
Author(s):  
Jesus Mendiola-Precoma ◽  
Karla Padilla ◽  
Alfredo Rodríguez-Cruz ◽  
Laura C. Berumen ◽  
Ricardo Miledi ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Angela M. Crist ◽  
Kelly M. Hinkle ◽  
Xue Wang ◽  
Christina M. Moloney ◽  
Billie J. Matchett ◽  
...  

AbstractSelective vulnerability of different brain regions is seen in many neurodegenerative disorders. The hippocampus and cortex are selectively vulnerable in Alzheimer’s disease (AD), however the degree of involvement of the different brain regions differs among patients. We classified corticolimbic patterns of neurofibrillary tangles in postmortem tissue to capture extreme and representative phenotypes. We combined bulk RNA sequencing with digital pathology to examine hippocampal vulnerability in AD. We identified hippocampal gene expression changes associated with hippocampal vulnerability and used machine learning to identify genes that were associated with AD neuropathology, including SERPINA5, RYBP, SLC38A2, FEM1B, and PYDC1. Further histologic and biochemical analyses suggested SERPINA5 expression is associated with tau expression in the brain. Our study highlights the importance of embracing heterogeneity of the human brain in disease to identify disease-relevant gene expression.


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