Suchergebnisse - "Beach, Thomas G"

PubPharm (920)

1

Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease

enthalten in: Alzheimer's & dementia : the journal of the Alzheimer's Association | 2024

von Xicota, L. | Cosentino, S. | Vardarajan, B. | +118

2

RNA sequencing of olfactory bulb in Parkinson's disease reveals gene alterations associated with olfactory dysfunction

enthalten in: Neurobiology of disease | 2024

von Tremblay, C. | Aslam, S. | Walker, J. | +13

3

Circular RNAs in the human brain are tailored to neuron identity and neuropsychiatric disease

enthalten in: bioRxiv.org | 2024

von Dong, X. | Bai, Y. | Liao, Z. | +9

4

Low circulating choline, a modifiable dietary factor, is associated with the pathological progression and metabolome dysfunction in Alzheimer’s disease

enthalten in: bioRxiv.org | 2024

von Judd, J. | Jasbi, P. | Winslow, W. | +4

5

Bridging the Gap: Multi-Omics Profiling of Brain Tissue in Alzheimer’s Disease and Older Controls in Multi-Ethnic Populations

enthalten in: bioRxiv.org | 2024

von Reddy, J. | Heath, L. | Linden, A. | +50

6

Bridging the Gap : Multi-Omics Profiling of Brain Tissue in Alzheimer's Disease and Older Controls in Multi-Ethnic Populations

enthalten in: bioRxiv : the preprint server for biology | 2024

von Reddy, J. | Heath, L. | Linden, A. | +50

7

APOE4/4 is linked to damaging lipid droplets in Alzheimer's disease microglia

enthalten in: Nature | 2024

von Haney, M. | Pálovics, R. | Munson, C. | +25

UpdateOf: bioRxiv. 2023 Jul 25;:. - PMID 37546938

8

Conjugal Synucleinopathies : A Clinicopathologic Study

enthalten in: Movement disorders : official journal of the Movement Disorder Society | 2024

von Adler, C. | Halverson, M. | Zhang, N. | +11

9

Profiling Protein-Protein Interactions in the Human Brain by Refined Cofractionation Mass Spectrometry

enthalten in: Journal of proteome research | 2024

von Shrestha, H. | Lee, D. | Wu, Z. | +6

10

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium : a genetic association study

enthalten in: The Lancet. Neurology | 2024

von Valentino, R. | Scotton, W. | Roemer, S. | +153

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