PAPER Gan-Or Z, Wood NW
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286387 RESULTS
PAPER Ong TL, Dal S, Williams LJ, Morales-Briceno H, Fung VS
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes.
Mov Disord. 2021 Oct;36(10):2452. PubMed.PAPER Kang X, Ploner A, Roelstraete B, Khalili H, Williams DM, Pedersen NL, Ludvigsson JF, Wirdefeldt K
Heterozygous and Homozygous Variants in SORL1 Gene in Alzheimer's Disease Patients: Clinical, Neuroimaging and Neuropathological Findings.
Mov Disord. 2021 Oct;36(10):2453. PubMed.SORL1 R122Ter
MUTATIONS SORL1 121340794 GRCh37/hg19 rs775517202 C T Exon 2 Coding Unknown; predicted to be protein truncating. Unknown, but amyloid-PET positive. Global atrophy, superficial siderosis, and subcortical microhemorrhages shown by MRI. R122Ter Alzheimer's Diseas
PAPER Guan H, Geng Z, Yuan W, Chang B
Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing.
Front Neurosci. 2021;15:755056. Epub 2021 Oct 1 PubMed.PAPER Peng Z, Zhou R, Liu D, Cui M, Yu K, Yang H, Li L, Liu J, Chen Y, Hong W, Huang J, Wang C, Ma J, Zhou H
SORL1 Polymorphisms in Mexican Patients with Alzheimer's Disease.
Front Aging Neurosci. 2021;13:722836. Epub 2021 Oct 1 PubMed.PAPER Li T, Cheng C, Jia C, Leng Y, Qian J, Yu H, Liu Y, Wang N, Yang Y, Al-Nusaif M, Le W
Relying on the relationship with known disease-causing variants in homologous proteins to predict pathogenicity of SORL1 variants in Alzheimer's disease
Front Aging Neurosci. 2021;13:736026. Epub 2021 Oct 1 PubMed.PAPER Dong BH, Niu ZQ, Zhang JT, Zhou YJ, Meng FM, Dong AQ
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
Dis Markers. 2021;2021:2148820. Epub 2021 Oct 7 PubMed.Helmholtz Antibody Collection
Other The following are selected lists of antibodies against microglial proteins that are available through the Monoclonal Antibody Core Facility at Helmholtz Munich. ABI3 | ApoE | CD33 | CLEC7A | CX3CR1 | P2Y12R | TMEM119 | TYROBP/DAP12 Tested Applications:
APOE C130R (ApoE4)
MUTATIONS APOE 45411941 GRCh37/hg19 rs429358 T C Exon 4 Coding Strongest known risk factor for AD. Implicated in Aβ and tau pathologies, as well as in multiple other neuronal and non-neuronal functions. C130R Alzheimer's Disease, Multiple Conditions This varia
ABI3 (clone 3C4)
Other Epitope: Immunogen: Peptide in C-terminus of murine Abi3 Clonality: Monoclonal Isotype: IgG2a Host: Rat Reactivity: Mouse RRID: Format: Source: Available through the antibody request page of the Monoclonal Antibody Core Facility at Helmholtz Center Muni
ABI3 (clone 30B7)
Other Epitope: Immunogen: Recombinant human Abi3 protein Clonality: Monoclonal Isotype: IgG1 Host: Mouse Reactivity: Human, Mouse RRID: AB_2905538 Format: Source: Available through the antibody request page of the Monoclonal Antibody Core Facility at Helmholtz
PAPER Baban B, Khodadadi H, Salles ÉL, Costigliola V, Morgan JC, Hess DC, Vaibhav K, Dhandapani KM, Yu JC
F-actin-dependent regulation of NESH dynamics in rat hippocampal neurons.
Ageing Res Rev. 2021 Dec;72:101487. Epub 2021 Oct 15 PubMed.PAPER Peterson CE, Silva A, Goben AH, Ongtengco NP, Hu EZ, Khanna D, Nussbaum ER, Jasenof IG, Kim SJ, Dykens JA
NESH regulates dendritic spine morphology and synapse formation.
Prev Med. 2021 Dec;153:106849. Epub 2021 Oct 15 PubMed.PAPER Muthuraman M, Palotai M, Jávor-Duray B, Kelemen A, Koirala N, Halász L, Erőss L, Fekete G, Bognár L, Deuschl G, Tamás G
The NESH/Abi-3-based WAVE2 complex is functionally distinct from the Abi-1-based WAVE2 complex.
Neuroimage Clin. 2021;32:102857. Epub 2021 Oct 13 PubMed.Current Filters
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