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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Intra-Familial Clinical Heterogeneity due to FTLD-U with TDP-43 Proteinopathy Caused by a Novel Deletion in Progranulin Gene (PGRN).
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 22, n. 4, p. 1123, doi. 10.3233/JAD-2010-101413
- By:
- Publication type:
- Article
Presenilin-1 Holoprotein is an Interacting Partner of Sarco Endoplasmic Reticulum Calcium-ATPase and Confers Resistance to Endoplasmic Reticulum Stress.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 20, n. 1, p. 261, doi. 10.3233/JAD-2010-1360
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- Publication type:
- Article
Genetic complexity of Alzheimer's disease: Successes and challenges.
- Published in:
- Journal of Alzheimer's Disease, 2006, v. 9, n. 3, p. 381, doi. 10.3233/JAD-2006-9S343
- By:
- Publication type:
- Article
Biomolecular condensate phase diagrams with a combinatorial microdroplet platform.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-35265-7
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- Publication type:
- Article
Does Soluble TREM2 Protect Against Alzheimer's Disease?
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2021.834697
- By:
- Publication type:
- Article
TREM2 shedding by cleavage at the H157-S158 bond is accelerated for the Alzheimer's disease-associated H157Y variant.
- Published in:
- EMBO Molecular Medicine, 2017, v. 9, n. 10, p. 1366, doi. 10.15252/emmm.201707673
- By:
- Publication type:
- Article
A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families.
- Published in:
- 2001
- By:
- Publication type:
- journal article
The APOE-ε4 Allele and Alzheimer Disease Among African Americans, Hispanics, and Whites.
- Published in:
- JAMA: Journal of the American Medical Association, 1998, v. 280, n. 19, p. 1661, doi. 10.1001/jama.280.19.1661
- By:
- Publication type:
- Article
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Biology of presenilins as causative molecules for Alzheimer disease.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 4, p. 219, doi. 10.1034/j.1399-0004.1999.550401.x
- By:
- Publication type:
- Article
MicroRNA‐128 suppresses tau phosphorylation and reduces amyloid‐beta accumulation by inhibiting the expression of GSK3β, APPBP2, and mTOR in Alzheimer's disease.
- Published in:
- CNS Neuroscience & Therapeutics, 2023, v. 29, n. 7, p. 1848, doi. 10.1111/cns.14143
- By:
- Publication type:
- Article
Amyloid-β toxicity modulates tau phosphorylation through the PAX6 signalling pathway.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Genetic and epigenetic study of an Alzheimer's disease family with monozygotic triplets.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Mutation of the ALS-/FTD-Associated RNA-Binding Protein FUS Affects Axonal Development.
- Published in:
- Journal of Neuroscience, 2024, v. 44, n. 27, p. 1, doi. 10.1523/JNEUROSCI.2148-23.2024
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- Publication type:
- Article
Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 2, p. 611, doi. 10.1002/alz.12686
- By:
- Publication type:
- Article
Genetic Insights from the ADSP into Drug Discovery In Alzheimer's Disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.066442
- By:
- Publication type:
- Article
Reactive or transgenic increase in microglial TYROBP reveals a TREM2‐independent TYROBP–APOE link in wild‐type and Alzheimer's‐related mice.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 2, p. 149, doi. 10.1002/alz.12256
- By:
- Publication type:
- Article
APOE‐ε4 associates with hippocampal volume, learning, and memory across the spectrum of Alzheimer's disease and dementia with Lewy bodies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, n. 9, p. 1137, doi. 10.1016/j.jalz.2018.04.005
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- Publication type:
- Article
P2‐131: ANALYSIS OF A FAMILY WITH IDENTICAL TRIPLETS DISCORDANT FOR ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P718, doi. 10.1016/j.jalz.2018.06.817
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- Publication type:
- Article
S1‐02‐03: GENETICS OF SORL1 AND ITS ROLE AS AN APP NEURONAL SORTING RECEPTOR.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P198, doi. 10.1016/j.jalz.2018.06.2300
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- Publication type:
- Article
γ-SECRETASE, NOTCH, Aβ AND ALZHEIMER'S DISEASE: WHERE DO THE PRESENILINS FIT IN?
- Published in:
- Nature Reviews Neuroscience, 2002, v. 3, n. 4, p. 281, doi. 10.1038/nrn785
- By:
- Publication type:
- Article
Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 9, p. 671, doi. 10.1038/jhg.2011.79
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- Publication type:
- Article
An exploration of cognitive subgroups in Alzheimer's disease.
- Published in:
- Journal of the International Neuropsychological Society, 2010, v. 16, n. 2, p. 233, doi. 10.1017/S1355617709991160
- By:
- Publication type:
- Article
Regulatory RNA goes awry in Alzheimer's disease.
- Published in:
- Nature Medicine, 2008, v. 14, n. 7, p. 711, doi. 10.1038/nm0708-711
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- Publication type:
- Article
Cyclohexanehexol inhibitors of Aβ aggregation prevent and reverse Alzheimer phenotype in a mouse model.
- Published in:
- Nature Medicine, 2006, v. 12, n. 7, p. 801, doi. 10.1038/nm1423
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- Publication type:
- Article
Regulation of membrane fluidity by RNF145‐triggered degradation of the lipid hydrolase ADIPOR2.
- Published in:
- EMBO Journal, 2022, v. 41, n. 19, p. 1, doi. 10.15252/embj.2022110777
- By:
- Publication type:
- Article
Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, n. 5, p. 520, doi. 10.1016/j.jalz.2016.08.014
- By:
- Publication type:
- Article
MUTATION ANALYSIS OF THE MS4A AND TREM GENE-CLUSTERS IN A CASE-CONTROL ALZHEIMER’S DISEASE DATASET.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P682, doi. 10.1016/j.jalz.2016.06.1340
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- Publication type:
- Article
A ROLE OF PTPN21 IN NEURON SURVIVAL AND DEGENERATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P651, doi. 10.1016/j.jalz.2016.06.1308
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- Publication type:
- Article
PATHOGENIC SORL1 MUTATIONS AND PARKINSONIAN FEATURES IN ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P451, doi. 10.1016/j.jalz.2016.06.874
- By:
- Publication type:
- Article
Massachusetts Alzheimer's Disease Research Center: Progress and challenges.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 10, p. 1241, doi. 10.1016/j.jalz.2015.06.1887
- By:
- Publication type:
- Article
Elucidating the gene expression changes that underpin cholinergic dysfunction in a mouse model of Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P328, doi. 10.1016/j.jalz.2015.07.476
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- Publication type:
- Article
Rare coding mutations identified by targeted sequencing of Alzheimer’s disease loci detected in genome-wide association studies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P252, doi. 10.1016/j.jalz.2015.07.313
- By:
- Publication type:
- Article
Genome wide analyses of runs of homozygosity among african americans revealed further evidence of recessive inheritance for Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P228, doi. 10.1016/j.jalz.2015.07.262
- By:
- Publication type:
- Article
Picalm but not bin1 alters the secretion of beta-amyloid peptide
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Candidate gene study in the endosome-to-Golgi retrieval pathway reveals association of retromer genes with Alzheimer's disease
- Published in:
- 2012
- By:
- Publication type:
- Abstract
ATP-binding cassette transporter A7 (ABCA7) effects on amyloid processing and relevance to Alzheimer's disease
- Published in:
- 2012
- By:
- Publication type:
- Abstract
A rare mutation in the CTNND2 gene is associated with increased Aβ42 secretion
- Published in:
- 2012
- By:
- Publication type:
- Abstract
δ-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer's-related structural and functional brain changes
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Genes Found by GWAS in Alzheimer’s Disease: Comparing VPS10-Containing Receptors with BIN1 and CALM1
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Genome-Wide Analysis of Large Rare Copy Number Variations in Alzheimer Disease Among Caribbean Hispanics
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress
- Published in:
- 2010
- By:
- Publication type:
- Abstract
Examination of TOMM40, APOE, and PCDH11X in Caribbean Hispanics with late-onset Alzheimer's disease
- Published in:
- 2009
- By:
- Publication type:
- Abstract
The sortilin-related receptor (SORL1) influences variation in memory in late-onset Alzheimer's disease
- Published in:
- 2009
- By:
- Publication type:
- Abstract
The sortilin-related receptor (SORL1) influences variation in memory in late-onset Alzheimer disease
- Published in:
- 2009
- By:
- Publication type:
- Abstract
A novel PS1 mutation in a large aboriginal kindred with early onset familial Alzheimer's disease from a remote community in northern British Columbia
- Published in:
- 2009
- By:
- Publication type:
- Abstract
P4-219: TMP21 association with the γ-secretase complex and its regulation of protease activity
- Published in:
- 2008
- By:
- Publication type:
- Abstract
P4-190: Role of gamma-secretase in lipoprotein endocytosis
- Published in:
- 2008
- By:
- Publication type:
- Abstract
P3-376: Gene expression profiling in a transgenic mouse model of Alzheimer's disease
- Published in:
- 2008
- By:
- Publication type:
- Abstract