Found: 19
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A Nuclear Function for the Presenilin 1 Neuronal Partner NPRAP/δ-Catenin.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 27, n. 2, p. 307, doi. 10.3233/JAD-2011-110536
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- Publication type:
- Article
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
- Published in:
- 1998
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- Publication type:
- journal article
A rare mutation in the CTNND2 gene is associated with increased Aβ42 secretion
- Published in:
- 2012
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- Publication type:
- Abstract
Hypothermia-induced hyperphosphorylation: A new model to study tau kinase inhibitors
- Published in:
- 2012
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- 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
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- Abstract
Interactome of NPRAP, a presenilin-1 neuronal partner
- Published in:
- 2010
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- Publication type:
- Abstract
P4-218: Functional role of BACE1 and presenilin-1 interaction
- Published in:
- 2008
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- Publication type:
- Abstract
Silencing of Amyloid Precursor Protein Expression Using a New Engineered Delta Ribozyme.
- Published in:
- 2012
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- Publication type:
- Journal Article
Silencing of Amyloid Precursor Protein Expression Using a New Engineered Delta Ribozyme.
- Published in:
- International Journal of Alzheimer's Disease, 2012, p. 1, doi. 10.1155/2012/947147
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- Publication type:
- Article
The Fanconi Anemia Group C Protein Interacts with Uncoordinated 5A and Delays Apoptosis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092811
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- Publication type:
- Article
δ-Catenin Is Genetically and Biologically Associated with Cortical Cataract and Future Alzheimer-Related Structural and Functional Brain Changes.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0043728
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- Publication type:
- Article
Identification of Novel NPRAP/d-Catenin-Interacting Proteins and the Direct Association of NPRAP with Dynamin 2.
- Published in:
- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025379
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- Publication type:
- Article
Detection of the peripheral nervous system (PNS)-type glial fibrillary acidic protein (GFAP) and its mRNA in human lymphocytes.
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- Journal of Neuroscience Research, 1997, v. 48, n. 1, p. 53, doi. 10.1002/(SICI)1097-4547(19970401)48:1<53::AID-JNR5>3.0.CO;2-D
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- Publication type:
- Article
Hyperinsulinemia and abdominal obesity affect the expression of hypertriglyceridemia in heterozygous familial lipoprotein lipase deficiency.
- Published in:
- 1997
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- Publication type:
- journal article
FANCC localizes with UNC5A at neurite outgrowth and promotes neuritogenesis.
- Published in:
- BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-3763-1
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- Publication type:
- Article
Fanconi anemia core complex-dependent HES1 mono-ubiquitination regulates its transcriptional activity.
- Published in:
- BMC Research Notes, 2018, v. 11, p. 1, doi. 10.1186/s13104-018-3243-7
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- Publication type:
- Article
Oligomerization of human presenilin-1 fragments
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- FEBS Letters, 2003, v. 550, n. 1-3, p. 30, doi. 10.1016/S0014-5793(03)00813-5
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- Publication type:
- Article
Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population.
- Published in:
- Human Mutation, 1998, v. 11, p. S148, doi. 10.1002/humu.1380110150
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- Publication type:
- Article
A rapid restriction site screening method for the Pro<sup>207</sup>→Leu mutation in the lipoprotein lipase gene.
- Published in:
- Human Mutation, 1994, v. 3, n. 4, p. 416, doi. 10.1002/humu.1380030419
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- Publication type:
- Article