Found: 11
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FE65 Constitutes the Functional Link between the Low-Density Lipoprotein Receptor-Related Protein and the Amyloid Precursor Protein.
- Published in:
- Journal of Neuroscience, 2004, v. 24, n. 17, p. 4259, doi. 10.1523/JNEUROSCI.5451-03.2004
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- Article
The cytoplasmic domain of the LDL receptor-related protein regulates multiple steps in APP processing.
- Published in:
- EMBO Journal, 2002, v. 21, n. 21, p. 5691, doi. 10.1093/emboj/cdf568
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- Article
SWI/SNF chromatin remodeling complexes and cancer.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 3, p. 350, doi. 10.1002/ajmg.c.31410
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- Article
P4-272: Proteomic profile of COX-1/2 double deficient cells treated with Aβ42 lowering NSAIDS
- Published in:
- 2006
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- Publication type:
- Abstract
P3-420: F-box only protein 11, a target of Aβ42 lowering NSAIDs, interacts with presenilin 1 and alters γ-secretase activity
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P4-272: Proteomic profile of COX-1/2 double deficient cells treated with Aβ42 lowering NSAIDS
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-420: F-box only protein 11, a target of Aβ42 lowering NSAIDs, interacts with presenilin 1 and alters γ-secretase activity
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Applying the Grossman et al. Theoretical Framework: The Case of Reading.
- Published in:
- Teachers College Record, 2011, v. 113, n. 12, p. 2897, doi. 10.1177/016146811111301203
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- Publication type:
- Article
Low-density lipoprotein receptor-related protein promotes amyloid precursor protein trafficking to lipid rafts in the endocytic pathway.
- Published in:
- FASEB Journal, 2007, v. 21, n. 11, p. 2742, doi. 10.1096/fj.07-8114com
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- Publication type:
- Article
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
- Published in:
- Genes, Chromosomes & Cancer, 2017, v. 56, n. 10, p. 730, doi. 10.1002/gcc.22477
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- Publication type:
- Article
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.
- Published in:
- Human Mutation, 2011, v. 32, n. 1, p. 91, doi. 10.1002/humu.21395
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- Article