Pierce™ IP Lysis Buffer, 100 mL - Citations

Pierce™ IP Lysis Buffer, 100 mL - Citations

View additional product information for Pierce™ IP Lysis Buffer - Citations (87788, 87787)

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Citations & References
Abstract
Rac1 augments Wnt signaling by stimulating ß-catenin-lymphoid enhancer factor-1 complex assembly independent of ß-catenin nuclear import.
AuthorsJamieson C, Lui C, Brocardo MG, Martino-Echarri E, Henderson BR
Journal
PubMed ID26403202
ß-Catenin transduces the Wnt signaling pathway and its nuclear accumulation leads to gene transactivation and cancer. Rac1 GTPase is known to stimulate ß-catenin-dependent transcription of Wnt target genes and we confirmed this activity. Here we tested the recent hypothesis that Rac1 augments Wnt signaling by enhancing ß-catenin nuclear import; however, ... More
Characterization of extracellular circulating microRNA.
AuthorsTurchinovich A, Weiz L, Langheinz A, Burwinkel B
JournalNucleic Acids Res
PubMed ID21609964
MicroRNAs (miRNAs), a class of post-transcriptional gene expression regulators, have recently been detected in human body fluids, including peripheral blood plasma as extracellular nuclease resistant entities. However, the origin and function of extracellular circulating miRNA remain essentially unknown. Here, we confirmed that circulating mature miRNA in contrast to mRNA or ... More
Increasing the Receptor Tyrosine Kinase EphB2 Prevents Amyloid-ß-induced Depletion of Cell Surface Glutamate Receptors by a Mechanism That Requires the PDZ-binding Motif of EphB2 and Neuronal Activity.
AuthorsMiyamoto T, Kim D, Knox JA, Johnson E, Mucke L
JournalJ Biol Chem
PubMed ID26589795
'Diverse lines of evidence suggest that amyloid-ß (Aß) peptides causally contribute to the pathogenesis of Alzheimer disease (AD), the most frequent neurodegenerative disorder. However, the mechanisms by which Aß impairs neuronal functions remain to be fully elucidated. Previous studies showed that soluble Aß oligomers interfere with synaptic functions by depleting ... More