Citations 58

Developing novel blood‐based biomarkers for Alzheimer's disease

Alzheimer's & Dementia | December 21, 2013 | Volume: 10 | Issue: 1 | Pages: 109-114

10.1016/j.jalz.2013.10.007 | PMID 24365657

AbstractAlzheimer's disease is the public health crisis of the 21st century. There is a clear need for a widely available, inexpensive and reliable method to diagnosis Alzheimer's disease in the earliest stages, track disease progression, and accelerate clinical development of new therapeutics. One avenue of research being explored is blood based biomarkers. In April 2012, the Alzheimer's Association and the Alzheimer's Drug Discovery Foundation convened top scientists from around the world to discuss the state of blood based biomarker development. This manuscript summarizes the meeting and the resultant discussion, including potential next steps to move this area of research forward.
P1–248: Identification of altered metabolic pathways in plasma and CSF in mild cognitive impairment and Alzheimer's disease using metabolomics

Alzheimer's & Dementia | October 9, 2013 | Volume: 9 | Issue: 4S_Part_6 | Pages: No page available

10.1016/j.jalz.2013.05.472

O3–07–04: Axonal trafficking inhibition in neurons depends on the aggregation state of Alzheimer's disease beta‐amyloid peptides and their binding to the plasma membrane

Alzheimer's & Dementia | October 9, 2013 | Volume: 9 | Issue: 4S_Part_13 | Pages: No page available

10.1016/j.jalz.2013.04.276

From Metabolic Pathways To Biomarkers: Where Are We Now With Metabolomics In Alzheimer‘s Disease?

Future Neurology | August 28, 2013 | Volume: 8 | Issue: 5 | Pages: 491-494

10.2217/fnl.13.36

P2‐077: Early mitochondrial dysfunction in the etiology of Alzheimer's disease

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_8 | Pages: No page available

10.1016/j.jalz.2012.05.781

Mutant Huntingtin Impairs Axonal Trafficking in Mammalian Neurons In Vivo and In Vitro

Molecular and Cellular Biology | August 31, 2004 | Volume: 24 | Issue: 18 | Pages: 8195-8209

10.1128/mcb.24.18.8195-8209.2004 | PMID 15340079

Microtubule destabilization and nuclear entry are sequential steps leading to toxicity in Huntington's disease

Proceedings of the National Academy of Sciences | October 14, 2003 | Volume: 100 | Issue: 21 | Pages: 12171-12176

10.1073/pnas.2034961100 | PMID 14527999

There has been a longstanding debate regarding the role of proteolysis in Huntington's disease. The toxic peptide theory posits that N-terminal cleavage fragments of mutant Huntington's disease protein [mutant huntingtin (mhtt)] enter the nucleus to cause transcriptional dysfunction. However, recent data suggest a second model in which proteolysis of full-length mhtt is inhibited. Importantly, the two competing theories differ with respect to subcellular distribution of mhtt at initiation of toxicity: nuclear if cleaved and cytoplasmic in the absence of cleavage. Using quantitative single-cell analysis and time-lapse imaging, we show here that transcriptional dysfunction is “downstream” of cytoplasmic dysfunction. Primary and reversible toxic events involve destabilization of microtubules mediated by full-length mhtt before cleavage. Restoration of microtubule structure by taxol inhibits nuclear entry and increases cell survival.
Effective and Reproducible Capillary Electrophoretic Separation of Thiols under Conditions Where Exceptionally High Current Is Generated

Analytical Chemistry | July 26, 2002 | Volume: 71 | Issue: 24 | Pages: 5569-5573

10.1021/ac990505b | PMID 10624160