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presenilin-1
2 studies tagged presenilin-1, dated 2007-11-01 to 2016-02-04. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- The dynamic mechanism of presenilin-1 function: Sensitive gate dynamics and loop unplugging control protein access 2016-02-04
- Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease 2007-11-01
Studies
2 studies carry this tag.
Date range
2007 to 2016
Top journals
- Neurobiology of disease 1
- The Journal of neuroscience : the official journal of the Society for Neuroscience 1
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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There is no molecular explanation for the many presenilin 1 (PSEN1) mutations causing Alzheimer's disease, but both gain of function relating to amyloid production and loss of isolated PSEN1 function have been implied.
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Mutations in the PSEN1 gene encoding presenilin 1 (PS1) are linked to a vast majority of pedigrees with early-onset, autosomal dominant forms of familial Alzheimer's disease (FAD).