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Newest in this topic

  1. Rapidly reversible persistent long-term potentiation inhibition by patient-derived brain tau and amyloid ß proteins 2024-06-10
  2. Reversible memory loss in a mouse transgenic model of Alzheimer's disease 2002-08-01
  3. Reversible phosphorylation of tau to form A68 in heat-shocked neuronal PC12 cells 1993-07-01

Studies

3 studies carry this tag.

Date range

1993 to 2024

Top journals

  • Brain research. Molecular brain research 1
  • Philosophical transactions of the Royal Society of London. Series B, Biological sciences 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.

  1. Rapidly reversible persistent long-term potentiation inhibition by patient-derived brain tau and amyloid ß proteins

    ✓ Peer-reviewed alzhub usefulness score 45 out of 100. Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2024-06-10 Drug development

    How the two pathognomonic proteins of Alzheimer's disease (AD); amyloid ß (Aß) and tau, cause synaptic failure remains enigmatic.

  2. Reversible memory loss in a mouse transgenic model of Alzheimer's disease

    ✓ Peer-reviewed alzhub usefulness score 36 out of 100. The Journal of neuroscience : the official journal of the Society for Neuroscience 2002-08-01 Risk genes beyond APOE

    Alzheimer's disease (AD) is a neurodegenerative condition, believed to be irreversible, characterized by inexorable deterioration of memory and intellect, with neuronal loss accompanying amyloid plaques and neurofibrillary tangles.

  3. Reversible phosphorylation of tau to form A68 in heat-shocked neuronal PC12 cells

    ✓ Peer-reviewed alzhub usefulness score 36 out of 100. Brain research. Molecular brain research 1993-07-01 Drug development

    A68, the primary protein constituent of Alzheimer's disease-associated neurofibrillary tangles, is an abnormally phosphorylated form of the microtubule-associated protein tau.

All topic tags with their study counts