ライフサイエンスコーパス: amyloid protein precursor

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1 3) being produced from the metabolism of the amyloid protein precursor.

2 Various mutations in the amyloid protein precursor and presenilin genes can lead

3 Mutations in the gene encoding the amyloid protein precursor (APP) cause autosomal dominant

4 oE4(Delta272-299) with mice expressing human amyloid protein precursor (APP) harboring familial AD mu

5 Although the Alzheimer amyloid protein precursor (APP) has been studied intense

6 In order to localize amyloid protein precursor (APP) in nerve terminals, we h

7 rted to cleave the tau protein (Tau) and the amyloid protein precursor (APP) to hinder the formation

8 om proteolytic processing of the Alzheimer's amyloid protein precursor (APP).

9 peptide, Abeta42, which is derived from the amyloid protein precursor (APP).

10 r patients, is derived by proteolysis of the amyloid protein precursor (APP).

11 beta-Amyloid protein precursors (APPs, 695-770 amino acids) a

12 stroglial excitatory amino acid transport by amyloid protein precursors could protect the brain again

13 Amyloid protein precursor-dependent stimulation of aspar

14 rted that a variety of mutations in the beta-amyloid protein precursor gene and the Presenilin-1 and

15 ssed with transgenic mice that produce human amyloid protein precursors (hAPP) and Ass in neurons.(4,

16 es to compare the effects of different human amyloid protein precursors (hAPP) and their products on

17 ived growth factor promoter to express human amyloid protein precursors (hAPPs) in neurons of transge

18 The amyloid protein precursor has been well conserved throug

19 Tau and the amyloid protein precursor have important roles in normal

20 At moderate levels of expression, human amyloid protein precursors increased glutamate/aspartate

21 Thus, tau- and amyloid protein precursor-knockout mice were protected a

22 netically interacts with the Drosophila beta-amyloid protein precursor-like (Appl) protein, the homol

23 Here, we demonstrate that the amyloid protein precursor may participate in the regulat

24 Historically, the ability to monitor the amyloid protein precursor protein has been crude.

25 ion with transmembrane domain mutants of the amyloid protein precursor that are cleaved by pharmacolo

26 ficient (RAP-/-) mice was crossed with human amyloid protein precursor transgenic (hAPP tg) mice, and

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