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Titlebook: N-Acetylaspartate; A Unique Neuronal Mo John R. Moffett,Suzannah B. Tieman,Aryan M. A. Nam Conference proceedings 2006 The Editor(s) (if ap

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樓主: Prehypertension
31#
發(fā)表于 2025-3-26 23:48:16 | 只看該作者
,Regulation of NAA-Synthesis in the Human Brain ,: Canavan’s Disease, Alzheimer’s Disease and Schizo
32#
發(fā)表于 2025-3-27 03:06:53 | 只看該作者
33#
發(fā)表于 2025-3-27 06:52:27 | 只看該作者
Conference proceedings 2006er injury, or slowly during neurodegenerative diseases, MRS has become a preferred method of analyzing nerve cell dysfunction and death without surgical intervention. ..The second reason that NAA has attracted attention in recent years is that a congenital genetic disorder of NAA metabolism has been
34#
發(fā)表于 2025-3-27 13:25:54 | 只看該作者
A Brief Overview of ,-Acetylaspartate and ,-Acetylaspartylglutamate,rence will attract a broader interest in these moieties, as they have been linked to serious disorders including schizophrenia, Alzheimer’s Disease and pain. Given their remarkably high concentrations in the brain, the current level of research on NAAG and NAA seems to underestimate their potential significance.
35#
發(fā)表于 2025-3-27 14:27:32 | 只看該作者
Conference proceedings 2006e of the most highly concentrated chemicals found in the brain of humans and animals, and yet the functions served by this brain-specific metabolite remain elusive, and controversial. Despite the uncertainties surrounding the functions of NAA in the development and operation of the nervous system, t
36#
發(fā)表于 2025-3-27 20:49:40 | 只看該作者
Canavan Disease: Studies on the Knockout Mouse,ular studies of the mouse brain showed abnormal expression of multiple genes in addition to ASPA deficiency. Adenoassociated virus mediated gene transfer and stem cell therapy in the knockout mouse are the latest attempts to alter pathophysiology in the CD mouse.
37#
發(fā)表于 2025-3-27 22:31:56 | 只看該作者
Mutation Analysis of the Aspartoacylase Gene in Non-Jewish Patients with Canavan Disease,on-Jewish persons with Canavan disease requires sequencing of all exons and their splice sites as well as a search for insertions and deletions. When mRNA cannot be found so that cDNA is unavailable for sequencing, it may be possible to use polymorphisms in place of the actual mutations for prenatal diagnosis.
38#
發(fā)表于 2025-3-28 02:15:42 | 只看該作者
39#
發(fā)表于 2025-3-28 07:19:02 | 只看該作者
ylated form of the amino acid aspartate, and it is present exclusively in the nervous system. Indeed, NAA is one of the most highly concentrated chemicals found in the brain of humans and animals, and yet the functions served by this brain-specific metabolite remain elusive, and controversial. Despi
40#
發(fā)表于 2025-3-28 11:15:31 | 只看該作者
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