Secondary NAD+ deficiency in the inherited defect of glutamine synthetase-Reference-Cited by-同舟云学术

Secondary NAD+ deficiency in the inherited defect of glutamine synthetase

Published:2015-04-21 Issue:6 Volume:38 Page:1075-1083
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Hu Liyan,Ibrahim Khalid,Stucki Martin,Frapolli Michele,Shahbeck Noora,Chaudhry Farrukh A.,Görg Boris,Häussinger Dieter,Penberthy W. Todd,Ben-Omran Tawfeg,Häberle Johannes

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-015-9846-4

Reference38 articles.

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4. Bruzzone S, Fruscione F, Morando S, Ferrando T, Poggi A, Garuti A, D’Urso A, Selmo M, Benvenuto F, Cea M, Zoppoli G, Moran E, Soncini D, Ballestrero A, Sordat B, Patrone F, Mostoslavsky R, Uccelli A, Nencioni A (2009) Catastrophic NAD(+) depletion in activated T lymphocytes through Nampt inhibition reduces demyelination and disability in EAE. PLoS One 4

5. Carlsson M, Carlsson A (1990) Interactions between glutamatergic and monoaminergic systems within the basal ganglia–implications for schizophrenia and Parkinson’s disease. Trends Neurosci 13:272–6

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