Type 2 Transglutaminase, mitochondria and Huntington's disease: Menage a trois-Reference-Cited by-同舟云学术

Type 2 Transglutaminase, mitochondria and Huntington's disease: Menage a trois

Published:2014-11 Issue: Volume:19 Page:97-104
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Altuntas Sara,D'Eletto Manuela,Rossin Federica,Hidalgo Laura Diaz,Farrace Maria Grazia,Falasca Laura,Piredda Lucia,Cocco Stefania,Mastroberardino Pier Giorgio,Piacentini Mauro,Campanella Michelangelo

Funder

MIUR

Compagnia di San Paolo

Ministry of Health of Italy

AIRC

Marie Curie Grant

Netherlands Genomics Initiative

FIRB

EBRI-Rita Levi Montalcini Foundation Research Programme in Metabolism in Brain Diseases

LAM-Bighi Research Grant on Brain Tumours

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference64 articles.

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2. Recent advances in the development of tissue transglutaminase (TG2) inhibitors;Badarau;Amino Acids,2013

3. p53 Mediates cellular dysfunction and behavioral abnormalities in Huntington's disease;Bae;Neuron,2005

4. Transglutaminase 2 ablation leads to defective function of mitochondrial respiratory complex I affecting neuronal vulnerability in experimental models of extrapyramidal disorders;Battaglia;J. Neurochem.,2007

5. The transglutaminase family: an overview: minireview article;Beninati;Amino Acids,2004

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