Pyruvate dehydrogenase E1β subunit (human mitochondrial), mouse IgG1, monoclonal 17A5 (anti-PDH E1β subunit) - UNCONJ - Citations

Pyruvate dehydrogenase E1β subunit (human mitochondrial), mouse IgG1, monoclonal 17A5 (anti-PDH E1β subunit) - UNCONJ - Citations

View additional product information for Pyruvate dehydrogenase E1β subunit (human mitochondrial), mouse IgG1, monoclonal 17A5 (anti-PDH E1β subunit) - UNCONJ - Citations (A21324)

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Citations & References
Abstract
Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fission.
AuthorsDagda RK, Cherra SJ, Kulich SM, Tandon A, Park D, Chu CT,
JournalJ Biol Chem
PubMed ID19279012
'Mitochondrial dysregulation is strongly implicated in Parkinson disease. Mutations in PTEN-induced kinase 1 (PINK1) are associated with familial parkinsonism and neuropsychiatric disorders. Although overexpressed PINK1 is neuroprotective, less is known about neuronal responses to loss of PINK1 function. We found that stable knockdown of PINK1 induced mitochondrial fragmentation and autophagy ... More
Coupling of the de novo fatty acid biosynthesis and lipoylation pathways in mammalian mitochondria.
AuthorsWitkowski A, Joshi AK, Smith S
JournalJ Biol Chem
PubMed ID17374604
'The objective of this study was to identify the products and possible role of a putative pathway for de novo fatty acid synthesis in mammalian mitochondria. Bovine heart mitochondrial matrix preparations were prepared free from contamination by proteins from other subcellular components and, using a combination of radioisotopic labeling and ... More
Detection of pyruvate dehydrogenase E1 alpha-subunit deficiencies in females by immunohistochemical demonstration of mosaicism in cultured fibroblasts.
AuthorsLib MY, Brown RM, Brown GK, Marusich MF, Capaldi RA
JournalJ Histochem Cytochem
PubMed ID12070266
Deficiency of the E1 alpha-subunit of the pyruvate dehydrogenase (PDH) complex is an X-linked inborn error of metabolism and one of the major causes of lactic acidosis in children. Although most heterozygous females manifest symptoms of the disease, it is often difficult to establish the diagnosis as results based on ... More