Acetyl-CoA-Carboxylase (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acetyl-CoA-Carboxylase" in German language version.

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6doi.org

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4nih.gov

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3zdb-katalog.de

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1portlandpress.com

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1uniprot.org

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doi.org

Geoffray Monteuuis, Fumi Suomi, Juha M. Kerätär, Ali J. Masud, Alexander J. Kastaniotis: A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. In: Biochemical Journal. Band 474, Nr. 22, 15. November 2017, ISSN 0264-6021, S. 3783–3797, doi:10.1042/BCJ20170416 (portlandpress.com).
Alexander J. Kastaniotis, Kaija J. Autio, Remya R. Nair: Mitochondrial Fatty Acids and Neurodegenerative Disorders. In: The Neuroscientist. Band 27, Nr. 2, April 2021, ISSN 1073-8584, S. 143–158, doi:10.1177/1073858420936162.
C. M. Phillips, L. Goumidi u. a.: ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat. In: Journal of lipid research Band 51, Nummer 12, Dezember 2010, S. 3500–3507. doi:10.1194/jlr.M008474. PMID 20855566. PMC 297572 (freier Volltext).
C. W. Kim, Y. A. Moon u. a.: Induced polymerization of mammalian acetyl-CoA carboxylase by MIG12 provides a tertiary level of regulation of fatty acid synthesis. In: Proceedings of the National Academy of Sciences of the United States of America Band 107, Nummer 21, Mai 2010, S. 9626–9631. doi:10.1073/pnas.1001292107. PMID 20457939. PMC 290688 (freier Volltext).
G. Gago, D. Kurth u. a.: Biochemical and structural characterization of an essential acyl coenzyme A carboxylase from Mycobacterium tuberculosis. In: Journal of bacteriology Band 188, Nummer 2, Januar 2006, S. 477–486. doi:10.1128/JB.188.2.477-486.2006. PMID 16385038. PMC 134727 (freier Volltext).
Sara Tucci: Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. In: Orphanet Journal of Rare Diseases. Band 15, Nr. 1, Dezember 2020, ISSN 1750-1172, doi:10.1186/s13023-020-1299-7, PMID 31969167, PMC 6977288 (freier Volltext).

nih.gov

ncbi.nlm.nih.gov

C. M. Phillips, L. Goumidi u. a.: ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat. In: Journal of lipid research Band 51, Nummer 12, Dezember 2010, S. 3500–3507. doi:10.1194/jlr.M008474. PMID 20855566. PMC 297572 (freier Volltext).
C. W. Kim, Y. A. Moon u. a.: Induced polymerization of mammalian acetyl-CoA carboxylase by MIG12 provides a tertiary level of regulation of fatty acid synthesis. In: Proceedings of the National Academy of Sciences of the United States of America Band 107, Nummer 21, Mai 2010, S. 9626–9631. doi:10.1073/pnas.1001292107. PMID 20457939. PMC 290688 (freier Volltext).
G. Gago, D. Kurth u. a.: Biochemical and structural characterization of an essential acyl coenzyme A carboxylase from Mycobacterium tuberculosis. In: Journal of bacteriology Band 188, Nummer 2, Januar 2006, S. 477–486. doi:10.1128/JB.188.2.477-486.2006. PMID 16385038. PMC 134727 (freier Volltext).
Sara Tucci: Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. In: Orphanet Journal of Rare Diseases. Band 15, Nr. 1, Dezember 2020, ISSN 1750-1172, doi:10.1186/s13023-020-1299-7, PMID 31969167, PMC 6977288 (freier Volltext).

portlandpress.com

Geoffray Monteuuis, Fumi Suomi, Juha M. Kerätär, Ali J. Masud, Alexander J. Kastaniotis: A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. In: Biochemical Journal. Band 474, Nr. 22, 15. November 2017, ISSN 0264-6021, S. 3783–3797, doi:10.1042/BCJ20170416 (portlandpress.com).

uniprot.org

UniProt O13085, UniProt O00763

zdb-katalog.de

Geoffray Monteuuis, Fumi Suomi, Juha M. Kerätär, Ali J. Masud, Alexander J. Kastaniotis: A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. In: Biochemical Journal. Band 474, Nr. 22, 15. November 2017, ISSN 0264-6021, S. 3783–3797, doi:10.1042/BCJ20170416 (portlandpress.com).
Alexander J. Kastaniotis, Kaija J. Autio, Remya R. Nair: Mitochondrial Fatty Acids and Neurodegenerative Disorders. In: The Neuroscientist. Band 27, Nr. 2, April 2021, ISSN 1073-8584, S. 143–158, doi:10.1177/1073858420936162.
Sara Tucci: Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. In: Orphanet Journal of Rare Diseases. Band 15, Nr. 1, Dezember 2020, ISSN 1750-1172, doi:10.1186/s13023-020-1299-7, PMID 31969167, PMC 6977288 (freier Volltext).