Α-Ketoglutarat-Dehydrogenase-Komplex (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Α-Ketoglutarat-Dehydrogenase-Komplex" in German language version.

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doi.org

  • Alina Levtova, Paula J. Waters, Daniela Buhas, Sébastien Lévesque, Christiane Auray‐Blais, Joe T.R. Clarke, Rachel Laframboise, Bruno Maranda, Grant A. Mitchell, Catherine Brunel‐Guitton, Nancy E. Braverman: Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. In: Journal of Inherited Metabolic Disease. Band 42, Nr. 1, Januar 2019, ISSN 0141-8955, S. 107–116, doi:10.1002/jimd.12032 (wiley.com).
  • Zeinab Wehbe, Sidney Behringer, Khaled Alatibi, David Watkins, David Rosenblatt, Ute Spiekerkoetter, Sara Tucci: The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism. In: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. Band 1864, Nr. 11, November 2019, S. 1629–1643, doi:10.1016/j.bbalip.2019.07.012 (elsevier.com).
  • Baughn AD, Garforth SJ, Vilchèze C, Jacobs WR: An anaerobic-type alpha-ketoglutarate ferredoxin oxidoreductase completes the oxidative tricarboxylic acid cycle of Mycobacterium tuberculosis. In: PLoS Pathog. 5. Jahrgang, Nr. 11, November 2009, S. e1000662, doi:10.1371/journal.ppat.1000662, PMID 19936047, PMC 2773412 (freier Volltext).
  • Tian J, Bryk R, Itoh M, Suematsu M, Nathan C: Variant tricarboxylic acid cycle in Mycobacterium tuberculosis: identification of alpha-ketoglutarate decarboxylase. In: Proc. Natl. Acad. Sci. USA. 102. Jahrgang, Nr. 30, Juli 2005, S. 10670–5, doi:10.1073/pnas.0501605102, PMID 16027371, PMC 1180764 (freier Volltext).

elsevier.com

linkinghub.elsevier.com

  • Zeinab Wehbe, Sidney Behringer, Khaled Alatibi, David Watkins, David Rosenblatt, Ute Spiekerkoetter, Sara Tucci: The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism. In: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. Band 1864, Nr. 11, November 2019, S. 1629–1643, doi:10.1016/j.bbalip.2019.07.012 (elsevier.com).

nih.gov

ncbi.nlm.nih.gov

  • Cordwell SJ: Microbial genomes and "missing" enzymes: redefining biochemical pathways. In: Arch. Microbiol. 172. Jahrgang, Nr. 5, November 1999, S. 269–79, PMID 10550468.
  • Mai, X. und Adams, MW. (1996): Characterization of a fourth type of 2-keto acid-oxidizing enzyme from a hyperthermophilic archaeon: 2-ketoglutarate ferredoxin oxidoreductase from Thermococcus litoralis. In: Journal of bacteriology. Band 178, Nummer 20, Oktober 1996, S. 5890–5896, PMID 8830683, PMC 178443 (freier Volltext).
  • Pitson SM, Mendz GL, Srinivasan S, Hazell SL: The tricarboxylic acid cycle of Helicobacter pylori. In: Eur J Biochem. 260. Jahrgang, Nr. 1, Februar 1999, S. 258–67, PMID 10091606.
  • Baughn AD, Garforth SJ, Vilchèze C, Jacobs WR: An anaerobic-type alpha-ketoglutarate ferredoxin oxidoreductase completes the oxidative tricarboxylic acid cycle of Mycobacterium tuberculosis. In: PLoS Pathog. 5. Jahrgang, Nr. 11, November 2009, S. e1000662, doi:10.1371/journal.ppat.1000662, PMID 19936047, PMC 2773412 (freier Volltext).
  • Tian J, Bryk R, Itoh M, Suematsu M, Nathan C: Variant tricarboxylic acid cycle in Mycobacterium tuberculosis: identification of alpha-ketoglutarate decarboxylase. In: Proc. Natl. Acad. Sci. USA. 102. Jahrgang, Nr. 30, Juli 2005, S. 10670–5, doi:10.1073/pnas.0501605102, PMID 16027371, PMC 1180764 (freier Volltext).

wiley.com

onlinelibrary.wiley.com

  • Alina Levtova, Paula J. Waters, Daniela Buhas, Sébastien Lévesque, Christiane Auray‐Blais, Joe T.R. Clarke, Rachel Laframboise, Bruno Maranda, Grant A. Mitchell, Catherine Brunel‐Guitton, Nancy E. Braverman: Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. In: Journal of Inherited Metabolic Disease. Band 42, Nr. 1, Januar 2019, ISSN 0141-8955, S. 107–116, doi:10.1002/jimd.12032 (wiley.com).

zdb-katalog.de

  • Alina Levtova, Paula J. Waters, Daniela Buhas, Sébastien Lévesque, Christiane Auray‐Blais, Joe T.R. Clarke, Rachel Laframboise, Bruno Maranda, Grant A. Mitchell, Catherine Brunel‐Guitton, Nancy E. Braverman: Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. In: Journal of Inherited Metabolic Disease. Band 42, Nr. 1, Januar 2019, ISSN 0141-8955, S. 107–116, doi:10.1002/jimd.12032 (wiley.com).