ACADS (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "ACADS" in English language version.

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aap.org

publications.aap.org

doi.org

ensembl.org

May2017.archive.ensembl.org

heartproteome.org

amino.heartproteome.org

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

  • "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • "Entrez Gene: Acyl-CoA dehydrogenase, C-2 to C-3 short chain".
  • Jethva R, Bennett MJ, Vockley J (December 2008). "Short-chain acyl-coenzyme A dehydrogenase deficiency". Molecular Genetics and Metabolism. 95 (4): 195–200. doi:10.1016/j.ymgme.2008.09.007. PMC 2720545. PMID 18977676.
  • Wolfe L, Jethva R, Oglesbee D, Vockley J (1993). "Short-Chain Acyl-CoA Dehydrogenase Deficiency". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Amemiya A (eds.). GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle. PMID 21938826.
  • Hornbak M, Banasik K, Justesen JM, Krarup NT, Sandholt CH, Andersson Å, et al. (January 2011). "The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load". BMC Medical Genetics. 12: 4. doi:10.1186/1471-2350-12-4. PMC 3022800. PMID 21211036.

semanticscholar.org

api.semanticscholar.org

  • Corydon MJ, Andresen BS, Bross P, Kjeldsen M, Andreasen PH, Eiberg H, et al. (December 1997). "Structural organization of the human short-chain acyl-CoA dehydrogenase gene". Mammalian Genome. 8 (12): 922–926. doi:10.1007/s003359900612. PMID 9383286. S2CID 9157185.
  • Okuyaz C, Ezgü FS, Biberoglu G, Zeviani M, Tiranti V, Yilgör E (June 2008). "Severe infantile hypotonia with ethylmalonic aciduria: case report". Journal of Child Neurology. 23 (6): 703–705. doi:10.1177/0883073807313048. PMID 18539996. S2CID 46624539.
  • Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, et al. (August 2008). "The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level". Human Genetics. 124 (1): 43–56. doi:10.1007/s00439-008-0521-9. PMID 18523805. S2CID 25491212.
  • Giurgiutiu DV, Espinoza LM, Wood TC, DuPont BR, Holden KR (January 2008). "Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant". Journal of Child Neurology. 23 (1): 112–117. doi:10.1177/0883073807307979. PMID 18184946. S2CID 31888136.

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