ACADS (English Wikipedia)

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

Last modified: 23:12:42, 6 February 2024 (UTC)

Ref.Un. Ref.Website

Global rank English rank

2217nih.gov

5^th place

1010doi.org

2^nd place

62ensembl.org

630^th place

326^th place

44semanticscholar.org

15^th place

8^th place

22web.archive.org

1^st place

22heartproteome.org

low place

11aap.org

low place

aap.org (Global: low place; English: low place)

publications.aap.org

Bok LA, Vreken P, Wijburg FA, Wanders RJ, Gregersen N, Corydon MJ, et al. (November 2003). "Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder" (PDF). Pediatrics. 112 (5): 1152–1155. doi:10.1542/peds.112.5.1152. PMID 14595061.

doi.org (Global: 2^nd place; English: 2^nd place)

Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, et al. (February 2008). "Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin". Molecular Genetics and Metabolism. 93 (2): 179–189. doi:10.1016/j.ymgme.2007.09.021. PMID 18054510.
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.
Schmidt SP, Corydon TJ, Pedersen CB, Bross P, Gregersen N (June 2010). "Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress". Molecular Genetics and Metabolism. 100 (2): 155–162. doi:10.1016/j.ymgme.2010.03.009. PMID 20371198.
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.
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.
Bok LA, Vreken P, Wijburg FA, Wanders RJ, Gregersen N, Corydon MJ, et al. (November 2003). "Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder" (PDF). Pediatrics. 112 (5): 1152–1155. doi:10.1542/peds.112.5.1152. PMID 14595061.
van Maldegem BT, Duran M, Wanders RJ, Waterham HR, Wijburg FA (March 2010). "Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency". Pediatric Research. 67 (3): 304–308. doi:10.1203/PDR.0b013e3181cbd57b. PMID 19952864.
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.
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.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000122971 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000029545 – Ensembl, May 2017

heartproteome.org (Global: low place; English: low place)

amino.heartproteome.org

"Protein Information: P16219". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 14 August 2016. Retrieved 23 July 2016.
"Protein Information: Q07417". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 14 August 2016. Retrieved 23 July 2016.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, et al. (February 2008). "Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin". Molecular Genetics and Metabolism. 93 (2): 179–189. doi:10.1016/j.ymgme.2007.09.021. PMID 18054510.
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.
Schmidt SP, Corydon TJ, Pedersen CB, Bross P, Gregersen N (June 2010). "Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress". Molecular Genetics and Metabolism. 100 (2): 155–162. doi:10.1016/j.ymgme.2010.03.009. PMID 20371198.
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.
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.
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.
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.
Bok LA, Vreken P, Wijburg FA, Wanders RJ, Gregersen N, Corydon MJ, et al. (November 2003). "Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder" (PDF). Pediatrics. 112 (5): 1152–1155. doi:10.1542/peds.112.5.1152. PMID 14595061.
van Maldegem BT, Duran M, Wanders RJ, Waterham HR, Wijburg FA (March 2010). "Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency". Pediatric Research. 67 (3): 304–308. doi:10.1203/PDR.0b013e3181cbd57b. PMID 19952864.
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.
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.

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 (Global: 15^th place; English: 8^th place)

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.

web.archive.org (Global: 1^st place; English: 1^st place)

"Protein Information: P16219". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 14 August 2016. Retrieved 23 July 2016.
"Protein Information: Q07417". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 14 August 2016. Retrieved 23 July 2016.