CEP89 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CEP89" in English language version.

refsWebsite

Global rank English rank

11nih.gov

4^th place

6doi.org

2^nd place

2uniprot.org

5,673^rd place

6,418^th place

2semanticscholar.org

11^th place

8^th place

1ensembl.org

1,626^th place

1,007^th place

1creativecommons.org

1,010^th place

612^th place

1web.archive.org

1^st place

1heartproteome.org

low place

1handle.net

102^nd place

76^th place

creativecommons.org

"CEP89 - Centrosomal protein of 89 kDa - Homo sapiens (Human) - CEP89 gene & protein". Retrieved 2018-08-07. This article incorporates text available under the CC BY 4.0 license.

doi.org

"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158 – D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
van Bon BW, Oortveld MA, Nijtmans LG, Fenckova M, Nijhof B, Besseling J, et al. (August 2013). "CEP89 is required for mitochondrial metabolism and neuronal function in man and fly". Human Molecular Genetics. 22 (15): 3138–3151. doi:10.1093/hmg/ddt170. PMID 23575228.
Sillibourne JE, Specht CG, Izeddin I, Hurbain I, Tran P, Triller A, et al. (November 2011). "Assessing the localization of centrosomal proteins by PALM/STORM nanoscopy". Cytoskeleton. 68 (11): 619–627. doi:10.1002/cm.20536. PMID 21976302. S2CID 33280582.
Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, et al. (March 2015). "Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature". Journal of Medical Genetics. 52 (3): 203–207. doi:10.1136/jmedgenet-2014-102914. PMID 25604084. S2CID 43018915.
Mick DU, Dennerlein S, Wiese H, Reinhold R, Pacheu-Grau D, Lorenzi I, et al. (December 2012). "MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulation". Cell. 151 (7): 1528–1541. doi:10.1016/j.cell.2012.11.053. hdl:11858/00-001M-0000-000E-DDDF-4. PMID 23260140.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000121289 – Ensembl, May 2017

handle.net

hdl.handle.net

Mick DU, Dennerlein S, Wiese H, Reinhold R, Pacheu-Grau D, Lorenzi I, et al. (December 2012). "MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulation". Cell. 151 (7): 1528–1541. doi:10.1016/j.cell.2012.11.053. hdl:11858/00-001M-0000-000E-DDDF-4. PMID 23260140.

heartproteome.org

amino.heartproteome.org

"Protein Cep89 homolog". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 2018-08-10. Retrieved 2018-08-09.

nih.gov

pubmed.ncbi.nlm.nih.gov

"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158 – D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
van Bon BW, Oortveld MA, Nijtmans LG, Fenckova M, Nijhof B, Besseling J, et al. (August 2013). "CEP89 is required for mitochondrial metabolism and neuronal function in man and fly". Human Molecular Genetics. 22 (15): 3138–3151. doi:10.1093/hmg/ddt170. PMID 23575228.
Sillibourne JE, Specht CG, Izeddin I, Hurbain I, Tran P, Triller A, et al. (November 2011). "Assessing the localization of centrosomal proteins by PALM/STORM nanoscopy". Cytoskeleton. 68 (11): 619–627. doi:10.1002/cm.20536. PMID 21976302. S2CID 33280582.
Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, et al. (March 2015). "Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature". Journal of Medical Genetics. 52 (3): 203–207. doi:10.1136/jmedgenet-2014-102914. PMID 25604084. S2CID 43018915.
Mick DU, Dennerlein S, Wiese H, Reinhold R, Pacheu-Grau D, Lorenzi I, et al. (December 2012). "MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulation". Cell. 151 (7): 1528–1541. doi:10.1016/j.cell.2012.11.053. hdl:11858/00-001M-0000-000E-DDDF-4. PMID 23260140.

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: Centrosomal protein 89". Retrieved 2018-08-09. This article incorporates text from this source, which is in the public domain.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158 – D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.

semanticscholar.org

api.semanticscholar.org

Sillibourne JE, Specht CG, Izeddin I, Hurbain I, Tran P, Triller A, et al. (November 2011). "Assessing the localization of centrosomal proteins by PALM/STORM nanoscopy". Cytoskeleton. 68 (11): 619–627. doi:10.1002/cm.20536. PMID 21976302. S2CID 33280582.
Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, et al. (March 2015). "Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature". Journal of Medical Genetics. 52 (3): 203–207. doi:10.1136/jmedgenet-2014-102914. PMID 25604084. S2CID 43018915.

uniprot.org

"CEP89 - Centrosomal protein of 89 kDa - Homo sapiens (Human) - CEP89 gene & protein". Retrieved 2018-08-07. This article incorporates text available under the CC BY 4.0 license.
"Mitochondrial complex IV deficiency". www.uniprot.org.

web.archive.org

"Protein Cep89 homolog". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 2018-08-10. Retrieved 2018-08-09.