Citokróm c-oxidáz, II. alegység (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Citokróm c-oxidáz, II. alegység" in Hungarian language version.

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16nih.gov

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10doi.org

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4archive.org

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2uniprot.org

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1heartproteome.org

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archive.org

García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (1994. szeptember). „The superfamily of heme-copper respiratory oxidases”. Journal of Bacteriology 176 (18), 5587–600. o. DOI:10.1128/jb.176.18.5587-5600.1994. PMID 8083153. PMC 196760.
Capaldi RA (1990). „Structure and function of cytochrome c oxidase”. Annual Review of Biochemistry 59, 569–596. o. DOI:10.1146/annurev.bi.59.070190.003033. PMID 2165384.
Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J (2001. szeptember). „Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene”. Annals of Neurology 50 (3), 409–413. o. DOI:10.1002/ana.1141. PMID 11558799.
Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM (1999. május). „An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy”. American Journal of Human Genetics 64 (5), 1330–1339. o. DOI:10.1086/302361. PMID 10205264. PMC 1377869.

doi.org

dx.doi.org

Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (2013. október). „Integration of cardiac proteome biology and medicine by a specialized knowledgebase”. Circulation Research 113 (9), 1043–53. o. DOI:10.1161/CIRCRESAHA.113.301151. PMID 23965338. PMC 4076475.
Capaldi RA, Malatesta F, Darley-Usmar VM (1983. július). „Structure of cytochrome c oxidase”. Biochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics 726 (2), 135–148. o. DOI:10.1016/0304-4173(83)90003-4. PMID 6307356.
García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (1994. szeptember). „The superfamily of heme-copper respiratory oxidases”. Journal of Bacteriology 176 (18), 5587–600. o. DOI:10.1128/jb.176.18.5587-5600.1994. PMID 8083153. PMC 196760.
Capaldi RA (1990). „Structure and function of cytochrome c oxidase”. Annual Review of Biochemistry 59, 569–596. o. DOI:10.1146/annurev.bi.59.070190.003033. PMID 2165384.
Hill BC (1993. április). „The sequence of electron carriers in the reaction of cytochrome c oxidase with oxygen”. Journal of Bioenergetics and Biomembranes 25 (2), 115–120. o. DOI:10.1007/bf00762853. PMID 8389744.
(2017. január 1.) „UniProt: the universal protein knowledgebase”. Nucleic Acids Research 45 (D1), D158–D169. o. DOI:10.1093/nar/gkw1099. PMID 27899622. PMC 5210571.
Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, Wibrand F, Shoubridge EA, Vissing J (2015. március). „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. o. DOI:10.1136/jmedgenet-2014-102914. PMID 25604084.
Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE (2008. február 1.). „Isolated cytochrome c oxidase deficiency as a cause of MELAS”. Journal of Medical Genetics 45 (2), 117–21. o. DOI:10.1136/jmg.2007.052076. PMID 18245391. PMC 3027970.
Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J (2001. szeptember). „Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene”. Annals of Neurology 50 (3), 409–413. o. DOI:10.1002/ana.1141. PMID 11558799.
Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM (1999. május). „An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy”. American Journal of Human Genetics 64 (5), 1330–1339. o. DOI:10.1086/302361. PMID 10205264. PMC 1377869.

heartproteome.org

amino.heartproteome.org

Cytochrome c oxidase subunit 2. Cardiac Organellar Protein Atlas Knowledgebase (COPaKB)^{[halott link]}

nih.gov

pubmed.ncbi.nlm.nih.gov

Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (2013. október). „Integration of cardiac proteome biology and medicine by a specialized knowledgebase”. Circulation Research 113 (9), 1043–53. o. DOI:10.1161/CIRCRESAHA.113.301151. PMID 23965338. PMC 4076475.
Capaldi RA, Malatesta F, Darley-Usmar VM (1983. július). „Structure of cytochrome c oxidase”. Biochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics 726 (2), 135–148. o. DOI:10.1016/0304-4173(83)90003-4. PMID 6307356.
García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (1994. szeptember). „The superfamily of heme-copper respiratory oxidases”. Journal of Bacteriology 176 (18), 5587–600. o. DOI:10.1128/jb.176.18.5587-5600.1994. PMID 8083153. PMC 196760.
Capaldi RA (1990). „Structure and function of cytochrome c oxidase”. Annual Review of Biochemistry 59, 569–596. o. DOI:10.1146/annurev.bi.59.070190.003033. PMID 2165384.
Hill BC (1993. április). „The sequence of electron carriers in the reaction of cytochrome c oxidase with oxygen”. Journal of Bioenergetics and Biomembranes 25 (2), 115–120. o. DOI:10.1007/bf00762853. PMID 8389744.
(2017. január 1.) „UniProt: the universal protein knowledgebase”. Nucleic Acids Research 45 (D1), D158–D169. o. DOI:10.1093/nar/gkw1099. PMID 27899622. PMC 5210571.
Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, Wibrand F, Shoubridge EA, Vissing J (2015. március). „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. o. DOI:10.1136/jmedgenet-2014-102914. PMID 25604084.
Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE (2008. február 1.). „Isolated cytochrome c oxidase deficiency as a cause of MELAS”. Journal of Medical Genetics 45 (2), 117–21. o. DOI:10.1136/jmg.2007.052076. PMID 18245391. PMC 3027970.
Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J (2001. szeptember). „Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene”. Annals of Neurology 50 (3), 409–413. o. DOI:10.1002/ana.1141. PMID 11558799.
Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM (1999. május). „An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy”. American Journal of Human Genetics 64 (5), 1330–1339. o. DOI:10.1086/302361. PMID 10205264. PMC 1377869.

ncbi.nlm.nih.gov

Entrez Gene: COX2 cytochrome c oxidase subunit II Ez a cikk ebből a forrásból származó szöveget tartalmaz, amely közkincs.
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (2013. október). „Integration of cardiac proteome biology and medicine by a specialized knowledgebase”. Circulation Research 113 (9), 1043–53. o. DOI:10.1161/CIRCRESAHA.113.301151. PMID 23965338. PMC 4076475.
García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (1994. szeptember). „The superfamily of heme-copper respiratory oxidases”. Journal of Bacteriology 176 (18), 5587–600. o. DOI:10.1128/jb.176.18.5587-5600.1994. PMID 8083153. PMC 196760.
(2017. január 1.) „UniProt: the universal protein knowledgebase”. Nucleic Acids Research 45 (D1), D158–D169. o. DOI:10.1093/nar/gkw1099. PMID 27899622. PMC 5210571.
Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE (2008. február 1.). „Isolated cytochrome c oxidase deficiency as a cause of MELAS”. Journal of Medical Genetics 45 (2), 117–21. o. DOI:10.1136/jmg.2007.052076. PMID 18245391. PMC 3027970.
Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM (1999. május). „An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy”. American Journal of Human Genetics 64 (5), 1330–1339. o. DOI:10.1086/302361. PMID 10205264. PMC 1377869.

uniprot.org

MT-CO2 - Cytochrome c oxidase subunit 2 - Homo sapiens (Human) - MT-CO2 gene & protein. (Hozzáférés: 2018. augusztus 7.) A szócikk e forrás CC BY-SA 4.0 licencű szövegét használja.
Mitochondrial complex IV deficiency (angol nyelven). www.uniprot.org