TMEM70 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "TMEM70" in English language version.

refsWebsite

Global rank English rank

12nih.gov

4^th place

7doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

2ensembl.org

1,626^th place

1,007^th place

1omim.org

4,380^th place

4,305^th place

1heartproteome.org

low place

1uniprot.org

5,673^rd place

6,418^th place

1creativecommons.org

1,010^th place

612^th place

1ugent.be

3,695^th place

3,560^th place

1handle.net

102^nd place

76^th place

1ebi.ac.uk

5,849^th place

7,886^th place

creativecommons.org (Global: 1,010^th place; English: 612^th place)

"TMEM70 - Transmembrane protein 70, mitochondrial precursor - Homo sapiens (Human) - TMEM70 gene & protein". www.uniprot.org. Retrieved 2018-08-15. This article incorporates text available under the CC BY 4.0 license.

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

Cameron JM, Levandovskiy V, Mackay N, Ackerley C, Chitayat D, Raiman J, et al. (January 2011). "Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization". Mitochondrion. 11 (1): 191–9. doi:10.1016/j.mito.2010.09.008. PMID 20920610.
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): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Cízková A, Stránecký V, Mayr JA, Tesarová M, Havlícková V, Paul J, et al. (November 2008). "TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy". Nature Genetics. 40 (11): 1288–90. doi:10.1038/ng.246. PMID 18953340. S2CID 34536246.
Catteruccia M, Verrigni D, Martinelli D, Torraco A, Agovino T, Bonafé L, et al. (March 2014). "Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patients". Molecular Genetics and Metabolism. 111 (3): 353–359. doi:10.1016/j.ymgme.2014.01.001. PMID 24485043.
Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, et al. (April 2010). "Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation". Archives of Disease in Childhood. 95 (4): 296–301. doi:10.1136/adc.2009.168096. hdl:1854/LU-987464. PMID 20335238. S2CID 2946094.
Spiegel R, Khayat M, Shalev SA, Horovitz Y, Mandel H, Hershkovitz E, et al. (March 2011). "TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome". Journal of Medical Genetics. 48 (3): 177–82. doi:10.1136/jmg.2010.084608. PMID 21147908. S2CID 8699153.

ebi.ac.uk (Global: 5,849^th place; English: 7,886^th place)

IntAct. "TMEM70 interactions". www.ebi.ac.uk. Retrieved 2018-08-16.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000175606 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000025940 – Ensembl, May 2017

handle.net (Global: 102^nd place; English: 76^th place)

hdl.handle.net

Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, et al. (April 2010). "Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation". Archives of Disease in Childhood. 95 (4): 296–301. doi:10.1136/adc.2009.168096. hdl:1854/LU-987464. PMID 20335238. S2CID 2946094.

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

amino.heartproteome.org

"TMEM70 - Transmembrane protein 70, mitochondrial". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB).^{[permanent dead link]}

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Cameron JM, Levandovskiy V, Mackay N, Ackerley C, Chitayat D, Raiman J, et al. (January 2011). "Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization". Mitochondrion. 11 (1): 191–9. doi:10.1016/j.mito.2010.09.008. PMID 20920610.
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): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Cízková A, Stránecký V, Mayr JA, Tesarová M, Havlícková V, Paul J, et al. (November 2008). "TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy". Nature Genetics. 40 (11): 1288–90. doi:10.1038/ng.246. PMID 18953340. S2CID 34536246.
Catteruccia M, Verrigni D, Martinelli D, Torraco A, Agovino T, Bonafé L, et al. (March 2014). "Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patients". Molecular Genetics and Metabolism. 111 (3): 353–359. doi:10.1016/j.ymgme.2014.01.001. PMID 24485043.
Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, et al. (April 2010). "Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation". Archives of Disease in Childhood. 95 (4): 296–301. doi:10.1136/adc.2009.168096. hdl:1854/LU-987464. PMID 20335238. S2CID 2946094.
Spiegel R, Khayat M, Shalev SA, Horovitz Y, Mandel H, Hershkovitz E, et al. (March 2011). "TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome". Journal of Medical Genetics. 48 (3): 177–82. doi:10.1136/jmg.2010.084608. PMID 21147908. S2CID 8699153.

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: Transmembrane protein 70". Retrieved 2018-08-14. This article incorporates text from this source, which is in the public domain.
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): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.

omim.org (Global: 4,380^th place; English: 4,305^th place)

Online Mendelian Inheritance in Man (OMIM): TMEM70 - 612418

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Cízková A, Stránecký V, Mayr JA, Tesarová M, Havlícková V, Paul J, et al. (November 2008). "TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy". Nature Genetics. 40 (11): 1288–90. doi:10.1038/ng.246. PMID 18953340. S2CID 34536246.
Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, et al. (April 2010). "Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation". Archives of Disease in Childhood. 95 (4): 296–301. doi:10.1136/adc.2009.168096. hdl:1854/LU-987464. PMID 20335238. S2CID 2946094.
Spiegel R, Khayat M, Shalev SA, Horovitz Y, Mandel H, Hershkovitz E, et al. (March 2011). "TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome". Journal of Medical Genetics. 48 (3): 177–82. doi:10.1136/jmg.2010.084608. PMID 21147908. S2CID 8699153.

ugent.be (Global: 3,695^th place; English: 3,560^th place)

biblio.ugent.be

Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, et al. (April 2010). "Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation". Archives of Disease in Childhood. 95 (4): 296–301. doi:10.1136/adc.2009.168096. hdl:1854/LU-987464. PMID 20335238. S2CID 2946094.

uniprot.org (Global: 5,673^rd place; English: 6,418^th place)

"TMEM70 - Transmembrane protein 70, mitochondrial precursor - Homo sapiens (Human) - TMEM70 gene & protein". www.uniprot.org. Retrieved 2018-08-15. This article incorporates text available under the CC BY 4.0 license.

TMEM70 (English Wikipedia)

creativecommons.org (Global: 1,010th place; English: 612th place)

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

ebi.ac.uk (Global: 5,849th place; English: 7,886th place)

ensembl.org (Global: 1,626th place; English: 1,007th place)