SLC25A22 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "SLC25A22" in English language version.

refsWebsite

Global rank English rank

4^th place

2^nd place

1,626^th place

1,007^th place

4,380^th place

4,305^th place

low place

5,673^rd place

6,418^th place

1,010^th place

612^th place

5,849^th place

7,886^th place

creativecommons.org

Wong CC, Qian Y, Li X, Xu J, Kang W, Tong JH, et al. (November 2016). "SLC25A22 Promotes Proliferation and Survival of Colorectal Cancer Cells With KRAS Mutations and Xenograft Tumor Progression in Mice via Intracellular Synthesis of Aspartate". Gastroenterology. 151 (5): 945–960.e6. doi:10.1053/j.gastro.2016.07.011. PMID 27451147.
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.
The UniProt Consortium (January 2017). "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Poduri A, Heinzen EL, Chitsazzadeh V, Lasorsa FM, Elhosary PC, LaCoursiere CM, et al. (December 2013). "SLC25A22 is a novel gene for migrating partial seizures in infancy". Annals of Neurology. 74 (6): 873–82. doi:10.1002/ana.23998. PMC 4031329. PMID 24596948.
Molinari F, Raas-Rothschild A, Rio M, Fiermonte G, Encha-Razavi F, Palmieri L, et al. (February 2005). "Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy". American Journal of Human Genetics. 76 (2): 334–9. doi:10.1086/427564. PMC 1196378. PMID 15592994.

"SLC25A22 - Mitochondrial glutamate carrier 1". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB).

"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: Solute carrier family 25 member 22". Retrieved 2016-10-15. 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.
The UniProt Consortium (January 2017). "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Poduri A, Heinzen EL, Chitsazzadeh V, Lasorsa FM, Elhosary PC, LaCoursiere CM, et al. (December 2013). "SLC25A22 is a novel gene for migrating partial seizures in infancy". Annals of Neurology. 74 (6): 873–82. doi:10.1002/ana.23998. PMC 4031329. PMID 24596948.
Molinari F, Raas-Rothschild A, Rio M, Fiermonte G, Encha-Razavi F, Palmieri L, et al. (February 2005). "Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy". American Journal of Human Genetics. 76 (2): 334–9. doi:10.1086/427564. PMC 1196378. PMID 15592994.

Wong CC, Qian Y, Li X, Xu J, Kang W, Tong JH, et al. (November 2016). "SLC25A22 Promotes Proliferation and Survival of Colorectal Cancer Cells With KRAS Mutations and Xenograft Tumor Progression in Mice via Intracellular Synthesis of Aspartate". Gastroenterology. 151 (5): 945–960.e6. doi:10.1053/j.gastro.2016.07.011. PMID 27451147.
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.
The UniProt Consortium (January 2017). "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Poduri A, Heinzen EL, Chitsazzadeh V, Lasorsa FM, Elhosary PC, LaCoursiere CM, et al. (December 2013). "SLC25A22 is a novel gene for migrating partial seizures in infancy". Annals of Neurology. 74 (6): 873–82. doi:10.1002/ana.23998. PMC 4031329. PMID 24596948.
Molinari F, Raas-Rothschild A, Rio M, Fiermonte G, Encha-Razavi F, Palmieri L, et al. (February 2005). "Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy". American Journal of Human Genetics. 76 (2): 334–9. doi:10.1086/427564. PMC 1196378. PMID 15592994.