ATP7A (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "ATP7A" in English language version.

refsWebsite

Global rank English rank

18nih.gov

4^th place

10doi.org

2^nd place

2ensembl.org

1,626^th place

1,007^th place

2semanticscholar.org

11^th place

8^th place

1harvard.edu

18^th place

17^th place

1igib.res.in

low place

doi.org

Tümer Z, Møller LB, Horn N (1999). "Mutation Spectrum of ATP7A, the Gene Defective in Menkes Disease". Copper Transport and Its Disorders. Advances in Experimental Medicine and Biology. Vol. 448. pp. 83–95. doi:10.1007/978-1-4615-4859-1_7. ISBN 978-1-4613-7204-2. PMID 10079817.
Kodama H, Murata Y (Aug 1999). "Molecular genetics and pathophysiology of Menkes disease". Pediatrics International. 41 (4): 430–5. doi:10.1046/j.1442-200x.1999.01091.x. PMID 10453200. S2CID 19509148.
Šimčíková D, Heneberg P (December 2019). "Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases". Scientific Reports. 9 (1): 18577. Bibcode:2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
Kaler SG (Jan 2011). "ATP7A-related copper transport diseases-emerging concepts and future trends". Nature Reviews. Neurology. 7 (1): 15–29. doi:10.1038/nrneurol.2010.180. PMC 4214867. PMID 21221114.
Lutsenko S, Gupta A, Burkhead JL, Zuzel V (Aug 2008). "Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance". Archives of Biochemistry and Biophysics. 476 (1): 22–32. doi:10.1016/j.abb.2008.05.005. PMC 2556376. PMID 18534184.
Crisponi G, Nurchi VM, Fanni D, Gerosa C, Nemolato S, Faa G (April 2010). "Copper-related diseases: From chemistry to molecular pathology". Coordination Chemistry Reviews. 254 (7–8): 876–889. doi:10.1016/j.ccr.2009.12.018.
Inesi G, Pilankatta R, Tadini-Buoninsegni F (Oct 2014). "Biochemical characterization of P-type copper ATPases". The Biochemical Journal. 463 (2): 167–76. doi:10.1042/BJ20140741. PMC 4179477. PMID 25242165.
Banci L, Bertini I, Cantini F, Ciofi-Baffoni S (Aug 2010). "Cellular copper distribution: a mechanistic systems biology approach". Cellular and Molecular Life Sciences. 67 (15): 2563–89. doi:10.1007/s00018-010-0330-x. PMC 11115773. PMID 20333435. S2CID 41967295.
Hordyjewska A, Popiołek Ł, Kocot J (August 2014). "The many "faces" of copper in medicine and treatment". Biometals. 27 (4): 611–21. doi:10.1007/s10534-014-9736-5. PMC 4113679. PMID 24748564.
Siggs OM, Cruite JT, Du X, Rutschmann S, Masliah E, Beutler B, Oldstone MB (August 2012). "Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease". Proc. Natl. Acad. Sci. U.S.A. 109 (34): 13733–8. doi:10.1073/pnas.1211499109. PMC 3427069. PMID 22869751.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000165240 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000033792 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Šimčíková D, Heneberg P (December 2019). "Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases". Scientific Reports. 9 (1): 18577. Bibcode:2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.

igib.res.in

clingen.igib.res.in

"ATP7Agen a comprehensive resource for clinically annotated variants in ATP7A Gene". clingen.igib.res.in. Retrieved 2020-07-06.

nih.gov

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.
Šimčíková D, Heneberg P (December 2019). "Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases". Scientific Reports. 9 (1): 18577. Bibcode:2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
Kaler SG (Jan 2011). "ATP7A-related copper transport diseases-emerging concepts and future trends". Nature Reviews. Neurology. 7 (1): 15–29. doi:10.1038/nrneurol.2010.180. PMC 4214867. PMID 21221114.
Lutsenko S, Gupta A, Burkhead JL, Zuzel V (Aug 2008). "Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance". Archives of Biochemistry and Biophysics. 476 (1): 22–32. doi:10.1016/j.abb.2008.05.005. PMC 2556376. PMID 18534184.
Inesi G, Pilankatta R, Tadini-Buoninsegni F (Oct 2014). "Biochemical characterization of P-type copper ATPases". The Biochemical Journal. 463 (2): 167–76. doi:10.1042/BJ20140741. PMC 4179477. PMID 25242165.
Banci L, Bertini I, Cantini F, Ciofi-Baffoni S (Aug 2010). "Cellular copper distribution: a mechanistic systems biology approach". Cellular and Molecular Life Sciences. 67 (15): 2563–89. doi:10.1007/s00018-010-0330-x. PMC 11115773. PMID 20333435. S2CID 41967295.
Hordyjewska A, Popiołek Ł, Kocot J (August 2014). "The many "faces" of copper in medicine and treatment". Biometals. 27 (4): 611–21. doi:10.1007/s10534-014-9736-5. PMC 4113679. PMID 24748564.
Siggs OM, Cruite JT, Du X, Rutschmann S, Masliah E, Beutler B, Oldstone MB (August 2012). "Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease". Proc. Natl. Acad. Sci. U.S.A. 109 (34): 13733–8. doi:10.1073/pnas.1211499109. PMC 3427069. PMID 22869751.

pubmed.ncbi.nlm.nih.gov

Tümer Z, Møller LB, Horn N (1999). "Mutation Spectrum of ATP7A, the Gene Defective in Menkes Disease". Copper Transport and Its Disorders. Advances in Experimental Medicine and Biology. Vol. 448. pp. 83–95. doi:10.1007/978-1-4615-4859-1_7. ISBN 978-1-4613-7204-2. PMID 10079817.
Kodama H, Murata Y (Aug 1999). "Molecular genetics and pathophysiology of Menkes disease". Pediatrics International. 41 (4): 430–5. doi:10.1046/j.1442-200x.1999.01091.x. PMID 10453200. S2CID 19509148.
Šimčíková D, Heneberg P (December 2019). "Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases". Scientific Reports. 9 (1): 18577. Bibcode:2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
Kaler SG (Jan 2011). "ATP7A-related copper transport diseases-emerging concepts and future trends". Nature Reviews. Neurology. 7 (1): 15–29. doi:10.1038/nrneurol.2010.180. PMC 4214867. PMID 21221114.
Lutsenko S, Gupta A, Burkhead JL, Zuzel V (Aug 2008). "Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance". Archives of Biochemistry and Biophysics. 476 (1): 22–32. doi:10.1016/j.abb.2008.05.005. PMC 2556376. PMID 18534184.
Inesi G, Pilankatta R, Tadini-Buoninsegni F (Oct 2014). "Biochemical characterization of P-type copper ATPases". The Biochemical Journal. 463 (2): 167–76. doi:10.1042/BJ20140741. PMC 4179477. PMID 25242165.
Banci L, Bertini I, Cantini F, Ciofi-Baffoni S (Aug 2010). "Cellular copper distribution: a mechanistic systems biology approach". Cellular and Molecular Life Sciences. 67 (15): 2563–89. doi:10.1007/s00018-010-0330-x. PMC 11115773. PMID 20333435. S2CID 41967295.
Hordyjewska A, Popiołek Ł, Kocot J (August 2014). "The many "faces" of copper in medicine and treatment". Biometals. 27 (4): 611–21. doi:10.1007/s10534-014-9736-5. PMC 4113679. PMID 24748564.
Siggs OM, Cruite JT, Du X, Rutschmann S, Masliah E, Beutler B, Oldstone MB (August 2012). "Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease". Proc. Natl. Acad. Sci. U.S.A. 109 (34): 13733–8. doi:10.1073/pnas.1211499109. PMC 3427069. PMID 22869751.

semanticscholar.org

api.semanticscholar.org

Kodama H, Murata Y (Aug 1999). "Molecular genetics and pathophysiology of Menkes disease". Pediatrics International. 41 (4): 430–5. doi:10.1046/j.1442-200x.1999.01091.x. PMID 10453200. S2CID 19509148.
Banci L, Bertini I, Cantini F, Ciofi-Baffoni S (Aug 2010). "Cellular copper distribution: a mechanistic systems biology approach". Cellular and Molecular Life Sciences. 67 (15): 2563–89. doi:10.1007/s00018-010-0330-x. PMC 11115773. PMID 20333435. S2CID 41967295.