| Year |
Citation |
Score |
| 2023 |
Mishra M, Saha S, Maji S, Rodriguez-Boulan E, Schreiner R, Gupta A. Regulation of the apico-basolateral trafficking polarity of the homologous copper-ATPases ATP7A and ATP7B. Journal of Cell Science. 137. PMID 38032054 DOI: 10.1242/jcs.261258 |
0.314 |
|
| 2023 |
Maji S, Pirozzi M, Pandey R, Ghosh T, Das S, Gupta A. Copper-independent lysosomal localisation of the Wilson disease protein ATP7B. Traffic (Copenhagen, Denmark). PMID 37846526 DOI: 10.1111/tra.12919 |
0.359 |
|
| 2020 |
Das S, Maji S, Raj R, Bhattacharya I, Saha T, Naskar N, Gupta A. Retromer retrieves the Wilson Disease protein ATP7B from endolysosomes in a copper-dependent mode. Journal of Cell Science. PMID 33268466 DOI: 10.1242/jcs.246819 |
0.344 |
|
| 2019 |
Purkait K, Ruturaj, Mukherjee A, Gupta A. ATP7B Binds Ruthenium(II) -Cymene Half-Sandwich Complexes: Role of Steric Hindrance and Ru-I Coordination in Rescuing the Sequestration. Inorganic Chemistry. PMID 31657924 DOI: 10.1021/Acs.Inorgchem.9B02780 |
0.308 |
|
| 2018 |
Gupta A, Das S, Ray K. A glimpse into the regulation of the Wilson disease protein, ATP7B, sheds light on the complexity of mammalian apical trafficking pathways. Metallomics : Integrated Biometal Science. PMID 29473088 DOI: 10.1039/C7Mt00314E |
0.413 |
|
| 2016 |
Biswas S, Sengupta S, Roy Chowdhury S, Jana S, Mandal G, Mandal PK, Saha N, Malhotra V, Gupta A, Kuprash DV, Bhattacharyya A. Erratum to: CXCL13-CXCR5 co-expression regulates epithelial to mesenchymal transition of breast cancer cells during lymph node metastasis. Breast Cancer Research and Treatment. PMID 26886560 DOI: 10.1007/S10549-016-3713-3 |
0.303 |
|
| 2016 |
Gupta A, Schell MJ, Bhattacharjee A, Lutsenko S, Hubbard AL. Myosin Vb mediates copper export in polarized hepatocytes. Journal of Cell Science. PMID 26823605 DOI: 10.1242/Jcs.175307 |
0.596 |
|
| 2015 |
Gupta A. Low-density oligonucleotide microarrays - A major step in Wilson's disease diagnosis. The Indian Journal of Medical Research. 141: 145-7. PMID 25900946 DOI: 10.4103/0971-5916.155534 |
0.347 |
|
| 2015 |
Braiterman LT, Gupta A, Chaerkady R, Cole RN, Hubbard AL. Communication between the N and C termini is required for copper-stimulated Ser/Thr phosphorylation of Cu(I)-ATPase (ATP7B). The Journal of Biological Chemistry. 290: 8803-19. PMID 25666620 DOI: 10.1074/Jbc.M114.627414 |
0.594 |
|
| 2014 |
Gupta A, Bhattacharjee A, Hasan N, Braiterman L, Lutsenko S, Hubbard AL. Genetic, metabolic and cellular factors influencing intracellular localization of the Wilson disease protein, ATP7B Molecular Cytogenetics. 7: P68. DOI: 10.1186/1755-8166-7-S1-P68 |
0.608 |
|
| 2012 |
Gupta A, Lutsenko S. Evolution of copper transporting ATPases in eukaryotic organisms. Current Genomics. 13: 124-33. PMID 23024604 DOI: 10.2174/138920212799860661 |
0.406 |
|
| 2012 |
Hasan NM, Gupta A, Polishchuk E, Yu CH, Polishchuk R, Dmitriev OY, Lutsenko S. Molecular events initiating exit of a copper-transporting ATPase ATP7B from the trans-Golgi network. The Journal of Biological Chemistry. 287: 36041-50. PMID 22898812 DOI: 10.1074/Jbc.M112.370403 |
0.408 |
|
| 2011 |
Gupta A, Bhattacharjee A, Dmitriev OY, Nokhrin S, Braiterman L, Hubbard AL, Lutsenko S. Cellular copper levels determine the phenotype of the Arg875 variant of ATP7B/Wilson disease protein. Proceedings of the National Academy of Sciences of the United States of America. 108: 5390-5. PMID 21406592 DOI: 10.1073/Pnas.1014959108 |
0.631 |
|
| 2010 |
Gupta A, Chattopadhyay I, Mukherjee S, Sengupta M, Das SK, Ray K. A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient. Behavioral and Brain Functions : Bbf. 6: 33. PMID 20550661 DOI: 10.1186/1744-9081-6-33 |
0.377 |
|
| 2009 |
Gupta A, Lutsenko S. Human copper transporters: mechanism, role in human diseases and therapeutic potential. Future Medicinal Chemistry. 1: 1125-42. PMID 20454597 DOI: 10.4155/Fmc.09.84 |
0.414 |
|
| 2009 |
Barnes N, Bartee MY, Braiterman L, Gupta A, Ustiyan V, Zuzel V, Kaplan JH, Hubbard AL, Lutsenko S. Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage. Traffic (Copenhagen, Denmark). 10: 767-79. PMID 19416479 DOI: 10.1111/J.1600-0854.2009.00901.X |
0.581 |
|
| 2008 |
Lutsenko S, Gupta A, Burkhead JL, Zuzel V. Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance. Archives of Biochemistry and Biophysics. 476: 22-32. PMID 18534184 DOI: 10.1016/J.Abb.2008.05.005 |
0.405 |
|
| 2007 |
Gupta A, Chattopadhyay I, Dey S, Nasipuri P, Das SK, Gangopadhyay PK, Ray K. Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis. Cellular and Molecular Neurobiology. 27: 1023-33. PMID 17823867 DOI: 10.1007/S10571-007-9192-7 |
0.312 |
|
| 2007 |
Gupta A, Maulik M, Nasipuri P, Chattopadhyay I, Das SK, Gangopadhyay PK, Ray K. Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers. Clinical Chemistry. 53: 1601-8. PMID 17634212 DOI: 10.1373/Clinchem.2007.086066 |
0.362 |
|
| 2006 |
Gupta A, Nasipuri P, Das SK, Ray K. Simple and effective strategies for detection of allele dropout in PCR-based diagnosis of Wilson disease. Clinical Chemistry. 52: 1611-2. PMID 16873303 DOI: 10.1373/Clinchem.2006.069989 |
0.32 |
|
| 2005 |
Gupta A, Aikath D, Neogi R, Datta S, Basu K, Maity B, Trivedi R, Ray J, Das SK, Gangopadhyay PK, Ray K. Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients. Human Genetics. 118: 49-57. PMID 16133174 DOI: 10.1007/S00439-005-0007-Y |
0.363 |
|
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