Elena Torban, Ph.D. - Publications

2000 McGill University, Montreal, QC, Canada 
Molecular Biology, Animal Physiology Biology

37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Wang IY, Chung CF, Babayeva S, Sogomonian T, Torban E. Loss of Planar Cell Polarity Effector Fuzzy Causes Renal Hypoplasia by Disrupting Several Signaling Pathways. Journal of Developmental Biology. 10. PMID 35076510 DOI: 10.3390/jdb10010001  0.445
2021 Torban E, Sokol SY. Planar cell polarity pathway in kidney development, function and disease. Nature Reviews. Nephrology. PMID 33547419 DOI: 10.1038/s41581-021-00395-6  0.371
2020 Derish I, Lee JKH, Wong-King-Cheong M, Babayeva S, Caplan J, Leung V, Shahinian C, Gravel M, Deans MR, Gros P, Torban E. Differential role of planar cell polarity gene Vangl2 in embryonic and adult mammalian kidneys. Plos One. 15: e0230586. PMID 32203543 DOI: 10.1371/Journal.Pone.0230586  0.486
2019 Torban E, Braun F, Wanner N, Takano T, Goodyer PR, Lennon R, Ronco P, Cybulsky AV, Huber TB. From podocyte biology to novel cures for glomerular disease. Kidney International. PMID 31420194 DOI: 10.1016/J.Kint.2019.05.015  0.596
2019 Chung CF, Kitzler T, Kachurina N, Pessina K, Babayeva S, Bitzan M, Kaskel F, Colmegna I, Alachkar N, Goodyer P, Cybulsky AV, Torban E. Intrinsic tumor necrosis factor-α pathway is activated in a subset of patients with focal segmental glomerulosclerosis. Plos One. 14: e0216426. PMID 31095586 DOI: 10.1371/Journal.Pone.0216426  0.625
2018 Kitzler TM, Kachurina N, Bitzan MM, Torban E, Goodyer PR. Use of genomic and functional analysis to characterize patients with steroid-resistant nephrotic syndrome. Pediatric Nephrology (Berlin, Germany). PMID 29982877 DOI: 10.1007/S00467-018-3995-2  0.619
2017 Cybulsky AV, Papillon J, Guillemette J, Belkina N, Patino-Lopez G, Torban E. Ste20-like Kinase, SLK, a Novel Mediator of Podocyte Integrity. American Journal of Physiology. Renal Physiology. ajprenal.00238.2017. PMID 29187370 DOI: 10.1152/Ajprenal.00238.2017  0.393
2016 Sequeira-Lopez ML, Torban E. New insights into precursors of renal endothelium. Kidney International. 90: 244-6. PMID 27418087 DOI: 10.1016/J.Kint.2016.03.043  0.416
2015 Kachurina N, Chung CF, Benderoff E, Babayeva S, Bitzan M, Goodyer PR, Kitzler T, Matar D, Cybulsky AV, Alachkar N, Torban E. NOVEL UNBIASED ASSAY FOR CIRCULATING PODOCYTE-TOXIC FACTORS ASSOCIATED WITH RECURRENT FOCAL SEGMENTAL GLOMERULOSCLEROSIS. American Journal of Physiology. Renal Physiology. ajprenal.00349.2015. PMID 26719363 DOI: 10.1152/Ajprenal.00349.2015  0.662
2015 Akpa MM, Chu LL, Thiébaut A, Jentoft I, Hammond L, Torban E, Goodyer PR. Wilms tumor suppressor, WT1, cooperates with microRNA-26a and microRNA-101 to suppress translation of the Polycomb protein, EZH2, in mesenchymal stem cells. The Journal of Biological Chemistry. PMID 26655220 DOI: 10.1074/Jbc.M115.678029  0.607
2015 Leung V, Iliescu A, Jolicoeur C, Gravel M, Apuzzo S, Torban E, Cayouette M, Gros P. The planar cell polarity protein Vangl2 is required for retinal axon guidance. Developmental Neurobiology. PMID 25990804 DOI: 10.1002/Dneu.22305  0.312
2015 Seo JH, Zilber Y, Babayeva S, Liu J, Kyriakopoulos P, De Marco P, Merello E, Capra V, Gros P, Torban E. Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans. Human Molecular Genetics. 24: 3893. PMID 25954026 DOI: 10.1093/Hmg/Ddv131  0.358
2015 Rocque BL, Babayeva S, Li J, Leung V, Nezvitsky L, Cybulsky AV, Gros P, Torban E. Deficiency of the planar cell polarity protein Vangl2 in podocytes affects glomerular morphogenesis and increases susceptibility to injury. Journal of the American Society of Nephrology : Jasn. 26: 576-86. PMID 25145929 DOI: 10.1681/Asn.2014040340  0.455
2013 Babayeva S, Rocque B, Aoudjit L, Zilber Y, Li J, Baldwin C, Kawachi H, Takano T, Torban E. Planar cell polarity pathway regulates nephrin endocytosis in developing podocytes. The Journal of Biological Chemistry. 288: 24035-48. PMID 23824190 DOI: 10.1074/Jbc.M113.452904  0.411
2013 Rink N, Bitzan M, O'Gorman G, Nagel M, Torban E, Goodyer P. Erratum to "endolymphatic sac enlargement in a girl with a novel mutation for distal renal tubular acidosis and severe deafness". Case Reports in Pediatrics. 2013: 356031. PMID 23691405 DOI: 10.1155/2013/356031  0.638
2012 Torban E, Iliescu A, Gros P. An expanding role of Vangl proteins in embryonic development. Current Topics in Developmental Biology. 101: 237-61. PMID 23140632 DOI: 10.1016/B978-0-12-394592-1.00005-3  0.412
2012 Bitzan M, Babayeva S, Vasudevan A, Goodyer P, Torban E. TNF α pathway blockade ameliorates toxic effects of FSGS plasma on podocyte cytoskeleton and β3 integrin activation Pediatric Nephrology. 27: 2217-2226. PMID 22538781 DOI: 10.1007/S00467-012-2163-3  0.612
2012 Torban E, Bitzan M, Goodyer P. Recurrent focal segmental glomerulosclerosis: a discrete clinical entity. International Journal of Nephrology. 2012: 246128. PMID 22288013 DOI: 10.1155/2012/246128  0.659
2011 Seo JH, Zilber Y, Babayeva S, Liu J, Kyriakopoulos P, De Marco P, Merello E, Capra V, Gros P, Torban E. Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans. Human Molecular Genetics. 20: 4324-33. PMID 21840926 DOI: 10.1093/Hmg/Ddr359  0.402
2011 Babayeva S, Miller M, Zilber Y, El Kares R, Bernard C, Bitzan M, Goodyer P, Torban E. Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes. Pediatric Nephrology (Berlin, Germany). 26: 1071-81. PMID 21380797 DOI: 10.1007/S00467-011-1831-Z  0.668
2011 Babayeva S, Zilber Y, Torban E. Planar cell polarity pathway regulates actin rearrangement, cell shape, motility, and nephrin distribution in podocytes. American Journal of Physiology. Renal Physiology. 300: F549-60. PMID 20534871 DOI: 10.1152/Ajprenal.00566.2009  0.404
2009 Torban E, Goodyer P. The kidney and ear: emerging parallel functions. Annual Review of Medicine. 60: 339-53. PMID 18976115 DOI: 10.1146/Annurev.Med.60.052307.120752  0.627
2008 Torban E, Patenaude AM, Leclerc S, Rakowiecki S, Gauthier S, Andelfinger G, Epstein DJ, Gros P. Genetic interaction between members of the Vangl family causes neural tube defects in mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 3449-54. PMID 18296642 DOI: 10.1073/Pnas.0712126105  0.4
2007 Kibar Z, Torban E, McDearmid JR, Reynolds A, Berghout J, Mathieu M, Kirillova I, De Marco P, Merello E, Hayes JM, Wallingford JB, Drapeau P, Capra V, Gros P. Mutations in VANGL1 associated with neural-tube defects. The New England Journal of Medicine. 356: 1432-7. PMID 17409324 DOI: 10.1056/Nejmoa060651  0.375
2007 Torban E, Wang HJ, Patenaude AM, Riccomagno M, Daniels E, Epstein D, Gros P. Tissue, cellular and sub-cellular localization of the Vangl2 protein during embryonic development: effect of the Lp mutation. Gene Expression Patterns : Gep. 7: 346-54. PMID 16962386 DOI: 10.1016/J.Modgep.2006.07.007  0.379
2006 Torban E, Dziarmaga A, Iglesias D, Chu LL, Vassilieva T, Little M, Eccles M, Discenza M, Pelletier J, Goodyer P. PAX2 activates WNT4 expression during mammalian kidney development. The Journal of Biological Chemistry. 281: 12705-12. PMID 16368682 DOI: 10.1074/Jbc.M513181200  0.69
2004 Torban E, Kor C, Gros P. Van Gogh-like2 (Strabismus) and its role in planar cell polarity and convergent extension in vertebrates. Trends in Genetics : Tig. 20: 570-7. PMID 15475117 DOI: 10.1016/J.Tig.2004.09.003  0.323
2004 Torban E, Wang HJ, Groulx N, Gros P. Independent mutations in mouse Vangl2 that cause neural tube defects in looptail mice impair interaction with members of the Dishevelled family. The Journal of Biological Chemistry. 279: 52703-13. PMID 15456783 DOI: 10.1074/Jbc.M408675200  0.398
2003 Dziarmaga A, Clark P, Stayner C, Julien JP, Torban E, Goodyer P, Eccles M. Ureteric bud apoptosis and renal hypoplasia in transgenic PAX2-Bax fetal mice mimics the renal-coloboma syndrome. Journal of the American Society of Nephrology : Jasn. 14: 2767-74. PMID 14569086 DOI: 10.1097/01.Asn.0000094082.11026.Ee  0.684
2000 Torban E, Eccles MR, Favor J, Goodyer PR. PAX2 suppresses apoptosis in renal collecting duct cells. The American Journal of Pathology. 157: 833-42. PMID 10980123 DOI: 10.1016/S0002-9440(10)64597-X  0.683
2000 Porteous S, Torban E, Cho NP, Cunliffe H, Chua L, McNoe L, Ward T, Souza C, Gus P, Giugliani R, Sato T, Yun K, Favor J, Sicotte M, Goodyer P, et al. Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice. Human Molecular Genetics. 9: 1-11. PMID 10587573 DOI: 10.1093/Hmg/9.1.1  0.705
1999 Kim J, Prawitt D, Bardeesy N, Torban E, Vicaner C, Goodyer P, Zabel B, Pelletier J. The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiation. Molecular and Cellular Biology. 19: 2289-99. PMID 10022915 DOI: 10.1128/Mcb.19.3.2289  0.628
1998 Torban E, Goodyer P. What PAX genes do in the kidney. Experimental Nephrology. 6: 7-11. PMID 9523167 DOI: 10.1159/000020498  0.689
1998 Torban E, Goodyer PR. Effects of PAX2 expression in a human fetal kidney (HEK293) cell line. Biochimica Et Biophysica Acta. 1401: 53-62. PMID 9459485  0.653
1997 Torban E, Pelletier J, Goodyer P. F329L polymorphism in the human PAX8 gene. American Journal of Medical Genetics. 72: 186-7. PMID 9382140 DOI: 10.1002/(Sici)1096-8628(19971017)72:2<186::Aid-Ajmg11>3.0.Co;2-J  0.61
1997 Vicanek C, Ferretti E, Goodyer C, Torban E, Moffett P, Pelletier J, Goodyer P. Regulation of renal EGF receptor expression is normal in Denys-Drash syndrome. Kidney International. 52: 614-9. PMID 9291179 DOI: 10.1038/Ki.1997.374  0.667
1995 Goodyer P, Dehbi M, Torban E, Bruening W, Pelletier J. Repression of the retinoic acid receptor-alpha gene by the Wilms' tumor suppressor gene product, wt1. Oncogene. 10: 1125-9. PMID 7700638  0.57
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