| Year |
Citation |
Score |
| 2023 |
Torban E, Goodyer P. Wilms Tumor Gene 1: Lessons from Kidney Development and Cancer. American Journal of Physiology. Renal Physiology. PMID 37916284 DOI: 10.1152/ajprenal.00248.2023 |
0.657 |
|
| 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 |
0.446 |
|
| 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 |
0.373 |
|
| 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 |
0.488 |
|
| 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 |
0.594 |
|
| 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 |
0.624 |
|
| 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 |
0.617 |
|
| 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 |
0.395 |
|
| 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 |
0.415 |
|
| 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 |
0.66 |
|
| 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 |
0.612 |
|
| 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 |
0.313 |
|
| 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 |
0.36 |
|
| 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 |
0.457 |
|
| 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 |
0.412 |
|
| 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 |
0.637 |
|
| 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 |
0.415 |
|
| 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 |
0.61 |
|
| 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 |
0.658 |
|
| 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 |
0.404 |
|
| 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 |
0.666 |
|
| 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 |
0.625 |
|
| 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 |
0.402 |
|
| 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 |
0.377 |
|
| 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 |
0.691 |
|
| 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 |
0.324 |
|
| 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 |
0.4 |
|
| 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 |
0.683 |
|
| 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 |
0.682 |
|
| 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 |
0.631 |
|
| 1998 |
Torban E, Goodyer P. What PAX genes do in the kidney. Experimental Nephrology. 6: 7-11. PMID 9523167 DOI: 10.1159/000020498 |
0.691 |
|
| 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 |
0.654 |
|
| 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 |
0.67 |
|
| 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 |
0.573 |
|
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