| 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 |
0.724 |
|
| 2019 |
Tokhmafshan F, Dickinson K, Akpa MM, Brasell E, Huertas P, Goodyer PR. A no-nonsense approach to hereditary kidney disease. Pediatric Nephrology (Berlin, Germany). PMID 31807928 DOI: 10.1007/s00467-019-04394-5 |
0.326 |
|
| 2019 |
Brasell EJ, Chu LL, Akpa MM, Eshkar-Oren I, Alroy I, Corsini R, Gilfix BM, Yamanaka Y, Huertas P, Goodyer P. The novel aminoglycoside, ELX-02, permits CTNSW138X translational read-through and restores lysosomal cystine efflux in cystinosis. Plos One. 14: e0223954. PMID 31800572 DOI: 10.1371/Journal.Pone.0223954 |
0.493 |
|
| 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 |
0.664 |
|
| 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 |
0.7 |
|
| 2019 |
Dickinson KK, Hammond LC, Karner CM, Hastie ND, Carroll TJ, Goodyer P. Molecular determinants of WNT9b responsiveness in nephron progenitor cells. Plos One. 14: e0215139. PMID 30978219 DOI: 10.1371/Journal.Pone.0215139 |
0.305 |
|
| 2018 |
Brasell EJ, Chu L, El Kares R, Seo JH, Loesch R, Iglesias DM, Goodyer P. The aminoglycoside geneticin permits translational readthrough of the CTNS W138X nonsense mutation in fibroblasts from patients with nephropathic cystinosis. Pediatric Nephrology (Berlin, Germany). PMID 30413946 DOI: 10.1007/S00467-018-4094-0 |
0.48 |
|
| 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 |
0.68 |
|
| 2016 |
Langman CB, Barshop BA, Deschênes G, Emma F, Goodyer P, Lipkin G, Midgley JP, Ottolenghi C, Servais A, Soliman NA, Thoene JG, Levtchenko EN. Controversies and research agenda in nephropathic cystinosis: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference. Kidney International. 89: 1192-203. PMID 27181776 DOI: 10.1016/J.Kint.2016.01.033 |
0.393 |
|
| 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 |
0.718 |
|
| 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 |
0.668 |
|
| 2015 |
Zhang Z, Iglesias DM, Corsini R, Chu L, Goodyer P. WNT/β-Catenin Signaling Is Required for Integration of CD24+ Renal Progenitor Cells into Glycerol-Damaged Adult Renal Tubules. Stem Cells International. 2015: 391043. PMID 26089915 DOI: 10.1155/2015/391043 |
0.354 |
|
| 2014 |
Emma F, Nesterova G, Langman C, Labbé A, Cherqui S, Goodyer P, Janssen MC, Greco M, Topaloglu R, Elenberg E, Dohil R, Trauner D, Antignac C, Cochat P, Kaskel F, et al. Nephropathic cystinosis: an international consensus document. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 29: iv87-94. PMID 25165189 DOI: 10.1093/Ndt/Gfu090 |
0.402 |
|
| 2014 |
Iglesias DM, Akpa MM, Goodyer P. Priming the renal progenitor cell. Pediatric Nephrology (Berlin, Germany). 29: 705-10. PMID 24414605 DOI: 10.1007/S00467-013-2685-3 |
0.379 |
|
| 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 |
0.72 |
|
| 2013 |
Wu MK, Sabbaghian N, Xu B, Addidou-Kalucki S, Bernard C, Zou D, Reeve AE, Eccles MR, Cole C, Choong CS, Charles A, Tan TY, Iglesias DM, Goodyer PR, Foulkes WD. Biallelic DICER1 mutations occur in Wilms tumours. The Journal of Pathology. 230: 154-64. PMID 23620094 DOI: 10.1002/Path.4196 |
0.341 |
|
| 2012 |
Iglesias DM, El-Kares R, Taranta A, Bellomo F, Emma F, Besouw M, Levtchenko E, Toelen J, van den Heuvel L, Chu L, Zhao J, Young YK, Eliopoulos N, Goodyer P. Stem cell microvesicles transfer cystinosin to human cystinotic cells and reduce cystine accumulation in vitro. Plos One. 7: e42840. PMID 22912749 DOI: 10.1371/Journal.Pone.0042840 |
0.339 |
|
| 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 |
0.688 |
|
| 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 |
0.727 |
|
| 2012 |
Grouls S, Iglesias DM, Wentzensen N, Moeller MJ, Bouchard M, Kemler R, Goodyer P, Niggli F, Gröne HJ, Kriz W, Koesters R. Lineage specification of parietal epithelial cells requires β-catenin/Wnt signaling Journal of the American Society of Nephrology. 23: 63-72. PMID 22021707 DOI: 10.1681/Asn.2010121257 |
0.368 |
|
| 2011 |
Goodyer P. The history of cystinosis: lessons for clinical management. International Journal of Nephrology. 2011: 929456. PMID 22013525 DOI: 10.4061/2011/929456 |
0.344 |
|
| 2011 |
Zhang Z, Iglesias D, Eliopoulos N, El Kares R, Chu L, Romagnani P, Goodyer P. A variant OSR1 allele which disturbs OSR1 mRNA expression in renal progenitor cells is associated with reduction of newborn kidney size and function. Human Molecular Genetics. 20: 4167-74. PMID 21821672 DOI: 10.1093/Hmg/Ddr341 |
0.378 |
|
| 2011 |
Midgley JP, El-Kares R, Mathieu F, Goodyer P. Natural history of adolescent-onset cystinosis. Pediatric Nephrology (Berlin, Germany). 26: 1335-7. PMID 21553323 DOI: 10.1007/S00467-011-1904-Z |
0.391 |
|
| 2011 |
Miller MM, Iglesias DM, Zhang Z, Corsini R, Chu L, Murawski I, Gupta I, Somlo S, Germino GG, Goodyer PR. T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney disease. Kidney International. 80: 146-53. PMID 21389971 DOI: 10.1038/Ki.2011.56 |
0.309 |
|
| 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 |
0.73 |
|
| 2010 |
El Kares R, Manolescu DC, Lakhal-Chaieb L, Montpetit A, Zhang Z, Bhat PV, Goodyer P. A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. Kidney International. 78: 96-102. PMID 20375987 DOI: 10.1038/Ki.2010.101 |
0.381 |
|
| 2010 |
Zhang Z, Pascuet E, Hueber PA, Chu L, Bichet DG, Lee TC, Threadgill DW, Goodyer P. Targeted inactivation of EGF receptor inhibits renal collecting duct development and function. Journal of the American Society of Nephrology : Jasn. 21: 573-8. PMID 20133479 DOI: 10.1681/Asn.2009070719 |
0.42 |
|
| 2009 |
Mauer M, Zinman B, Gardiner R, Suissa S, Sinaiko A, Strand T, Drummond K, Donnelly S, Goodyer P, Gubler MC, Klein R. Renal and retinal effects of enalapril and losartan in type 1 diabetes. The New England Journal of Medicine. 361: 40-51. PMID 19571282 DOI: 10.1056/Nejmoa0808400 |
0.306 |
|
| 2009 |
El-Kares R, Hueber PA, Blumenkrantz M, Iglesias D, Ma K, Jabado N, Bichet DG, Goodyer P. Wilms tumor arising in a child with X-linked nephrogenic diabetes insipidus. Pediatric Nephrology (Berlin, Germany). 24: 1313-9. PMID 19294427 DOI: 10.1007/S00467-009-1147-4 |
0.382 |
|
| 2009 |
Zhang Z, Quinlan J, Grote D, Lemire M, Hudson T, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Houghton F, Bouchard M, Goodyer P. Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn. Pediatric Nephrology (Berlin, Germany). 24: 1151-7. PMID 19184120 DOI: 10.1007/S00467-008-1097-2 |
0.457 |
|
| 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 |
0.7 |
|
| 2009 |
Hueber PA, Fukuzawa R, Elkares R, Chu L, Blumentkrantz M, He SJ, Anaka MR, Reeve AE, Eccles M, Jabado N, Iglesias DM, Goodyer PR. PAX3 is expressed in the stromal compartment of the developing kidney and in Wilms tumors with myogenic phenotype. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 12: 347-54. PMID 18666806 DOI: 10.2350/08-05-0466.1 |
0.365 |
|
| 2008 |
Zhang Z, Quinlan J, Hoy W, Hughson MD, Lemire M, Hudson T, Hueber PA, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Houghton F, Bertram J, Goodyer P. A common RET variant is associated with reduced newborn kidney size and function. Journal of the American Society of Nephrology : Jasn. 19: 2027-34. PMID 18820179 DOI: 10.1681/Asn.2007101098 |
0.44 |
|
| 2008 |
Hueber PA, Iglesias D, Chu LL, Eccles M, Goodyer P. In vivo validation of PAX2 as a target for renal cancer therapy. Cancer Letters. 265: 148-55. PMID 18439754 DOI: 10.1016/J.Canlet.2008.02.016 |
0.442 |
|
| 2008 |
Donnelly S, Goodyer P, Mauer M. Comparing the automated versus manual method of needle biopsy for renal histology artefacts Nephrology Dialysis Transplantation. 23: 2098-2100. PMID 18332067 DOI: 10.1093/Ndt/Gfn061 |
0.394 |
|
| 2007 |
Quinlan J, Kaplan F, Sweezey N, Goodyer P. LGL1, a novel branching morphogen in developing kidney, is induced by retinoic acid. American Journal of Physiology. Renal Physiology. 293: F987-93. PMID 17670908 DOI: 10.1152/Ajprenal.00098.2007 |
0.356 |
|
| 2007 |
Quinlan J, Lemire M, Hudson T, Qu H, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Zhang Z, Houghton F, Goodyer P. A common variant of the PAX2 gene is associated with reduced newborn kidney size. Journal of the American Society of Nephrology : Jasn. 18: 1915-21. PMID 17513325 DOI: 10.1681/Asn.2006101107 |
0.516 |
|
| 2007 |
Cohen T, Loutochin O, Amin M, Capolicchio JP, Goodyer P, Jednak R. PAX2 is reactivated in urinary tract obstruction and partially protects collecting duct cells from programmed cell death. American Journal of Physiology. Renal Physiology. 292: F1267-73. PMID 17164400 DOI: 10.1152/Ajprenal.00281.2006 |
0.374 |
|
| 2006 |
Stayner C, Iglesias DM, Goodyer PR, Ellis L, Germino G, Zhou J, Eccles MR. Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease. Human Molecular Genetics. 15: 3520-8. PMID 17082250 DOI: 10.1093/hmg/ddl428 |
0.39 |
|
| 2006 |
Dziarmaga A, Hueber PA, Iglesias D, Hache N, Jeffs A, Gendron N, Mackenzie A, Eccles M, Goodyer P. Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2. American Journal of Physiology. Renal Physiology. 291: F913-20. PMID 16735463 DOI: 10.1152/Ajprenal.00004.2006 |
0.451 |
|
| 2006 |
Dziarmaga A, Eccles M, Goodyer P. Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice. Journal of the American Society of Nephrology : Jasn. 17: 1568-75. PMID 16672320 DOI: 10.1681/Asn.2005101074 |
0.462 |
|
| 2006 |
Hueber P-, Waters P, Clarke P, Eccles M, Goodyer P. PAX2 inactivation enhances cisplatin-induced apoptosis in renal carcinoma cells. Kidney International. 69: 1139-1145. PMID 16609680 DOI: 10.1038/Sj.Ki.5000136 |
0.435 |
|
| 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 |
0.744 |
|
| 2006 |
Dziarmaga A, Quinlan J, Goodyer P. Renal hypoplasia: lessons from Pax2. Pediatric Nephrology (Berlin, Germany). 21: 26-31. PMID 16273412 DOI: 10.1007/S00467-005-2039-X |
0.481 |
|
| 2006 |
Goodyer P. The molecular basis of cystinuria. Nephron. Experimental Nephrology. 98: e45-9. PMID 15499206 DOI: 10.1159/000080255 |
0.314 |
|
| 2005 |
Boutros M, Vicanek C, Rozen R, Goodyer P. Transient neonatal cystinuria. Kidney International. 67: 443-8. PMID 15673291 DOI: 10.1111/J.1523-1755.2005.67100.X |
0.393 |
|
| 2004 |
Clark P, Dziarmaga A, Eccles M, Goodyer P. Rescue of defective branching nephrogenesis in renal-coloboma syndrome by the caspase inhibitor, Z-VAD-fmk. Journal of the American Society of Nephrology : Jasn. 15: 299-305. PMID 14747376 DOI: 10.1097/01.Asn.0000111248.23454.19 |
0.462 |
|
| 2003 |
Discenza MT, He S, Lee TH, Chu LL, Bolon B, Goodyer P, Eccles M, Pelletier J. WT1 is a modifier of the Pax2 mutant phenotype: cooperation and interaction between WT1 and Pax2. Oncogene. 22: 8145-55. PMID 14603255 DOI: 10.1038/Sj.Onc.1206997 |
0.523 |
|
| 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 |
0.747 |
|
| 2003 |
Muratovska A, Zhou C, He S, Goodyer P, Eccles MR. Paired-Box genes are frequently expressed in cancer and often required for cancer cell survival. Oncogene. 22: 7989-97. PMID 12970747 DOI: 10.1038/Sj.Onc.1206766 |
0.371 |
|
| 2003 |
Goodyer P. Big Problems from Little Kidneys Pediatric Research. 54: 152-152. DOI: 10.1203/01.Pdr.0000082992.69946.62 |
0.325 |
|
| 2002 |
Raja KA, Schurman S, D'mello RG, Blowey D, Goodyer P, Van Why S, Ploutz-Snyder RJ, Asplin J, Scheinman SJ. Responsiveness of hypercalciuria to thiazide in Dent's disease. Journal of the American Society of Nephrology : Jasn. 13: 2938-44. PMID 12444212 DOI: 10.1097/01.Asn.0000036869.82685.F6 |
0.301 |
|
| 2002 |
Parvex P, Pippi-Salle JL, Goodyer PR. Rapid loss of renal parenchyma after acute obstruction. Pediatric Nephrology (Berlin, Germany). 16: 1076-9. PMID 11793104 DOI: 10.1007/s004670100031 |
0.36 |
|
| 2000 |
Goodyer P, Langlois V, Geary D, Murray L, Champoux S, Hébert D. Polyuria and proteinuria in cystinosis have no impact on renal transplantation. A report of the North American Pediatric Renal Transplant Cooperative Study. Pediatric Nephrology. 15: 7-10. PMID 11095001 DOI: 10.1007/S004670000429 |
0.384 |
|
| 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 |
0.73 |
|
| 2000 |
Goodyer P, Boutros M, Rozen R. The molecular basis of cystinuria: An update Experimental Nephrology. 8: 123-127. PMID 10810228 DOI: 10.1159/000020659 |
0.446 |
|
| 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 |
0.765 |
|
| 1999 |
McGowan-Jordan J, Stoddard K, Podolsky L, Orrbine E, McLaine P, Town M, Goodyer P, MacKenzie A, Heick H. Molecular analysis of cystinosis: probable Irish origin of the most common French Canadian mutation. European Journal of Human Genetics : Ejhg. 7: 671-8. PMID 10482956 DOI: 10.1038/Sj.Ejhg.5200349 |
0.364 |
|
| 1999 |
Cox JP, Yamamoto K, Christie PT, Wooding C, Feest T, Flinter FA, Goodyer PR, Leumann E, Neuhaus T, Reid C, Williams PF, Wrong O, Thakker RV. Renal chloride channel, CLCN5, mutations in Dent's disease. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 14: 1536-42. PMID 10469281 DOI: 10.1359/jbmr.1999.14.9.1536 |
0.339 |
|
| 1999 |
Blydt-Hansen TD, Tenenhouse HS, Goodyer P. PHEX expression in parathyroid gland and parathyroid hormone dysregulation in X-linked hypophosphatemia. Pediatric Nephrology (Berlin, Germany). 13: 607-11. PMID 10460513 DOI: 10.1007/S004670050669 |
0.424 |
|
| 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 |
0.697 |
|
| 1998 |
Langlois V, Bernard C, Scheinman SJ, Thakker RV, Cox JP, Goodyer PR. Clinical features of X-linked nephrolithiasis in childhood. Pediatric Nephrology (Berlin, Germany). 12: 625-9. PMID 9811383 DOI: 10.1007/s004670050516 |
0.362 |
|
| 1998 |
Hoopes RR, Hueber PA, Reid RJ, Braden GL, Goodyer PR, Melnyk AR, Midgley JP, Moel DI, Neu AM, VanWhy SK, Scheinman SJ. CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis. Kidney International. 54: 698-705. PMID 9734595 DOI: 10.1046/J.1523-1755.1998.00061.X |
0.308 |
|
| 1998 |
Goodyer P, Saadi I, Ong P, Elkas G, Rozen R. Cystinuria subtype and the risk of nephrolithiasis. Kidney International. 54: 56-61. PMID 9648063 DOI: 10.1046/J.1523-1755.1998.00957.X |
0.307 |
|
| 1998 |
Saadi I, Chen XZ, Hediger M, Ong P, Pereira P, Goodyer P, Rozen R. Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotype. Kidney International. 54: 48-55. PMID 9648062 DOI: 10.1046/J.1523-1755.1998.00956.X |
0.402 |
|
| 1998 |
Torban E, Goodyer P. What PAX genes do in the kidney. Experimental Nephrology. 6: 7-11. PMID 9523167 DOI: 10.1159/000020498 |
0.751 |
|
| 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 |
0.723 |
|
| 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 |
0.691 |
|
| 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 |
0.735 |
|
| 1996 |
Lloyd SE, Pearce SH, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SP, Wrong O, Jentsch TJ, Craig IW, Thakker RV. A common molecular basis for three inherited kidney stone diseases. Nature. 379: 445-9. PMID 8559248 DOI: 10.1038/379445A0 |
0.477 |
|
| 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 |
0.663 |
|
| 1991 |
Goodyer PR, Mulligan L, Goodyer CG. Expression of growth-related genes in human fetal kidney. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 17: 608-10. PMID 2042631 DOI: 10.1016/S0272-6386(12)80331-3 |
0.31 |
|
| 1986 |
Jequier S, Cramer B, Goodyer P, Kronick J, Reade T. Renal ultrasound in metabolic bone disease. Pediatric Radiology. 16: 135-139. PMID 3513110 DOI: 10.1007/Bf02386638 |
0.36 |
|
| 1984 |
Kronick J, Goodyer P, Jequier S, Reade T. Ultrasound Diagnosis Of Nephrocalcinosis During Treatment Of Hereditary Rickets Pediatric Research. 18: 364-364. DOI: 10.1203/00006450-198404001-01626 |
0.323 |
|
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