Lisa M. Guay-Woodford - Publications

Affiliations: 
Cell Biology University of Alabama, Birmingham, Birmingham, AL, United States 
Area:
Genetics, Cell Biology

107 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
2017 Kaimori JY, Lin CC, Outeda P, Garcia-Gonzalez MA, Menezes LF, Hartung EA, Li A, Wu G, Fujita H, Sato Y, Nakanuma Y, Yamamoto S, Ichimaru N, Takahara S, Isaka Y, ... ... Guay-Woodford LM, et al. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports. 7: 7733. PMID 28798345 DOI: 10.1038/s41598-017-08284-4  0.4
2015 Mrug M, Zhou J, Yang C, Aronow BJ, Cui X, Schoeb TR, Siegal GP, Yoder BK, Guay-Woodford LM. Genetic and Informatic Analyses Implicate Kif12 as a Candidate Gene within the Mpkd2 Locus That Modulates Renal Cystic Disease Severity in the Cys1cpk Mouse. Plos One. 10: e0135678. PMID 26295839 DOI: 10.1371/journal.pone.0135678  0.4
2015 Cramer MT, Guay-Woodford LM. Cystic Kidney Disease: A Primer. Advances in Chronic Kidney Disease. 22: 297-305. PMID 26088074 DOI: 10.1053/j.ackd.2015.04.001  0.4
2015 Kopp JB, Winkler CA, Zhao X, Radeva MK, Gassman JJ, D'Agati VD, Nast CC, Wei C, Reiser J, Guay-Woodford LM, Pollak MR, Hildebrandt F, Moxey-Mims M, Gipson DS, Trachtman H, et al. Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial. Journal of the American Society of Nephrology : Jasn. 26: 1443-8. PMID 25573908 DOI: 10.1681/ASN.2013111242  0.4
2015 Lambie L, Amin R, Essop F, Cnaan A, Krause A, Guay-Woodford LM. Clinical and genetic characterization of a founder PKHD1 mutation in Afrikaners with ARPKD. Pediatric Nephrology (Berlin, Germany). 30: 273-9. PMID 25193386 DOI: 10.1007/s00467-014-2917-1  0.4
2014 Mrug M, Zhou J, Mrug S, Guay-Woodford LM, Yoder BK, Szalai AJ. Complement C3 activation in cyst fluid and urine from autosomal dominant polycystic kidney disease patients. Journal of Internal Medicine. 276: 539-40. PMID 25205519 DOI: 10.1111/joim.12307  0.4
2014 Hartung EA, Guay-Woodford LM. Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects. Pediatrics. 134: e833-45. PMID 25113295 DOI: 10.1542/peds.2013-3646  0.4
2014 Guay-Woodford LM, Bissler JJ, Braun MC, Bockenhauer D, Cadnapaphornchai MA, Dell KM, Kerecuk L, Liebau MC, Alonso-Peclet MH, Shneider B, Emre S, Heller T, Kamath BM, Murray KF, Moise K, et al. Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference. The Journal of Pediatrics. 165: 611-7. PMID 25015577 DOI: 10.1016/j.jpeds.2014.06.015  0.4
2014 Boddu R, Yang C, O'Connor AK, Hendrickson RC, Boone B, Cui X, Garcia-Gonzalez M, Igarashi P, Onuchic LF, Germino GG, Guay-Woodford LM. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. Journal of Molecular Medicine (Berlin, Germany). 92: 1045-56. PMID 24984783 DOI: 10.1007/s00109-014-1185-7  0.4
2014 Guay-Woodford LM, Henske E, Igarashi P, Perrone RD, Reed-Gitomer B, Somlo S, Torres VE, Ketchum CJ, Star RA, Flessner MF, Rasooly RS. Filling the holes in cystic kidney disease research. Clinical Journal of the American Society of Nephrology : Cjasn. 9: 1799-801. PMID 24903391 DOI: 10.2215/CJN.03410414  0.4
2014 Hartung EA, Matheson M, Lande MB, Dell KM, Guay-Woodford LM, Gerson AC, Warady BA, Hooper SR, Furth SL. Neurocognition in children with autosomal recessive polycystic kidney disease in the CKiD cohort study. Pediatric Nephrology (Berlin, Germany). 29: 1957-65. PMID 24828609 DOI: 10.1007/s00467-014-2816-5  0.4
2014 Cramer MT, Charlton JR, Fogo AB, Fathallah-Shaykh SA, Askenazi DJ, Guay-Woodford LM. Expanding the phenotype of proteinuria in Dent disease. A case series. Pediatric Nephrology (Berlin, Germany). 29: 2051-4. PMID 24810952 DOI: 10.1007/s00467-014-2824-5  0.4
2013 Mrug M, Zhou J, Guay-Woodford LM, Smythies LE. Renal macrophages in autosomal recessive polycystic kidney disease. Nephrology (Carlton, Vic.). 18: 746. PMID 24571748 DOI: 10.1111/nep.12153  0.4
2013 Wu M, Yang C, Tao B, Bu S, Guay-Woodford LM. The ciliary protein cystin forms a regulatory complex with necdin to modulate Myc expression. Plos One. 8: e83062. PMID 24349431 DOI: 10.1371/journal.pone.0083062  0.4
2013 Gill HS, Dutcher L, Boron WF, Patel S, Guay-Woodford LM. X-ray diffraction studies on merohedrally twinned Δ1-62NtNBCe1-A crystals of the sodium/bicarbonate cotransporter. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 69: 796-9. PMID 23832211 DOI: 10.1107/S1744309113016710  0.4
2011 Raynaud P, Tate J, Callens C, Cordi S, Vandersmissen P, Carpentier R, Sempoux C, Devuyst O, Pierreux CE, Courtoy P, Dahan K, Delbecque K, Lepreux S, Pontoglio M, Guay-Woodford LM, et al. A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis. Hepatology (Baltimore, Md.). 53: 1959-66. PMID 21391226 DOI: 10.1002/hep.24292  0.4
2011 Guay-Woodford LM. Hereditary Nephropathies and Developmental Abnormalities of the Urinary Tract Goldman's Cecil Medicine: Twenty Fourth Edition. 1: 800-805. DOI: 10.1016/B978-1-4377-1604-7.00130-5  0.4
2010 Otto EA, Hurd TW, Airik R, Chaki M, Zhou W, Stoetzel C, Patil SB, Levy S, Ghosh AK, Murga-Zamalloa CA, van Reeuwijk J, Letteboer SJ, Sang L, Giles RH, Liu Q, ... ... Guay-Woodford LM, et al. Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. Nature Genetics. 42: 840-50. PMID 20835237 DOI: 10.1038/ng.662  0.4
2010 Boyer O, Benoit G, Gribouval O, Nevo F, Pawtowski A, Bilge I, Bircan Z, Deschênes G, Guay-Woodford LM, Hall M, Macher MA, Soulami K, Stefanidis CJ, Weiss R, Loirat C, et al. Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome. Journal of Medical Genetics. 47: 445-52. PMID 20591883 DOI: 10.1136/jmg.2009.076166  0.4
2010 Zhou J, Ouyang X, Cui X, Schoeb TR, Smythies LE, Johnson MR, Guay-Woodford LM, Chapman AB, Mrug M. Renal CD14 expression correlates with the progression of cystic kidney disease. Kidney International. 78: 550-60. PMID 20555320 DOI: 10.1038/ki.2010.175  0.4
2010 Gunay-Aygun M, Font-Montgomery E, Lukose L, Tuchman M, Graf J, Bryant JC, Kleta R, Garcia A, Edwards H, Piwnica-Worms K, Adams D, Bernardini I, Fischer RE, Krasnewich D, Oden N, ... ... Guay-Woodford LM, et al. Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease. Clinical Journal of the American Society of Nephrology : Cjasn. 5: 972-84. PMID 20413436 DOI: 10.2215/CJN.07141009  0.4
2010 Murawski IJ, Maina RW, Malo D, Guay-Woodford LM, Gros P, Fujiwara M, Morgan K, Gupta IR. The C3H/HeJ inbred mouse is a model of vesico-ureteric reflux with a susceptibility locus on chromosome 12. Kidney International. 78: 269-78. PMID 20407478 DOI: 10.1038/ki.2010.110  0.4
2010 Guay-Woodford LM. Other Cystic Kidney Diseases Comprehensive Clinical Nephrology. 543-559. DOI: 10.1016/B978-0-323-05876-6.00045-9  0.4
2009 Tao B, Bu S, Yang Z, Siroky B, Kappes JC, Kispert A, Guay-Woodford LM. Cystin localizes to primary cilia via membrane microdomains and a targeting motif. Journal of the American Society of Nephrology : Jasn. 20: 2570-80. PMID 19850956 DOI: 10.1681/ASN.2009020188  0.4
2009 Guay-Woodford LM, Knoers NV. Genetic testing: considerations for pediatric nephrologists. Seminars in Nephrology. 29: 338-48. PMID 19615555 DOI: 10.1016/j.semnephrol.2009.03.010  0.4
2009 Chapman AB, Guay-Woodford LM. Renal volume in children with ADPKD: size matters. Clinical Journal of the American Society of Nephrology : Cjasn. 4: 698-9. PMID 19339418 DOI: 10.2215/CJN.01410209  0.4
2009 Bae KT, Tao C, Zhu F, Bost JE, Chapman AB, Grantham JJ, Torres VE, Guay-Woodford LM, Meyers CM, Bennett WM. MRI-based kidney volume measurements in ADPKD: reliability and effect of gadolinium enhancement. Clinical Journal of the American Society of Nephrology : Cjasn. 4: 719-25. PMID 19339416 DOI: 10.2215/CJN.03750708  0.4
2009 Somlo S, Guay-Woodford LM. Polycystic Kidney Disease Genetic Diseases of the Kidney. 393-424. DOI: 10.1016/B978-0-12-449851-8.00024-3  0.4
2009 Guay-Woodford LM, Knoers NVAM. Clinical Applications of Genetics Genetic Diseases of the Kidney. 25-36. DOI: 10.1016/B978-0-12-449851-8.00002-4  0.4
2008 Chapman AB, Guay-Woodford LM. Nurturing passion in a time of academic climate change: the modern-day challenge of junior faculty development. Clinical Journal of the American Society of Nephrology : Cjasn. 3: 1878-83. PMID 18945997 DOI: 10.2215/CJN.04240808  0.4
2008 Consugar MB, Wong WC, Lundquist PA, Rossetti S, Kubly VJ, Walker DL, Rangel LJ, Aspinwall R, Niaudet WP, Ozen S, David A, Velinov M, Bergstralh EJ, Bae KT, Chapman AB, ... Guay-Woodford LM, et al. Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome. Kidney International. 74: 1468-79. PMID 18818683 DOI: 10.1038/ki.2008.485  0.4
2008 Grantham JJ, Cook LT, Torres VE, Bost JE, Chapman AB, Harris PC, Guay-Woodford LM, Bae KT. Determinants of renal volume in autosomal-dominant polycystic kidney disease. Kidney International. 73: 108-16. PMID 17960141 DOI: 10.1038/sj.ki.5002624  0.4
2008 Mrug M, Zhou J, Woo Y, Cui X, Szalai AJ, Novak J, Churchill GA, Guay-Woodford LM. Overexpression of innate immune response genes in a model of recessive polycystic kidney disease Kidney International. 73: 63-76. PMID 17960140 DOI: 10.1038/sj.ki.5002627  0.4
2008 Bae KT, Commean PK, Brunsden BS, Baumgarten DA, King BF, Wetzel LH, Kenney PJ, Chapman AB, Torres VE, Grantham JJ, Guay-Woodford LM, Tao C, Miller JP, Meyers CM, Bennett WM. Segmentation and volumetric measurement of renal cysts and parenchyma from MR images of polycystic kidneys using multi-spectral analysis method Progress in Biomedical Optics and Imaging - Proceedings of Spie. 6914. DOI: 10.1117/12.770934  0.4
2008 Mrug M, Zhou J, Woo Y, Cui X, Szalai AJ, Novak J, Churchill GA, Guay-Woodford LM. Response to 'Overexpression of complement-component genes in Han:SPRD rats a model of polycystic kidney disease' Kidney International. 73: 1325. DOI: 10.1038/ki.2008.52  0.4
2007 Guay-Woodford LM. Autosomal recessive PKD in the early years. Nephrology News & Issues. 21: 39. PMID 18038751  0.4
2007 Torres VE, King BF, Chapman AB, Brummer ME, Bae KT, Glockner JF, Arya K, Risk D, Felmlee JP, Grantham JJ, Guay-Woodford LM, Bennett WM, Klahr S, Meyers CM, Zhang X, et al. Magnetic resonance measurements of renal blood flow and disease progression in autosomal dominant polycystic kidney disease. Clinical Journal of the American Society of Nephrology : Cjasn. 2: 112-20. PMID 17699395 DOI: 10.2215/CJN.00910306  0.4
2007 Rossetti S, Consugar MB, Chapman AB, Torres VE, Guay-Woodford LM, Grantham JJ, Bennett WM, Meyers CM, Walker DL, Bae K, Zhang QJ, Thompson PA, Miller JP, Harris PC. Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease. Journal of the American Society of Nephrology : Jasn. 18: 2143-60. PMID 17582161 DOI: 10.1681/ASN.2006121387  0.4
2007 Garcia-Gonzalez MA, Menezes LF, Piontek KB, Kaimori J, Huso DL, Watnick T, Onuchic LF, Guay-Woodford LM, Germino GG. Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway. Human Molecular Genetics. 16: 1940-50. PMID 17575307 DOI: 10.1093/hmg/ddm141  0.4
2007 Kaimori JY, Nagasawa Y, Menezes LF, Garcia-Gonzalez MA, Deng J, Imai E, Onuchic LF, Guay-Woodford LM, Germino GG. Polyductin undergoes notch-like processing and regulated release from primary cilia. Human Molecular Genetics. 16: 942-56. PMID 17470460 DOI: 10.1093/hmg/ddm039  0.4
2006 Bae KT, Zhu F, Chapman AB, Torres VE, Grantham JJ, Guay-Woodford LM, Baumgarten DA, King BF, Wetzel LH, Kenney PJ, Brummer ME, Bennett WM, Klahr S, Meyers CM, Zhang X, et al. Magnetic resonance imaging evaluation of hepatic cysts in early autosomal-dominant polycystic kidney disease: the Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease cohort. Clinical Journal of the American Society of Nephrology : Cjasn. 1: 64-9. PMID 17699192 DOI: 10.2215/CJN.00080605  0.4
2006 Harris PC, Bae KT, Rossetti S, Torres VE, Grantham JJ, Chapman AB, Guay-Woodford LM, King BF, Wetzel LH, Baumgarten DA, Kenney PJ, Consugar M, Klahr S, Bennett WM, Meyers CM, et al. Cyst number but not the rate of cystic growth is associated with the mutated gene in autosomal dominant polycystic kidney disease. Journal of the American Society of Nephrology : Jasn. 17: 3013-9. PMID 17035604 DOI: 10.1681/ASN.2006080835  0.4
2006 Guay-Woodford LM. Renal cystic diseases: diverse phenotypes converge on the cilium/centrosome complex. Pediatric Nephrology (Berlin, Germany). 21: 1369-76. PMID 16823577 DOI: 10.1007/s00467-006-0164-9  0.4
2006 Grantham JJ, Torres VE, Chapman AB, Guay-Woodford LM, Bae KT, King BF, Wetzel LH, Baumgarten DA, Kenney PJ, Harris PC, Klahr S, Bennett WM, Hirschman GN, Meyers CM, Zhang X, et al. Volume progression in polycystic kidney disease. The New England Journal of Medicine. 354: 2122-30. PMID 16707749 DOI: 10.1056/NEJMoa054341  0.4
2006 Siroky BJ, Guay-Woodford LM. Renal cystic disease: the role of the primary cilium/centrosome complex in pathogenesis. Advances in Chronic Kidney Disease. 13: 131-7. PMID 16580614 DOI: 10.1053/j.ackd.2006.01.021  0.4
2006 Rule AD, Torres VE, Chapman AB, Grantham JJ, Guay-Woodford LM, Bae KT, Klahr S, Bennett WM, Meyers CM, Thompson PA, Miller JP. Comparison of methods for determining renal function decline in early autosomal dominant polycystic kidney disease: the consortium of radiologic imaging studies of polycystic kidney disease cohort. Journal of the American Society of Nephrology : Jasn. 17: 854-62. PMID 16452494 DOI: 10.1681/ASN.2005070697  0.4
2006 Siroky BJ, Ferguson WB, Fuson AL, Xie Y, Fintha A, Komlosi P, Yoder BK, Schwiebert EM, Guay-Woodford LM, Bell PD. Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells. American Journal of Physiology. Renal Physiology. 290: F1320-8. PMID 16396941 DOI: 10.1152/ajprenal.00463.2005  0.4
2006 Olteanu D, Yoder BK, Liu W, Croyle MJ, Welty EA, Rosborough K, Wyss JM, Bell PD, Guay-Woodford LM, Bevensee MO, Satlin LM, Schwiebert EM. Heightened epithelial Na+ channel-mediated Na+ absorption in a murine polycystic kidney disease model epithelium lacking apical monocilia. American Journal of Physiology. Cell Physiology. 290: C952-63. PMID 16207792 DOI: 10.1152/ajpcell.00339.2005  0.4
2005 O'Neill WC, Robbin ML, Bae KT, Grantham JJ, Chapman AB, Guay-Woodford LM, Torres VE, King BF, Wetzel LH, Thompson PA, Miller JP. Sonographic assessment of the severity and progression of autosomal dominant polycystic kidney disease: the Consortium of Renal Imaging Studies in Polycystic Kidney Disease (CRISP). American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 46: 1058-64. PMID 16310571 DOI: 10.1053/j.ajkd.2005.08.026  0.4
2005 Sharp AM, Messiaen LM, Page G, Antignac C, Gubler MC, Onuchic LF, Somlo S, Germino GG, Guay-Woodford LM. Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts Journal of Medical Genetics. 42: 336-349. PMID 15805161 DOI: 10.1136/jmg.2004.024489  0.4
2005 Kleta R, Kaskel F, Dohil R, Goodyer P, Guay-Woodford LM, Harms E, Ingelfinger JR, Koch VH, Langman CB, Leonard MB, Mannon RB, Sarwal M, Schneider JA, Skovby F, Sonies BC, et al. First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and future. Pediatric Nephrology (Berlin, Germany). 20: 452-4. PMID 15747161 DOI: 10.1007/s00467-004-1777-5  0.4
2005 Mrug M, Li R, Cui X, Schoeb TR, Churchill GA, Guay-Woodford LM. Kinesin family member 12 is a candidate polycystic kidney disease modifier in the cpk mouse. Journal of the American Society of Nephrology : Jasn. 16: 905-16. PMID 15728779 DOI: 10.1681/ASN.2004121083  0.4
2004 Guay-Woodford LM. RIP-ed and ready to dance: new mechanisms for polycystin-1 signaling. The Journal of Clinical Investigation. 114: 1404-6. PMID 15545988 DOI: 10.1172/JCI23544  0.4
2004 Menezes LF, Cai Y, Nagasawa Y, Silva AM, Watkins ML, Da Silva AM, Somlo S, Guay-Woodford LM, Germino GG, Onuchic LF. Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm. Kidney International. 66: 1345-55. PMID 15458427 DOI: 10.1111/j.1523-1755.2004.00844.x  0.4
2004 Li JB, Gerdes JM, Haycraft CJ, Fan Y, Teslovich TM, May-Simera H, Li H, Blacque OE, Li L, Leitch CC, Lewis RA, Green JS, Parfrey PS, Leroux MR, Davidson WS, ... ... Guay-Woodford LM, et al. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell. 117: 541-52. PMID 15137946 DOI: 10.1016/S0092-8674(04)00450-7  0.4
2003 King BF, Torres VE, Brummer ME, Chapman AB, Bae KT, Glockner JF, Arya K, Felmlee JP, Grantham JJ, Guay-Woodford LM, Bennett WM, Klahr S, Hirschman GH, Kimmel PL, Thompson PA, et al. Magnetic resonance measurements of renal blood flow as a marker of disease severity in autosomal-dominant polycystic kidney disease. Kidney International. 64: 2214-21. PMID 14633145 DOI: 10.1046/j.1523-1755.2003.00326.x  0.4
2003 Guay-Woodford LM. Murine models of polycystic kidney disease: molecular and therapeutic insights. American Journal of Physiology. Renal Physiology. 285: F1034-49. PMID 14600027 DOI: 10.1152/ajprenal.00195.2003  0.4
2003 Chapman AB, Guay-Woodford LM, Grantham JJ, Torres VE, Bae KT, Baumgarten DA, Kenney PJ, King BF, Glockner JF, Wetzel LH, Brummer ME, O'Neill WC, Robbin ML, Bennett WM, Klahr S, et al. Renal structure in early autosomal-dominant polycystic kidney disease (ADPKD): The Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease (CRISP) cohort. Kidney International. 64: 1035-45. PMID 12911554 DOI: 10.1046/j.1523-1755.2003.00185.x  0.4
2003 Furu L, Onuchic LF, Gharavi A, Hou X, Esquivel EL, Nagasawa Y, Bergmann C, Senderek J, Avner E, Zerres K, Germino GG, Guay-Woodford LM, Somlo S. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations. Journal of the American Society of Nephrology : Jasn. 14: 2004-14. PMID 12874454 DOI: 10.1097/01.ASN.0000078805.87038.05  0.4
2003 Guay-Woodford LM, Desmond RA. Autosomal recessive polycystic kidney disease: the clinical experience in North America. Pediatrics. 111: 1072-80. PMID 12728091 DOI: 10.1542/peds.111.5.1072  0.4
2003 Cogswell C, Price SJ, Hou X, Guay-Woodford LM, Flaherty L, Bryda EC. Positional cloning of jcpk/bpk locus of the mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 242-9. PMID 12682776 DOI: 10.1007/s00335-002-2241-0  0.4
2003 Cho JT, Guay-Woodford LM. Heterozygous Mutations of The Gene for Kir 1.1 (ROMK) in Antenatal Bartter Syndrome Presenting with Transient Hyperkalemia, Evolving to a Benign Course Journal of Korean Medical Science. 18: 65-68. PMID 12589089  0.4
2003 Capisonda R, Phan V, Traubuci J, Daneman A, Balfe JW, Guay-Woodford LM. Autosomal recessive polycystic kidney disease: outcomes from a single-center experience. Pediatric Nephrology (Berlin, Germany). 18: 119-26. PMID 12579400 DOI: 10.1007/s00467-002-1021-0  0.4
2002 Price SJ, Chittenden LR, Flaherty L, O'Dell B, Guay-Woodford LM, Stubbs L, Bryda EC. Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10. Cytogenetic and Genome Research. 98: 61-6. PMID 12584442 DOI: 10.1159/000068534  0.4
2002 Guay-Woodford LM. Autosomal recessive polycystic kidney disease (ARPKD): new insights from the identification of the ARPKD gene, PKHD1. Pediatric Research. 52: 830-1. PMID 12438655 DOI: 10.1203/00006450-200212000-00002  0.4
2002 Yoder BK, Hou X, Guay-Woodford LM. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. Journal of the American Society of Nephrology : Jasn. 13: 2508-16. PMID 12239239 DOI: 10.1097/01.ASN.0000029587.47950.25  0.4
2002 Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo S, Nagasawa Y, Germino GG, Guay-Woodford LM. Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. American Journal of Medical Genetics. 110: 346-52. PMID 12116208 DOI: 10.1002/ajmg.10468  0.4
2002 Onuchic LF, Furu L, Nagasawa Y, Hou X, Eggermann T, Ren Z, Bergmann C, Senderek J, Esquivel E, Zeltner R, Rudnik-Schöneborn S, Mrug M, Sweeney W, Avner ED, Zerres K, ... Guay-Woodford LM, et al. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. American Journal of Human Genetics. 70: 1305-17. PMID 11898128 DOI: 10.1086/340448  0.4
2002 Schwiebert EM, Wallace DP, Braunstein GM, King SR, Peti-Peterdi J, Hanaoka K, Guggino WB, Guay-Woodford LM, Bell PD, Sullivan LP, Grantham JJ, Taylor AL. Autocrine extracellular purinergic signaling in epithelial cells derived from polycystic kidneys. American Journal of Physiology. Renal Physiology. 282: F763-75. PMID 11880338 DOI: 10.1152/ajprenal.0337.2000  0.4
2002 Hou X, Mrug M, Yoder BK, Lefkowitz EJ, Kremmidiotis G, D'Eustachio P, Beier DR, Guay-Woodford LM. Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. The Journal of Clinical Investigation. 109: 533-40. PMID 11854326 DOI: 10.1172/JCI14099  0.4
2001 Mrug M, Green WJ, DasGupta S, Beier DR, Lu W, D'Eustachio P, Guay-Woodford LM. An integrated genetic and physical map of the 650-kb region containing the congenital polycystic kidney (cpk) locus on mouse chromosome 12. Cytogenetics and Cell Genetics. 94: 55-61. PMID 11701955  0.4
2000 Mrug M, Stockwin J, Ẅuthrich RP, Gasser DL, Guay-Woodford LM. Mapping of mouse α1(XIII) collagen to chromosome 10 and its exclusion as a kd candidate gene Biochemical Genetics. 38: 337-340. PMID 11129527  0.4
2000 Nauta J, Goedbloed MA, Herck HV, Hesselink DA, Visser P, Willemsen R, Dokkum RP, Wright CJ, Guay-Woodford LM. New rat model that phenotypically resembles autosomal recessive polycystic kidney disease. Journal of the American Society of Nephrology : Jasn. 11: 2272-84. PMID 11095650  0.4
2000 Guay-Woodford LM, Wright CJ, Walz G, Churchill GA. Quantitative trait loci modulate renal cystic disease severity in the mouse bpk model. Journal of the American Society of Nephrology : Jasn. 11: 1253-60. PMID 10864581  0.4
2000 Vollmer M, Jeck N, Lemmink HH, Vargas R, Feldmann D, Konrad M, Beekmann F, Van Den Heuvel LPWJ, Deschenes G, Guay-Woodford LM, Antignac C, Seyberth HW, Hildebrandt F, Knoers NVAM. Antenatal Bartter syndrome with sensorineural deafness: Refinement of the locus on chromosome 1p31 Nephrology Dialysis Transplantation. 15: 970-974. PMID 10862633  0.4
2000 Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay-Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF. Genomic structure of the gene for the human p1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease European Journal of Human Genetics. 8: 163-166. PMID 10780780 DOI: 10.1038/sj.ejhg.5200426  0.4
2000 Nakanishi K, Sweeney WE, Zerres K, Guay-Woodford LM, Avner ED. Proximal tubular cysts in fetal human autosomal recessive polycystic kidney disease Journal of the American Society of Nephrology. 11: 760-763. PMID 10752536  0.4
2000 Guay-Woodford LM, Green WJ, Lindsey JR, Beier DR. Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated. Human Molecular Genetics. 9: 769-78. PMID 10749984  0.4
1999 Onuchic LF, Mrug M, Lakings AL, Muecher G, Becker J, Zerres K, Avner ED, Dixit M, Somlo S, Germino GG, Guay-Woodford LM. Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene Mammalian Genome. 10: 1175-1178. PMID 10594243 DOI: 10.1007/s003359901186  0.4
1999 Dell KM, Guay-Woodford LM. Inherited tubular transport disorders Seminars in Nephrology. 19: 364-373. PMID 10435674  0.4
1999 Guay-Woodford LM. Overview: The genetics of renal disease Seminars in Nephrology. 19: 312-318. PMID 10435669  0.4
1999 Guay-Woodford LM. Phenotypic variability in PKD1: The family as a starting point Kidney International. 56: 344-346. PMID 10411712 DOI: 10.1046/j.1523-1755.1999.00552.x  0.4
1999 Scheinman SJ, Guay-Woodford LM, Thakker RV, Warnock DG. Mechanisms of Disease: Genetic disorders of renal electrolyte transport New England Journal of Medicine. 340: 1177-1187. PMID 10202170 DOI: 10.1056/NEJM199904153401507  0.4
1998 Loh NY, Ambrose HJ, Guay-Woodford LM, DasGupta S, Nawrotzki RA, Blake DJ, Davies KE. Genomic organization and refined mapping of the mouse beta-dystrobrevin gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 857-62. PMID 9799833 DOI: 10.1007/s003359900883  0.4
1998 Lemmink HH, Knoers NVAM, Karolyi L, Van Dijk H, Niaudet P, Antignac C, Guay-Woodford LM, Goodyer PR, Carel JC, Hermes A, Seyberth HW, Monnens LAH, Van Den Heuvel LPWJ. Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C- terminal domain Kidney International. 54: 720-730. PMID 9734597 DOI: 10.1046/j.1523-1755.1998.00070.x  0.4
1998 Guay-Woodford LM. Bartter syndrome: Unraveling the pathophysiologic enigma American Journal of Medicine. 105: 151-161. PMID 9727823 DOI: 10.1016/S0002-9343(98)00196-X  0.4
1998 Guay-Woodford LM, Galliani CA, Musulman-Mroczek E, Spear GS, Guillot AP, Bernstein J. Diffuse renal cystic disease in children: morphologic and genetic correlations. Pediatric Nephrology (Berlin, Germany). 12: 173-82. PMID 9630032 DOI: 10.1007/s004670050431  0.4
1998 Vargas-Poussou R, Feldmann D, Vollmer M, Konrad M, Kelly L, Van Den Heuvel LPWJ, Tebourbi L, Brandis M, Karolyi L, Hebert SC, Lemmink HH, Deschênes G, Hildebrandt F, Seyberth HW, Guay-Woodford LM, et al. Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome American Journal of Human Genetics. 62: 1332-1340. PMID 9585600 DOI: 10.1086/301872  0.4
1998 Zerres K, Mücher G, Becker J, Steinkamm C, Rudnik-Schöneborn S, Heikkilä P, Rapola J, Salonen R, Germino GG, Onuchic L, Somlo S, Avner ED, Harman LA, Stockwin JM, Guay-Woodford LM. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology American Journal of Medical Genetics. 76: 137-144. PMID 9511976 DOI: 10.1002/(SICI)1096-8628(19980305)76:2<137::AID-AJMG6>3.0.CO;2-Q  0.4
1998 Jarolim P, Shayakul C, Prabakaran D, Jiang L, Stuart-Tilley A, Rubin HL, Simova S, Zavadil J, Herrin JT, Brouillette J, Somers MJG, Seemanova E, Brugnara C, Guay-Woodford LM, Alper SL. Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (Band 3) Cl- /HCO3/- exchanger Journal of Biological Chemistry. 273: 6380-6388. PMID 9497368 DOI: 10.1074/jbc.273.11.6380  0.4
1997 Kurtz CL, Karolyi L, Seyberth HW, Koch MC, Vargas R, Feldmann D, Vollmer M, Knoers NVAM, Madrigal G, Guay-Woodford LM. A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: Evidence for a founder effect Journal of the American Society of Nephrology. 8: 1706-1711. PMID 9355073  0.4
1997 Yiu VWY, Dluhy RP, Lifton RP, Guay-Woodford LM. Low periperal plasma renin activity as a marker in pediatric hypertension Pediatric Nephrology. 11: 343-346. PMID 9203188 DOI: 10.1007/s004670050292  0.4
1997 Madrigal G, Saborio P, Mora F, Rincon G, Guay-Woodford LM. Bartter syndrome in Costa Rica: A description of 20 cases Pediatric Nephrology. 11: 296-301. PMID 9203176 DOI: 10.1007/s004670050280  0.4
1997 Sharp CK, Bergman SM, Stockwin JM, Robbin ML, Galliani C, Guay-Woodford LM. Dominantly transmitted glomerulocystic kidney disease A distinct genetic entity Journal of the American Society of Nephrology. 8: 77-84. PMID 9013451  0.4
1997 Károlyi L, Konrad M, Köckerling A, Ziegler A, Zimmermann DK, Roth B, Wieg C, Grzeschik KH, Koch MC, Seyberth HW, Vargas R, Forestier L, Jean G, Deschaux M, Rizzoni GF, ... ... Guay-Woodford LM, et al. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity Human Molecular Genetics. 6: 17-26. PMID 9002665 DOI: 10.1093/hmg/6.1.17  0.4
1996 Guay-Woodford LM, Bryda EC, Christine B, Lindsey JR, Collier WR, Avner ED, D'Eustachio P, Flaherty L. Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Kidney International. 50: 1158-65. PMID 8887273  0.4
1995 Onuchic LF, Schrick JJ, Ma J, Hudson T, Guay-Woodford LM, Zerres K, Woychik RP, Reeders ST. Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease Mammalian Genome. 6: 805-808. PMID 8597639 DOI: 10.1007/BF00539009  0.4
1995 Guay-Woodford LM, Muecher G, Hopkins SD, Avner ED, Germino GG, Guillot AP, Herrin J, Holleman R, Irons DA, Primack W. The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling. American Journal of Human Genetics. 56: 1101-7. PMID 7726165  0.4
1995 Guay-Woodford LM. Molecular insights into the pathogenesis of inherited renal tubular disorders Current Opinion in Nephrology and Hypertension. 4: 121-129. PMID 7600042  0.4
1994 Simon EA, Cook S, Davisson MT, D'Eustachio P, Guay-Woodford LM. The mouse congenital polycystic kidney (cpk) locus maps within 1.3 cM of the chromosome 12 marker D12Nyu2 Genomics. 21: 415-418. PMID 8088836 DOI: 10.1006/geno.1994.1285  0.4
1994 Guay-Woodford LM, Bruns GAP, D'Eustachio P. Identification of a simple sequence polymorphism within the mouse locus D12Nyu2 Mammalian Genome. 5: 251-252. PMID 8012120 DOI: 10.1007/BF00360558  0.4
1994 D'Agata ID, Jonas MM, Perez-Atayde AR, Guay-Woodford LM. Combined cystic disease of the liver and kidney. Seminars in Liver Disease. 14: 215-28. PMID 7939783 DOI: 10.1055/s-2007-1007313  0.4
1994 Guay-Woodford LM, Bruns GAP, D'Eustachio P. Identification of a sequence polymorphism within the mouse locus D12Nyu2 Mammalian Genome. 5: 658. DOI: 10.1007/BF00411468  0.4
1993 Holtzman EJ, Harris HW, Kolakowski LF, Guay-Woodford LM, Botelho B, Ausiello DA. Brief report: A molecular defect in the vasopressin V2-receptor gene causing nephrogenic diabetes insipidus New England Journal of Medicine. 328: 1534-1537. PMID 8479490 DOI: 10.1056/NEJM199305273282105  0.4
1993 Lande MB, Kim MS, Bartlett C, Guay-Woodford LM. Reversible Fanconi syndrome associated with valproate therapy The Journal of Pediatrics. 123: 320-322. PMID 7688423 DOI: 10.1016/S0022-3476(05)81712-3  0.4
1991 Davisson MT, Guay-Woodford LM, Harris HW, D'Eustachio P. The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12 Genomics. 9: 778-781. PMID 2037305 DOI: 10.1016/0888-7543(91)90376-P  0.4
1991 Guay-Woodford LM, Platt O, Harris HW. Toad urinary bladder epithelial cells contain an analogue of cytoskeletal protein 4.1 American Journal of Physiology - Cell Physiology. 260. PMID 1905484  0.4
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