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Select item 59274871.

The Spectrum of Histopathological Changes in the Renal Allograft - a 12 Months Protocol Biopsy Study

Galina Severova-Andreevska, Ladislava Grcevska, Gordana Petrushevska, Koco Cakalaroski, Aleksandar Sikole, Olivera Stojceva–Taneva, Ilina Danilovska, Ninoslav Ivanovski

Open Access Maced J Med Sci. 2018 Apr 15; 6(4): 606–612. Published online 2018 Mar 30. doi: 10.3889/oamjms.2018.162

PMCID:: PMC5927487

Abstract Article PDF–439K

Select item 44978572.

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 Confer Risk for Congenital Anomalies of the Kidney and Urinary Tract

Daw-Yang Hwang, Stefan Kohl, Xueping Fan, Asaf Vivante, Stefanie Chan, Gabriel C Dworschak, Julian Schulz, Albertien M van Eerde, Alina C Hilger, Heon Yung Gee, Tracie Pennimpede, Bernhard G Herrmann, Glenn van de Hoek, Kirsten Y Renkema, Christoph Schell, Tobias B Huber, Heiko M Reutter, Neveen A Soliman, Natasa Stajic, Radovan Bogdanovic, Elijah O Kehinde, Richard P Lifton, Velibor Tasic, Weining Lu, Friedhelm Hildebrandt

Hum Genet. Author manuscript; available in PMC 2016 Aug 1.

Published in final edited form as: Hum Genet. 2015 Aug; 134(8): 905–916. Published online 2015 May 31. doi: 10.1007/s00439-015-1570-5

PMCID:: PMC4497857

Abstract Article PDF–2.5M

Select item 3130983.

Molecular epidemiology of adhesin and hemolysin virulence factors among uropathogenic Escherichia coli.

M Arthur, C E Johnson, R H Rubin, R D Arbeit, C Campanelli, C Kim, S Steinbach, M Agarwal, R Wilkinson, R Goldstein

Infect Immun. 1989 Feb; 57(2): 303–313. doi: 10.1128/iai.57.2.303-313.1989

PMCID:: PMC313098

Summary Page Browse PDF–2.9M

Select item 18182364.

Chronic renal failure in children.

J. G. Mongeau, P. Robitaille, M. M. Grall

Can Med Assoc J. 1978 Apr 22; 118(8): 907-10, 913.

PMCID:: PMC1818236

Summary Page Browse PDF–2.1M

Select item 18527145.

Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux

Weining Lu, Albertien M. van Eerde, Xueping Fan, Fabiola Quintero-Rivera, Shashikant Kulkarni, Heather Ferguson, Hyung-Goo Kim, Yanli Fan, Qiongchao Xi, Qing-gang Li, Damien Sanlaville, William Andrews, Vasi Sundaresan, Weimin Bi, Jiong Yan, Jacques C. Giltay, Cisca Wijmenga, Tom P. V. M. de Jong, Sally A. Feather, Adrian S. Woolf, Yi Rao, James R. Lupski, Michael R. Eccles, Bradley J. Quade, James F. Gusella, Cynthia C. Morton, Richard L. Maas

Am J Hum Genet. 2007 Apr; 80(4): 616–632. Published online 2007 Feb 14. doi: 10.1086/512735

PMCID:: PMC1852714

Abstract Article PDF–1.0M

Select item 27992866.

Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux

Heather J. Cordell, Rebecca Darlay, Pimphen Charoen, Aisling Stewart, Ambrose M. Gullett, Heather J. Lambert, Sue Malcolm, Sally A. Feather, Timothy H.J. Goodship, Adrian S. Woolf, Rajko B. Kenda, Judith A. Goodship, for the UK VUR Study Group

J Am Soc Nephrol. 2010 Jan; 21(1): 113–123. doi: 10.1681/ASN.2009060624

PMCID:: PMC2799286

Abstract Article

Select item 28385887.

Angiotensin II AT₂ receptor regulates ureteric bud morphogenesis

Renfang Song, Melissa Spera, Colleen Garrett, Samir S. El-Dahr, Ihor V. Yosypiv

Am J Physiol Renal Physiol. 2010 Mar; 298(3): F807–F817. Published online 2009 Dec 23. doi: 10.1152/ajprenal.00147.2009

PMCID:: PMC2838588

Abstract Article

Select item 30058988.

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype

Sally H. Cross, Lisa McKie, Katrine West, Emma L. Coghill, Jack Favor, Shoumo Bhattacharya, Steve D.M. Brown, Ian J. Jackson

Hum Mol Genet. 2011 Jan 15; 20(2): 223–234. Published online 2010 Oct 13. doi: 10.1093/hmg/ddq457

PMCID:: PMC3005898

Abstract Article PDF–486K

Select item 33387439.

Genes in the Ureteric Budding Pathway: Association Study on Vesico-Ureteral Reflux Patients

Albertien M. van Eerde, Karen Duran, Els van Riel, Carolien G. F. de Kovel, Bobby P. C. Koeleman, Nine V. A. M. Knoers, Kirsten Y. Renkema, Henricus J. R. van der Horst, Arend Bökenkamp, Johanna M. van Hagen, Leonard H. van den Berg, Katja P. Wolffenbuttel, Joop van den Hoek, Wouter F. Feitz, Tom P. V. M. de Jong, Jacques C. Giltay, Cisca Wijmenga

PLoS One. 2012; 7(4): e31327. Published online 2012 Apr 27. doi: 10.1371/journal.pone.0031327

PMCID:: PMC3338743

Abstract Article PDF–161K

Select item 356707310.

Deletion of Fibroblast Growth Factor Receptor 2 from the Peri-Wolffian Duct Stroma Leads to Ureteric Induction Abnormalities and Vesicoureteral Reflux

Kenneth A. Walker, Sunder Sims-Lucas, Valeria E. Di Giovanni, Caitlin Schaefer, Whitney M. Sunseri, Tatiana Novitskaya, Mark P. de Caestecker, Feng Chen, Carlton M. Bates

PLoS One. 2013; 8(2): e56062. Published online 2013 Feb 7. doi: 10.1371/journal.pone.0056062

Correction in:: PLoS One. 2016; 11(11): e0167191.

PMCID:: PMC3567073

Abstract Article PDF–1.3M

Select item 365770411.

High incidence of vesico-ureteral reflux in mice with deletion of fibroblast growth factor receptor 2 in kidney mesenchyme

David S. Hains, Sunder Sims-Lucas, Ashley Carpenter, Monalee Saha, Inga Murawski, Kayle Kish, Indra Gupta, Kirk McHugh, Carlton M. Bates

J Urol. Author manuscript; available in PMC 2013 May 20.

Published in final edited form as: J Urol. 2010 May; 183(5): 2077–2084. Published online 2010 Mar 19. doi: 10.1016/j.juro.2009.12.095

PMCID:: PMC3657704

Abstract Article PDF–1.6M

Select item 404014812.

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

Daw-Yang Hwang, Gabriel C. Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C. Hilger, Heiko M. Reutter, Neveen A. Soliman, Radovan Bogdanovic, Elijah O. Kehinde, Velibor Tasic, Friedhelm Hildebrandt

Kidney Int. Author manuscript; available in PMC 2014 Dec 1.

Published in final edited form as: Kidney Int. 2014 Jun; 85(6): 1429–1433. Published online 2014 Jan 15. doi: 10.1038/ki.2013.508

PMCID:: PMC4040148

Abstract Article PDF–305K

Select item 968356213.

Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux

Zsuzsa I. Bartik, Ulla Sillén, Anna Djos, Anna Lindholm, Susanne Fransson

PLoS One. 2022; 17(11): e0277524. Published online 2022 Nov 23. doi: 10.1371/journal.pone.0277524

PMCID:: PMC9683562

Abstract Article PDF–1.8M

Select item 472164514.

Wnt5a Deficiency Leads to Anomalies in Ureteric Tree Development, Tubular Epithelial Cell Organization and Basement Membrane Integrity Pointing to a Role in Kidney Collecting Duct Patterning

Ilkka Pietilä, Renata Prunskaite-Hyyryläinen, Susanna Kaisto, Elisavet Tika, Albertien M. van Eerde, Antti M. Salo, Leonardo Garma, Ilkka Miinalainen, Wout F. Feitz, Ernie M. H. F. Bongers, André Juffer, Nine V. A. M. Knoers, Kirsten Y. Renkema, Johanna Myllyharju, Seppo J. Vainio

PLoS One. 2016; 11(1): e0147171. Published online 2016 Jan 21. doi: 10.1371/journal.pone.0147171

PMCID:: PMC4721645

Abstract Article PDF–5.2M

Select item 474710815.

RARE VARIANTS IN TENASCIN GENES IN A COHORT OF CHILDREN WITH PRIMARY VESICOURETERIC REFLUX

Shan Elahi, Alison Homstad, Himani Vaidya, Jennifer Stout, Gentzon Hall, Guanghong Wu, Peter Conlon, jr, Jonathan C. Routh, John S. Wiener, Sherry S. Ross, Shashi Nagaraj, Delbert Wigfall, John Foreman, Adebowale Adeyemo, Indra R. Gupta, Patrick D. Brophy, C. Egla Rabinovich, Rasheed A. Gbadegesin

Pediatr Nephrol. Author manuscript; available in PMC 2016 May 1.

Published in final edited form as: Pediatr Nephrol. 2016 Feb; 31(2): 247–253. Published online 2015 Sep 25. doi: 10.1007/s00467-015-3203-6

PMCID:: PMC4747108

Abstract Article PDF–655K

Select item 496238316.

New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon

Jialu Liu, Li Sun, Qian Shen, Xiaohui Wu, Hong Xu

BMC Nephrol. 2016; 17: 98. Published online 2016 Jul 26. doi: 10.1186/s12882-016-0308-5

PMCID:: PMC4962383

Abstract Article PDF–3.0M

Select item 532169217.

Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux

Marcin Życzkowski, Joanna Żywiec, Krzysztof Nowakowski, Andrzej Paradysz, Władyslaw Grzeszczak, Janusz Gumprecht

Int Urol Nephrol. 2017; 49(3): 387–397. Published online 2016 Dec 17. doi: 10.1007/s11255-016-1483-9

PMCID:: PMC5321692

Abstract Article PDF–492K

Select item 639092518.

Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS

Tony Yao, Khalil Udwan, Rohan John, Akanchaya Rana, Amirreza Haghighi, Lizhen Xu, Saidah Hack, Heather N. Reich, Michelle Adrienne Hladunewich, Daniel C. Cattran, Andrew D. Paterson, York Pei, Moumita Barua

Clin J Am Soc Nephrol. 2019 Feb 7; 14(2): 213–223. Published online 2019 Jan 15. doi: 10.2215/CJN.08750718

PMCID:: PMC6390925

Abstract Article

Select item 767618819.

Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing

Xiaoyan Zhou, Yan Wang, Binbin Shao, Chen Wang, Ping Hu, Fengchang Qiao, Zhengfeng Xu

J Clin Lab Anal. 2020 Nov; 34(11): e23480. Published online 2020 Aug 11. doi: 10.1002/jcla.23480

PMCID:: PMC7676188

Abstract Article PDF–296K

Select item 778487420.

Rare heterozygous GDF6 variants in patients with renal anomalies

Helge Martens, Imke Hennies, Maike Getwan, Anne Christians, Anna-Carina Weiss, Frank Brand, Ann Christin Gjerstad, Arne Christians, Zoran Gucev, Robert Geffers, Tomáš Seeman, Andreas Kispert, Velibor Tasic, Anna Bjerre, Soeren S. Lienkamp, Dieter Haffner, Ruthild G. Weber

Eur J Hum Genet. 2020 Dec; 28(12): 1681–1693. Published online 2020 Jul 31. doi: 10.1038/s41431-020-0678-9

PMCID:: PMC7784874

Abstract Article PDF–10M

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