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Items: 1 to 20 of 47

1.

Children with vesico-ureteric reflux have joint hypermobility and occasional TNXB sequence variants.

Tokhmafshan F, El Andalousi J, Murugapoopathy V, Fillion ML, Campillo S, Capolicchio JP, Jednak R, El Sherbiny M, Turpin S, Schalkwijk J, Matsumoto KI, Brophy PD, Gbadegesin RA, Gupta IR.

Can Urol Assoc J. 2019 Nov 5. doi: 10.5489/cuaj.6068. [Epub ahead of print]

PMID:
31702543
2.

Temporal Effects of Quercetin on Tight Junction Barrier Properties and Claudin Expression and Localization in MDCK II Cells.

Gamero-Estevez E, Andonian S, Jean-Claude B, Gupta I, Ryan AK.

Int J Mol Sci. 2019 Oct 2;20(19). pii: E4889. doi: 10.3390/ijms20194889.

3.

Regulatory interaction between the ZPBP2-ORMDL3/Zpbp2-Ormdl3 region and the circadian clock.

Chang ML, Moussette S, Gamero-Estevez E, Gálvez JH, Chiwara V, Gupta IR, Ryan AK, Naumova AK.

PLoS One. 2019 Sep 27;14(9):e0223212. doi: 10.1371/journal.pone.0223212. eCollection 2019.

4.

The pathogenesis and management of renal scarring in children with vesicoureteric reflux and pyelonephritis.

Murugapoopathy V, McCusker C, Gupta IR.

Pediatr Nephrol. 2020 Mar;35(3):349-357. doi: 10.1007/s00467-018-4187-9. Epub 2019 Mar 7. Review.

PMID:
30847554
5.

Recessive mutation in CD2AP causes focal segmental glomerulosclerosis in humans and mice.

Takano T, Bareke E, Takeda N, Aoudjit L, Baldwin C, Pisano P, Matsuda J, El Andalousi J, Muhtadie L, Bernard C, Majewski J, Miyazaki T, Yamamura KI, Gupta IR.

Kidney Int. 2019 Jan;95(1):57-61. doi: 10.1016/j.kint.2018.08.014. Epub 2018 Oct 26.

PMID:
30612599
6.

Acute and Chronic Management in an Atypical Case of Ethylmalonic Encephalopathy.

Kitzler TM, Gupta IR, Osterman B, Poulin C, Trakadis Y, Waters PJ, Buhas DC.

JIMD Rep. 2019;45:57-63. doi: 10.1007/8904_2018_136. Epub 2018 Oct 23.

7.

Renal tubular dysgenesis and microcolon, a novel association. Report of three cases.

Saskin A, Alfares A, Bernard C, Blumenkrantz M, Braverman N, Gupta I, Brosnihan KB, Antignac C, Gubler MC, Morinière V, De Bie I, Bitzan M.

Eur J Med Genet. 2019 Apr;62(4):254-258. doi: 10.1016/j.ejmg.2018.07.024. Epub 2018 Jul 31.

PMID:
30071301
8.

Claudins in morphogenesis: Forming an epithelial tube.

Baumholtz AI, Gupta IR, Ryan AK.

Tissue Barriers. 2017 Oct 2;5(4):e1361899. doi: 10.1080/21688370.2017.1361899. Epub 2017 Aug 24. Review.

9.

Heterozygous loss-of-function mutation in Odd-skipped related 1 (Osr1) is associated with vesicoureteric reflux, duplex systems, and hydronephrosis.

Fillion ML, El Andalousi J, Tokhmafshan F, Murugapoopathy V, Watt CL, Murawski IJ, Capolicchio JP, El-Sherbiny M, Jednak R, Gupta IR.

Am J Physiol Renal Physiol. 2017 Nov 1;313(5):F1106-F1115. doi: 10.1152/ajprenal.00107.2017. Epub 2017 Jul 19.

10.

Rac1 activation in podocytes induces the spectrum of nephrotic syndrome.

Robins R, Baldwin C, Aoudjit L, Côté JF, Gupta IR, Takano T.

Kidney Int. 2017 Aug;92(2):349-364. doi: 10.1016/j.kint.2017.03.010. Epub 2017 May 6.

PMID:
28483380
11.

Donor Quality in the Eye of the Beholder: Interactions between Nonimmunologic Recipient and Donor Factors as Determinants of Graft Survival.

Foster BJ, Gupta IR.

Clin J Am Soc Nephrol. 2017 Apr 3;12(4):565-567. doi: 10.2215/CJN.02180217. Epub 2017 Mar 30. No abstract available.

12.

Vesicoureteral reflux and the extracellular matrix connection.

Tokhmafshan F, Brophy PD, Gbadegesin RA, Gupta IR.

Pediatr Nephrol. 2017 Apr;32(4):565-576. doi: 10.1007/s00467-016-3386-5. Epub 2016 May 2. Review.

13.

Disease-causing mutations of RhoGDIα induce Rac1 hyperactivation in podocytes.

Auguste D, Maier M, Baldwin C, Aoudjit L, Robins R, Gupta IR, Takano T.

Small GTPases. 2016 Apr 2;7(2):107-21. doi: 10.1080/21541248.2015.1113353. Epub 2016 Jan 4.

14.

Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.

Elahi S, Homstad A, Vaidya H, Stout J, Hall G, Wu G, Conlon P Jr, Routh JC, Wiener JS, Ross SS, Nagaraj S, Wigfall D, Foreman J, Adeyemo A, Gupta IR, Brophy PD, Rabinovich CE, Gbadegesin RA.

Pediatr Nephrol. 2016 Feb;31(2):247-53. doi: 10.1007/s00467-015-3203-6. Epub 2015 Sep 25.

15.

Claudin-7, -16, and -19 during mouse kidney development.

Khairallah H, El Andalousi J, Simard A, Haddad N, Chen YH, Hou J, Ryan AK, Gupta IR.

Tissue Barriers. 2014 Aug 8;2(4):e964547. doi: 10.4161/21688362.2014.964547. eCollection 2014.

16.

Loss of Rho-GDIα sensitizes podocytes to lipopolysaccharide-mediated injury.

Robins R, Baldwin C, Aoudjit L, Gupta IR, Takano T.

Am J Physiol Renal Physiol. 2015 Jun 1;308(11):F1207-16. doi: 10.1152/ajprenal.00225.2014. Epub 2014 Dec 10.

17.

Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.

Fillion ML, Watt CL, Gupta IR.

Pediatr Nephrol. 2014 Apr;29(4):757-66. doi: 10.1007/s00467-014-2761-3. Epub 2014 Feb 6. Review.

PMID:
24500705
18.

Segmentation, feature extraction, and multiclass brain tumor classification.

Sachdeva J, Kumar V, Gupta I, Khandelwal N, Ahuja CK.

J Digit Imaging. 2013 Dec;26(6):1141-50. doi: 10.1007/s10278-013-9600-0.

19.

TNXB mutations can cause vesicoureteral reflux.

Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP.

J Am Soc Nephrol. 2013 Jul;24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25.

20.

A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

El Andalousi J, Murawski IJ, Capolicchio JP, El-Sherbiny M, Jednak R, Gupta IR.

Pediatr Nephrol. 2013 Sep;28(9):1813-9. doi: 10.1007/s00467-013-2440-9. Epub 2013 Mar 26.

PMID:
23529638

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