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1.

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasa M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simoes-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S.

Nat Genet. 2019 Apr;51(4):764. doi: 10.1038/s41588-019-0376-0.

PMID:
30816350
2.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasà M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simões-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S.

Nat Genet. 2019 Jan;51(1):117-127. doi: 10.1038/s41588-018-0281-y. Epub 2018 Dec 21. Erratum in: Nat Genet. 2019 Apr;51(4):764.

3.

The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.

Rasouly HM, Groopman EE, Heyman-Kantor R, Fasel DA, Mitrotti A, Westland R, Bier L, Weng C, Ren Z, Copeland B, Krithivasan P, Chung WK, Sanna-Cherchi S, Goldstein DB, Gharavi AG.

Ann Intern Med. 2019 Jan 1;170(1):11-21. doi: 10.7326/M18-1241. Epub 2018 Nov 27.

PMID:
30476936
4.

Genetic basis of human congenital anomalies of the kidney and urinary tract.

Sanna-Cherchi S, Westland R, Ghiggeri GM, Gharavi AG.

J Clin Invest. 2018 Jan 2;128(1):4-15. doi: 10.1172/JCI95300. Epub 2018 Jan 2. Review.

5.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

Sanna-Cherchi S, Khan K, Westland R, Krithivasan P, Fievet L, Rasouly HM, Ionita-Laza I, Capone VP, Fasel DA, Kiryluk K, Kamalakaran S, Bodria M, Otto EA, Sampson MG, Gillies CE, Vega-Warner V, Vukojevic K, Pediaditakis I, Makar GS, Mitrotti A, Verbitsky M, Martino J, Liu Q, Na YJ, Goj V, Ardissino G, Gigante M, Gesualdo L, Janezcko M, Zaniew M, Mendelsohn CL, Shril S, Hildebrandt F, van Wijk JAE, Arapovic A, Saraga M, Allegri L, Izzi C, Scolari F, Tasic V, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Mane S, Goldstein DB, Lifton RP, Katsanis N, Davis EE, Gharavi AG.

Am J Hum Genet. 2017 Dec 7;101(6):1034. doi: 10.1016/j.ajhg.2017.11.003. No abstract available.

6.

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.

Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, Rasouly H, Mitrotti A, Westland R, Verbitsky M, Nestor J, Slater LM, D'Agati V, Zaniew M, Materna-Kiryluk A, Lugani F, Caridi G, Rampoldi L, Mattoo A, Newton CA, Rao MK, Radhakrishnan J, Ahn W, Canetta PA, Bomback AS, Appel GB, Antignac C, Markowitz GS, Garcia CK, Kiryluk K, Sanna-Cherchi S, Gharavi AG.

Ann Intern Med. 2018 Jan 16;168(2):100-109. doi: 10.7326/M17-1319. Epub 2017 Dec 5. Erratum in: Ann Intern Med. 2018 Feb 20;168(4):308.

7.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

Sanna-Cherchi S, Khan K, Westland R, Krithivasan P, Fievet L, Rasouly HM, Ionita-Laza I, Capone VP, Fasel DA, Kiryluk K, Kamalakaran S, Bodria M, Otto EA, Sampson MG, Gillies CE, Vega-Warner V, Vukojevic K, Pediaditakis I, Makar GS, Mitrotti A, Verbitsky M, Martino J, Liu Q, Na YJ, Goj V, Ardissino G, Gigante M, Gesualdo L, Janezcko M, Zaniew M, Mendelsohn CL, Shril S, Hildebrandt F, van Wijk JAE, Arapovic A, Saraga M, Allegri L, Izzi C, Scolari F, Tasic V, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Mane S, Goldstein DB, Lifton RP, Katsanis N, Davis EE, Gharavi AG.

Am J Hum Genet. 2017 Nov 2;101(5):789-802. doi: 10.1016/j.ajhg.2017.09.018. Erratum in: Am J Hum Genet. 2017 Dec 7;101(6):1034.

8.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.

Lopez-Rivera E, Liu YP, Verbitsky M, Anderson BR, Capone VP, Otto EA, Yan Z, Mitrotti A, Martino J, Steers NJ, Fasel DA, Vukojevic K, Deng R, Racedo SE, Liu Q, Werth M, Westland R, Vivante A, Makar GS, Bodria M, Sampson MG, Gillies CE, Vega-Warner V, Maiorana M, Petrey DS, Honig B, Lozanovski VJ, Salomon R, Heidet L, Carpentier W, Gaillard D, Carrea A, Gesualdo L, Cusi D, Izzi C, Scolari F, van Wijk JA, Arapovic A, Saraga-Babic M, Saraga M, Kunac N, Samii A, McDonald-McGinn DM, Crowley TB, Zackai EH, Drozdz D, Miklaszewska M, Tkaczyk M, Sikora P, Szczepanska M, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Darlow JM, Puri P, Barton D, Casolari E, Furth SL, Warady BA, Gucev Z, Hakonarson H, Flogelova H, Tasic V, Latos-Bielenska A, Materna-Kiryluk A, Allegri L, Wong CS, Drummond IA, D'Agati V, Imamoto A, Barasch JM, Hildebrandt F, Kiryluk K, Lifton RP, Morrow BE, Jeanpierre C, Papaioannou VE, Ghiggeri GM, Gharavi AG, Katsanis N, Sanna-Cherchi S.

N Engl J Med. 2017 Feb 23;376(8):742-754. doi: 10.1056/NEJMoa1609009. Epub 2017 Jan 25.

9.

Long-term follow-up of blood pressure and glomerular filtration rate in patients with a solitary functioning kidney: a comparison between Wilms tumor survivors and nephrectomy for other reasons.

Mavinkurve-Groothuis AM, van de Kracht F, Westland R, van Wijk JA, Loonen JJ, Schreuder MF.

Pediatr Nephrol. 2016 Mar;31(3):435-41. doi: 10.1007/s00467-015-3215-2. Epub 2015 Oct 19.

10.

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.

Westland R, Verbitsky M, Vukojevic K, Perry BJ, Fasel DA, Zwijnenburg PJ, Bökenkamp A, Gille JJ, Saraga-Babic M, Ghiggeri GM, D'Agati VD, Schreuder MF, Gharavi AG, van Wijk JA, Sanna-Cherchi S.

Kidney Int. 2015 Dec;88(6):1402-1410. doi: 10.1038/ki.2015.239. Epub 2015 Sep 9.

11.

Ambulatory blood pressure monitoring is recommended in the clinical management of children with a solitary functioning kidney.

Westland R, Schreuder MF, van der Lof DF, Vermeulen A, Dekker-van der Meer IM, Bökenkamp A, van Wijk JA.

Pediatr Nephrol. 2014 Nov;29(11):2205-11. doi: 10.1007/s00467-014-2853-0. Epub 2014 Jun 9.

PMID:
24908323
12.

Recessive mutations in CAKUT and VACTERL association.

Westland R, Sanna-Cherchi S.

Kidney Int. 2014 Jun;85(6):1253-5. doi: 10.1038/ki.2013.495.

13.

Phenotypic expansion of DGKE-associated diseases.

Westland R, Bodria M, Carrea A, Lata S, Scolari F, Fremeaux-Bacchi V, D'Agati VD, Lifton RP, Gharavi AG, Ghiggeri GM, Sanna-Cherchi S.

J Am Soc Nephrol. 2014 Jul;25(7):1408-14. doi: 10.1681/ASN.2013080886. Epub 2014 Feb 7.

14.

Clinical implications of the solitary functioning kidney.

Westland R, Schreuder MF, van Goudoever JB, Sanna-Cherchi S, van Wijk JA.

Clin J Am Soc Nephrol. 2014 May;9(5):978-86. doi: 10.2215/CJN.08900813. Epub 2013 Dec 26. Review.

15.

Height-independent estimation of glomerular filtration rate in children: an alternative to the Schwartz equation.

Blufpand HN, Westland R, van Wijk JA, Roelandse-Koop EA, Kaspers GJ, Bökenkamp A.

J Pediatr. 2013 Dec;163(6):1722-7. doi: 10.1016/j.jpeds.2013.08.031. Epub 2013 Oct 2.

16.

Gender differences in solitary functioning kidney: do they affect renal outcome?

Westland R, Schreuder MF.

Pediatr Nephrol. 2014 Nov;29(11):2243-4. doi: 10.1007/s00467-013-2473-0. Epub 2013 Apr 11. No abstract available.

PMID:
23576193
17.

Unilateral renal agenesis: a systematic review on associated anomalies and renal injury.

Westland R, Schreuder MF, Ket JC, van Wijk JA.

Nephrol Dial Transplant. 2013 Jul;28(7):1844-55. doi: 10.1093/ndt/gft012. Epub 2013 Feb 28. Review.

PMID:
23449343
18.

Precision of estimating equations for GFR in children with a solitary functioning kidney: the KIMONO study.

Westland R, Abraham Y, Bökenkamp A, Stoffel-Wagner B, Schreuder MF, van Wijk JA.

Clin J Am Soc Nephrol. 2013 May;8(5):764-72. doi: 10.2215/CJN.07870812. Epub 2013 Jan 31.

19.

Risk factors for renal injury in children with a solitary functioning kidney.

Westland R, Kurvers RA, van Wijk JA, Schreuder MF.

Pediatrics. 2013 Feb;131(2):e478-85. doi: 10.1542/peds.2012-2088. Epub 2013 Jan 14.

PMID:
23319536
20.

Bartter syndrome type III and congenital anomalies of the kidney and urinary tract: an antenatal presentation.

Westland R, Hack WW, van der Horst HJ, Uittenbogaard LB, van Hagen JM, van der Valk P, Kamsteeg EJ, van den Heuvel LP, van Wijk JA.

Clin Nephrol. 2012 Dec;78(6):492-6.

PMID:
23164417
21.

The reason why mother nature provided us with two kidneys: the risks of a congenital solitary functioning kidney.

Westland R, van Wijk JA, Schreuder MF.

Nephrol Dial Transplant. 2012 Jun;27(6):2603-4. doi: 10.1093/ndt/gfr625. Epub 2011 Nov 5. No abstract available.

PMID:
22058171
22.

Renal injury in children with a solitary functioning kidney--the KIMONO study.

Westland R, Schreuder MF, Bökenkamp A, Spreeuwenberg MD, van Wijk JA.

Nephrol Dial Transplant. 2011 May;26(5):1533-41. doi: 10.1093/ndt/gfq844. Epub 2011 Mar 21.

PMID:
21427076
23.

Unilateral multicystic dysplastic kidney: a meta-analysis of observational studies on the incidence, associated urinary tract malformations and the contralateral kidney.

Schreuder MF, Westland R, van Wijk JA.

Nephrol Dial Transplant. 2009 Jun;24(6):1810-8. doi: 10.1093/ndt/gfn777. Epub 2009 Jan 26.

PMID:
19171687
24.

Limited beta2-adrenoceptor haplotypes display different agonist mediated airway responses in asthmatics.

van Veen A, Wierenga EA, Westland R, Weller FR, Hart GA, Jansen HM, Jonkers RE.

Respir Res. 2006 Jan 31;7:19.

25.

Limited impact of multiple 5' single-nucleotide polymorphisms on the transcriptional control of the human beta 2-adrenoceptor gene.

Westland R, van Veen A, Jansen HM, Jonkers RE, Wierenga EA.

Immunogenetics. 2004 Dec;56(9):625-30. Epub 2004 Nov 17.

PMID:
15578262
26.

A novel polymorphic GATA site in the human IL-12Rbeta2 promoter region affects transcriptional activity.

van Rietschoten JG, Westland R, van den Bogaard R, Nieste-Otter MA, van Veen A, Jonkers RE, van der Pouw Kraan TC, den Hartog MT, Wierenga EA.

Tissue Antigens. 2004 Jun;63(6):538-46.

PMID:
15140029
27.

Commensal Gram-negative bacteria prime human dendritic cells for enhanced IL-23 and IL-27 expression and enhanced Th1 development.

Smits HH, van Beelen AJ, Hessle C, Westland R, de Jong E, Soeteman E, Wold A, Wierenga EA, Kapsenberg ML.

Eur J Immunol. 2004 May;34(5):1371-80.

28.

Silencer activity of NFATc2 in the interleukin-12 receptor beta 2 proximal promoter in human T helper cells.

van Rietschoten JG, Smits HH, van de Wetering D, Westland R, Verweij CL, den Hartog MT, Wierenga EA.

J Biol Chem. 2001 Sep 14;276(37):34509-16. Epub 2001 Jul 3.

29.

Genomic organization of the human interleukin-12 receptor beta2-chain gene.

van Rietschoten JG, Smits HH, Westland R, Verweij CL, den Hartog MT, Wierenga EA.

Immunogenetics. 2000 Jan;51(1):30-6.

PMID:
10663559
30.

Gastric inhibitory polypeptide in obesity and diabetes mellitus.

Service FJ, Rizza RA, Westland RE, Hall LD, Gerich JE, Go VL.

J Clin Endocrinol Metab. 1984 Jun;58(6):1133-40.

PMID:
6373812
31.

Prandial insulin requirements in insulin-dependent diabetics: effects of size, time of day, and sequence of meals.

Service FJ, Rizza RA, Hall LD, Westland RE, O'Brien PC, Clemens AH, Haymond MW, Gerich JE.

J Clin Endocrinol Metab. 1983 Nov;57(5):931-6.

PMID:
6352728
32.

Effects of size, time of day and sequence of meal ingestion on carbohydrate tolerance in normal subjects.

Service FJ, Hall LD, Westland RE, O'Brien PC, Go VL, Haymond MW, Rizza RA.

Diabetologia. 1983 Oct;25(4):316-21.

PMID:
6357914
33.
34.

Subcutaneous versus intraperitoneal administration of insulin on post-prandial hyperglycaemia and glucose turnover in alloxan diabetic dogs.

Rizza RA, Westland RE, Hall LD, Patton G, Haymond MW, Clemens AH, Gerich JE, Service FJ.

Diabetologia. 1982 Jul;23(1):61-4.

PMID:
6749587
35.

Effect of peripheral versus portal venous administration of insulin on postprandial hyperglycemia and glucose turnover in alloxan-diabetic dogs.

Rizza RA, Westland RE, Hall LD, Patton GS, Haymond MW, Clemens AH, Gerich JE, Service FJ.

Mayo Clin Proc. 1981 Jul;56(7):434-8.

PMID:
7019592
36.
37.

Glucose clamping using the Biostator GCIIS.

Verdonk CA, Rizza RA, Westland RE, Nelson RL, Gerich JE, Service FJ.

Horm Metab Res. 1980 Apr;12(4):133-5.

PMID:
6993319
38.

Considerations for the programming of an open-loop insulin infusion device from the biostator glucose controller.

Service FJ, Rizza RA, Westland RE, Hall LD, Nelson RL, Haymond MW, Clemens AH, Gerich JE.

Diabetes Care. 1980 Mar-Apr;3(2):278-84.

PMID:
6993141
39.

Carbon-13 N.M.R. spectra of the antibiotic butirosin A, and related aminoglycosides.

Woo PW, Westland RD.

Carbohydr Res. 1973 Nov;31(1):27-36. No abstract available.

PMID:
4774677
40.

The preparation and biological activity of novel amino acid analogs of butirosin.

Haskell TH, Rodebaugh R, Plessas N, Watson D, Westland RD.

Carbohydr Res. 1973 Jun;28(2):263-80. No abstract available.

PMID:
4201448
41.

Antiradiation agents. 3-[(Alkylthio)alkyl]thiazolidines and substituted 2-([(3-thiazolidinyl)alkyl]thio)pyridines and -quinolines.

Westland RD, Lin MH, Cooley RA Jr, Zwiesler ML, Grenan MM.

J Med Chem. 1973 Apr;16(4):328-31. No abstract available.

PMID:
4716176
43.

2-Mercaptoacetamidine and derivatives as antiradiation agents.

Westland RD, Merz MM, Alexander SM, Newton LS, Bauer L, Conway TT, Barton JM, Khullar KK, Devdhar PB, Grenan MM.

J Med Chem. 1972 Dec;15(12):1313-21. No abstract available.

PMID:
4635980
45.

Novel schistosomicides. S-2-((2-(2-thiazolylcarbamoyl)ethyl)amino)ethyl hydrogen thiosulfate and related compounds.

Westland RD, Werbel LM, Dice JR, Holmes JL, Zahm BG.

J Med Chem. 1971 Oct;14(10):916-20. No abstract available.

PMID:
5000519
46.

Growth pattern in children with congenital heart disease.

Banik ND, Westland R, Falkner F.

Indian J Pediatr. 1969 Apr;36(255):112-6. No abstract available.

PMID:
5354915
47.

N-substituted S-2-aminoethyl thiosulfates as antiradiation agents.

Westland RD, Holmes JL, Mouk ML, Marsh DD, Cooley RA Jr, Dice JR.

J Med Chem. 1968 Nov;11(6):1190-201. No abstract available.

PMID:
5680035
48.

N-substituted derivatives of 2-aminoethanethiol and 2-hydrazinoethanethiol.

Westland RD, Holmes JL, Green B, Dice JR.

J Med Chem. 1968 Jul;11(4):824-9. No abstract available.

PMID:
5671249
49.

1-Alkyl-1-(2-mercaptoethyl)guanidines and the corresponding thioureas, disulfides, and thiosulfates as antibacterial agents.

Westland RD, Karger ER, Green B, Dice JR.

J Med Chem. 1968 Jan;11(1):84-6. No abstract available.

PMID:
4384131
50.

Potential antiviral agents. Carbobenzoxy di- and tripeptides active against measles and herpes viruses.

Nicolaides E, DeWald H, Lipnik M, Westland R, Posler J.

J Med Chem. 1968 Jan;11(1):74-9. No abstract available.

PMID:
4295313

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