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Onur Cil, MD, PhD

TitleClinical Fellow
SchoolUCSF School of Medicine
DepartmentPediatrics
Address550 16th. Street
San Francisco CA 94158
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Cil O, Phuan PW, Gillespie AM, Lee S, Tradtrantip L, Yin J, Tse M, Zachos NC, Lin R, Donowitz M, Verkman AS. Benzopyrimido-pyrrolo-oxazine-dione CFTR inhibitor (R)-BPO-27 for anti-secretory therapy of diarrheas caused by bacterial enterotoxins. FASEB J. 2016 Nov 8. PMID: 27871064.
      View in: PubMed
    2. Cil O, Phuan PW, Son JH, Zhu JS, Ku CK, Tabib NA, Teuthorn AP, Ferrera L, Zachos NC, Lin R, Galietta LJ, Donowitz M, Kurth MJ, Verkman AS. Phenylquinoxalinone CFTR activator as potential prosecretory therapy for constipation. Transl Res. 2016 Oct 15. PMID: 27815136.
      View in: PubMed
    3. Cil O, Haggie PM, Phuan PW, Tan JA, Verkman AS, et al. Small-Molecule Inhibitors of Pendrin Potentiate the Diuretic Action of Furosemide. J Am Soc Nephrol. 2016 May 6. PMID: 27153921.
      View in: PubMed
    4. Cil O, Phuan PW, Lee S, Tan J, Haggie PM, Levin MH, Sun L, Thiagarajah JR, Ma T, Verkman AS, et al. CFTR activator increases intestinal fluid secretion and normalizes stool output in a mouse model of constipation. Cell Mol Gastroenterol Hepatol. 2016 May; 2(3):317-327. PMID: 27127798.
      View in: PubMed
    5. Besbas N, Kalyoncu M, Cil O, Ozgul RK, Bakkaloglu A, Ozaltin F. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis. Ren Fail. 2015 Oct; 37(9):1435-9. PMID: 26335292.
      View in: PubMed
    6. Cil O, Esteva-Font C, Tas ST, Su T, Lee S, Anderson MO, Ertunc M, Verkman AS. Salt-sparing diuretic action of a water-soluble urea analog inhibitor of urea transporters UT-A and UT-B in rats. Kidney Int. 2015 Aug; 88(2):311-20. PMID: 25993324; PMCID: PMC4523423 [Available on 02/01/16].
    7. Cil O, Besbas N, Duzova A, Topaloglu R, Peco-Antic A, Korkmaz E, Ozaltin F. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome. Pediatr Nephrol. 2015 Aug; 30(8):1279-87. PMID: 25720465.
      View in: PubMed
    8. Esteva-Font C, Cil O, Phuan PW, Su T, Lee S, Anderson MO, Verkman AS. Diuresis and reduced urinary osmolality in rats produced by small-molecule UT-A-selective urea transport inhibitors. FASEB J. 2014 Sep; 28(9):3878-90. PMID: 24843071; PMCID: PMC4139901.
    9. Verkman AS, Esteva-Font C, Cil O, Anderson MO, Li F, Li M, Lei T, Ren H, Yang B. Small-molecule inhibitors of urea transporters. Subcell Biochem. 2014; 73:165-77. PMID: 25298345; PMCID: PMC4306426.
    10. Unal S, Gumruk F, Yigit S, Tuncer M, Tavil B, Cil O, Takci S, Urata M, Hotta T, Kang D, Cetin M. A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period. Pediatr Blood Cancer. 2014 Apr; 61(4):763-4. PMID: 24115609.
      View in: PubMed
    11. Celebi N, Cil H, Cil O, Canbay O, Onur R, Aypar U. Protective effect of coenzyme Q10 in paclitaxel-induced peripheral neuropathy in rats. Neurosciences (Riyadh). 2013 Apr; 18(2):133-7. PMID: 23545610.
      View in: PubMed
    12. Ozaltin F, Besbas N, Iskit AB, Cil O, Akcoren Z, Kale G, Bakkaloglu A. Role of CXCR1 (CKR-1) in inflammation of experimental mesangioproliferative glomerulonephritis. Ren Fail. 2013; 35(3):380-5. PMID: 23336303.
      View in: PubMed
    13. Cil O, Ertunc M, Gucer KS, Ozaltin F, Iskit AB, Onur R. Endothelial dysfunction and increased responses to renal nerve stimulation in rat kidneys during rhabdomyolysis-induced acute renal failure: role of hydroxyl radical. Ren Fail. 2012; 34(2):211-20. PMID: 22229548.
      View in: PubMed
    14. Barua M, Cil O, Paterson AD, Wang K, He N, Dicks E, Parfrey P, Pei Y. Family history of renal disease severity predicts the mutated gene in ADPKD. J Am Soc Nephrol. 2009 Aug; 20(8):1833-8. PMID: 19443633; PMCID: PMC2723982.
    15. Wang K, Zhao X, Chan S, Cil O, He N, Song X, Paterson AD, Pei Y. Evidence for pathogenicity of atypical splice mutations in autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol. 2009 Feb; 4(2):442-9. PMID: 19158373; PMCID: PMC2637591.
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