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Inherited renal acidoses.
Fry AC, Karet FE. Fry AC, et al. Among authors: karet fe. Physiology (Bethesda). 2007 Jun;22:202-11. doi: 10.1152/physiol.00044.2006. Physiology (Bethesda). 2007. PMID: 17557941 Review.
Selective downregulation of ETA receptor mRNA in renal transplant recipients on cyclosporin A revealed by quantitative RT-PCR.
Karet FE, Davenport AP. Karet FE, et al. Nephrol Dial Transplant. 1996 Oct;11(10):1976-82. doi: 10.1093/oxfordjournals.ndt.a027084. Nephrol Dial Transplant. 1996. PMID: 8918710
Endothelin peptides and receptors in human kidney.
Karet FE. Karet FE. Clin Sci (Lond). 1996 Sep;91(3):267-73. doi: 10.1042/cs0910267. Clin Sci (Lond). 1996. PMID: 8869408
Comparative quantification of endothelin receptor mRNA in human kidney: new tools for direct investigation of human tissue.
Karet FE, Davenport AP. Karet FE, et al. J Cardiovasc Pharmacol. 1995;26 Suppl 3:S268-71. J Cardiovasc Pharmacol. 1995. PMID: 8587385
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Välimäki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, Tucci JR, Stockigt JR, Keppler-Noreuil KM, Porter CC, Anand SK, Whiteford ML, Davis ID, Dewar SB, Bettinelli A, Fadrowski JJ, Belsha CW, Hunley TE, Nelson RD, Trachtman H, Cole TR, Pinsk M, Bockenhauer D, Shenoy M, Vaidyanathan P, Foreman JW, Rasoulpour M, Thameem F, Al-Shahrouri HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP. Boyden LM, et al. Among authors: karet fe. Nature. 2012 Jan 22;482(7383):98-102. doi: 10.1038/nature10814. Nature. 2012. PMID: 22266938 Free PMC article.
Salt handling and hypertension.
O'Shaughnessy KM, Karet FE. O'Shaughnessy KM, et al. Among authors: karet fe. Annu Rev Nutr. 2006;26:343-65. doi: 10.1146/annurev.nutr.26.061505.111316. Annu Rev Nutr. 2006. PMID: 16602929 Review.
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis.
Karet FE, Gainza FJ, Györy AZ, Unwin RJ, Wrong O, Tanner MJ, Nayir A, Alpay H, Santos F, Hulton SA, Bakkaloglu A, Ozen S, Cunningham MJ, di Pietro A, Walker WG, Lifton RP. Karet FE, et al. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6337-42. doi: 10.1073/pnas.95.11.6337. Proc Natl Acad Sci U S A. 1998. PMID: 9600966 Free PMC article.
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.
Borthwick KJ, Kandemir N, Topaloglu R, Kornak U, Bakkaloglu A, Yordam N, Ozen S, Mocan H, Shah GN, Sly WS, Karet FE. Borthwick KJ, et al. Among authors: karet fe. J Med Genet. 2003 Feb;40(2):115-21. doi: 10.1136/jmg.40.2.115. J Med Genet. 2003. PMID: 12566520 Free PMC article.
Inherited renal tubular acidosis.
Karet FE. Karet FE. Adv Nephrol Necker Hosp. 2000;30:147-62. Adv Nephrol Necker Hosp. 2000. PMID: 11068640 Review. No abstract available.
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.
Karet FE, Finberg KE, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Medina JF, Lifton RP. Karet FE, et al. Am J Hum Genet. 1999 Dec;65(6):1656-65. doi: 10.1086/302679. Am J Hum Genet. 1999. PMID: 10577919 Free PMC article.
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