Publications by authors named "Nicole C Meyer"

29Publications

CPR in medical TV shows: non-health care student perspective.

Adv Med Educ Pract 2018 7;9:85-91. Epub 2018 Feb 7.

Department of Allied Health Studies, School of Allied Health Professions, Loma Linda University, Loma Linda, CA, USA.

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http://dx.doi.org/10.2147/AMEP.S146149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808693PMC
February 2018

C4 Nephritic Factors in C3 Glomerulopathy: A Case Series.

Am J Kidney Dis 2017 Dec 24;70(6):834-843. Epub 2017 Aug 24.

Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, IA; Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA. Electronic address:

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http://dx.doi.org/10.1053/j.ajkd.2017.07.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701858PMC
December 2017

PDZD7 and hearing loss: More than just a modifier.

Am J Med Genet A 2015 Dec 29;167A(12):2957-65. Epub 2015 Sep 29.

Department of Otolaryngology-Head Neck Surgery, Molecular Otolaryngology Renal Research Laboratories, University of Iowa, Iowa City, Iowa.

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http://doi.wiley.com/10.1002/ajmg.a.37274
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http://dx.doi.org/10.1002/ajmg.a.37274DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741280PMC
December 2015

High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies.

J Am Soc Nephrol 2016 Apr 17;27(4):1245-53. Epub 2015 Aug 17.

Molecular Otolaryngology and Renal Research Laboratories, Iowa Institute of Human Genetics, Division of Nephrology, Department of Internal Medicine and Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa

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http://dx.doi.org/10.1681/ASN.2015040385DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814193PMC
April 2016

Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndrome.

Am J Kidney Dis 2015 Jun 25;65(6):968-9. Epub 2015 Mar 25.

University of Iowa, Iowa City, Iowa. Electronic address:

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http://dx.doi.org/10.1053/j.ajkd.2015.02.326DOI Listing
June 2015

Defining the complement biomarker profile of C3 glomerulopathy.

Clin J Am Soc Nephrol 2014 Nov 23;9(11):1876-82. Epub 2014 Oct 23.

Molecular Otolaryngology and Renal Research Laboratories, Division of Nephrology, Department of Internal Medicine, Division of Nephrology, Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa;

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http://dx.doi.org/10.2215/CJN.01820214DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220750PMC
November 2014

Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.

Otol Neurotol 2014 Mar;35(3):395-400

*Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa, U.S.A.; †Department of Medical Genetics, University of Antwerp, Antwerp, Belgium; and ‡Department of Otorhinolaryngology, University of Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1097/MAO.0000000000000244DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945298PMC
March 2014

Soluble CR1 therapy improves complement regulation in C3 glomerulopathy.

J Am Soc Nephrol 2013 Nov 1;24(11):1820-9. Epub 2013 Aug 1.

Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, Iowa;

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http://dx.doi.org/10.1681/ASN.2013010045DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810083PMC
November 2013

A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome.

Pediatr Nephrol 2013 Nov 24;28(11):2221-5. Epub 2013 Jul 24.

Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, 5270 CBRB Building, Iowa City, IA, 52242, USA.

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http://dx.doi.org/10.1007/s00467-013-2560-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433496PMC
November 2013

Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.

Kidney Int 2013 Feb 12;83(2):293-9. Epub 2012 Dec 12.

Division of Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1038/ki.2012.384DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561505PMC
February 2013

Causes of alternative pathway dysregulation in dense deposit disease.

Clin J Am Soc Nephrol 2012 Feb 5;7(2):265-74. Epub 2012 Jan 5.

Department of Otolaryngology-Head & Neck Surgery, Caver College of Medicine, University of Iowa, 5270 CBRB Building, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.2215/CJN.07900811DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280037PMC
February 2012

The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.

Laryngoscope 2011 Jun 14;121(6):1184-6. Epub 2011 Apr 14.

Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa 52242, USA.

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http://doi.wiley.com/10.1002/lary.21778
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http://dx.doi.org/10.1002/lary.21778DOI Listing
June 2011

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.

Nephrol Dial Transplant 2011 Feb 25;26(2):739-41. Epub 2010 Oct 25.

Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.

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http://ndt.oxfordjournals.org/content/26/2/739.full.pdf
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http://ndt.oxfordjournals.org/cgi/doi/10.1093/ndt/gfq658
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http://dx.doi.org/10.1093/ndt/gfq658DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937010PMC
February 2011

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population.

Am J Med Genet A 2010 Jan;152A(1):67-74

Molecular Otolaryngology Research Laboratories, Department of Otolaryngology - Head and Neck Surgery, University of Iowa, Iowa City, IA 52242, USA.

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http://doi.wiley.com/10.1002/ajmg.a.33114
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http://dx.doi.org/10.1002/ajmg.a.33114DOI Listing
January 2010

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

Hum Genet 2010 Feb 22;127(2):155-62. Epub 2009 Oct 22.

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00439-009-0754-2DOI Listing
February 2010

Human male infertility caused by mutations in the CATSPER1 channel protein.

Am J Hum Genet 2009 Apr 2;84(4):505-10. Epub 2009 Apr 2.

Department of Human Genetics, University of Michigan School of Medicine, Ann Arbor, MI 48109-0618, USA.

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http://dx.doi.org/10.1016/j.ajhg.2009.03.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667975PMC
April 2009

Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences.

Hum Mutat 2004 Jun;23(6):582-9

Molecular Otolaryngology Research Labs, University of Iowa, Iowa City, Iowa 52242, USA.

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http://dx.doi.org/10.1002/humu.20048DOI Listing
June 2004