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Page 1
Polycystin-1 maturation requires polycystin-2 in a dose-dependent manner.
J Clin Invest. 2015 Feb;125(2):607-20. doi: 10.1172/JCI76972. Epub 2015 Jan 9.
J Clin Invest. 2015.
PMID: 25574838
Free PMC article.
Tolvaptan plus pasireotide shows enhanced efficacy in a PKD1 model.
Hopp K, Hommerding CJ, Wang X, Ye H, Harris PC, Torres VE.
Hopp K, et al. Among authors: hommerding cj.
J Am Soc Nephrol. 2015 Jan;26(1):39-47. doi: 10.1681/ASN.2013121312. Epub 2014 Jul 3.
J Am Soc Nephrol. 2015.
PMID: 24994926
Free PMC article.
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Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.
Hopp K, Ward CJ, Hommerding CJ, Nasr SH, Tuan HF, Gainullin VG, Rossetti S, Torres VE, Harris PC.
Hopp K, et al. Among authors: hommerding cj.
J Clin Invest. 2012 Nov;122(11):4257-73. doi: 10.1172/JCI64313. Epub 2012 Oct 15.
J Clin Invest. 2012.
PMID: 23064367
Free PMC article.
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Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3.
Consugar MB, Kubly VJ, Lager DJ, Hommerding CJ, Wong WC, Bakker E, Gattone VH 2nd, Torres VE, Breuning MH, Harris PC.
Consugar MB, et al. Among authors: hommerding cj.
Hum Genet. 2007 Jun;121(5):591-9. doi: 10.1007/s00439-007-0341-3. Epub 2007 Mar 22.
Hum Genet. 2007.
PMID: 17377820
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B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.
Hopp K, Heyer CM, Hommerding CJ, Henke SA, Sundsbak JL, Patel S, Patel P, Consugar MB, Czarnecki PG, Gliem TJ, Torres VE, Rossetti S, Harris PC.
Hopp K, et al. Among authors: hommerding cj.
Hum Mol Genet. 2011 Jul 1;20(13):2524-34. doi: 10.1093/hmg/ddr151. Epub 2011 Apr 14.
Hum Mol Genet. 2011.
PMID: 21493627
Free PMC article.
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The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity.
Leightner AC, Hommerding CJ, Peng Y, Salisbury JL, Gainullin VG, Czarnecki PG, Sussman CR, Harris PC.
Leightner AC, et al. Among authors: hommerding cj.
Hum Mol Genet. 2013 May 15;22(10):2024-40. doi: 10.1093/hmg/ddt054. Epub 2013 Feb 7.
Hum Mol Genet. 2013.
PMID: 23393159
Free PMC article.
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Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.
Tammachote R, Hommerding CJ, Sinders RM, Miller CA, Czarnecki PG, Leightner AC, Salisbury JL, Ward CJ, Torres VE, Gattone VH 2nd, Harris PC.
Tammachote R, et al. Among authors: hommerding cj.
Hum Mol Genet. 2009 Sep 1;18(17):3311-23. doi: 10.1093/hmg/ddp272. Epub 2009 Jun 10.
Hum Mol Genet. 2009.
PMID: 19515853
Free PMC article.
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