Pei Y - Search Results

1

Molecular diagnosis of autosomal dominant polycystic kidney disease.

Song X, Haghighi A, Iliuta IA, Pei Y. Song X, et al. Among authors: pei y. Expert Rev Mol Diagn. 2017 Oct;17(10):885-895. doi: 10.1080/14737159.2017.1358088. Epub 2017 Aug 13. Expert Rev Mol Diagn. 2017. PMID: 28724316 Review.

2

A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene.

Pei Y, Wang K, Kasenda M, Paterson AD, Liang Y, Huang E, Lian J, Rogovea E, Somlo S, St George-Hyslop P. Pei Y, et al. Kidney Int. 1998 May;53(5):1127-32. doi: 10.1046/j.1523-1755.1998.00890.x. Kidney Int. 1998. PMID: 9573526 Free article.

3

A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindreds.

Pei Y, He N, Wang K, Kasenda M, Paterson AD, Chan G, Liang Y, Roscoe J, Brissenden J, Hefferton D, Parfrey P, Somlo S, St George-Hyslop P. Pei Y, et al. J Am Soc Nephrol. 1998 Oct;9(10):1853-60. doi: 10.1681/ASN.V9101853. J Am Soc Nephrol. 1998. PMID: 9773786 Clinical Trial.

4

Somatic PKD2 mutations in individual kidney and liver cysts support a "two-hit" model of cystogenesis in type 2 autosomal dominant polycystic kidney disease.

Pei Y, Watnick T, He N, Wang K, Liang Y, Parfrey P, Germino G, St George-Hyslop P. Pei Y, et al. J Am Soc Nephrol. 1999 Jul;10(7):1524-9. doi: 10.1681/ASN.V1071524. J Am Soc Nephrol. 1999. PMID: 10405208

5

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.

Pei Y, Paterson AD, Wang KR, He N, Hefferton D, Watnick T, Germino GG, Parfrey P, Somlo S, St George-Hyslop P. Pei Y, et al. Am J Hum Genet. 2001 Feb;68(2):355-63. doi: 10.1086/318188. Epub 2001 Jan 10. Am J Hum Genet. 2001. PMID: 11156533 Free PMC article.

6

A "two-hit" model of cystogenesis in autosomal dominant polycystic kidney disease?

Pei Y. Pei Y. Trends Mol Med. 2001 Apr;7(4):151-6. doi: 10.1016/s1471-4914(01)01953-0. Trends Mol Med. 2001. PMID: 11286938

7

Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype.

Rossetti S, Chauveau D, Kubly V, Slezak JM, Saggar-Malik AK, Pei Y, Ong AC, Stewart F, Watson ML, Bergstralh EJ, Winearls CG, Torres VE, Harris PC. Rossetti S, et al. Among authors: pei y. Lancet. 2003 Jun 28;361(9376):2196-201. doi: 10.1016/S0140-6736(03)13773-7. Lancet. 2003. PMID: 12842373

8

Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease.

Garcia-Gonzalez MA, Jones JG, Allen SK, Palatucci CM, Batish SD, Seltzer WK, Lan Z, Allen E, Qian F, Lens XM, Pei Y, Germino GG, Watnick TJ. Garcia-Gonzalez MA, et al. Among authors: pei y. Mol Genet Metab. 2007 Sep-Oct;92(1-2):160-7. doi: 10.1016/j.ymgme.2007.05.004. Epub 2007 Jun 18. Mol Genet Metab. 2007. PMID: 17574468 Free PMC article.

9

Polycystin-1 C-terminal tail associates with beta-catenin and inhibits canonical Wnt signaling.

Lal M, Song X, Pluznick JL, Di Giovanni V, Merrick DM, Rosenblum ND, Chauvet V, Gottardi CJ, Pei Y, Caplan MJ. Lal M, et al. Among authors: pei y. Hum Mol Genet. 2008 Oct 15;17(20):3105-17. doi: 10.1093/hmg/ddn208. Epub 2008 Jul 16. Hum Mol Genet. 2008. PMID: 18632682 Free PMC article.

10

Characterization of the intrarenal renin-angiotensin system in experimental alport syndrome.

Bae EH, Konvalinka A, Fang F, Zhou X, Williams V, Maksimowski N, Song X, Zhang SL, John R, Oudit GY, Pei Y, Scholey JW. Bae EH, et al. Among authors: pei y. Am J Pathol. 2015 May;185(5):1423-35. doi: 10.1016/j.ajpath.2015.01.021. Epub 2015 Mar 14. Am J Pathol. 2015. PMID: 25777062 Free article.

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