Pei Y - Search Results

1

LAMA2 and LOXL4 are candidate FSGS genes.

Vijayan P, Hack S, Yao T, Qureshi MA, Paterson AD, John R, Davenport B, Lennon R, Pei Y, Barua M. Vijayan P, et al. Among authors: pei y. BMC Nephrol. 2021 Sep 26;22(1):320. doi: 10.1186/s12882-021-02524-6. BMC Nephrol. 2021. PMID: 34565340 Free PMC article.

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

Is there a third gene for autosomal dominant polycystic kidney disease?

Paterson AD, Pei Y. Paterson AD, et al. Among authors: pei y. Kidney Int. 1998 Nov;54(5):1759-61. doi: 10.1046/j.1523-1755.1998.00166.x. Kidney Int. 1998. PMID: 9844156 Free article. No abstract available.

5

PKD3-to be or not to be?

Paterson AD, Pei Y. Paterson AD, et al. Among authors: pei y. Nephrol Dial Transplant. 1999 Dec;14(12):2965-6. doi: 10.1093/ndt/14.12.2965. Nephrol Dial Transplant. 1999. PMID: 10570111 No abstract available.

6

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.

7

Murine recombinant angiotensin-converting enzyme 2 attenuates kidney injury in experimental Alport syndrome.

Bae EH, Fang F, Williams VR, Konvalinka A, Zhou X, Patel VB, Song X, John R, Oudit GY, Pei Y, Scholey JW. Bae EH, et al. Among authors: pei y. Kidney Int. 2017 Jun;91(6):1347-1361. doi: 10.1016/j.kint.2016.12.022. Epub 2017 Feb 27. Kidney Int. 2017. PMID: 28249676 Free article.

8

X-Linked Glomerulopathy Due to COL4A5 Founder Variant.

Barua M, John R, Stella L, Li W, Roslin NM, Sharif B, Hack S, Lajoie-Starkell G, Schwaderer AL, Becknell B, Wuttke M, Köttgen A, Cattran D, Paterson AD, Pei Y. Barua M, et al. Among authors: pei y. Am J Kidney Dis. 2018 Mar;71(3):441-445. doi: 10.1053/j.ajkd.2017.09.005. Epub 2017 Dec 1. Am J Kidney Dis. 2018. PMID: 29198386 Review.

9

Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing.

Lanktree MB, Haghighi A, Guiard E, Iliuta IA, Song X, Harris PC, Paterson AD, Pei Y. Lanktree MB, et al. Among authors: pei y. J Am Soc Nephrol. 2018 Oct;29(10):2593-2600. doi: 10.1681/ASN.2018050493. Epub 2018 Aug 22. J Am Soc Nephrol. 2018. PMID: 30135240 Free PMC article.

10

Evolving role of genetic testing for the clinical management of autosomal dominant polycystic kidney disease.

Lanktree MB, Iliuta IA, Haghighi A, Song X, Pei Y. Lanktree MB, et al. Among authors: pei y. Nephrol Dial Transplant. 2019 Sep 1;34(9):1453-1460. doi: 10.1093/ndt/gfy261. Nephrol Dial Transplant. 2019. PMID: 30165646 Review.

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