He N - Search Results

1

Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.

Zhao X, Paterson AD, Zahirieh A, He N, Wang K, Pei Y. Zhao X, et al. Among authors: he n. Clin J Am Soc Nephrol. 2008 Jan;3(1):146-52. doi: 10.2215/CJN.03430807. Epub 2007 Dec 12. Clin J Am Soc Nephrol. 2008. PMID: 18077784 Free PMC article. Clinical Trial.

2

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. Among authors: he n. J Am Soc Nephrol. 1998 Oct;9(10):1853-60. doi: 10.1681/ASN.V9101853. J Am Soc Nephrol. 1998. PMID: 9773786 Clinical Trial.

3

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. Among authors: he n. J Am Soc Nephrol. 1999 Jul;10(7):1524-9. doi: 10.1681/ASN.V1071524. J Am Soc Nephrol. 1999. PMID: 10405208

4

Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations.

Watnick T, He N, Wang K, Liang Y, Parfrey P, Hefferton D, St George-Hyslop P, Germino G, Pei Y. Watnick T, et al. Among authors: he n. Nat Genet. 2000 Jun;25(2):143-4. doi: 10.1038/75981. Nat Genet. 2000. PMID: 10835625

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. Among authors: he n. 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

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.

Magistroni R, He N, Wang K, Andrew R, Johnson A, Gabow P, Dicks E, Parfrey P, Torra R, San-Millan JL, Coto E, Van Dijk M, Breuning M, Peters D, Bogdanova N, Ligabue G, Albertazzi A, Hateboer N, Demetriou K, Pierides A, Deltas C, St George-Hyslop P, Ravine D, Pei Y. Magistroni R, et al. Among authors: he n. J Am Soc Nephrol. 2003 May;14(5):1164-74. doi: 10.1097/01.asn.0000061774.90975.25. J Am Soc Nephrol. 2003. PMID: 12707387 Free article.

7

Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease.

Paterson AD, Magistroni R, He N, Wang K, Johnson A, Fain PR, Dicks E, Parfrey P, St George-Hyslop P, Pei Y. Paterson AD, et al. Among authors: he n. J Am Soc Nephrol. 2005 Mar;16(3):755-62. doi: 10.1681/ASN.2004090758. Epub 2005 Jan 26. J Am Soc Nephrol. 2005. PMID: 15677307

8

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

Zahirieh A, Nesbit MA, Ali A, Wang K, He N, Stangou M, Bamichas G, Sombolos K, Thakker RV, Pei Y. Zahirieh A, et al. Among authors: he n. J Clin Endocrinol Metab. 2005 Apr;90(4):2445-50. doi: 10.1210/jc.2004-1969. Epub 2005 Feb 10. J Clin Endocrinol Metab. 2005. PMID: 15705923

9

Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.

He N, Zahirieh A, Mei Y, Lee B, Senthilnathan S, Wong B, Mucha B, Hildebrandt F, Cole DE, Cattran D, Pei Y. He N, et al. Clin J Am Soc Nephrol. 2007 Jan;2(1):31-7. doi: 10.2215/CJN.02690806. Epub 2006 Oct 25. Clin J Am Soc Nephrol. 2007. PMID: 17699384

10

IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathy.

Liu XQ, Paterson AD, He N, St George-Hyslop P, Rauta V, Gronhagen-Riska C, Laakso M, Thibaudin L, Berthoux F, Cattran D, Pei Y. Liu XQ, et al. Among authors: he n. J Am Soc Nephrol. 2008 May;19(5):1025-33. doi: 10.1681/ASN.2007091013. Epub 2008 Feb 6. J Am Soc Nephrol. 2008. PMID: 18256354 Free PMC article.

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