Watnick TJ - Search Results

1

Gene conversion is a likely cause of mutation in PKD1.

Watnick TJ, Gandolph MA, Weber H, Neumann HP, Germino GG. Watnick TJ, et al. Hum Mol Genet. 1998 Aug;7(8):1239-43. doi: 10.1093/hmg/7.8.1239. Hum Mol Genet. 1998. PMID: 9668165

2

The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.

Qian F, Watnick TJ, Onuchic LF, Germino GG. Qian F, et al. Among authors: watnick tj. Cell. 1996 Dec 13;87(6):979-87. doi: 10.1016/s0092-8674(00)81793-6. Cell. 1996. PMID: 8978603 Free article.

3

Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein.

Ibraghimov-Beskrovnaya O, Dackowski WR, Foggensteiner L, Coleman N, Thiru S, Petry LR, Burn TC, Connors TD, Van Raay T, Bradley J, Qian F, Onuchic LF, Watnick TJ, Piontek K, Hakim RM, Landes GM, Germino GG, Sandford R, Klinger KW. Ibraghimov-Beskrovnaya O, et al. Among authors: watnick tj. Proc Natl Acad Sci U S A. 1997 Jun 10;94(12):6397-402. doi: 10.1073/pnas.94.12.6397. Proc Natl Acad Sci U S A. 1997. PMID: 9177229 Free PMC article.

4

An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detection.

Watnick TJ, Piontek KB, Cordal TM, Weber H, Gandolph MA, Qian F, Lens XM, Neumann HP, Germino GG. Watnick TJ, et al. Hum Mol Genet. 1997 Sep;6(9):1473-81. doi: 10.1093/hmg/6.9.1473. Hum Mol Genet. 1997. PMID: 9285784

5

Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominant polycystic kidney disease.

Watnick TJ, Torres VE, Gandolph MA, Qian F, Onuchic LF, Klinger KW, Landes G, Germino GG. Watnick TJ, et al. Mol Cell. 1998 Aug;2(2):247-51. doi: 10.1016/s1097-2765(00)80135-5. Mol Cell. 1998. PMID: 9734362 Free article.

6

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

7

Molecular basis of autosomal dominant polycystic kidney disease.

Watnick T, Germino GG. Watnick T, et al. Semin Nephrol. 1999 Jul;19(4):327-43. Semin Nephrol. 1999. PMID: 10435671 Review.

8

Somatic mutation as mechanism for cyst formation in autosomal dominant polycystic kidney disease.

Qian F, Watnick TJ. Qian F, et al. Among authors: watnick tj. Mol Genet Metab. 1999 Oct;68(2):237-42. doi: 10.1006/mgme.1999.2896. Mol Genet Metab. 1999. PMID: 10527675 Free article. Review. No abstract available.

9

Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease.

Reynolds DM, Hayashi T, Cai Y, Veldhuisen B, Watnick TJ, Lens XM, Mochizuki T, Qian F, Maeda Y, Li L, Fossdal R, Coto E, Wu G, Breuning MH, Germino GG, Peters DJ, Somlo S. Reynolds DM, et al. Among authors: watnick tj. J Am Soc Nephrol. 1999 Nov;10(11):2342-51. doi: 10.1681/ASN.V10112342. J Am Soc Nephrol. 1999. PMID: 10541293

10

Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease.

Watnick T, Phakdeekitcharoen B, Johnson A, Gandolph M, Wang M, Briefel G, Klinger KW, Kimberling W, Gabow P, Germino GG. Watnick T, et al. Am J Hum Genet. 1999 Dec;65(6):1561-71. doi: 10.1086/302657. Am J Hum Genet. 1999. PMID: 10577909 Free PMC article.

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