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Items: 1 to 20 of 184

1.

Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations.

Qian F, Boletta A, Bhunia AK, Xu H, Liu L, Ahrabi AK, Watnick TJ, Zhou F, Germino GG.

Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16981-6. Epub 2002 Dec 13.

2.

Characterization of cis-autoproteolysis of polycystin-1, the product of human polycystic kidney disease 1 gene.

Wei W, Hackmann K, Xu H, Germino G, Qian F.

J Biol Chem. 2007 Jul 27;282(30):21729-37. Epub 2007 May 24.

3.

Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein.

Hughes J, Ward CJ, Aspinwall R, Butler R, Harris PC.

Hum Mol Genet. 1999 Mar;8(3):543-9.

4.

Autosomal dominant polycystic kidney disease: clues to pathogenesis.

Harris PC.

Hum Mol Genet. 1999;8(10):1861-6. Review.

5.

The structure of a PKD domain from polycystin-1: implications for polycystic kidney disease.

Bycroft M, Bateman A, Clarke J, Hamill SJ, Sandford R, Thomas RL, Chothia C.

EMBO J. 1999 Jan 15;18(2):297-305.

6.

Polycystin-1L2 is a novel G-protein-binding protein.

Yuasa T, Takakura A, Denker BM, Venugopal B, Zhou J.

Genomics. 2004 Jul;84(1):126-38.

PMID:
15203210
7.

Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2).

Veldhuisen B, Spruit L, Dauwerse HG, Breuning MH, Peters DJ.

Eur J Hum Genet. 1999 Dec;7(8):860-72.

8.

Characterization and cell distribution of polycystin, the product of autosomal dominant polycystic kidney disease gene 1.

Palsson R, Sharma CP, Kim K, McLaughlin M, Brown D, Arnaout MA.

Mol Med. 1996 Nov;2(6):702-11.

9.

Polycystins: what polycystic kidney disease tells us about sperm.

Kierszenbaum AL.

Mol Reprod Dev. 2004 Apr;67(4):385-8. Review.

PMID:
14991728
10.

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents.

Hanaoka K, Qian F, Boletta A, Bhunia AK, Piontek K, Tsiokas L, Sukhatme VP, Guggino WB, Germino GG.

Nature. 2000 Dec 21-28;408(6815):990-4.

PMID:
11140688
11.

Novel mutations of PKD1 gene in Chinese patients with autosomal dominant polycystic kidney disease.

Ding L, Zhang S, Qiu W, Xiao C, Wu S, Zhang G, Cheng L, Zhang S.

Nephrol Dial Transplant. 2002 Jan;17(1):75-80.

12.

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1.

Ibraghimov-Beskrovnaya O, Bukanov NO, Donohue LC, Dackowski WR, Klinger KW, Landes GM.

Hum Mol Genet. 2000 Jul 1;9(11):1641-9.

13.

Molecular basis of autosomal-dominant polycystic kidney disease.

Gallagher AR, Hidaka S, Gretz N, Witzgall R.

Cell Mol Life Sci. 2002 Apr;59(4):682-93. Review.

PMID:
12022474
17.

Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1.

Harris PC.

Curr Opin Nephrol Hypertens. 2002 May;11(3):309-14. Review.

PMID:
11981261
18.

The sea urchin sperm receptor for egg jelly is a modular protein with extensive homology to the human polycystic kidney disease protein, PKD1.

Moy GW, Mendoza LM, Schulz JR, Swanson WJ, Glabe CG, Vacquier VD.

J Cell Biol. 1996 May;133(4):809-17.

19.

In vitro cystogenesis: the search for drugs antagonizing cyst development.

Ibraghimov-Beskrovnaya O, Bukanov NO.

Nephrol Ther. 2006 Jan;2 Suppl 2:S109-14.

PMID:
17373209
20.

Functional polycystin-1 expression is developmentally regulated during epithelial morphogenesis in vitro: downregulation and loss of membrane localization during cystogenesis.

O Bukanov N, Husson H, Dackowski WR, Lawrence BD, Clow PA, Roberts BL, Klinger KW, Ibraghimov-Beskrovnaya O.

Hum Mol Genet. 2002 Apr 15;11(8):923-36.

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