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

By Ibraghimov-Beskrovnaya Oxana   Bukanov Nikolay O.   Donohue Lincoln C.   Dackowski William R.   Klinger Katherine W.   Landes Gregory M.  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1641-1649

Oxford University Press

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Wolfram syndrome 1 gene ( WFS1 ) product localizes to secretory granules and determines granule acidification in pancreatic -cells

By Hatanaka Masayuki   Tanabe Katsuya   Yanai Akie   Ohta Yasuharu   Kondo Manabu   Akiyama Masaru   Shinoda Koh   Oka Yoshitomo   Tanizawa Yukio  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1274-1284

Oxford University Press

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Loss of Tsc1 , but not Pten , in renal tubular cells causes polycystic kidney disease by activating mTORC1

By Zhou Jing   Brugarolas James   Parada Luis F.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4428-4441

Oxford University Press

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RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin

By Shu X.  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1183-1197

Oxford University Press

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PKHDL1 , a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression

By Hogan M.C.   Griffin M.D.   Rossetti S.   Torres V.E.   Ward C.J.   Harris P.C.  

Human Molecular Genetics, Vol. 12, Iss. 6, 2003-03 ,pp. : 685-698

Oxford University Press

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