Comparison of Pkd1- targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects

By Genest D.R.  

Human Molecular Genetics, Vol. 10, Iss. 21, 2001-10 ,pp. : 2385-2396

Oxford University Press

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Loss of polycystin-1 or polycystin-2 results in dysregulated apolipoprotein expression in murine tissues via alterations in nuclear hormone receptors

By Allen Erica   Piontek Klaus B.   Garrett-Mayer Elizabeth   Garcia-Gonzalez Miguel   Gorelick Kerry Lee   Germino Gregory G.  

Human Molecular Genetics, Vol. 15, Iss. 1, 2006-01 ,pp. : 11-21

Oxford University Press

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Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma

By Dimaras Helen   Khetan Vikas   Halliday William   Orlic Marija   Prigoda Nadia L.   Piovesan Beata   Marrano Paula   Corson Timothy W.   Eagle Ralph C.   Squire Jeremy A.   Gallie Brenda L.  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1363-1372

Oxford University Press

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

By O. Bukanov N.   Husson H.   Dackowski W.R.   Lawrence B.D.   Clow P.A.   Roberts B.L.   Klinger K.W.   Ibraghimov-Beskrovnaya O.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 923-936

Oxford University Press

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DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

By Morris J.A.   Kandpal G.   Ma L.   Austin C.P.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1591-1608

Oxford University Press

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