Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells

By Scheffers Martijn S.   vander Bent Paola   Prins Frans   Spruit Lia   Breuning MartijnH.   Litvinov SergeyV.   deHeer Emile   Peters DorienJ.M.  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2743-2750

Oxford University Press

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Alstrm Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity

By Jagger Daniel   Collin Gayle   Kelly John   Towers Emily   Nevill Graham   Longo-Guess Chantal   Benson Jennifer   Halsey Karin   Dolan David   Marshall Jan   Naggert Jrgen   Forge Andrew  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 466-481

Oxford University Press

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Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration

By Zhang Q.  

Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 993-1003

Oxford University Press

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Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species

By Mavlyutov T.A.   Zhao H.   Ferreira P.A.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1899-1907

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SALL1, the gene mutated in Townes–Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin

By Netzer Christian   Rieger Leonie   Brero Alessandro   Zhang Chang-Dong   Hinzke Markus   Kohlhase Jürgen   Bohlander StefanK.  

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