Mutations in the diastrophic dysplasia sulfate transporter ( DTDST ) gene: correlation between sulfate transport activity and chondrodysplasia phenotype

By Karniski L.P.  

Human Molecular Genetics, Vol. 10, Iss. 14, 2001-07 ,pp. : 1485-1490

Oxford University Press

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Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter ( DTDST ) gene mutations in HEK cells

By Karniski Lawrence P.  

Human Molecular Genetics, Vol. 13, Iss. 19, 2004-10 ,pp. : 2165-2171

Oxford University Press

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The Testis Anion Transporter 1 (Slc26a8) is required for sperm terminal differentiation and male fertility in the mouse

By Tour Aminata   Lhuillier Pierre   Gossen Jan A.   Kuil Cor W.   Lhte David   Jgou Bernard   Escalier Denise   Gacon Grard  

Human Molecular Genetics, Vol. 16, Iss. 15, 2007-08 ,pp. : 1783-1793

Oxford University Press

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A Runx2 threshold for the cleidocranial dysplasia phenotype

By Lou Yang   Javed Amjad   Hussain Sadiq   Colby Jennifer   Frederick Dana   Pratap Jitesh   Xie Ronglin   Gaur Tripti   van Wijnen Andre J.   Jones Stephen N.   Stein Gary S.   Lian Jane B.   Stein Janet L.  

Human Molecular Genetics, Vol. 18, Iss. 3, 2009-02 ,pp. : 556-568

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Variation in the uric acid transporter gene ( SLC2A9 ) and memory performance

By Houlihan Lorna M.   Wyatt Niki D.   Harris Sarah E.   Hayward Caroline   Gow Alan J.   Marioni Riccardo E.   Strachan Mark W.J.   Price Jackie F.   Starr John M.   Wright Alan F.   Deary Ian J.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2321-2330

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