Targeted disruption of Slc19a2 , the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice

By Forrest D.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2951-2960

Oxford University Press

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Mutation of the gene encoding fibrillin-2 results in syndactyly in mice

By Chaudhry S.S.  

Human Molecular Genetics, Vol. 10, Iss. 8, 2001-04 ,pp. : 835-843

Oxford University Press

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Targeted disruption of the Wnk4 gene decreases phosphorylation of Na-Cl cotransporter, increases Na excretion and lowers blood pressure

By Ohta Akihito   Rai Tatemitsu   Yui Naofumi   Chiga Motoko   Yang Sung-Sen   Lin Shih-Hua   Sohara Eisei   Sasaki Sei   Uchida Shinichi  

Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3978-3986

Oxford University Press

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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

Oxford University Press

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Suppression of the deafness and thyroid dysfunction in Thrb -null mice by an independent mutation in the Thra thyroid hormone receptor α gene

By Rüsch A.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2701-2708

Oxford University Press

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