Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

By Dixon Michael J.   Gazzard James  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1579-1584

Oxford University Press

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Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study

By Newhouse Stephen J.  

Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1805-1814

Oxford University Press

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Downregulation of NCC and NKCC2 cotransporters by kidney-specific WNK1 revealed by gene disruption and transgenic mouse models

By Liu Zhen   Xie Jian   Wu Tao   Truong Thao   Auchus Richard J.   Huang Chou-Long  

Human Molecular Genetics, Vol. 20, Iss. 5, 2011-03 ,pp. : 855-866

Oxford University Press

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The targeted disruption of the MYPT1 gene results in embryonic lethality

By Okamoto Ryuji  

Transgenic Research, Vol. 14, Iss. 3, 2005-06 ,pp. : 337-340

Springer Publishing Company

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Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure

By Fava C.   Montagnana M.   Rosberg L.   Burri P.   Almgren P.   Jnsson A.   Wanby P.   Lippi G.   Minuz P.   Hulthn L.U.   Aurell M.   Melander O.  

Human Molecular Genetics, Vol. 17, Iss. 3, 2008-02 ,pp. : 413-418

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