Molecular basis of the functional podocin–nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

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Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3397-3405

Oxford University Press

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Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation

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Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1219-1226

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Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice

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Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein

By Moore Yuki   Lambracht-Washington Doris   Tabaczewski Piotr   Fischer Lindahl Kirsten  

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Springer Publishing Company

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The Murine Homologue of HIRA, a DiGeorge Syndrome Candidate Gene, Is Expressed in Embryonic Structures Affected in Human CATCH22 Patients

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