PKHDL1 , a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression

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Human Molecular Genetics, Vol. 12, Iss. 6, 2003-03 ,pp. : 685-698

Oxford University Press

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Mutational analysis of genes encoding chromatin proteins in the archaeon Methanococcus voltae indicates their involvement in the regulation of gene expression

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Molecular Genetics and Genomics, Vol. 272, Iss. 1, 2004-08 ,pp. : 76-87

Springer Publishing Company

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Repeat induced point mutation in two asexual fungi, Aspergillus niger and Penicillium chrysogenum

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Current Genetics, Vol. 53, Iss. 5, 2008-05 ,pp. : 287-297

Springer Publishing Company

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

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

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ES2 , a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene

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