The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader–Willi region

By Boccaccio Irène   Glatt-Deeley Heather   Watrin Françoise   Roëckel Nathalie   Lalande Marc   Muscatelli Françoise  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2497-2505

Oxford University Press

Access to resources Recommend Favorite

Functional interaction between −629C/A, −971G/A and −1337C/T polymorphisms in the CETP gene is a major determinant of promoter activity and plasma CETP concentration in the REGRESS Study

By Frisdal Eric  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2607-2618

Oxford University Press

Access to resources Recommend Favorite

Association of acetylated histones with paternally expressed genes in the Prader–Willi deletion region

By B.Fulmer-Smentek S.   Francke U.  

Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 645-652

Oxford University Press

Access to resources Recommend Favorite

Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3

By Kim J.   Kollhoff A.   Bergmann A.   Stubbs L.  

Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 233-245

Oxford University Press

Access to resources Recommend Favorite

Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

By Cheetham M.E.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 3065-3074

Oxford University Press

Access to resources Recommend Favorite