Contrasting effects on HIF-1α regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease

By Clifford S.C.  

Human Molecular Genetics, Vol. 10, Iss. 10, 2001-05 ,pp. : 1029-1038

Oxford University Press

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Genotype–phenotype correlation in von Hippel-Lindau syndrome

By A.Friedrich C.  

Human Molecular Genetics, Vol. 10, Iss. 7, 2001-04 ,pp. : 763-767

Oxford University Press

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Expression of the Von Hippel—Lindau Disease Tumour Suppressor Gene during Human Embryogenesis

By Richards Frances M.   Schofield Paul N.   Fleming Stewart   Maher Eamonn R.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 639-644

Oxford University Press

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von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF

By Hoffman M.A.  

Human Molecular Genetics, Vol. 10, Iss. 10, 2001-05 ,pp. : 1019-1027

Oxford University Press

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Comparison of the Human and Mouse Genes Encoding the Telomeric Protein, TRF1: Chromosomal Localization, Expression and Conserved Protein Domains

By Broccoli Dominique   Chong Laura   Oelmann Stefan   Fernald Anthony A.   Marziliano Nicola   van Steensel Bas   Kipling David   Le Beau Michelle M.   de Lange Titia  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 69-76

Oxford University Press

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