Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphase

By Earle Elizabeth   Saxena Alka   MacDonald Andrew   Hudson Damien F.   Shaffer Lisa G.   Saffery Richard   Cancilla Michael R.   Cutts Suzanne M.   Howman Emily   Choo K. H. Andy  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 187-194

Oxford University Press

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Aprataxin, poly-ADP ribose polymerase 1 (PARP-1) and apurinic endonuclease 1 (APE1) function together to protect the genome against oxidative damage

By Harris Janelle L.   Jakob Burkhard   Taucher-Scholz Gisela   Dianov Grigory L.   Becherel Olivier J.   Lavin Martin F.  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4102-4117

Oxford University Press

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In vivo misregulation of genes involved in apoptosis, development and oxidative stress in mice lacking both functional Werner syndrome protein and poly(ADP-ribose) polymerase-1

By Deschênes François   Massip Laurent   Lebel Michel  

Human Molecular Genetics, Vol. 14, Iss. 21, 2005-11 ,pp. : 3293-3308

Oxford University Press

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Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere–kinetochore complexes

By Sugata Naoko  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2919-2926

Oxford University Press

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SALL1, the gene mutated in Townes–Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin

By Netzer Christian   Rieger Leonie   Brero Alessandro   Zhang Chang-Dong   Hinzke Markus   Kohlhase Jürgen   Bohlander StefanK.  

Human Molecular Genetics, Vol. 10, Iss. 26, 2001-12 ,pp. : 3017-3024

Oxford University Press

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