The Bloom syndrome helicase BLM interacts with TRF2 in ALT cells and promotes telomeric DNA synthesis

By Stavropoulos Dimitrios J.  

Human Molecular Genetics, Vol. 11, Iss. 25, 2002-12 ,pp. : 3135-3144

Oxford University Press

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TRF1 is a critical trans -acting factor required for de novo telomere formation in human cells

By Okabe Jun   Eguchi Akiko   Masago Akinori   Hayakawa Takao   Nakanishi Mahito  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2639-2650

Oxford University Press

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Limited capacity of the nuclear matrix to bind telomere repeat binding factor TRF1 may restrict the proliferation of mortal human fibroblasts

By Okabe Jun  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 285-293

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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Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia

By Badell I.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 439-444

Oxford University Press

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