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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Characterization of a New BLM Mutation Associated with a Topoisomerase Ilα Defect in a Patient with Bloom's Syndrome

By Foucault Frédéric   Vaury Christelle   Barakat Abdelhamid   Thibout Déborah   Planchon Philippe   Jaulin Christian   Praz Françoise   Amor-Guéret Mounira  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1427-1434

Oxford University Press

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Loss of Bloom syndrome protein destabilizes human gene cluster architecture

By Killen Michael W.   Stults Dawn M.   Adachi Noritaka   Hanakahi Les   Pierce Andrew J.  

Human Molecular Genetics, Vol. 18, Iss. 18, 2009-09 ,pp. : 3417-3428

Oxford University Press

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First Two Cases of Bloom Syndrome in Russia: Lack of Skin Manifestations in a BLM c.1642C>T (p.Q548X) Homozygote as a Likely Cause of Underdiagnosis

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Molecular Syndromology, Vol. 8, Iss. 2, 2017-01 ,pp. : 103-106

Karger

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Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2

By Lillard-Wetherell Kate  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1919-1932

Oxford University Press

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