‘Mitotic drive’ of expanded CTG repeats in myotonic dystrophy type 1 (DM1)

By Khajavi M.  

Human Molecular Genetics, Vol. 10, Iss. 8, 2001-04 ,pp. : 855-863

Oxford University Press

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Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients

By Fernandez-Costa Juan M.   Garcia-Lopez Amparo   Zuñiga Sheila   Fernandez-Pedrosa Victoria   Felipo-Benavent Amelia   Mata Manuel   Jaka Oihane   Aiastui Ana   Hernandez-Torres Francisco   Aguado Begoña   Perez-Alonso Manuel   Vilchez Jesus J.   Lopez de Munain Adolfo   Artero Ruben D.  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 704-716

Oxford University Press

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Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression

By Korade-Mirnics Zeljka   Tarleton Jack  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1017-1023

Oxford University Press

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Compound heterozygous myotonic dystrophy type 1

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1952-1953

John Wiley & Sons Inc

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Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients

By Braida Claudia   Stefanatos Rhoda K.A.   Adam Berit   Mahajan Navdeep   Smeets Hubert J.M.   Niel Florence   Goizet Cyril   Arveiler Benoit   Koenig Michel   Lagier-Tourenne Clotilde   Mandel Jean-Louis   Faber Catharina G.   de Die-Smulders Christine E.M.   Spaans Frank   Monckton Darren G.  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1399-1412

Oxford University Press

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