Origin of alternative splicing by tandem exon duplication

By Kondrashov F.A.   Koonin E.V.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2661-2669

Oxford University Press

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Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/–KTS splice isoforms

By Klamt B.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 709-714

Oxford University Press

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An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects

By Fernandez Alanis Eugenio   Pinotti Mirko   Dal Mas Andrea   Balestra Dario   Cavallari Nicola   Rogalska Malgorzata E.   Bernardi Francesco   Pagani Franco  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2389-2398

Oxford University Press

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A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

By Bardoni Barbara   Schenck Annette   Mandel Jean Louis  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2557-2566

Oxford University Press

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Nucleocytoplasmic transfer of the NF2 tumor suppressor protein merlin is regulated by exon 2 and a CRM1-dependent nuclear export signal in exon 15

By Kressel M.  

Human Molecular Genetics, Vol. 11, Iss. 19, 2002-07 ,pp. : 2269-2278

Oxford University Press

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