Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays

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Human Molecular Genetics, Vol. 14, Iss. 22, 2005-11 ,pp. : 3379-3388

Oxford University Press

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TCF7L2 splice variants have distinct effects on -cell turnover and function

By Le Bacquer Olivier   Shu Luan   Marchand Marion   Neve Bernadette   Paroni Federico   Kerr Conte Julie   Pattou Francois   Froguel Philippe   Maedler Kathrin  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 1906-1915

Oxford University Press

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Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa

By Linder Bastian   Dill Holger   Hirmer Anja   Brocher Jan   Lee Gek Ping   Mathavan Sinnakaruppan   Bolz Hanno Jrn   Winkler Christoph   Laggerbauer Bernhard   Fischer Utz  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 368-377

Oxford University Press

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Up-regulation of the ubiquitous alternative splicing factor Tra2 causes inclusion of a germ cell-specific exon

By Venables Julian P.  

Human Molecular Genetics, Vol. 14, Iss. 16, 2005-08 ,pp. : 2289-2303

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Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathway

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Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 196-207

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