ERMM: Discovery
Discovery
FRZB and melusin, overexpressed in LGMD2A, regulate integrin β1D isoform replacement altering myoblast fusion and the integrin-signalling pathway
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- Journal:
- Expert Reviews in Molecular Medicine / Volume 19 / 2017
- Published online by Cambridge University Press:
- 16 March 2017, e2
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The microRNA miR-124 suppresses seizure activity and regulates CREB1 activity
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- Expert Reviews in Molecular Medicine / Volume 18 / 2016
- Published online by Cambridge University Press:
- 21 March 2016, e4
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Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle
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- Expert Reviews in Molecular Medicine / Volume 18 / 2016
- Published online by Cambridge University Press:
- 08 April 2016, e7
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Simplified strategy for rapid first-line screening of fragile X syndrome: closed-tube triplet-primed PCR and amplicon melt peak analysis
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- Expert Reviews in Molecular Medicine / Volume 17 / 2015
- Published online by Cambridge University Press:
- 04 May 2015, e7
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FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
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- Expert Reviews in Molecular Medicine / Volume 19 / 2017
- Published online by Cambridge University Press:
- 19 July 2017, e10
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Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
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- Journal:
- Expert Reviews in Molecular Medicine / Volume 17 / 2015
- Published online by Cambridge University Press:
- 01 July 2015, e13
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