Search results (20)
« Back to PublicationsDystrophin involvement in peripheral circadian SRF signalling.
Journal article
Betts CA. et al, (2021), Life Sci Alliance, 4
Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology.
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van Westering TLE. et al, (2020), J Cachexia Sarcopenia Muscle, 11, 578 - 593
Comprehensive RNA-Sequencing Analysis in Serum and Muscle Reveals Novel Small RNA Signatures with Biomarker Potential for DMD.
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Coenen-Stass AML. et al, (2018), Mol Ther Nucleic Acids, 13, 1 - 15
Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice.
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Walter LM. et al, (2018), Hum Mol Genet, 27, 3582 - 3597
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.
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Davies B. et al, (2017), Hum Mol Genet, 26, 3869 - 3882
Genomic Rearrangements in Arabidopsis Considered as Quantitative Traits.
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Imprialou M. et al, (2017), Genetics, 205, 1425 - 1441
The Amount of Mitochondrial DNA in Blood Reflects the Course of a Depressive Episode.
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Nicod J. et al, (2016), Biol Psychiatry, 80, e41 - e42
Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing.
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Nicod J. et al, (2016), Nat Genet, 48, 912 - 918
The fine-scale architecture of structural variants in 17 mouse genomes.
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Yalcin B. et al, (2012), Genome Biol, 13
Mouse genomic variation and its effect on phenotypes and gene regulation.
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Keane TM. et al, (2011), Nature, 477, 289 - 294
Sequence-based characterization of structural variation in the mouse genome.
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Yalcin B. et al, (2011), Nature, 477, 326 - 329
Elusive copy number variation in the mouse genome.
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Agam A. et al, (2010), PLoS One, 5
Commercially available outbred mice for genome-wide association studies.
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Yalcin B. et al, (2010), PLoS Genet, 6
Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locus.
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Fullerton JM. et al, (2008), Biol Psychiatry, 63, 874 - 883