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Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locus

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Genome Wide Conditional Mouse Knockout Resources.

Tissue chips - innovative tools for drug development and disease modeling.

Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk.

Analysis of yeast artificial chromosome clones.

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility.

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

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CRISPR/dCas9-mediated tuning of DMPK transcription reveals a quantitative relationship between toxic repeat RNA expression and MBNL1 activity in myotonic dystrophy.

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

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Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locus

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