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- A Synonymous Mutation Upstream of the Gene Encoding a Weak-Link Enzyme Causes an Ultrasensitive Response in Growth Rate Journal Article
- A hypomorphic allele reveals an important role of inturned in mouse skeletal development Journal Article
- A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice Journal Article
- An Automated Data-Driven Pipeline for Improving Heterologous Enzyme Expression Journal Article
- Cardiac myosin heavy chains lacking the light chain binding domain cause hypertrophic cardiomyopathy in mice. Journal Article
- Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy Journal Article
- Efficient differentiation of murine embryonic stem cells requires the binding of CXXC finger protein 1 to DNA or methylated histone H3-Lys4 Journal Article
- Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC Journal Article
- Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T Journal Article
- Inherent properties of adenylosuccinate lyase could explain S-Ado/SAICAr ratio due to homozygous R426H and R303C mutations. Journal Article
- Intrinsically active variants of Erk oncogenically transform cells and disclose unexpected autophosphorylation capability that is independent of TEY phosphorylation Journal Article
- Label-free detection of missense mutations and methylation differences in the p53 gene using optically diffracting hydrogels Journal Article
- Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human beta-cardiac myosin motor function Journal Article
- Morphological and functional alterations in ventricular myocytes from male transgenic mice with hypertrophic cardiomyopathy Journal Article
- Mps1 activation loop autophosphorylation enhances kinase activity Journal Article
- Myosin motor domains carrying mutations implicated in early or late onset hypertrophic cardiomyopathy have similar properties Journal Article
- Regulation of CED-3 caspase localization and activation by C-elegans nuclear-membrane protein NPP-14 Journal Article
- SKR-1, a homolog of Skp1 and a member of the SCFSEL-10 complex, regulates sex-determination and LIN-12/Notch signaling in C. elegans Journal Article
- Salmonella enterica Causes More Severe Inflammatory Disease in C57/BL6 Nramp 1(G169) Mice Than Sv129S6 Mice Journal Article
- Structural Insights into Apoptotic DNA Degradation by CED-3 Protease Suppressor-6 (CPS-6) from Caenorhabditis elegans Journal Article
- Structure of Est3 reveals a bimodal surface with differential roles in telomere replication Journal Article
- TSPAN12 Is a Norrin Co-receptor that Amplifies Frizzled4 Ligand Selectivity and Signaling Journal Article
- The Transcription Factor Spn1 Regulates Gene Expression via a Highly Conserved Novel Structural Motif Journal Article