Mira Holliday

发表

Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia

William J. Astle, Warren S. Alexander, Edna C. Hardeman, 2017, The Journal of clinical investigation.

Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates.

Nolan J Hoffman, David E James, Sean J Humphrey, 2015, Cell metabolism.

Terminal Galactosylation and Sialylation Switching on Membrane Glycoproteins upon TNF-Alpha-Induced Insulin Resistance in Adipocytes*

David E James, Nicolle H Packer, Benjamin L Parker, 2015, Molecular & Cellular Proteomics.

Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy

C. Semsarian, L. Hool, H. Cserne Szappanos, 2023, Scientific reports.

Parallel assembly of actin and tropomyosin, but not myosin II, during de novo actin filament formation in live mice

Nicole S. Bryce, E. Hardeman, P. Gunning, 2018, Journal of Cell Science.

Transcriptome Sequencing of Patients With Hypertrophic Cardiomyopathy Reveals Novel Splice-Altering Variants in MYBPC3

C. Semsarian, J. Ingles, S. Lal, 2021, Circulation. Genomic and precision medicine.

Slow conduction and spatial dispersion of repolarization are intrinsic properties of cardiomyocyte electrophysiology that contribute to proarrhythmia in an iPSC model of hypertrophic cardiomyopathy

C. Semsarian, L. Hool, A. Hill, 2023, bioRxiv.

The Expression of Inflammatory Genes in 3T3-L1 Adipocytes Exhibits a Memory to Stimulation by Macrophage Secretions

G. Denyer, N. Yuwono, D. Hancock, 2018, bioRxiv.

Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln.

C. Semsarian, L. Hool, A. Hill, 2018, Stem cell research.

The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death

L. Yeates, C. Semsarian, J. Ingles, 2023, NPJ genomic medicine.

Reduced connexin-43 expression, slow conduction and repolarisation dispersion in a model of hypertrophic cardiomyopathy

H. Cserne Szappanos, Seakcheng Lim, M. Mangala, 2024, Disease models & mechanisms.

Generation of an induced pluripotent stem cell line from a hypertrophic cardiomyopathy patient with a pathogenic myosin binding protein C (MYBPC3) p.Arg502Trp mutation.

C. Semsarian, Seakcheng Lim, S. Ross, 2018, Stem cell research.