Found: 19
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5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 3, p. 1364, doi. 10.1172/JCI70108
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- Publication type:
- Article
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.
- Published in:
- 2010
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- Publication type:
- journal article
GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm.
- Published in:
- eLife, 2020, p. 1, doi. 10.7554/eLife.53278
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- Publication type:
- Article
An RNA-seq protocol to identify mRNA expression changes in mouse diaphyseal bone: Applications in mice with bone property altering Lrp5 mutations.
- Published in:
- Journal of Bone & Mineral Research, 2013, v. 28, n. 10, p. 2081, doi. 10.1002/jbmr.1946
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- Publication type:
- Article
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
- Published in:
- Nature Genetics, 2009, v. 41, n. 8, p. 931, doi. 10.1038/ng.415
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- Publication type:
- Article
Robust identification of mosaic variants in congenital heart disease.
- Published in:
- Human Genetics, 2018, v. 137, n. 2, p. 183, doi. 10.1007/s00439-018-1871-6
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- Publication type:
- Article
Myc targeted CDK18 promotes ATR and homologous recombination to mediate PARP inhibitor resistance in glioblastoma.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10993-5
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- Publication type:
- Article
Joint analysis of left ventricular expression and circulating plasma levels of Omentin after myocardial ischemia.
- Published in:
- Cardiovascular Diabetology, 2017, v. 16, p. 1, doi. 10.1186/s12933-017-0567-x
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- Publication type:
- Article
The extracellular matrix proteoglycan lumican improves survival and counteracts cardiac dilatation and failure in mice subjected to pressure overload.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45651-9
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- Publication type:
- Article
Dissecting spatio-temporal protein networks driving human heart development and related disorders.
- Published in:
- Molecular Systems Biology, 2010, v. 6, n. 1, p. 1, doi. 10.1038/msb.2010.36
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- Publication type:
- Article
Loss of RNA expression and allele-specific expression associated with congenital heart disease.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12824, doi. 10.1038/ncomms12824
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- Publication type:
- Article
Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin.
- Published in:
- Science Translational Medicine, 2019, v. 11, n. 476, p. N.PAG, doi. 10.1126/scitranslmed.aat1199
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- Publication type:
- Article
Cardiomyopathy: Consequences of Impaired Autophagy in the Heart.
- Published in:
- 2021
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- Publication type:
- journal article
Sex differences in gene expression in response to ischemia in the human left ventricular myocardium.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 10, p. 1682, doi. 10.1093/hmg/ddz014
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- Publication type:
- Article
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 1, p. 209, doi. 10.1093/hmg/ddt412
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- Publication type:
- Article
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.
- Published in:
- Human Mutation, 2018, v. 39, n. 6, p. 870, doi. 10.1002/humu.23419
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- Publication type:
- Article
Multiplexed Single‐Nucleus RNA Sequencing Using Lipid‐Oligo Barcodes.
- Published in:
- Current Protocols, 2022, v. 2, n. 10, p. 1, doi. 10.1002/cpz1.579
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- Publication type:
- Article
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00738-1
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- Publication type:
- Article
ViroFind: A novel target-enrichment deep-sequencing platform reveals a complex JC virus population in the brain of PML patients.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0186945
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- Publication type:
- Article