Found: 53
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The Kids Heart BioBank: supporting 20 years of patient care and research into CHD.
- Published in:
- Cardiology in the Young, 2024, v. 34, n. 8, p. 1645, doi. 10.1017/S1047951124025654
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- Publication type:
- Article
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy.
- Published in:
- EMBO Molecular Medicine, 2015, v. 7, n. 5, p. 562, doi. 10.15252/emmm.201505047
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- Publication type:
- Article
Epistatic and Independent Effects on Schizophrenia-Related Phenotypes Following Co-disruption of the Risk Factors Neuregulin-1 x DISC1.
- Published in:
- Schizophrenia Bulletin, 2017, v. 43, n. 1, p. 214, doi. 10.1093/schbul/sbw120
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- Publication type:
- Article
Nkx2.5 marks angioblasts that contribute to hemogenic endothelium of the endocardium and dorsal aorta.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.20994
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- Publication type:
- Article
Platelet-derived growth factor (PDGF) signaling directs cardiomyocyte movement toward the midline during heart tube assembly.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.21172
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- Publication type:
- Article
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets.
- Published in:
- eLife, 2015, p. 1, doi. 10.7554/eLife.06942
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- Publication type:
- Article
Pressure Overload by Transverse Aortic Constriction Induces Maladaptive Hypertrophy in a Titin-Truncated Mouse Model.
- Published in:
- 2015
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- Publication type:
- journal article
c-Kit Function Is Necessary for In Vitro Myogenic Differentiation of Bone Marrow Hematopoietic Cells.
- Published in:
- Stem Cells, 2009, v. 27, n. 8, p. 1911, doi. 10.1002/stem.106
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- Publication type:
- Article
RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression.
- Published in:
- Nature Genetics, 2008, v. 40, n. 1, p. 61, doi. 10.1038/ng.2007.28
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- Publication type:
- Article
The Hlx homeobox transcription factor is required early in enteric nervous system development.
- Published in:
- BMC Developmental Biology, 2006, v. 6, p. 33, doi. 10.1186/1471-213X-6-33
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- Publication type:
- Article
Correction: Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy.
- Published in:
- 2018
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- Publication type:
- Correction Notice
Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy.
- Published in:
- PLoS Genetics, 2018, p. 1, doi. 10.1371/journal.pgen.1007502
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- Publication type:
- Article
Conditional (loxP‐flanked) allele for the gene encoding the retinoic acid‐synthesizing enzyme retinaldehyde dehydrogenase 2 (RALDH2).
- Published in:
- Genesis: The Journal of Genetics & Development, 2006, v. 44, n. 3, p. 155, doi. 10.1002/gene.20195
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- Publication type:
- Article
Targeted insertion of a lacZ reporter gene into the mouse Cer1 locus reveals complex and dynamic expression during embryogenesis.
- Published in:
- Genesis: The Journal of Genetics & Development, 2000, v. 26, n. 4, p. 259, doi. 10.1002/(SICI)1526-968X(200004)26:4<259::AID-GENE70>3.0.CO;2-V
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- Publication type:
- Article
epicardin: A novel basic helix-loop-helix transcription factor gene expressed in epicardium, branchial arch myoblasts, and mesenchyme of developing lung, gut, kidney, and gonads.
- Published in:
- Developmental Dynamics, 1998, v. 213, n. 1, p. 105, doi. 10.1002/(SICI)1097-0177(199809)213:1<105::AID-AJA10>3.0.CO;2-1
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- Publication type:
- Article
The Small Muscle-specific Protein Csl Modifies Cell Shape and Promotes Myocyte Fusion in an...
- Published in:
- Journal of Cell Biology, 2001, v. 153, n. 5, p. 985, doi. 10.1083/jcb.153.5.985
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- Publication type:
- Article
A rapid co-culture stamping device for studying intercellular communication.
- Published in:
- Scientific Reports, 2016, p. 35618, doi. 10.1038/srep35618
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- Publication type:
- Article
Lack of Genetic Interaction between <i>Tbx20</i> and <i>Tbx3</i> in Early Mouse Heart Development.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0070149
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- Publication type:
- Article
Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024812
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- Publication type:
- Article
Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA4.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020711
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- Publication type:
- Article
Cardiac Deletion of Smyd2 Is Dispensable for Mouse Heart Development.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009748
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- Publication type:
- Article
Patterning the vertebrate heart.
- Published in:
- 2002
- By:
- Publication type:
- review
A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem Cells.
- Published in:
- Stem Cells Translational Medicine, 2015, v. 4, n. 12, p. 1482, doi. 10.5966/sctm.2014-0275
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- Publication type:
- Article
Molecular pathways in myocardial development: a stem cell perspective
- Published in:
- Cardiovascular Research, 2003, v. 58, n. 2, p. 264, doi. 10.1016/S0008-6363(03)00286-4
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- Publication type:
- Article
CompGO: an R package for comparing and visualizing Gene Ontology enrichment differences between DNA binding experiments.
- Published in:
- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0701-2
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- Publication type:
- Article
CompGO: an R package for comparing and visualizing Gene Ontology enrichment differences between DNA binding experiments.
- Published in:
- BMC Bioinformatics, 2015, v. 16, n. 1, p. 275, doi. 10.1186/s12859-015-0701-2
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- Publication type:
- Article
Regenerative medicine: Heart redevelopment.
- Published in:
- Nature, 2010, v. 467, n. 7311, p. 39, doi. 10.1038/467039a
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- Publication type:
- Article
The Creation of an Historical Meteorological Database for Environmental Dose Assessment.
- Published in:
- Environmental Monitoring & Assessment, 2003, v. 83, n. 3, p. 255, doi. 10.1023/A:1022624821528
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- Publication type:
- Article
ERBB2 triggers mammalian heart regeneration by promoting cardiomyocyte dedifferentiation and proliferation.
- Published in:
- Nature Cell Biology, 2015, v. 17, n. 5, p. 627, doi. 10.1038/ncb3149
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- Publication type:
- Article
Heart field origin of great vessel precursors relies on nkx2.5-mediated vasculogenesis.
- Published in:
- Nature Cell Biology, 2013, v. 15, n. 11, p. 1362, doi. 10.1038/ncb2862
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- Publication type:
- Article
Cardiac fibroblast heterogeneity and dynamics through the lens of single-cell dual 'omics.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 6, p. 1380, doi. 10.1093/cvr/cvac037
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- Publication type:
- Article
Congenital heart disease: current knowledge about causes and inheritance.
- Published in:
- Medical Journal of Australia, 2012, v. 197, n. 3, p. 155, doi. 10.5694/mja12.10811
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- Publication type:
- Article
Congenital heart disease: current knowledge about causes and inheritance.
- Published in:
- Medical Journal of Australia, 2012, v. 197, n. 3, p. 155, doi. 10.5694/mja12.10811
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- Publication type:
- Article
Progress and challenges in the genetics of congenital heart disease.
- Published in:
- Medical Journal of Australia, 2005, v. 182, n. 3, p. 100, doi. 10.5694/j.1326-5377.2005.tb06604.x
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- Publication type:
- Article
Haemogenic endocardium contributes to transient definitive haematopoiesis.
- Published in:
- Nature Communications, 2013, v. 4, n. 3, p. 1564, doi. 10.1038/ncomms2569
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- Publication type:
- Article
Characterization of Pitx2c expression in the mouse heart using a reporter transgene.
- Published in:
- Developmental Dynamics, 2011, v. 240, n. 1, p. 195, doi. 10.1002/dvdy.22492
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- Publication type:
- Article
Expression of Slit and Robo genes in the developing mouse heart.
- Published in:
- Developmental Dynamics, 2010, v. 239, n. 12, p. 3303, doi. 10.1002/dvdy.22449
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- Publication type:
- Article
Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species.
- Published in:
- Journal of Cell Biology, 2011, v. 193, n. 7, p. 1181, doi. 10.1083/jcb.201006114
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- Publication type:
- Article
Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line.
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.83606
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- Publication type:
- Article
Platelet-Derived Growth Factor Receptor Type α Activation Drives Pulmonary Vascular Remodeling Via Progenitor Cell Proliferation and Induces Pulmonary Hypertension.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Structural and functional characterization of the mouse Hlx homeobox gene.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 10, p. 836, doi. 10.1007/s003350010179
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- Publication type:
- Article
Conserved linkage of NK-2 homeobox gene pairs Nkx2-2/2-4 and Nkx2-1/2-9 in mammals.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 6, p. 466, doi. 10.1007/s003350010089
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- Publication type:
- Article
Uncontrolled angiogenic precursor expansion causes coronary artery anomalies in mice lacking Pofut1.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00654-w
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- Publication type:
- Article
Somatic mutations in NKX2-5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 10, p. 2416, doi. 10.1002/ajmg.a.34187
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- Publication type:
- Article
Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations.
- Published in:
- Congenital Heart Disease, 2012, v. 7, n. 2, p. 151, doi. 10.1111/j.1747-0803.2011.00573.x
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- Publication type:
- Article
Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 6, p. 1097, doi. 10.1093/hmg/ddq554
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- Publication type:
- Article
α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 20, p. 4007, doi. 10.1093/hmg/ddq315
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- Publication type:
- Article
Epithelial to mesenchymal transition as a portal to stem cell characters embedded in gene networks.
- Published in:
- BioEssays, 2013, v. 35, n. 3, p. 191, doi. 10.1002/bies.201200089
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- Publication type:
- Article
Sierra: discovery of differential transcript usage from polyA-captured single-cell RNA-seq data.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-02071-7
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- Publication type:
- Article
Skeletal muscle hypertrophy is mediated by a Ca2+ -dependent calcineurin signalling pathway.
- Published in:
- Nature, 1999, v. 400, n. 6744, p. 576, doi. 10.1038/23054
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- Publication type:
- Article