Found: 29
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Systemic Dosing of Thymosin Beta 4 before and after Ischemia Does Not Attenuate Global Myocardial Ischemia-Reperfusion Injury in Pigs.
- Published in:
- Frontiers in Pharmacology, 2016, p. 1, doi. 10.3389/fphar.2016.00115
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- Publication type:
- Article
Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure.
- Published in:
- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0203422
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- Publication type:
- Article
Loss of Bone Morphogenetic Protein Receptor 2 Is Associated with Abnormal DNA Repair in Pulmonary Arterial Hypertension.
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- American Journal of Respiratory Cell & Molecular Biology, 2014, v. 50, n. 6, p. 1118, doi. 10.1165/rcmb.2013-0349OC
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- Publication type:
- Article
BMP promotes motility and represses growth of smooth muscle cells by activation of tandem Wnt pathways.
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- Journal of Cell Biology, 2011, v. 192, n. 1, p. 171, doi. 10.1083/jcb.201008060
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- Article
Bone morphogenetic protein 2 induces pulmonary angiogenesis via Wnt-β-catenin and Wnt-RhoA-Rac1 pathways.
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- Journal of Cell Biology, 2009, v. 184, n. 1, p. 83, doi. 10.1083/jcb.200806049
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- Publication type:
- Article
Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39911-x
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- Publication type:
- Article
Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosis.
- Published in:
- PLoS ONE, 2021, v. 16, n. 9, p. 1, doi. 10.1371/journal.pone.0255933
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- Publication type:
- Article
Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.
- Published in:
- BMC Medical Genetics, 2017, v. 18, n. 1, p. 1, doi. 10.1186/s12881-017-0442-3
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- Article
DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0955-z
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- Article
Therapeutic potential of thymosin β4 in myocardial infarct and heart failure.
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- Annals of the New York Academy of Sciences, 2012, v. 1269, n. 1, p. 117, doi. 10.1111/j.1749-6632.2012.06695.x
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- Article
GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.786705
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- Article
Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice.
- Published in:
- EMBO Journal, 2002, v. 21, n. 11, p. 2591, doi. 10.1093/emboj/21.11.2591
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- Publication type:
- Article
Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice.
- Published in:
- EMBO Journal, 2002, v. 21, n. 11, p. 2591, doi. 10.1093/emboj/21.11.2591
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- Publication type:
- Article
Whole-Exome Sequencing Reveals TopBP1 as a Novel Gene in Idiopathic Pulmonary Arterial Hypertension.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 189, n. 10, p. 1260, doi. 10.1164/rccm.201310-1749OC
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- Publication type:
- Article
WHOLE EXOME SEQUENCING REVEALS TOPBP1 AS A NOVEL GENE IN IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION.
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- American Journal of Respiratory & Critical Care Medicine, 2014, v. 189, n. 10, p. E8, doi. 10.1164/rccm.201310-1749oc
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- Publication type:
- Article
Autophagic protein LC3B confers resistance against hypoxia-induced pulmonary hypertension.
- Published in:
- 2011
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- Publication type:
- journal article
Disruption of PPARγ/β-catenin-mediated regulation of apelin impairs BMP-induced mouse and human pulmonary arterial EC survival.
- Published in:
- 2011
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- Publication type:
- journal article
An antiproliferative BMP-2/PPARgamma/apoE axis in human and murine SMCs and its role in pulmonary hypertension.
- Published in:
- 2008
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- Publication type:
- journal article
Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
- Published in:
- 2021
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- Publication type:
- journal article
LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging.
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- Human Mutation, 2015, v. 36, n. 7, p. 694, doi. 10.1002/humu.22793
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- Publication type:
- Article
The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1433, doi. 10.1002/ajmg.a.37596
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- Article
Expanding the phenotype of Timothy syndrome type 2: An adolescent with ventricular fibrillation but normal development.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 3, p. 629, doi. 10.1002/ajmg.a.36924
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- Publication type:
- Article
A comparison of echocardiography to invasive measurement in the evaluation of pulmonary arterial hypertension in a rat model.
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- International Journal of Cardiovascular Imaging, 2010, v. 26, n. 5, p. 509, doi. 10.1007/s10554-010-9596-1
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- Publication type:
- Article
Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 4, p. 354, doi. 10.1002/mgg3.147
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- Publication type:
- Article
Prevalence of Titin Truncating Variants in General Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0145284
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- Article
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
- Published in:
- European Heart Journal, 2015, v. 36, n. 34, p. 2327, doi. 10.1093/eurheartj/ehv253
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- Publication type:
- Article
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
- Published in:
- 2022
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- Publication type:
- corrected article
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
- Published in:
- 2021
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- Publication type:
- journal article