Found: 27
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High prevalence of cardiovascular risk factors in children and adolescents with Williams-Beuren syndrome.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Comparison of protein behavior between wild-type and G601S hERG in living cells by fluorescence correlation spectroscopy.
- Published in:
- Journal of Physiological Sciences, 2011, v. 61, n. 4, p. 313, doi. 10.1007/s12576-011-0150-2
- By:
- Publication type:
- Article
Hot water extract of Agaricus blazei Murrill specifically inhibits growth and induces apoptosis in human pancreatic cancer cells.
- Published in:
- BMC Complementary & Alternative Medicine, 2018, v. 18, n. 1, p. 1, doi. 10.1186/s12906-018-2385-4
- By:
- Publication type:
- Article
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 6, p. 543, doi. 10.1007/s10038-007-0149-y
- By:
- Publication type:
- Article
Characterization of a novel KRAS mutation identified in Noonan syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 3, p. 524, doi. 10.1002/ajmg.a.34419
- By:
- Publication type:
- Article
The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 11, p. 2641, doi. 10.1002/ajmg.a.34285
- By:
- Publication type:
- Article
Changes in myosin heavy chain and its localization in rat heart in association with hypobaric hypoxia-induced pulmonary hypertension.
- Published in:
- Journal of Pathology, 2002, v. 197, n. 3, p. 380, doi. 10.1002/path.1132
- By:
- Publication type:
- Article
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
- Published in:
- Nature Genetics, 2007, v. 39, n. 8, p. 1013, doi. 10.1038/ng2078
- By:
- Publication type:
- Article
Evidence for the expression of neonatal skeletal myosin heavy chain in primary myocardium and cardiac conduction tissue in the developing chick heart.
- Published in:
- Developmental Dynamics, 2000, v. 217, n. 1, p. 37, doi. 10.1002/(SICI)1097-0177(200001)217:1<37::AID-DVDY4>3.0.CO;2-3
- By:
- Publication type:
- Article
Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients.
- Published in:
- Cardiology in the Young, 1999, v. 9, n. 5, p. 463, doi. 10.1017/S1047951100005357
- By:
- Publication type:
- Article
c-kit<sup>pos</sup> GATA-4 High Rat Cardiac Stem Cells Foster Adult Cardiomyocyte Survival through IGF-1 Paracrine Signalling.
- Published in:
- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014297
- By:
- Publication type:
- Article
Myogenic differentiation in atrium-derived adult cardiac pluripotent cells and the transcriptional regulation of GATA4 and myogenin on ANP promoter.
- Published in:
- Genes to Cells, 2010, v. 15, n. 5, p. 439, doi. 10.1111/j.1365-2443.2010.01394.x
- By:
- Publication type:
- Article
Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity?
- Published in:
- Pediatric Cardiology, 2016, v. 37, n. 5, p. 962, doi. 10.1007/s00246-016-1378-7
- By:
- Publication type:
- Article
Determination of Normal Ranges of Mitochondrial Respiratory Activities by mtDNA Transfer from 54 Human Subjects to mtDNA-less HeLa Cells for Identification of the Pathogenicities of Mutated mtDNAs.
- Published in:
- Journal of Biochemistry, 2004, v. 135, n. 2, p. 237, doi. 10.1093/jb/mvh028
- By:
- Publication type:
- Article
Teratogenic Effect of Tedral (Theophylline, Ephedrine, and Phenobarbital) on Cardiac Development in Chick Embryos.
- Published in:
- Congenital Anomalies, 1992, v. 32, n. 1, p. 65, doi. 10.1111/j.1741-4520.1992.tb00781.x
- By:
- Publication type:
- Article
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
- Published in:
- Nature, 2003, v. 424, n. 6947, p. 443, doi. 10.1038/nature01827
- By:
- Publication type:
- Article
Induced Pluripotent Stem Cell-Derived Cardiomyocytes with SCN5A R1623Q Mutation Associated with Severe Long QT Syndrome in Fetuses and Neonates Recapitulates Pathophysiological Phenotypes.
- Published in:
- Biology (2079-7737), 2021, v. 10, n. 10, p. 1062, doi. 10.3390/biology10101062
- By:
- Publication type:
- Article
Akt and PKC are involved not only in upregulation of telomerase activity but also in cell differentiation-related function via mTORC2 in leukemia cells.
- Published in:
- Histochemistry & Cell Biology, 2010, v. 134, n. 6, p. 555, doi. 10.1007/s00418-010-0764-0
- By:
- Publication type:
- Article
Coronary Artery Dilatation in LEOPARD Syndrome. A Child Case and Literature Review.
- Published in:
- Congenital Heart Disease, 2009, v. 4, n. 1, p. 38, doi. 10.1111/j.1747-0803.2008.00243.x
- By:
- Publication type:
- Article
Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy.
- Published in:
- Heart & Vessels, 2013, v. 28, n. 6, p. 785, doi. 10.1007/s00380-013-0332-3
- By:
- Publication type:
- Article
The role of the large-conductance voltage-dependent and calcium-activated potassium (BK) channels in the regulation of rat ductus arteriosus tone.
- Published in:
- Heart & Vessels, 2010, v. 25, n. 6, p. 556, doi. 10.1007/s00380-010-0008-1
- By:
- Publication type:
- Article
Developmental changes in the expression of voltage-gated potassium channels in the ductus arteriosus of the fetal rat.
- Published in:
- Heart & Vessels, 2007, v. 22, n. 1, p. 34, doi. 10.1007/s00380-006-0926-0
- By:
- Publication type:
- Article
VI. Genome Structure and Cognitive Map of Williams Syndrome.
- Published in:
- Journal of Cognitive Neuroscience, 2000, v. 12, n. S1, p. 89, doi. 10.1162/089892900562002
- By:
- Publication type:
- Article
A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT syndrome.
- Published in:
- Human Mutation, 1998, v. 11, n. 6, p. 481, doi. 10.1002/(SICI)1098-1004(1998)11:6<481::AID-HUMU12>3.0.CO;2-Q
- By:
- Publication type:
- Article
Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family.
- Published in:
- Human Mutation, 1998, v. 11, p. S184, doi. 10.1002/humu.1380110159
- By:
- Publication type:
- Article
The teratogenic effect of phenobarbital on the embryonic chick heart.
- Published in:
- Journal of Applied Toxicology, 1986, v. 6, n. 2, p. 91, doi. 10.1002/jat.2550060205
- By:
- Publication type:
- Article
Myelomonoblastic leukaemia cells carrying the PEBP2β/MYH11 fusion gene are CD34<sup>+</sup>, c-KIT<sup>+</sup> immature cells.
- Published in:
- British Journal of Haematology, 1997, v. 97, n. 3, p. 656, doi. 10.1046/j.1365-2141.1997.1012917.x
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- Publication type:
- Article