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Angiogenic Factor AGGF1-Primed Endothelial Progenitor Cells Repair Vascular Defect in Diabetic Mice.
- Published in:
- 2019
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- Publication type:
- journal article
AGGF1 therapy inhibits thoracic aortic aneurysms by enhancing integrin α7-mediated inhibition of TGF-β1 maturation and ERK1/2 signaling.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37809-x
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- Publication type:
- Article
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
- Published in:
- Nature Genetics, 2005, v. 37, n. 7, p. 733, doi. 10.1038/ng1585
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- Publication type:
- Article
Hyperlipidemia patients carrying LDLR splicing mutation c.1187-2A>G respond favorably to rosuvastatin and PCSK9 inhibitor evolocumab.
- Published in:
- Molecular Genetics & Genomics, 2022, v. 297, n. 3, p. 833, doi. 10.1007/s00438-022-01892-4
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- Publication type:
- Article
Identification of a mutation in <italic>CNNM4</italic> by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.
- Published in:
- Molecular Genetics & Genomics, 2018, v. 293, n. 3, p. 699, doi. 10.1007/s00438-018-1417-6
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- Publication type:
- Article
Significant genetic association of a functional <italic>TFPI</italic> variant with circulating fibrinogen levels and coronary artery disease.
- Published in:
- Molecular Genetics & Genomics, 2018, v. 293, n. 1, p. 119, doi. 10.1007/s00438-017-1365-6
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- Publication type:
- Article
Up-regulation of miR-95-3p in hepatocellular carcinoma promotes tumorigenesis by targeting p21 expression.
- Published in:
- Scientific Reports, 2016, p. 34034, doi. 10.1038/srep34034
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- Publication type:
- Article
Cardiac sodium channel regulator MOG1 regulates cardiac morphogenesis and rhythm.
- Published in:
- Scientific Reports, 2016, p. 21538, doi. 10.1038/srep21538
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- Publication type:
- Article
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125926
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- Publication type:
- Article
Genome-Wide Linkage Scan Identifies Two Novel Genetic Loci for Coronary Artery Disease: In GeneQuest Families.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113935
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- Publication type:
- Article
Cloning and Functional Characterization of Novel Variants and Tissue-Specific Expression of Alternative Amino and Carboxyl Termini of Products of <i>Slc4a10</i>.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055974
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- Publication type:
- Article
Genetic Variants at Newly Identified Lipid Loci Are Associated with Coronary Heart Disease in a Chinese Han Population.
- Published in:
- PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027481
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- Publication type:
- Article
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.
- Published in:
- Human Genetics, 2020, v. 139, n. 4, p. 545, doi. 10.1007/s00439-020-02123-9
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- Publication type:
- Article
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33.
- Published in:
- Human Genetics, 2008, v. 124, n. 4, p. 423, doi. 10.1007/s00439-008-0566-9
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- Publication type:
- Article
Identification of a genetic locus for autosomal dominant disseminated superficial actinic porokeratosis on chromosome 1p31.3–p31.1.
- Published in:
- Human Genetics, 2008, v. 123, n. 5, p. 507, doi. 10.1007/s00439-008-0504-x
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- Publication type:
- Article
phlda3 overexpression impairs specification of hemangioblasts and vascular development.
- Published in:
- FEBS Journal, 2018, v. 285, n. 21, p. 4071, doi. 10.1111/febs.14653
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- Publication type:
- Article
Genetic Variant R952Q in LRP8 is Associated with Increased Plasma Triglyceride Levels in Patients with Early-Onset CAD and MI.
- Published in:
- Annals of Human Genetics, 2012, v. 76, n. 3, p. 193, doi. 10.1111/j.1469-1809.2012.00705.x
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- Publication type:
- Article
Endothelial cell metabolic memory causes cardiovascular dysfunction in diabetes.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 1, p. 196, doi. 10.1093/cvr/cvab013
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- Publication type:
- Article
ADAMTS16 activates latent TGF-β, accentuating fibrosis and dysfunction of the pressure-overloaded heart.
- Published in:
- Cardiovascular Research, 2020, v. 116, n. 5, p. 956, doi. 10.1093/cvr/cvz187
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- Publication type:
- Article
Lysosomal membrane protein TMEM106B modulates hematopoietic stem and progenitor cell proliferation and differentiation by regulating LAMP2A stability.
- Published in:
- FASEB Journal, 2024, v. 38, n. 15, p. 1, doi. 10.1096/fj.202400727R
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- Publication type:
- Article
Identification and characterization of a special type of subnuclear structure: AGGF1‐coated paraspeckles.
- Published in:
- FASEB Journal, 2022, v. 36, n. 6, p. 1, doi. 10.1096/fj.202101690RR
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- Publication type:
- Article
Role of epigenetic m<sup>6</sup>A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling.
- Published in:
- FASEB Journal, 2021, v. 35, n. 5, p. 1, doi. 10.1096/fj.202000516RR
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- Publication type:
- Article
Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat model.
- Published in:
- FASEB Journal, 2019, v. 33, n. 8, p. 8878, doi. 10.1096/fj.201802455RRR
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- Publication type:
- Article
Losartan protects against myocardial ischemia and reperfusion injury via vascular integrity preservation.
- Published in:
- FASEB Journal, 2019, v. 33, n. 7, p. 8555, doi. 10.1096/fj.201900060R
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- Publication type:
- Article
A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five‐generation Chinese family.
- Published in:
- Clinical Case Reports, 2018, v. 6, n. 8, p. 1612, doi. 10.1002/ccr3.1693
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- Publication type:
- Article
Loss of heterozygosity in human aberrant crypt foci (ACF), a putative precursor of colon cancer.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 6, p. 1153
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- Publication type:
- Article
A non-canonical pathway regulates ER stress signaling and blocks ER stress-induced apoptosis and heart failure.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00171-w
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- Publication type:
- Article
Analysis of causal effect of APOA5 variants on premature coronary artery disease.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 437, doi. 10.1111/ahg.12273
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- Publication type:
- Article
Identification of a Genetic Locus for Ichthyosis Vulgaris on Chromosome 10q22.3–q24.2.
- Published in:
- Journal of Investigative Dermatology, 2008, v. 128, n. 6, p. 1418, doi. 10.1038/sj.jid.5701191
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- Publication type:
- Article
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang–Wang syndrome.
- Published in:
- Acta Physiologica, 2022, v. 235, n. 1, p. 1, doi. 10.1111/apha.13800
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- Publication type:
- Article
Integrative Analysis of miRNA and mRNA Expression Profiles Associated With Human Atrial Aging.
- Published in:
- Frontiers in Physiology, 2019, p. 1, doi. 10.3389/fphys.2019.01226
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- Publication type:
- Article
Identification of a p.Trp403* nonsense variant in PHEX causing X‐linked hypophosphatemia by inhibiting p38 MAPK signaling.
- Published in:
- Human Mutation, 2019, v. 40, n. 7, p. 879, doi. 10.1002/humu.23743
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- Publication type:
- Article
Protein therapy of skeletal muscle atrophy and mechanism by angiogenic factor AGGF1.
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- Journal of Cachexia, Sarcopenia & Muscle, 2023, v. 14, n. 2, p. 978, doi. 10.1002/jcsm.13179
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- Publication type:
- Article
Genetic susceptibility to myocardial infarction and coronary artery disease.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 2, p. r117, doi. 10.1093/hmg/ddl183
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- Publication type:
- Article
Genetic susceptibility to myocardial infarction and coronary artery disease.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R117, doi. 10.1093/hmg/ddl183
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- Publication type:
- Article
Gene therapy targeting protein trafficking regulator MOG1 in mouse models of Brugada syndrome, arrhythmias, and mild cardiomyopathy.
- Published in:
- Science Translational Medicine, 2022, v. 14, n. 648, p. 1, doi. 10.1126/scitranslmed.abf3136
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- Publication type:
- Article
NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling.
- Published in:
- Obesity (19307381), 2023, v. 31, n. 1, p. 123, doi. 10.1002/oby.23580
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- Publication type:
- Article
TAGAP instructs Th17 differentiation by bridging Dectin activation to EPHB2 signaling in innate antifungal response.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15564-7
- By:
- Publication type:
- Article
Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 121, doi. 10.1186/1471-2350-11-121
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- Publication type:
- Article
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-87
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- Publication type:
- Article
A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 1, doi. 10.1186/1471-2350-8-52
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- Publication type:
- Article