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1	Material Type: Article	Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot Genetics in medicine, 2019-04, Vol.21 (4), p.1001-1007 [Peer Reviewed Journal] 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0260-9 ;PMID: 30232381 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	Growth and development of children under 5 years of age with tetralogy of Fallot in a Chinese population Scientific reports, 2021-07, Vol.11 (1), p.14255-14255, Article 14255 [Peer Reviewed Journal] The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-93726-3 ;PMID: 34244570 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	Altered brain structure in preschool-aged children with tetralogy of Fallot Pediatric research, 2023-04, Vol.93 (5), p.1321-1327 [Peer Reviewed Journal] 2022. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc. ;The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc 2022. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-022-01987-z ;PMID: 35194163 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Biventricular shape modes discriminate pulmonary valve replacement in tetralogy of Fallot better than imaging indices Scientific reports, 2023-02, Vol.13 (1), p.2335-2335, Article 2335 [Peer Reviewed Journal] 2023. The Author(s). ;The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-023-28358-w ;PMID: 36759522 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Sexual difference of small RNA expression in Tetralogy of Fallot Scientific reports, 2018-08, Vol.8 (1), p.12847-8, Article 12847 [Peer Reviewed Journal] 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-31243-6 ;PMID: 30150777 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot Genetics in medicine, 2021-10, Vol.23 (10), p.1952-1960 [Peer Reviewed Journal] 2021 The Author(s) ;2021. The Author(s). ;The Author(s) 2021. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021, corrected publication 2021 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01212-y ;PMID: 34113005 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	Altered microRNA and target gene expression related to Tetralogy of Fallot Scientific reports, 2019-12, Vol.9 (1), p.19063-12, Article 19063 [Peer Reviewed Journal] 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-019-55570-4 ;PMID: 31836860 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	Circulation derived from 4D flow MRI correlates with right ventricular dysfunction in patients with tetralogy of Fallot Scientific reports, 2021-06, Vol.11 (1), p.11623-11623, Article 11623 [Peer Reviewed Journal] The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-91125-2 ;PMID: 34079023 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation Scientific reports, 2020-07, Vol.10 (1), p.10921, Article 10921 [Peer Reviewed Journal] The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-67872-z ;PMID: 32616843 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
10	Material Type: Article	Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot Journal of human genetics, 2022-10, Vol.67 (10), p.613-615 [Peer Reviewed Journal] 2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-022-01051-y ;PMID: 35718831 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
11	Material Type: Article	Insights Image for "Dysregulation of Notch signaling in cardiac mesenchymal cells of patients with Tetralogy of Fallot" Pediatric research, 2020-07, Vol.88 (1), p.139-139 [Peer Reviewed Journal] International Pediatric Research Foundation, Inc 2020. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-0848-z ;PMID: 32170193 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	A quantitative assessment of aorta root rotation in patients with tetralogy of Fallot evaluated by MSCT Scientific reports, 2021-07, Vol.11 (1), p.14336-14336, Article 14336 [Peer Reviewed Journal] The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-93814-4 ;PMID: 34253813 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	Material Type: Article	BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis Scientific reports, 2020-08, Vol.10 (1), p.14167-14167, Article 14167 [Peer Reviewed Journal] The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-70806-4 ;PMID: 32843646 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
14	Material Type: Article	Dysregulation of Notch signaling in cardiac mesenchymal cells of patients with tetralogy of Fallot Pediatric research, 2020-07, Vol.88 (1), p.38-47 [Peer Reviewed Journal] International Pediatric Research Foundation, Inc 2020. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-0760-6 ;PMID: 31952074 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot public 629918;All rights reserved ;ISSN: 1530-0366 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01212-y Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot Genetics in medicine, 2021-10, Vol.23 (10), p.2013-2013 [Peer Reviewed Journal] 2021 The Author(s) ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01279-7 ;PMID: 34522030 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
17	Material Type: Article	A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect Journal of human genetics, 2010-10, Vol.55 (10), p.662-667 [Peer Reviewed Journal] The Japan Society of Human Genetics 2010. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2010.84 ;PMID: 20631719 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	CpG island shore methylation of ZFPM2 is identified in tetralogy of fallot samples Pediatric research, 2016-07, Vol.80 (1), p.151-158 [Peer Reviewed Journal] Copyright Nature Publishing Group Jul 2016 ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/pr.2016.42 ;PMID: 26959486 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair Pediatric research, 2012-10, Vol.72 (4), p.407-413 [Peer Reviewed Journal] 2015 INIST-CNRS ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/pr.2012.95 ;PMID: 22797143 ;CODEN: PEREBL Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	Abnormal developmental trajectory and vulnerability to cardiac arrhythmias in tetralogy of Fallot with DiGeorge syndrome Communications biology, 2023-09, Vol.6 (1), p.969-969, Article 969 [Peer Reviewed Journal] The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Springer Nature Limited 2023 ;ISSN: 2399-3642 ;EISSN: 2399-3642 ;DOI: 10.1038/s42003-023-05344-6 ;PMID: 37740059 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by

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Results 1 - 20 of 582 for All Library Resources

2022. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc. ;The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc 2022. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-022-01987-z ;PMID: 35194163

International Pediatric Research Foundation, Inc 2020. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-0848-z ;PMID: 32170193

International Pediatric Research Foundation, Inc 2020. ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-0760-6 ;PMID: 31952074

public 629918;All rights reserved ;ISSN: 1530-0366 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01212-y

The Japan Society of Human Genetics 2010. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2010.84 ;PMID: 20631719

Copyright Nature Publishing Group Jul 2016 ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/pr.2016.42 ;PMID: 26959486

2015 INIST-CNRS ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/pr.2012.95 ;PMID: 22797143 ;CODEN: PEREBL

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