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1
Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)
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Correction: Genetic evaluation of cardiomyopathy: a clinicalpractice resource of the American College of Medical Genetics and Genomics(ACMG)

Genetics in medicine, 2019-10, Vol.21 (10), p.2406-2409 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0521-2

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2
Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx mice
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Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx mice

Scientific reports, 2015-03, Vol.5 (1), p.8986-8986, Article 8986 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2015 ;Copyright © 2015, Macmillan Publishers Limited. All rights reserved 2015 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep08986 ;PMID: 25758104

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3
Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling
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Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling

Scientific reports, 2018-01, Vol.8 (1), p.1998-11, Article 1998 [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/s41598-018-20114-9 ;PMID: 29386531

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4
Silencing long non-coding RNA Kcnq1ot1 alleviates pyroptosis and fibrosis in diabetic cardiomyopathy
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Silencing long non-coding RNA Kcnq1ot1 alleviates pyroptosis and fibrosis in diabetic cardiomyopathy

Cell death & disease, 2018-09, Vol.9 (10), p.1000-13, Article 1000 [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: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/s41419-018-1029-4 ;PMID: 30250027

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5
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
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Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy

Nature communications, 2020-05, Vol.11 (1), p.2254-2254, Article 2254 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-15823-7 ;PMID: 32382064

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6
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
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Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

Genetics in medicine, 2021-05, Vol.23 (5), p.856-864 [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: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-01049-x ;PMID: 33500567

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7
Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy
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Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy

Genetics in medicine, 2018-11, Vol.20 (11), p.1374-1386 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2018.9 ;PMID: 29517769

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8
Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
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Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals

Genetics in medicine, 2010-11, Vol.12 (11), p.655-667 [Peer Reviewed Journal]

2010 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1097/GIM.0b013e3181f2481f ;PMID: 20864896

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9
Myocardial tissue-specific Dnmt1 knockout in rats protects against pathological injury induced by Adriamycin
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Myocardial tissue-specific Dnmt1 knockout in rats protects against pathological injury induced by Adriamycin

Laboratory investigation, 2020-07, Vol.100 (7), p.974-985 [Peer Reviewed Journal]

2020 United States & Canadian Academy of Pathology ;The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2020. ;The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2020 ;ISSN: 0023-6837 ;EISSN: 1530-0307 ;DOI: 10.1038/s41374-020-0402-y ;PMID: 32051532

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10
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity
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Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity

Genetics in medicine, 2015-11, Vol.17 (11), p.880-888 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2015 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2014.205 ;PMID: 25611685

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11
WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
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WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling

Nature communications, 2019-08, Vol.10 (1), p.3616-19, Article 3616 [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. ;Attribution ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11551-9 ;PMID: 31399586

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12
Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging
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Homogeneous 2D and 3D alignment of cardiomyocyte in dilated cardiomyopathy revealed by intravital heart imaging

Scientific reports, 2021-07, Vol.11 (1), p.14698-14698, Article 14698 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-94100-z ;PMID: 34282197

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13
Correction: Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy
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Correction: Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy

Laboratory investigation, 2020-06, Vol.100 (6), p.900-900 [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. This work is published under https://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: 0023-6837 ;EISSN: 1530-0307 ;DOI: 10.1038/s41374-020-0414-7 ;PMID: 32203148

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14
Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy
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Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy

Nature communications, 2023-06, Vol.14 (1), p.3714-3714, Article 3714 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-023-39352-1 ;PMID: 37349314

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15
Investigation of diets associated with dilated cardiomyopathy in dogs using foodomics analysis
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Investigation of diets associated with dilated cardiomyopathy in dogs using foodomics analysis

Scientific reports, 2021-08, Vol.11 (1), p.15881-12, Article 15881 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-94464-2 ;PMID: 34354102

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16
Intergenerational inheritance of high fat diet-induced cardiac lipotoxicity in Drosophila
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Intergenerational inheritance of high fat diet-induced cardiac lipotoxicity in Drosophila

Nature communications, 2019-01, Vol.10 (1), p.193-14, Article 193 [Peer Reviewed Journal]

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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-08128-3 ;PMID: 30643137

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17
Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy
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Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy

European journal of human genetics : EJHG, 2023-01, Vol.31 (1), p.97-104 [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: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-022-01204-9 ;PMID: 36253531

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18
Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy
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Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy

European journal of human genetics : EJHG, 2023-07, Vol.31 (7), p.776-783 [Peer Reviewed Journal]

2023. The Author(s), under exclusive licence to European Society of Human Genetics. ;The Author(s), under exclusive licence to European Society of Human Genetics 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-023-01384-y ;PMID: 37198425

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19
Propionic acidemia as a cause of adult-onset dilated cardiomyopathy
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Propionic acidemia as a cause of adult-onset dilated cardiomyopathy

European journal of human genetics : EJHG, 2017-11, Vol.25 (11), p.1195-1201 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2017 ;Copyright © 2017 Macmillan Publishers Limited, part of Springer Nature. 2017 Macmillan Publishers Limited, part of Springer Nature. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2017.127 ;PMID: 28853722

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20
Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy
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Phospholamban antisense oligonucleotides improve cardiac function in murine cardiomyopathy

Nature communications, 2021-08, Vol.12 (1), p.5180-5180, Article 5180 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-25439-0 ;PMID: 34462437

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