Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Congenital diaphragmatic hernias: from genes to mechanisms to therapiesDisease models & mechanisms, 2017-08, Vol.10 (8), p.955-970 [Peer Reviewed Journal]2017. Published by The Company of Biologists Ltd. ;2017. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017. Published by The Company of Biologists Ltd 2017 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.028365 ;PMID: 28768736Full text available |
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2 |
Material Type: Article
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The clinical manifestations, molecular mechanisms and treatment of craniosynostosisDisease models & mechanisms, 2022-04, Vol.15 (4) [Peer Reviewed Journal]2022. Published by The Company of Biologists Ltd. ;2022. This work is licensed 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. ;2022. Published by The Company of Biologists Ltd 2022 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049390 ;PMID: 35451466Full text available |
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3 |
Material Type: Article
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The RASopathies: from pathogenetics to therapeuticsDisease models & mechanisms, 2022-02, Vol.15 (2) [Peer Reviewed Journal]2022. Published by The Company of Biologists Ltd. ;2022. This work is licensed 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. ;2022. Published by The Company of Biologists Ltd 2022 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049107 ;PMID: 35178568Full text available |
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4 |
Material Type: Article
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Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disordersDisease models & mechanisms, 2018-10, Vol.11 (10) [Peer Reviewed Journal]2018. Published by The Company of Biologists Ltd. ;2018. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018. Published by The Company of Biologists Ltd 2018 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.035469 ;PMID: 30355756Full text available |
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5 |
Material Type: Article
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Advancing congenital defect phenotyping using HREM imagingDisease models & mechanisms, 2014-10, Vol.7 (10), p.e1002-e1002 [Peer Reviewed Journal]2014. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2014. Published by The Company of Biologists Ltd 2014 ;ISSN: 1754-8403 ;EISSN: 1754-8411Full text available |
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6 |
Material Type: Article
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The zebrafish as a tool to identify novel therapies for human cardiovascular diseaseDisease models & mechanisms, 2014-07, Vol.7 (7), p.763-767 [Peer Reviewed Journal]2014. Published by The Company of Biologists Ltd. ;2014. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2014. Published by The Company of Biologists Ltd 2014 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.016170 ;PMID: 24973746Full text available |
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7 |
Material Type: Article
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First person – Rebecca RolfeDisease models & mechanisms, 2021-04, Vol.14 (4) [Peer Reviewed Journal]2021. This work is licensed 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. ;2021. Published by The Company of Biologists Ltd 2021 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049040Full text available |
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8 |
Material Type: Article
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Preclinical research in Rett syndrome: setting the foundation for translational successDisease models & mechanisms, 2012-11, Vol.5 (6), p.733-745 [Peer Reviewed Journal]2012. This work is licensed under http://creativecommons.org/licenses/by-nc-sa/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2012. Published by The Company of Biologists Ltd 2012 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.011007 ;PMID: 23115203Full text available |
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9 |
Material Type: Article
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Ribosomopathies: how a common root can cause a tree of pathologiesDisease models & mechanisms, 2015-09, Vol.8 (9), p.1013-1026 [Peer Reviewed Journal]2015. Published by The Company of Biologists Ltd. ;2015. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015. Published by The Company of Biologists Ltd 2015 ;ISSN: 1754-8403 ;ISSN: 1754-8411 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.020529 ;PMID: 26398160Full text available |
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10 |
Material Type: Article
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Collagen VI in healthy and diseased nervous systemDisease models & mechanisms, 2018-06, Vol.11 (6) [Peer Reviewed Journal]2018. Published by The Company of Biologists Ltd. ;2018. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018. Published by The Company of Biologists Ltd 2018 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.032946 ;PMID: 29728408Full text available |
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11 |
Material Type: Article
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The predictive value of models of neuromuscular disorders to potentiate clinical translationDisease models & mechanisms, 2022-07, Vol.15 (7) [Peer Reviewed Journal]2022. This work is licensed 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. ;2022. Published by The Company of Biologists Ltd 2022 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049788 ;PMID: 35912512Full text available |
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12 |
Material Type: Article
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Repurposing the aldose reductase inhibitor and diabetic neuropathy drug epalrestat for the congenital disorder of glycosylation PMM2-CDGDisease models & mechanisms, 2019-11, Vol.12 (11) [Peer Reviewed Journal]2019. Published by The Company of Biologists Ltd. ;2019. This work is licensed 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. ;2019. Published by The Company of Biologists Ltd 2019 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.040584 ;PMID: 31636082Full text available |
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13 |
Material Type: Article
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The Finnish genetic heritage in 2022 – from diagnosis to translational researchDisease models & mechanisms, 2022-10, Vol.15 (10) [Peer Reviewed Journal]2022. This work is licensed 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. ;2022. Published by The Company of Biologists Ltd 2022 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049490 ;PMID: 36285626Full text available |
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14 |
Material Type: Article
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Functional loss of Ccdc151 leads to hydrocephalus in a mouse model of primary ciliary dyskinesiaDisease models & mechanisms, 2019-08, Vol.12 (8) [Peer Reviewed Journal]2019. This work is licensed 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. ;2019. Published by The Company of Biologists Ltd 2019 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.038489 ;PMID: 31383820Full text available |
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15 |
Material Type: Article
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Functional testing of a human PBX3 variant in zebrafish reveals a potential modifier role in congenital heart defectsDisease models & mechanisms, 2018-10, Vol.11 (10) [Peer Reviewed Journal]2018. Published by The Company of Biologists Ltd. ;2018. This work is licensed under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018. Published by The Company of Biologists Ltd 2018 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.035972 ;PMID: 30355621Full text available |
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16 |
Material Type: Article
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Collagen VI deficiency causes behavioral abnormalities and cortical dopaminergic dysfunctionDisease models & mechanisms, 2022-09, Vol.15 (9) [Peer Reviewed Journal]2022. This work is licensed 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. ;2022. Published by The Company of Biologists Ltd 2022 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049481 ;PMID: 35946603Full text available |
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17 |
Material Type: Article
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First person – Emilie Auxerre-Plantié and Tanja NielsenDisease models & mechanisms, 2020-12, Vol.13 (12) [Peer Reviewed Journal]2020. This work is licensed 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. ;2020. Published by The Company of Biologists Ltd 2020 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.047902Full text available |
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18 |
Material Type: Article
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Mending a broken heart: In vitro , in vivo and in silico models of congenital heart diseaseDisease models & mechanisms, 2021-03, Vol.14 (3) [Peer Reviewed Journal]2021. Published by The Company of Biologists Ltd. ;2021. This work is licensed 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. ;2021. Published by The Company of Biologists Ltd 2021 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.047522 ;PMID: 33787508Full text available |
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19 |
Material Type: Article
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‘Big issues’ in neurodevelopment for children and adults with congenital heart diseaseOpen heart, 2019, Vol.6 (2), p.e000998-e000998 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019 ;ISSN: 2053-3624 ;ISSN: 2398-595X ;EISSN: 2053-3624 ;DOI: 10.1136/openhrt-2018-000998 ;PMID: 31354955Full text available |
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20 |
Material Type: Article
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Developmental disorders Journal Meeting: a collaboration between Development and Disease Models & MechanismsDisease models & mechanisms, 2021-09, Vol.14 (9) [Peer Reviewed Journal]2021. This work is licensed 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. ;2021. Published by The Company of Biologists Ltd 2021 ;ISSN: 1754-8403 ;EISSN: 1754-8411 ;DOI: 10.1242/dmm.049268 ;PMID: 34515289Full text available |