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1
Increased risk for inflammatory bowel disease in congenital hypothyroidism supports the existence of a shared susceptibility factor
Increased risk for inflammatory bowel disease in congenital hypothyroidism supports the existence of a shared susceptibility factor
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Increased risk for inflammatory bowel disease in congenital hypothyroidism supports the existence of a shared susceptibility factor

Scientific reports, 2018-07, Vol.8 (1), p.10158-6, Article 10158 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2018 ;The Author(s) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-28586-5 ;PMID: 29977049

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2
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
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Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus

Scientific reports, 2019-04, Vol.9 (1), p.6196-6196, Article 6196 [Peer Reviewed Journal]

The Author(s) 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/s41598-019-42549-4 ;PMID: 30996265

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3
Toxicity of internalized polyalanine to cells depends on aggregation
Toxicity of internalized polyalanine to cells depends on aggregation
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Toxicity of internalized polyalanine to cells depends on aggregation

Scientific reports, 2021-12, Vol.11 (1), p.23441-23441, Article 23441 [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/s41598-021-02889-6 ;PMID: 34873226

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4
Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors

Scientific reports, 2020-09, Vol.10 (1), p.14859, Article 14859 [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/s41598-020-71844-8 ;PMID: 32908229

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5
Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies
Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies
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Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies

Scientific reports, 2019-08, Vol.9 (1), p.11842-11, Article 11842 [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/s41598-019-48156-7 ;PMID: 31413358

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6
In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus
In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus
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In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus

Scientific reports, 2018-01, Vol.8 (1), p.1-1, Article 1 [Peer Reviewed Journal]

2017. 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) 2017 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-017-17765-5 ;PMID: 29311619

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7
Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome
Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome
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Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome

Scientific reports, 2016-09, Vol.6 (1), p.33974-33974, Article 33974 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2016 ;Copyright © 2016, The Author(s) 2016 The Author(s) ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep33974 ;PMID: 27687499

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8
Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression
Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression
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Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression

Scientific reports, 2015-02, Vol.5 (1), p.8316-8316, Article 8316 [Peer Reviewed Journal]

Copyright Nature Publishing Group Feb 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/srep08316 ;PMID: 25661440

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9
Fontan-associated liver disease and hepatocellular carcinoma in adults
Fontan-associated liver disease and hepatocellular carcinoma in adults
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Fontan-associated liver disease and hepatocellular carcinoma in adults

Scientific reports, 2020-12, Vol.10 (1), p.21742-21742, Article 21742 [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/s41598-020-78840-y ;PMID: 33303924

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10
The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice
The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice
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The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice

Scientific reports, 2022-07, Vol.12 (1), p.11259-11259, Article 11259 [Peer Reviewed Journal]

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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-15151-4 ;PMID: 35788623

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11
Identifying Ear Abnormality from 2D Photographs Using Convolutional Neural Networks
Identifying Ear Abnormality from 2D Photographs Using Convolutional Neural Networks
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Identifying Ear Abnormality from 2D Photographs Using Convolutional Neural Networks

Scientific reports, 2019-12, Vol.9 (1), p.18198-6, Article 18198 [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/s41598-019-54779-7 ;PMID: 31796839

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12
Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome
Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome
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Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome

Scientific reports, 2017-04, Vol.7 (1), p.46565-46565, Article 46565 [Peer Reviewed Journal]

Copyright Nature Publishing Group Apr 2017 ;Copyright © 2017, The Author(s) 2017 The Author(s) ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep46565 ;PMID: 28422173

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13
Longitudinal morphological changes during recovery from brain deformation due to idiopathic normal pressure hydrocephalus after ventriculoperitoneal shunt surgery
Longitudinal morphological changes during recovery from brain deformation due to idiopathic normal pressure hydrocephalus after ventriculoperitoneal shunt surgery
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Longitudinal morphological changes during recovery from brain deformation due to idiopathic normal pressure hydrocephalus after ventriculoperitoneal shunt surgery

Scientific reports, 2019-11, Vol.9 (1), p.17318-13, Article 17318 [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/s41598-019-53888-7 ;PMID: 31754171

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14
A novel index equivalent to the myocardial performance index for right ventricular functional assessment in children and adolescent patients
A novel index equivalent to the myocardial performance index for right ventricular functional assessment in children and adolescent patients
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A novel index equivalent to the myocardial performance index for right ventricular functional assessment in children and adolescent patients

Scientific reports, 2019-12, Vol.9 (1), p.19975-10, Article 19975 [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/s41598-019-56564-y ;PMID: 31882794

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15
Structural basis for misregulation of kinesin KIF21A autoinhibition by CFEOM1 disease mutations
Structural basis for misregulation of kinesin KIF21A autoinhibition by CFEOM1 disease mutations
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Structural basis for misregulation of kinesin KIF21A autoinhibition by CFEOM1 disease mutations

Scientific reports, 2016-08, Vol.6 (1), p.30668-30668, Article 30668 [Peer Reviewed Journal]

Copyright Nature Publishing Group Aug 2016 ;Copyright © 2016, The Author(s) 2016 The Author(s) ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep30668 ;PMID: 27485312

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16
Six3 regulates optic nerve development via multiple mechanisms
Six3 regulates optic nerve development via multiple mechanisms
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Six3 regulates optic nerve development via multiple mechanisms

Scientific reports, 2016-01, Vol.6 (1), p.20267-20267, Article 20267 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jan 2016 ;Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep20267 ;PMID: 26822689

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17
Isolated Congenital Anosmia and CNGA2 Mutation
Isolated Congenital Anosmia and CNGA2 Mutation
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Isolated Congenital Anosmia and CNGA2 Mutation

Scientific reports, 2017-06, Vol.7 (1), p.2667-5, Article 2667 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2017 ;The Author(s) 2017 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-017-02947-y ;PMID: 28572688

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18
A palindromic motif in the -2084 to -2078 upstream region is essential for ABCA12 promoter function in cultured human keratinocytes
A palindromic motif in the -2084 to -2078 upstream region is essential for ABCA12 promoter function in cultured human keratinocytes
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A palindromic motif in the -2084 to -2078 upstream region is essential for ABCA12 promoter function in cultured human keratinocytes

Scientific reports, 2014-10, Vol.4 (1), p.6737, Article 6737 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2014 ;Copyright © 2014, Macmillan Publishers Limited. All rights reserved 2014 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep06737 ;PMID: 25338618

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19
Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use
Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use
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Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use

Scientific reports, 2018-05, Vol.8 (1), p.8443-7, Article 8443 [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/s41598-018-26723-8 ;PMID: 29855564

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20
Consequences of in utero exposure to Zika virus in offspring of AG129 mice
Consequences of in utero exposure to Zika virus in offspring of AG129 mice
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Consequences of in utero exposure to Zika virus in offspring of AG129 mice

Scientific reports, 2018-06, Vol.8 (1), p.9384-11, Article 9384 [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/s41598-018-27611-x ;PMID: 29925850

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