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Results 1 - 20 of 67,949  for All Library Resources

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1
Role of Epigenetics in Cardiac Development and Congenital Diseases
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Role of Epigenetics in Cardiac Development and Congenital Diseases

Physiological reviews, 2018-10, Vol.98 (4), p.2453-2475 [Peer Reviewed Journal]

Copyright American Physiological Society Oct 2018 ;ISSN: 0031-9333 ;EISSN: 1522-1210 ;DOI: 10.1152/physrev.00048.2017 ;PMID: 30156497

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2
Exogestation for treating premature births and congenital diseases: Artificial womb technology edges towards first trials in humans
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Exogestation for treating premature births and congenital diseases: Artificial womb technology edges towards first trials in humans

EMBO reports, 2024-01, Vol.25 (1), p.17-20 [Peer Reviewed Journal]

The Author(s) 2024 ;EISSN: 1469-3178 ;DOI: 10.1038/s44319-023-00022-4

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3
Winner of 2023 Wakley–Wu Lien Teh Prize: are congenital diseases a curse?
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Winner of 2023 Wakley–Wu Lien Teh Prize: are congenital diseases a curse?

The Lancet (British edition), 2024-02, Vol.403 (10425), p.419-419 [Peer Reviewed Journal]

2024 Elsevier Ltd ;2024. Elsevier Ltd ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(24)00130-2 ;PMID: 38309771

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4
Deubiquitylases in developmental ubiquitin signaling and congenital diseases
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Deubiquitylases in developmental ubiquitin signaling and congenital diseases

Cell death and differentiation, 2021-02, Vol.28 (2), p.538-556 [Peer Reviewed Journal]

This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 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. ;This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 ;ISSN: 1350-9047 ;EISSN: 1476-5403 ;DOI: 10.1038/s41418-020-00697-5 ;PMID: 33335288

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5
Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms
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Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms

International journal of molecular sciences, 2021-01, Vol.22 (2), p.911 [Peer Reviewed Journal]

2021. 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. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms22020911 ;PMID: 33477564

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6
Pre-Ribosomal RNA Processing in Human Cells: From Mechanisms to Congenital Diseases
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Pre-Ribosomal RNA Processing in Human Cells: From Mechanisms to Congenital Diseases

Biomolecules (Basel, Switzerland), 2018-10, Vol.8 (4), p.123 [Peer Reviewed Journal]

2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;2018 by the authors. 2018 ;ISSN: 2218-273X ;EISSN: 2218-273X ;DOI: 10.3390/biom8040123 ;PMID: 30356013

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7
Some congenital diseases may just show up later
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Some congenital diseases may just show up later

Journal of clinical sleep medicine, 2020-11, Vol.16 (11), p.1835-1836

2020 American Academy of Sleep Medicine 2020 ;ISSN: 1550-9389 ;EISSN: 1550-9397 ;DOI: 10.5664/jcsm.8850 ;PMID: 32990200

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8
Infants with Congenital Diseases Identified through Newborn Screening-United States, 2018-2020
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Infants with Congenital Diseases Identified through Newborn Screening-United States, 2018-2020

International journal of neonatal screening, 2023-04, Vol.9 (2), p.23 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 2409-515X ;EISSN: 2409-515X ;DOI: 10.3390/ijns9020023 ;PMID: 37092517

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9
Bone fragility in patients affected by congenital diseases non skeletal in origin
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Bone fragility in patients affected by congenital diseases non skeletal in origin

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.11-11, Article 11 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed 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: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-020-01611-5 ;PMID: 33407701

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10
Mutations of small heat shock proteins and human congenital diseases
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Mutations of small heat shock proteins and human congenital diseases

Biochemistry (Moscow), 2012-12, Vol.77 (13), p.1500-1514 [Peer Reviewed Journal]

Pleiades Publishing, Ltd. 2012 ;COPYRIGHT 2012 Springer ;ISSN: 0006-2979 ;EISSN: 1608-3040 ;DOI: 10.1134/S0006297912130081 ;PMID: 23379525

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11
Congenital Diseases in Harbor Seals (Phoca vitulina richardsii) from the Salish Sea
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Congenital Diseases in Harbor Seals (Phoca vitulina richardsii) from the Salish Sea

Journal of wildlife diseases, 2021-07, Vol.57 (3), p.672-677 [Peer Reviewed Journal]

Wildlife Disease Association 2021 ;Wildlife Disease Association 2021. ;ISSN: 0090-3558 ;EISSN: 1943-3700 ;DOI: 10.7589/JWD-D-20-00179 ;PMID: 34015807

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12
Congenital diseases caused by defective O-glycosylation of Notch receptors
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Congenital diseases caused by defective O-glycosylation of Notch receptors

Nagoya journal of medical science, 2018-08, Vol.80 (3), p.299-307

ISSN: 0027-7622 ;EISSN: 2186-3326 ;DOI: 10.18999/nagjms.80.3.299 ;PMID: 30214079

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13
New insights into the roles for DYRK family in mammalian development and congenital diseases
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New insights into the roles for DYRK family in mammalian development and congenital diseases

Genes & diseases, 2023-05, Vol.10 (3), p.758-770 [Peer Reviewed Journal]

2022 Chongqing Medical University ;2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. ;2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. 2022 Chongqing Medical University ;ISSN: 2352-3042 ;ISSN: 2352-4820 ;EISSN: 2352-3042 ;DOI: 10.1016/j.gendis.2021.12.004 ;PMID: 37396550

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14
Epigenetic deregulation of imprinting in congenital diseases of aberrant growth
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Epigenetic deregulation of imprinting in congenital diseases of aberrant growth

BioEssays, 2006-05, Vol.28 (5), p.453-459 [Peer Reviewed Journal]

Copyright © 2006 Wiley Periodicals, Inc. ;2006 Wiley Periodicals, Inc. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0265-9247 ;EISSN: 1521-1878 ;DOI: 10.1002/bies.20407 ;PMID: 16615080

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15
Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome
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Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome

Cardiovascular innovations and applications, 2024-01, Vol.9 (1), p.984 [Peer Reviewed Journal]

ISSN: 2009-8618 ;EISSN: 2009-8782 ;DOI: 10.15212/CVIA.2024.0005

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16
The impact of neighborhood to industrial areas on health in Uzbekistan: an ecological analysis of congenital diseases, infant mortality, and lung cancer
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Article
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The impact of neighborhood to industrial areas on health in Uzbekistan: an ecological analysis of congenital diseases, infant mortality, and lung cancer

Environmental science and pollution research international, 2020-05, Vol.27 (14), p.17243-17249 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 0944-1344 ;EISSN: 1614-7499 ;DOI: 10.1007/s11356-020-08190-9 ;PMID: 32152854

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17
Klinefelterʼs Syndrome-Associated Alpha-1 Antitrypsin Cholestatic Phenotype: A Genetic Linkage Between Two Congenital Diseases: 2005
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Klinefelterʼs Syndrome-Associated Alpha-1 Antitrypsin Cholestatic Phenotype: A Genetic Linkage Between Two Congenital Diseases: 2005

The American journal of gastroenterology, 2016-10, Vol.111, p.S955-S956 [Peer Reviewed Journal]

ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/00000434-201610001-02005

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18
Correlation of Folic Acid Metabolism Gene Polymorphism with Maternal Delivery Outcomes and Neonatal Congenital Diseases During Pregnancy
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Article
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Correlation of Folic Acid Metabolism Gene Polymorphism with Maternal Delivery Outcomes and Neonatal Congenital Diseases During Pregnancy

International journal of pharmacology, 2022-05, Vol.18 (5), p.869-876

ISSN: 1811-7775 ;EISSN: 1812-5700 ;DOI: 10.3923/ijp.2022.869.876

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19
S2676 Abnormal Liver Enzymes Secondary to Congenital Hepatic Fibrosis with Multiple Biliary Cysts
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S2676 Abnormal Liver Enzymes Secondary to Congenital Hepatic Fibrosis with Multiple Biliary Cysts

The American journal of gastroenterology, 2021-10, Vol.116 (1), p.S1122-S1122 [Peer Reviewed Journal]

2021 by The American College of Gastroenterology ;ISSN: 0002-9270 ;EISSN: 1572-0241 ;DOI: 10.14309/01.ajg.0000784236.02409.43

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20
Congenital diseases with multi-organ expression as an indication for liver transplantation in children during the first years of life: Integrative approach to improve the outcomes
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Congenital diseases with multi-organ expression as an indication for liver transplantation in children during the first years of life: Integrative approach to improve the outcomes

Journal of liver transplantation, 2024-05, Vol.14, Article 100216 [Peer Reviewed Journal]

2024 The Author(s) ;ISSN: 2666-9676 ;EISSN: 2666-9676 ;DOI: 10.1016/j.liver.2024.100216

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