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Results 1 - 20 of 45,986  for All Library Resources

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1
Higher Incidence of Chromosomal Aberrations in Operators Performing a Large Volume of Endovascular Procedures
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Higher Incidence of Chromosomal Aberrations in Operators Performing a Large Volume of Endovascular Procedures

Circulation (New York, N.Y.), 2022-06, Vol.145 (24), p.1808-1810 [Peer Reviewed Journal]

ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.121.058139 ;PMID: 35696458

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2
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
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Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes

Genetics in medicine, 2019-09, Vol.21 (9), p.1998-2006 [Peer Reviewed Journal]

2019 The Author(s) ;2019© American College of Medical Genetics and Genomics 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0467-4 ;PMID: 30828085

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3
Quality control and quality assurance in genotypic data for genome-wide association studies
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Quality control and quality assurance in genotypic data for genome-wide association studies

Genetic epidemiology, 2010-09, Vol.34 (6), p.591-602 [Peer Reviewed Journal]

2010 Wiley‐Liss, Inc. ;(c) 2010 Wiley-Liss, Inc. ;ISSN: 0741-0395 ;ISSN: 1098-2272 ;EISSN: 1098-2272 ;DOI: 10.1002/gepi.20516 ;PMID: 20718045

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4
Micronuclei and Genome Chaos: Changing the System Inheritance
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Micronuclei and Genome Chaos: Changing the System Inheritance

Genes, 2019-05, Vol.10 (5), p.366 [Peer Reviewed Journal]

2019 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. ;2019 by the authors. 2019 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes10050366 ;PMID: 31086101

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5
Combined PARP and ATR inhibition potentiates genome instability and cell death in ATM-deficient cancer cells
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Combined PARP and ATR inhibition potentiates genome instability and cell death in ATM-deficient cancer cells

Oncogene, 2020-06, Vol.39 (25), p.4869-4883 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;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: 0950-9232 ;EISSN: 1476-5594 ;DOI: 10.1038/s41388-020-1328-y ;PMID: 32444694

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6
Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma
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Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (50), p.20007-20012 [Peer Reviewed Journal]

Copyright 2007 The National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Dec 11, 2007 ;2007 by The National Academy of Sciences of the USA 2007 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0710052104 ;PMID: 18077431

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7
The cytogenetic constitution of human blastocysts: insights from comprehensive chromosome screening strategies
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The cytogenetic constitution of human blastocysts: insights from comprehensive chromosome screening strategies

Human reproduction update, 2019-01, Vol.25 (1), p.15-33 [Peer Reviewed Journal]

The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2018 ;ISSN: 1355-4786 ;EISSN: 1460-2369 ;DOI: 10.1093/humupd/dmy036 ;PMID: 30395265

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8
The genomic landscape of pediatric acute lymphoblastic leukemia
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Article
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The genomic landscape of pediatric acute lymphoblastic leukemia

Nature genetics, 2022-09, Vol.54 (9), p.1376-1389 [Peer Reviewed Journal]

2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Sep 2022 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01159-z ;PMID: 36050548

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9
Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases
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Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases

Genetics in medicine, 2017-02, Vol.19 (2), p.169-175 [Peer Reviewed Journal]

2017 The Author(s) ;Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017 Official journal of the American College of Medical Genetics and Genomics 2017 Official journal of the American College of Medical Genetics and Genomics ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2016.72 ;PMID: 27362910

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10
Molecular mechanisms and topological consequences of drastic chromosomal rearrangements of muntjac deer
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Molecular mechanisms and topological consequences of drastic chromosomal rearrangements of muntjac deer

Nature communications, 2021-11, Vol.12 (1), p.6858-6858, Article 6858 [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/s41467-021-27091-0 ;PMID: 34824214

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11
Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing
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Article
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Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing

Nature biotechnology, 2022-05, Vol.40 (5), p.731-740 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;The Author(s), under exclusive licence to Springer Nature America, Inc. 2021. Springer Nature or its licensor 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: 1087-0156 ;EISSN: 1546-1696 ;DOI: 10.1038/s41587-021-01133-w ;PMID: 34887556

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12
Genomic and Functional Approaches to Understanding Cancer Aneuploidy
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Genomic and Functional Approaches to Understanding Cancer Aneuploidy

Cancer cell, 2018-04, Vol.33 (4), p.676-689.e3 [Peer Reviewed Journal]

2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 1535-6108 ;EISSN: 1878-3686 ;DOI: 10.1016/j.ccell.2018.03.007 ;PMID: 29622463

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13
The relationship between blastocyst morphology, chromosomal abnormality, and embryo gender
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The relationship between blastocyst morphology, chromosomal abnormality, and embryo gender

Fertility and sterility, 2011-02, Vol.95 (2), p.520-524 [Peer Reviewed Journal]

American Society for Reproductive Medicine ;2011 American Society for Reproductive Medicine ;2015 INIST-CNRS ;Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved. ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2010.04.003 ;PMID: 20537630 ;CODEN: FESTAS

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14
Revised International Staging System for Multiple Myeloma: A Report From International Myeloma Working Group
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Article
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Revised International Staging System for Multiple Myeloma: A Report From International Myeloma Working Group

Journal of clinical oncology, 2015-09, Vol.33 (26), p.2863-2869 [Peer Reviewed Journal]

2015 by American Society of Clinical Oncology. ;2015 by American Society of Clinical Oncology 2015 American Society of Clinical Oncology ;ISSN: 0732-183X ;EISSN: 1527-7755 ;DOI: 10.1200/jco.2015.61.2267 ;PMID: 26240224

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15
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
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Article
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

Nature neuroscience, 2017-04, Vol.20 (4), p.602-611 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2017 ;ISSN: 1097-6256 ;EISSN: 1546-1726 ;DOI: 10.1038/nn.4524 ;PMID: 28263302 ;CODEN: NANEFN

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16
Assessing the combined toxic effects of metaldehyde mollucide
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Article
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Assessing the combined toxic effects of metaldehyde mollucide

Scientific reports, 2023-03, Vol.13 (1), p.4888-4888, Article 4888 [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/s41598-023-32183-6 ;PMID: 36966255

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17
Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation
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Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation

International journal of molecular sciences, 2018-12, Vol.20 (1), p.43 [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. ;2018 by the authors. 2018 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms20010043 ;PMID: 30583489

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18
Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group
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Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group

Blood, 2016-06, Vol.127 (24), p.2955-2962 [Peer Reviewed Journal]

2016 American Society of Hematology ;2016 by The American Society of Hematology. ;2016 by The American Society of Hematology 2016 ;ISSN: 0006-4971 ;ISSN: 1528-0020 ;EISSN: 1528-0020 ;DOI: 10.1182/blood-2016-01-631200 ;PMID: 27002115

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19
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0976-2 ;PMID: 30642344

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20
Unravelling tumour heterogeneity by single-cell profiling of circulating tumour cells
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Unravelling tumour heterogeneity by single-cell profiling of circulating tumour cells

Nature reviews. Cancer, 2019-10, Vol.19 (10), p.553-567 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2019 ;ISSN: 1474-175X ;EISSN: 1474-1768 ;DOI: 10.1038/s41568-019-0180-2 ;PMID: 31455893

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