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1
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-12869-0 ;PMID: 31653860

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2
Work-related COVID-19 transmission in six Asian countries/areas: A follow-up study
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Work-related COVID-19 transmission in six Asian countries/areas: A follow-up study

PloS one, 2020-05, Vol.15 (5), p.e0233588 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Lan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 Lan et al 2020 Lan et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0233588 ;PMID: 32428031

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3
Gut Microbiota in Hypertension and Atherosclerosis: A Review
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Gut Microbiota in Hypertension and Atherosclerosis: A Review

Nutrients, 2020-09, Vol.12 (10), p.2982 [Peer Reviewed Journal]

2020 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. ;2020 by the authors. 2020 ;ISSN: 2072-6643 ;EISSN: 2072-6643 ;DOI: 10.3390/nu12102982 ;PMID: 33003455

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4
Establishment of cholangiocarcinoma cell lines from patients in the endemic area of liver fluke infection in Thailand
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Article
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Establishment of cholangiocarcinoma cell lines from patients in the endemic area of liver fluke infection in Thailand

Tumor biology, 2017-11, Vol.39 (11), p.1010428317725925-1010428317725925 [Peer Reviewed Journal]

The Author(s) 2017 ;ISSN: 1010-4283 ;EISSN: 1423-0380 ;DOI: 10.1177/1010428317725925 ;PMID: 29110582

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5
Glycemic control by the SGLT2 inhibitor empagliflozin decreases aortic stiffness, renal resistivity index and kidney injury
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Glycemic control by the SGLT2 inhibitor empagliflozin decreases aortic stiffness, renal resistivity index and kidney injury

Cardiovascular diabetology, 2018-07, Vol.17 (1), p.108-108, Article 108 [Peer Reviewed Journal]

Copyright © 2018. 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) 2018 ;ISSN: 1475-2840 ;EISSN: 1475-2840 ;DOI: 10.1186/s12933-018-0750-8 ;PMID: 30060748

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6
The Potential Role of SGLT2 Inhibitors in the Treatment of Type 1 Diabetes Mellitus
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The Potential Role of SGLT2 Inhibitors in the Treatment of Type 1 Diabetes Mellitus

Drugs (New York, N.Y.), 2018-05, Vol.78 (7), p.717-726 [Peer Reviewed Journal]

Springer International Publishing AG, part of Springer Nature 2018 ;Copyright Springer Science & Business Media May 2018 ;ISSN: 0012-6667 ;EISSN: 1179-1950 ;DOI: 10.1007/s40265-018-0901-y ;PMID: 29663292

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7
Effects of Estrogen Therapies on Outcomes in Turner Syndrome: Assessment of Induction of Puberty and Adult Estrogen Use
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Article
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Effects of Estrogen Therapies on Outcomes in Turner Syndrome: Assessment of Induction of Puberty and Adult Estrogen Use

The journal of clinical endocrinology and metabolism, 2019-07, Vol.104 (7), p.2820-2826 [Peer Reviewed Journal]

Copyright © 2019 Endocrine Society 2019 ;Copyright © Oxford University Press 2015 ;Copyright © 2019 Endocrine Society. ;COPYRIGHT 2019 Oxford University Press ;Copyright © 2019 Endocrine Society ;ISSN: 0021-972X ;EISSN: 1945-7197 ;DOI: 10.1210/jc.2018-02137 ;PMID: 30726925

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8
Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
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Article
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Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases

Journal of assisted reproduction and genetics, 2018-02, Vol.35 (2), p.265-271 [Peer Reviewed Journal]

Springer Science+Business Media, LLC 2017 ;Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-017-1069-1 ;PMID: 29086320

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9
Breast tissue composition and its dependence on demographic risk factors for breast cancer: non-invasive assessment by time domain diffuse optical spectroscopy
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Breast tissue composition and its dependence on demographic risk factors for breast cancer: non-invasive assessment by time domain diffuse optical spectroscopy

PloS one, 2015-06, Vol.10 (6), p.e0128941-e0128941 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Taroni et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Taroni et al 2015 Taroni et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0128941 ;PMID: 26029912

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10
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
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Article
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Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.521-526 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group May 2012 ;Copyright © 2012 Macmillan Publishers Limited 2012 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.246 ;PMID: 22234154

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11
Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations
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Article
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Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations

Journal of human genetics, 2015-03, Vol.60 (3), p.133-137 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2014.116 ;PMID: 25566756

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12
Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients
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Article
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Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients

Biology of sex differences, 2017-08, Vol.8 (1), p.25-25, Article 25 [Peer Reviewed Journal]

Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 2042-6410 ;EISSN: 2042-6410 ;DOI: 10.1186/s13293-017-0146-6 ;PMID: 28789696

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13
Genetic analysis of products of conception using a HLPA/SNP-array strategy
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Article
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Genetic analysis of products of conception using a HLPA/SNP-array strategy

Molecular cytogenetics, 2019-09, Vol.12 (1), p.40-40, Article 40 [Peer Reviewed Journal]

The Author(s). 2019. ;COPYRIGHT 2019 BioMed Central Ltd. ;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: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0452-2 ;PMID: 31687045

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