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1
Identification and Molecular Characterization of HNF1B Gene Mutations in Indian Diabetic Patients with Renal Abnormalities
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Identification and Molecular Characterization of HNF1B Gene Mutations in Indian Diabetic Patients with Renal Abnormalities

Annals of human genetics, 2015-01, Vol.79 (1), p.10-19 [Peer Reviewed Journal]

2014 John Wiley & Sons Ltd/University College London ;2014 John Wiley & Sons Ltd/University College London. ;Copyright © 2014 John Wiley & Sons Ltd/University College London ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1111/ahg.12093 ;PMID: 25441779 ;CODEN: ANHGAA

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2
Signatures of tumour immunity distinguish Asian and non-Asian gastric adenocarcinomas
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Signatures of tumour immunity distinguish Asian and non-Asian gastric adenocarcinomas

Gut, 2015-11, Vol.64 (11), p.1721-1731 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Copyright: 2015 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2015 ;ISSN: 0017-5749 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2014-308252 ;PMID: 25385008 ;CODEN: GUTTAK

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3
Adult Moyamoya Disease: A Burden of Intracranial Stenosis in East Asians?
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Adult Moyamoya Disease: A Burden of Intracranial Stenosis in East Asians?

PloS one, 2015-06, Vol.10 (6), p.e0130663-e0130663 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Bang 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 Bang et al 2015 Bang et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0130663 ;PMID: 26125557

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4
High Blood Pressure and Its Association With Incident Diabetes Over 10 Years in the Korean Genome and Epidemiology Study (KoGES)
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High Blood Pressure and Its Association With Incident Diabetes Over 10 Years in the Korean Genome and Epidemiology Study (KoGES)

Diabetes care, 2015-07, Vol.38 (7), p.1333-1338 [Peer Reviewed Journal]

2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. ;Copyright American Diabetes Association Jul 2015 ;ISSN: 0149-5992 ;EISSN: 1935-5548 ;DOI: 10.2337/dc14-1931 ;PMID: 25986660 ;CODEN: DICAD2

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5
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes
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Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

Brain (London, England : 1878), 2014-09, Vol.137 (Pt 9), p.2444-2455 [Peer Reviewed Journal]

2015 INIST-CNRS ;The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2014 ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/awu174 ;PMID: 24972706

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6
Comprehensive Characterization of Oncogenic Drivers in Asian Lung Adenocarcinoma
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Comprehensive Characterization of Oncogenic Drivers in Asian Lung Adenocarcinoma

Journal of thoracic oncology, 2016-12, Vol.11 (12), p.2129-2140 [Peer Reviewed Journal]

2016 International Association for the Study of Lung Cancer ;Copyright © 2016 by the International Association for the Study of Lung Cancer ;Copyright © 2016 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved. ;ISSN: 1556-0864 ;EISSN: 1556-1380 ;DOI: 10.1016/j.jtho.2016.08.142 ;PMID: 27615396

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7
Variants conferring risk of atrial fibrillation on chromosome 4q25
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Variants conferring risk of atrial fibrillation on chromosome 4q25

Nature, 2007-07, Vol.448 (7151), p.353-357 [Peer Reviewed Journal]

2007 INIST-CNRS ;COPYRIGHT 2007 Nature Publishing Group ;COPYRIGHT 2007 Nature Publishing Group ;Copyright Nature Publishing Group Jul 19, 2007 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;EISSN: 1476-4679 ;DOI: 10.1038/nature06007 ;PMID: 17603472 ;CODEN: NATUAS

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8
HLA‐B alleles associated with severe cutaneous reactions to antiepileptic drugs in Han Chinese
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HLA‐B alleles associated with severe cutaneous reactions to antiepileptic drugs in Han Chinese

Epilepsia (Copenhagen), 2013-07, Vol.54 (7), p.1307-1314 [Peer Reviewed Journal]

Wiley Periodicals, Inc. © 2013 International League Against Epilepsy ;Wiley Periodicals, Inc. © 2013 International League Against Epilepsy. ;Copyright © 2013 International League Against Epilepsy ;ISSN: 0013-9580 ;EISSN: 1528-1167 ;DOI: 10.1111/epi.12217 ;PMID: 23692434 ;CODEN: EPILAK

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9
Discoveries beyond BRCA1/2: Multigene testing in an Asian multi-ethnic cohort suspected of hereditary breast cancer syndrome in the real world
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Discoveries beyond BRCA1/2: Multigene testing in an Asian multi-ethnic cohort suspected of hereditary breast cancer syndrome in the real world

PloS one, 2019-03, Vol.14 (3), p.e0213746-e0213746 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Ow 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. ;2019 Ow et al 2019 Ow et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0213746 ;PMID: 30875412

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10
The (−1486T/C) promoter polymorphism of the TLR-9 gene is associated with end-stage knee osteoarthritis in a Chinese population
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The (−1486T/C) promoter polymorphism of the TLR-9 gene is associated with end-stage knee osteoarthritis in a Chinese population

Journal of orthopaedic research, 2012-01, Vol.30 (1), p.9-14 [Peer Reviewed Journal]

Copyright © 2011 Orthopaedic Research Society ;Copyright © 2011 Orthopaedic Research Society. ;ISSN: 0736-0266 ;EISSN: 1554-527X ;DOI: 10.1002/jor.21494 ;PMID: 21748790

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11
Genomic landscape of lung adenocarcinoma in East Asians
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Article
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Genomic landscape of lung adenocarcinoma in East Asians

Nature genetics, 2020-02, Vol.52 (2), p.177-186 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0569-6 ;PMID: 32015526

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12
Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls
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Article
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Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls

Nature communications, 2018-10, Vol.9 (1), p.4083-7, Article 4083 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-06581-8 ;PMID: 30287823

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13
Association between the APOA2 promoter polymorphism and body weight in Mediterranean and Asian populations: replication of a gene–saturated fat interaction
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Article
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Association between the APOA2 promoter polymorphism and body weight in Mediterranean and Asian populations: replication of a gene–saturated fat interaction

International Journal of Obesity, 2011-05, Vol.35 (5), p.666-675 [Peer Reviewed Journal]

COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group May 2011 ;ISSN: 0307-0565 ;EISSN: 1476-5497 ;DOI: 10.1038/ijo.2010.187 ;PMID: 20975728

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14
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor
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Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor

Brain (London, England : 1878), 2020-01, Vol.143 (1), p.222-233 [Peer Reviewed Journal]

The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/awz372 ;PMID: 31819945

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15
Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations
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Article
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Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations

Neurologia medico-chirurgica, 2012, Vol.52(5), pp.299-303 [Peer Reviewed Journal]

2012 by The Japan Neurosurgical Society ;ISSN: 0470-8105 ;EISSN: 1349-8029 ;DOI: 10.2176/nmc.52.299

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16
European bone mineral density loci are also associated with BMD in East-Asian populations
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Article
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European bone mineral density loci are also associated with BMD in East-Asian populations

PloS one, 2010-10, Vol.5 (10), p.e13217-e13217 [Peer Reviewed Journal]

COPYRIGHT 2010 Public Library of Science ;COPYRIGHT 2010 Public Library of Science ;2010 Styrkarsdottir et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. ;Styrkarsdottir et al. 2010 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0013217 ;PMID: 20949110

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17
Association between HLA‐B1502 and carbamazepine‐induced severe cutaneous adverse drug reactions in a Thai population
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Article
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Association between HLA‐B1502 and carbamazepine‐induced severe cutaneous adverse drug reactions in a Thai population

Epilepsia (Copenhagen), 2010-05, Vol.51 (5), p.926-930 [Peer Reviewed Journal]

Wiley Periodicals, Inc. © 2010 International League Against Epilepsy ;2015 INIST-CNRS ;ISSN: 0013-9580 ;EISSN: 1528-1167 ;DOI: 10.1111/j.1528-1167.2010.02533.x ;PMID: 20345939 ;CODEN: EPILAK

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18
EGFR Mutation Subtypes Influence Survival Outcomes following First-Line Gefitinib Therapy in Advanced Asian NSCLC Patients
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EGFR Mutation Subtypes Influence Survival Outcomes following First-Line Gefitinib Therapy in Advanced Asian NSCLC Patients

Journal of thoracic oncology, 2017-03, Vol.12 (3), p.529-538 [Peer Reviewed Journal]

2016 International Association for the Study of Lung Cancer ;Copyright © 2017 by the International Association for the Study of Lung Cancer ;Copyright © 2016 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved. ;ISSN: 1556-0864 ;EISSN: 1556-1380 ;DOI: 10.1016/j.jtho.2016.11.2225 ;PMID: 27908825

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19
APP, PSEN1 , and PSEN2 Mutations in Asian Patients with Early-Onset Alzheimer Disease
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APP, PSEN1 , and PSEN2 Mutations in Asian Patients with Early-Onset Alzheimer Disease

International journal of molecular sciences, 2019-09, Vol.20 (19), p.4757 [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: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms20194757 ;PMID: 31557888

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20
Genetic association of the cytochrome c oxidase-related genes with Alzheimer's disease in Han Chinese
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Genetic association of the cytochrome c oxidase-related genes with Alzheimer's disease in Han Chinese

Neuropsychopharmacology (New York, N.Y.), 2018-10, Vol.43 (11), p.2264-2276 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2018 ;American College of Neuropsychopharmacology 2018 ;ISSN: 0893-133X ;EISSN: 1740-634X ;DOI: 10.1038/s41386-018-0144-3 ;PMID: 30054583

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