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1
Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations
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Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations

Hereditas, 2018-04, Vol.155 (1), p.19-19, Article 19 [Peer Reviewed Journal]

The Author(s) 2018 ;ISSN: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-018-0057-5 ;PMID: 29636655

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2
NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population
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NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population

Cell reports (Cambridge), 2021-11, Vol.37 (7), p.110017-110017, Article 110017 [Peer Reviewed Journal]

2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 2211-1247 ;EISSN: 2211-1247 ;DOI: 10.1016/j.celrep.2021.110017 ;PMID: 34788621

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3
Genetic Origins and Sex-Biased Admixture of the Huis
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Genetic Origins and Sex-Biased Admixture of the Huis

Molecular biology and evolution, 2021-09, Vol.38 (9), p.3804-3819 [Peer Reviewed Journal]

The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 1537-1719 ;ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/molbev/msab158 ;PMID: 34021754

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4
Association between RECQL5 genetic polymorphisms and susceptibility to breast cancer
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Association between RECQL5 genetic polymorphisms and susceptibility to breast cancer

Tumor biology, 2014-12, Vol.35 (12), p.12201-12204 [Peer Reviewed Journal]

International Society of Oncology and BioMarkers (ISOBM) 2014 ;ISSN: 1010-4283 ;EISSN: 1423-0380 ;DOI: 10.1007/s13277-014-2528-2 ;PMID: 25394896

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5
Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
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Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese

Hereditas, 2019, Vol.156 (1), p.4-4, Article 4 [Peer Reviewed Journal]

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: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-018-0078-0 ;PMID: 30679935

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6
Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencing
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Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencing

Scientific reports, 2021-11, Vol.11 (1), p.21830-21830, Article 21830 [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/s41598-021-01194-6 ;PMID: 34750414

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7
Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han population
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Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han population

BMC psychiatry, 2022-03, Vol.22 (1), p.171-171, Article 171 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1471-244X ;EISSN: 1471-244X ;DOI: 10.1186/s12888-022-03799-1 ;PMID: 35260124

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8
Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese Children
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Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese Children

Hereditas, 2019-05, Vol.156 (1), p.15-15, Article 15 [Peer Reviewed Journal]

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: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-019-0092-x ;PMID: 31148953

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9
Effect of CYP2C19 polymorphisms on serum valproic level acid in Chinese Han patients with schizophrenia
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Article
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Effect of CYP2C19 polymorphisms on serum valproic level acid in Chinese Han patients with schizophrenia

Scientific reports, 2021-11, Vol.11 (1), p.23150-23150, Article 23150 [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/s41598-021-02628-x ;PMID: 34848811

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10
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
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Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis

Genetics in medicine, 2019-10, Vol.21 (10), p.2345-2354 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0507-0 ;PMID: 31000793

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11
Genetic variation of pharmacogenomic VIP variants in the Chinese Li population: an updated research
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Article
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Genetic variation of pharmacogenomic VIP variants in the Chinese Li population: an updated research

Molecular genetics and genomics : MGG, 2022-03, Vol.297 (2), p.407-417 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 ;2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. ;ISSN: 1617-4615 ;EISSN: 1617-4623 ;DOI: 10.1007/s00438-022-01855-9 ;PMID: 35146537

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12
Vitamin D Receptor Genetic Variations May Associate with the Risk of Developing Late Fracture-Related Infection in the Chinese Han Population
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Vitamin D Receptor Genetic Variations May Associate with the Risk of Developing Late Fracture-Related Infection in the Chinese Han Population

Journal of immunology research, 2022-02, Vol.2022, p.9025354-8 [Peer Reviewed Journal]

Copyright © 2022 Xing-qi Zhao et al. ;Copyright © 2022 Xing-qi Zhao et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2022 Xing-qi Zhao et al. 2022 ;ISSN: 2314-8861 ;EISSN: 2314-7156 ;DOI: 10.1155/2022/9025354 ;PMID: 35242885

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13
Association of lncRNA PVT1 Gene Polymorphisms with the Risk of Essential Hypertension in Chinese Population
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Article
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Association of lncRNA PVT1 Gene Polymorphisms with the Risk of Essential Hypertension in Chinese Population

BioMed research international, 2022, Vol.2022, p.9976909-9 [Peer Reviewed Journal]

Copyright © 2022 Rong Li et al. ;Copyright © 2022 Rong Li et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2022 Rong Li et al. 2022 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2022/9976909 ;PMID: 35036445

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14
Genome-wide association study of survival in patients with pancreatic adenocarcinoma
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Article
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Genome-wide association study of survival in patients with pancreatic adenocarcinoma

Gut, 2014-01, Vol.63 (1), p.152-160 [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 ;Copyright: 2014 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 ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2012-303477 ;PMID: 23180869 ;CODEN: GUTTAK

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15
Effect of gene polymorphism on bleeding complications in Chinese Han patients taking warfarin
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Effect of gene polymorphism on bleeding complications in Chinese Han patients taking warfarin

European journal of clinical pharmacology, 2022-02, Vol.78 (2), p.205-214 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 ;2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021. ;ISSN: 0031-6970 ;EISSN: 1432-1041 ;DOI: 10.1007/s00228-021-03204-y ;PMID: 34596727

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16
Genome-wide association study of serum tumor markers in Southern Chinese Han population
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Article
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Genome-wide association study of serum tumor markers in Southern Chinese Han population

BMC cancer, 2022-02, Vol.22 (1), p.160-160, Article 160 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-022-09236-6 ;PMID: 35144566

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17
Relationships of interleukin-17 polymorphisms with recurrent aphthous ulcer risk in a Han Chinese population
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Relationships of interleukin-17 polymorphisms with recurrent aphthous ulcer risk in a Han Chinese population

Journal of international medical research, 2020-12, Vol.48 (12), p.300060520976833-300060520976833 [Peer Reviewed Journal]

The Author(s) 2020 ;The Author(s) 2020. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/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 2020 SAGE Publications ;ISSN: 0300-0605 ;EISSN: 1473-2300 ;DOI: 10.1177/0300060520976833 ;PMID: 33351682

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18
The rs9953490 polymorphism of DAL-1 gene is associated with gastric cancer risk in the Han population in Northeast China
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The rs9953490 polymorphism of DAL-1 gene is associated with gastric cancer risk in the Han population in Northeast China

BMC gastroenterology, 2021-09, Vol.21 (1), p.354-354, Article 354 [Peer Reviewed Journal]

2021. The Author(s). ;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: 1471-230X ;EISSN: 1471-230X ;DOI: 10.1186/s12876-021-01929-9 ;PMID: 34579655

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19
Glutathione S-transferase Omega 2 DD genotype is associated with an increased risk of sporadic amyotrophic lateral sclerosis in Chinese men
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Article
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Glutathione S-transferase Omega 2 DD genotype is associated with an increased risk of sporadic amyotrophic lateral sclerosis in Chinese men

Journal of international medical research, 2021-07, Vol.49 (7), p.3000605211033219-3000605211033219 [Peer Reviewed Journal]

The Author(s) 2021 ;The Author(s) 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/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 2021 SAGE Publications ;ISSN: 0300-0605 ;EISSN: 1473-2300 ;DOI: 10.1177/03000605211033219 ;PMID: 34311603

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20
Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population
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Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population

Hereditas, 2021-07, Vol.158 (1), p.24-24, Article 24 [Peer Reviewed Journal]

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: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-021-00189-7 ;PMID: 34238381

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