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1
Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case report
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Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient: A case report

Medicine (Baltimore), 2020-07, Vol.99 (28), p.e20813-e20813 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020813 ;PMID: 32664073

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2
Acupuncture and weight loss in Asians: A PRISMA-compliant systematic review and meta-analysis
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Acupuncture and weight loss in Asians: A PRISMA-compliant systematic review and meta-analysis

Medicine (Baltimore), 2019-08, Vol.98 (33), p.e16815-e16815 [Peer Reviewed Journal]

Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000016815 ;PMID: 31415397

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3
Assessment of HBV Preventive Services in a Medically Underserved Asian and Pacific Islander Population Using Provider and Patient Data
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Assessment of HBV Preventive Services in a Medically Underserved Asian and Pacific Islander Population Using Provider and Patient Data

Journal of general internal medicine : JGIM, 2015-01, Vol.30 (1), p.68-74 [Peer Reviewed Journal]

Society of General Internal Medicine 2014 ;Society of General Internal Medicine 2015 ;ISSN: 0884-8734 ;EISSN: 1525-1497 ;DOI: 10.1007/s11606-014-3057-9 ;PMID: 25324148

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4
Cell cycle-related lncRNAs and mRNAs in osteoarthritis chondrocytes in a Northwest Chinese Han Population
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Cell cycle-related lncRNAs and mRNAs in osteoarthritis chondrocytes in a Northwest Chinese Han Population

Medicine (Baltimore), 2020-06, Vol.99 (24), p.e19905-e19905 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;ISSN: 1536-5964 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000019905 ;PMID: 32541446

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5
Development of a physiologically based pharmacokinetic (PBPK) population model for Chinese elderly subjects
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Development of a physiologically based pharmacokinetic (PBPK) population model for Chinese elderly subjects

British journal of clinical pharmacology, 2021-07, Vol.87 (7), p.2711-2722 [Peer Reviewed Journal]

2020 The Authors. published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. ;2020 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. ;ISSN: 0306-5251 ;EISSN: 1365-2125 ;DOI: 10.1111/bcp.14609 ;PMID: 33068053

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6
Gastric mucosal microbiota in a Mongolian population with gastric cancer and precursor conditions
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Gastric mucosal microbiota in a Mongolian population with gastric cancer and precursor conditions

Alimentary pharmacology & therapeutics, 2020-04, Vol.51 (8), p.770-780 [Peer Reviewed Journal]

2020 John Wiley & Sons Ltd ;2020 John Wiley & Sons Ltd. ;Copyright © 2020 John Wiley & Sons Ltd ;ISSN: 0269-2813 ;EISSN: 1365-2036 ;DOI: 10.1111/apt.15675 ;PMID: 32133670

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7
A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy
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A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy

Medicine (Baltimore), 2020-10, Vol.99 (41), p.e22663 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000022663 ;PMID: 33031330

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8
Editorial: opposite effects of genetic polymorphisms known to induce NAFLD on hepatic and cardiovascular outcomes in Chinese population
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Editorial: opposite effects of genetic polymorphisms known to induce NAFLD on hepatic and cardiovascular outcomes in Chinese population

Alimentary pharmacology & therapeutics, 2022-04, Vol.55 (7), p.876-877 [Peer Reviewed Journal]

2022 John Wiley & Sons Ltd ;Copyright © 2022 John Wiley & Sons Ltd ;ISSN: 0269-2813 ;EISSN: 1365-2036 ;DOI: 10.1111/apt.16818 ;PMID: 35315107

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9
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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10
Identification of RET fusions in a Chinese multicancer retrospective analysis by next‐generation sequencing
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Identification of RET fusions in a Chinese multicancer retrospective analysis by next‐generation sequencing

Cancer science, 2022-01, Vol.113 (1), p.308-318 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.15181 ;PMID: 34710947

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11
Association of CYP2C192 and associated haplotypes with lower norendoxifen concentrations in tamoxifen‐treated Asian breast cancer patients
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Association of CYP2C192 and associated haplotypes with lower norendoxifen concentrations in tamoxifen‐treated Asian breast cancer patients

British journal of clinical pharmacology, 2016-06, Vol.81 (6), p.1142-1152 [Peer Reviewed Journal]

2016 The British Pharmacological Society ;ISSN: 0306-5251 ;EISSN: 1365-2125 ;DOI: 10.1111/bcp.12886 ;PMID: 26799162

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12
CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia
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CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia

Medicine (Baltimore), 2021-12, Vol.100 (51), p.e28275-e28275 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000028275 ;PMID: 34941110

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13
Population pharmacokinetics of bedaquiline in patients with drug-resistant TB
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Population pharmacokinetics of bedaquiline in patients with drug-resistant TB

The international journal of tuberculosis and lung disease, 2021-12, Vol.25 (12), p.1006-1012 [Peer Reviewed Journal]

ISSN: 1027-3719 ;EISSN: 1815-7920 ;DOI: 10.5588/ijtld.21.0158 ;PMID: 34886931

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14
Comparison of the HAS‐BLED versus ORBIT scores in predicting major bleeding among Asians receiving direct‐acting oral anticoagulants
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Comparison of the HAS‐BLED versus ORBIT scores in predicting major bleeding among Asians receiving direct‐acting oral anticoagulants

British journal of clinical pharmacology, 2022-05, Vol.88 (5), p.2203-2212 [Peer Reviewed Journal]

2021 British Pharmacological Society ;2021 British Pharmacological Society. ;ISSN: 0306-5251 ;EISSN: 1365-2125 ;DOI: 10.1111/bcp.15145 ;PMID: 34783372

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15
Association of the VEGFR2 single nucleotide polymorphism rs2305948 with glioma risk
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Association of the VEGFR2 single nucleotide polymorphism rs2305948 with glioma risk

Medicine (Baltimore), 2022-01, Vol.101 (1), p.e28454-e28454 [Peer Reviewed Journal]

Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000028454 ;PMID: 35029892

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16
Osimertinib in Japanese patients with EGFR T790M mutation‐positive advanced non‐small‐cell lung cancer: AURA3 trial
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Osimertinib in Japanese patients with EGFR T790M mutation‐positive advanced non‐small‐cell lung cancer: AURA3 trial

Cancer science, 2018-06, Vol.109 (6), p.1930-1938 [Peer Reviewed Journal]

2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.13623 ;PMID: 29697876

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17
The association between 5, 10 - methylenetetrahydrofolate reductase and the risk of unexplained recurrent pregnancy loss in China: A Meta-analysis
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The association between 5, 10 - methylenetetrahydrofolate reductase and the risk of unexplained recurrent pregnancy loss in China: A Meta-analysis

Medicine (Baltimore), 2021-04, Vol.100 (17), p.e25487-e25487 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000025487 ;PMID: 33907097

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18
Total cholesterol and mortality from ischemic heart disease and overall cardiovascular disease in Korean adults
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Total cholesterol and mortality from ischemic heart disease and overall cardiovascular disease in Korean adults

Medicine (Baltimore), 2019-09, Vol.98 (36), p.e17013 [Peer Reviewed Journal]

Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/md.0000000000017013 ;PMID: 31490384

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19
Age-specific reference values for the 5th generation cardiac troponin T assay in Chinese children
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Age-specific reference values for the 5th generation cardiac troponin T assay in Chinese children

Medicine (Baltimore), 2022-03, Vol.101 (11) [Peer Reviewed Journal]

Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000029101 ;PMID: 35356945

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20
A case report and literature review: Identification of a novel AIRE gene mutation associated with Autoimmune Polyendocrine Syndrome Type 1 in East Asians
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A case report and literature review: Identification of a novel AIRE gene mutation associated with Autoimmune Polyendocrine Syndrome Type 1 in East Asians

Medicine (Baltimore), 2020-05, Vol.99 (18), p.e20000-e20000 [Peer Reviewed Journal]

ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020000 ;PMID: 32358377

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