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1
GLUT3 inhibitor discovery through in silico ligand screening and in vivo validation in eukaryotic expression systems
GLUT3 inhibitor discovery through in silico ligand screening and in vivo validation in eukaryotic expression systems
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GLUT3 inhibitor discovery through in silico ligand screening and in vivo validation in eukaryotic expression systems

Scientific reports, 2022-01, Vol.12 (1), p.1429-1429, Article 1429 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. 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) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-05383-9 ;PMID: 35082341

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2
The role of SGLT1 and GLUT2 in intestinal glucose transport and sensing
The role of SGLT1 and GLUT2 in intestinal glucose transport and sensing
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The role of SGLT1 and GLUT2 in intestinal glucose transport and sensing

PloS one, 2014-02, Vol.9 (2), p.e89977 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Röder 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. ;2014 Röder et al 2014 Röder et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0089977 ;PMID: 24587162

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3
Screening for Glucose Perturbations and Risk Factor Management in Dysglycemic Patients With Coronary Artery Disease-A Persistent Challenge in Need of Substantial Improvement: A Report From ESC EORP EUROASPIRE V
Screening for Glucose Perturbations and Risk Factor Management in Dysglycemic Patients With Coronary Artery Disease-A Persistent Challenge in Need of Substantial Improvement: A Report From ESC EORP EUROASPIRE V
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Screening for Glucose Perturbations and Risk Factor Management in Dysglycemic Patients With Coronary Artery Disease-A Persistent Challenge in Need of Substantial Improvement: A Report From ESC EORP EUROASPIRE V

Diabetes care, 2020-04, Vol.43 (4), p.726-733 [Peer Reviewed Journal]

2020 by the American Diabetes Association. ;Copyright American Diabetes Association Apr 1, 2020 ;ISSN: 0149-5992 ;ISSN: 1935-5548 ;EISSN: 1935-5548 ;DOI: 10.2337/dc19-2165 ;PMID: 32079627

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4
Physiology of renal glucose handling via SGLT1, SGLT2 and GLUT2
Physiology of renal glucose handling via SGLT1, SGLT2 and GLUT2
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Physiology of renal glucose handling via SGLT1, SGLT2 and GLUT2

Diabetologia, 2018-10, Vol.61 (10), p.2087-2097 [Peer Reviewed Journal]

The Author(s) 2018 ;Diabetologia is a copyright of Springer, (2018). All Rights Reserved. © 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. ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-018-4656-5 ;PMID: 30132032

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5
A First-in-Human Study of GLY-200, an Oral, Gut- Restricted, Pharmacologic Duodenal Exclusion Therapy
A First-in-Human Study of GLY-200, an Oral, Gut- Restricted, Pharmacologic Duodenal Exclusion Therapy
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A First-in-Human Study of GLY-200, an Oral, Gut- Restricted, Pharmacologic Duodenal Exclusion Therapy

Obesity (Silver Spring, Md.), 2022-11, Vol.30, p.19-19 [Peer Reviewed Journal]

Copyright Blackwell Publishing Ltd. Nov 2022 ;ISSN: 1930-7381 ;EISSN: 1930-739X

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6
Development of SGLT1 and SGLT2 inhibitors
Development of SGLT1 and SGLT2 inhibitors
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Development of SGLT1 and SGLT2 inhibitors

Diabetologia, 2018-10, Vol.61 (10), p.2079-2086 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2018 ;Diabetologia is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-018-4654-7 ;PMID: 30132033

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7
Glucose transporters in the small intestine in health and disease
Glucose transporters in the small intestine in health and disease
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Glucose transporters in the small intestine in health and disease

Pflügers Archiv, 2020-09, Vol.472 (9), p.1207-1248 [Peer Reviewed Journal]

The Author(s) 2020 ;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. ;ISSN: 0031-6768 ;EISSN: 1432-2013 ;DOI: 10.1007/s00424-020-02439-5 ;PMID: 32829466

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8
SGLT2 inhibition and renal urate excretion: role of luminal glucose, GLUT9, and URAT1
SGLT2 inhibition and renal urate excretion: role of luminal glucose, GLUT9, and URAT1
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SGLT2 inhibition and renal urate excretion: role of luminal glucose, GLUT9, and URAT1

American journal of physiology. Renal physiology, 2019-01, Vol.316 (1), p.F173-F185 [Peer Reviewed Journal]

Copyright American Physiological Society Jan 2019 ;ISSN: 1931-857X ;EISSN: 1522-1466 ;DOI: 10.1152/ajprenal.00462.2018 ;PMID: 30427222

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9
Effect of canagliflozin on renal threshold for glucose, glycemia, and body weight in normal and diabetic animal models
Effect of canagliflozin on renal threshold for glucose, glycemia, and body weight in normal and diabetic animal models
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Effect of canagliflozin on renal threshold for glucose, glycemia, and body weight in normal and diabetic animal models

PloS one, 2012-02, Vol.7 (2), p.e30555-e30555 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Liang 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. ;Liang et al. 2012 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0030555 ;PMID: 22355316

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10
Comparative study of expression and activity of glucose transporters between stem cell-derived brain microvascular endothelial cells and hCMEC/D3 cells
Comparative study of expression and activity of glucose transporters between stem cell-derived brain microvascular endothelial cells and hCMEC/D3 cells
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Comparative study of expression and activity of glucose transporters between stem cell-derived brain microvascular endothelial cells and hCMEC/D3 cells

American Journal of Physiology: Cell Physiology, 2017-10, Vol.313 (4), p.C421-C429 [Peer Reviewed Journal]

Copyright © 2017 the American Physiological Society. ;Copyright American Physiological Society Oct 2017 ;Copyright © 2017 the American Physiological Society 2017 American Physiological Society ;ISSN: 0363-6143 ;EISSN: 1522-1563 ;DOI: 10.1152/ajpcell.00116.2017 ;PMID: 28993322

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11
1-deoxynojirimycin inhibits glucose absorption and accelerates glucose metabolism in streptozotocin-induced diabetic mice
1-deoxynojirimycin inhibits glucose absorption and accelerates glucose metabolism in streptozotocin-induced diabetic mice
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1-deoxynojirimycin inhibits glucose absorption and accelerates glucose metabolism in streptozotocin-induced diabetic mice

Scientific reports, 2013-03, Vol.3 (1), p.1377, Article 1377 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2013 ;Copyright © 2013, Macmillan Publishers Limited. All rights reserved 2013 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep01377 ;PMID: 23536174

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12
Natural Products as Lead Compounds for Sodium Glucose Cotransporter (SGLT) Inhibitors
Natural Products as Lead Compounds for Sodium Glucose Cotransporter (SGLT) Inhibitors
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Natural Products as Lead Compounds for Sodium Glucose Cotransporter (SGLT) Inhibitors

Planta medica, 2017-08, Vol.83 (12/13), p.985-993 [Peer Reviewed Journal]

ISSN: 0032-0943 ;EISSN: 1439-0221 ;DOI: 10.1055/s-0043-106050

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13
Insulin resistance and systemic metabolic changes in oral glucose tolerance test in 5340 individuals: an interventional study
Insulin resistance and systemic metabolic changes in oral glucose tolerance test in 5340 individuals: an interventional study
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Insulin resistance and systemic metabolic changes in oral glucose tolerance test in 5340 individuals: an interventional study

BMC medicine, 2019-11, Vol.17 (1), p.217-217, Article 217 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;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: 1741-7015 ;EISSN: 1741-7015 ;DOI: 10.1186/s12916-019-1440-4 ;PMID: 31779625

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14
Metformin and Insulin Resistance: A Review of the Underlying Mechanisms behind Changes in GLUT4-Mediated Glucose Transport
Metformin and Insulin Resistance: A Review of the Underlying Mechanisms behind Changes in GLUT4-Mediated Glucose Transport
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Metformin and Insulin Resistance: A Review of the Underlying Mechanisms behind Changes in GLUT4-Mediated Glucose Transport

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1264 [Peer Reviewed Journal]

2022 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 (https://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. ;2022 by the authors. 2022 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms23031264 ;PMID: 35163187

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15
Increase in SGLT1-mediated transport explains renal glucose reabsorption during genetic and pharmacological SGLT2 inhibition in euglycemia
Increase in SGLT1-mediated transport explains renal glucose reabsorption during genetic and pharmacological SGLT2 inhibition in euglycemia
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Increase in SGLT1-mediated transport explains renal glucose reabsorption during genetic and pharmacological SGLT2 inhibition in euglycemia

American journal of physiology. Renal physiology, 2014-01, Vol.306 (2), p.F188-F193 [Peer Reviewed Journal]

Copyright American Physiological Society Jan 15, 2014 ;ISSN: 1931-857X ;EISSN: 1522-1466 ;DOI: 10.1152/ajprenal.00518.2013 ;PMID: 24226519

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16
The role of the kidneys in glucose homeostasis: a new path towards normalizing glycaemia
The role of the kidneys in glucose homeostasis: a new path towards normalizing glycaemia
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The role of the kidneys in glucose homeostasis: a new path towards normalizing glycaemia

Diabetes, obesity & metabolism, 2012-01, Vol.14 (1), p.5-14

2011 Blackwell Publishing Ltd ;2011 Blackwell Publishing Ltd. ;ISSN: 1462-8902 ;EISSN: 1463-1326 ;DOI: 10.1111/j.1463-1326.2011.01511.x ;PMID: 21955459

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17
Oral glucose tolerance test is needed for appropriate classification of glucose regulation in patients with coronary artery disease: a report from the Euro Heart Survey on Diabetes and the Heart
Oral glucose tolerance test is needed for appropriate classification of glucose regulation in patients with coronary artery disease: a report from the Euro Heart Survey on Diabetes and the Heart
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Oral glucose tolerance test is needed for appropriate classification of glucose regulation in patients with coronary artery disease: a report from the Euro Heart Survey on Diabetes and the Heart

Heart (British Cardiac Society), 2007-01, Vol.93 (1), p.72-77 [Peer Reviewed Journal]

Copyright 2007 by Heart ;2007 INIST-CNRS ;Copyright: 2007 Copyright 2007 by Heart ;Copyright © 2007 BMJ Publishing Group and British Cardiovascular Society ;ISSN: 1355-6037 ;ISSN: 1468-201X ;EISSN: 1468-201X ;DOI: 10.1136/hrt.2005.086975 ;PMID: 16905628

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18
Insulin secretion and action in subjects with impaired fasting glucose and impaired glucose tolerance : Results from the veterans administration genetic epidemiology study
Insulin secretion and action in subjects with impaired fasting glucose and impaired glucose tolerance : Results from the veterans administration genetic epidemiology study
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Insulin secretion and action in subjects with impaired fasting glucose and impaired glucose tolerance : Results from the veterans administration genetic epidemiology study

Diabetes (New York, N.Y.), 2006-05, Vol.55 (5), p.1430-1435 [Peer Reviewed Journal]

2006 INIST-CNRS ;COPYRIGHT 2006 American Diabetes Association ;Copyright American Diabetes Association May 2006 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/db05-1200 ;PMID: 16644701 ;CODEN: DIAEAZ

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19
‘Smart’ insulin-delivery technologies and intrinsic glucose-responsive insulin analogues
‘Smart’ insulin-delivery technologies and intrinsic glucose-responsive insulin analogues
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‘Smart’ insulin-delivery technologies and intrinsic glucose-responsive insulin analogues

Diabetologia, 2021-05, Vol.64 (5), p.1016-1029 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 ;COPYRIGHT 2021 Springer ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021. ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-021-05422-6 ;PMID: 33710398

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20
Canagliflozin Lowers Postprandial Glucose and Insulin by Delaying Intestinal Glucose Absorption in Addition to Increasing Urinary Glucose Excretion: Results of a randomized, placebo-controlled study
Canagliflozin Lowers Postprandial Glucose and Insulin by Delaying Intestinal Glucose Absorption in Addition to Increasing Urinary Glucose Excretion: Results of a randomized, placebo-controlled study
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Canagliflozin Lowers Postprandial Glucose and Insulin by Delaying Intestinal Glucose Absorption in Addition to Increasing Urinary Glucose Excretion: Results of a randomized, placebo-controlled study

Diabetes care, 2013-08, Vol.36 (8), p.2154-2161 [Peer Reviewed Journal]

2014 INIST-CNRS ;COPYRIGHT 2013 American Diabetes Association ;Copyright American Diabetes Association Aug 2013 ;2013 by the American Diabetes Association. 2013 ;ISSN: 0149-5992 ;EISSN: 1935-5548 ;DOI: 10.2337/dc12-2391 ;PMID: 23412078 ;CODEN: DICAD2

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