Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 36 of 38035 entries
Sorted by: Best Match Show Resources per page
Insights from ecological niche modeling on the taxonomic distinction and niche differentiation between the black-spotted and red-spotted tokay geckoes (Gekko gecko).

Ecology and evolution

Zhang Y, Chen C, Li L, Zhao C, Chen W, Huang Y.
PMID: 25535555
Ecol Evol. 2014 Sep;4(17):3383-94. doi: 10.1002/ece3.1183. Epub 2014 Aug 18.

The black-spotted tokay and the red-spotted tokay are morphologically distinct and have largely allopatric distributions. The black-spotted tokay is characterized by a small body size and dark skin with sundry spots, while the red-spotted tokay has a relatively large...

Cite
Zhang Y, Chen C, Li L, et al. Insights from ecological niche modeling on the taxonomic distinction and niche differentiation between the black-spotted and red-spotted tokay geckoes (Gekko gecko). Ecol Evol. 2014;4(17):3383-94doi: 10.1002/ece3.1183.
Zhang, Y., Chen, C., Li, L., Zhao, C., Chen, W., & Huang, Y. (2014). Insights from ecological niche modeling on the taxonomic distinction and niche differentiation between the black-spotted and red-spotted tokay geckoes (Gekko gecko). Ecology and evolution, 4(17), 3383-94. https://doi.org/10.1002/ece3.1183
Zhang, Yueyun, et al. "Insights from ecological niche modeling on the taxonomic distinction and niche differentiation between the black-spotted and red-spotted tokay geckoes (Gekko gecko)." Ecology and evolution vol. 4,17 (2014): 3383-94. doi: https://doi.org/10.1002/ece3.1183
Zhang Y, Chen C, Li L, Zhao C, Chen W, Huang Y. Insights from ecological niche modeling on the taxonomic distinction and niche differentiation between the black-spotted and red-spotted tokay geckoes (Gekko gecko). Ecol Evol. 2014 Sep;4(17):3383-94. doi: 10.1002/ece3.1183. Epub 2014 Aug 18. PMID: 25535555; PMCID: PMC4228613.
Copy Download .nbib Format: NLM
Peroxisome Proliferator-Activated Receptor γ Regulates the Expression of Lipid Phosphate Phosphohydrolase 1 in Human Vascular Endothelial Cells.

PPAR research

Huang Y, Zhao B, Liu Y, Wang N.
PMID: 24955089
PPAR Res. 2014;2014:740121. doi: 10.1155/2014/740121. Epub 2014 May 12.

Lipid phosphate phosphohydrolase 1 (LPP1), a membrane ectophosphohydrolase regulating the availability of bioactive lipid phosphates, plays important roles in cellular signaling and physiological processes such as angiogenesis and endothelial migration. However, the regulated expression of LPP1 remains largely unknown....

Cite
Huang Y, Zhao B, Liu Y, et al. Peroxisome Proliferator-Activated Receptor γ Regulates the Expression of Lipid Phosphate Phosphohydrolase 1 in Human Vascular Endothelial Cells. PPAR Res. 2014;2014:740121doi: 10.1155/2014/740121.
Huang, Y., Zhao, B., Liu, Y., & Wang, N. (2014). Peroxisome Proliferator-Activated Receptor γ Regulates the Expression of Lipid Phosphate Phosphohydrolase 1 in Human Vascular Endothelial Cells. PPAR research, 2014740121. https://doi.org/10.1155/2014/740121
Huang, Yazi, et al. "Peroxisome Proliferator-Activated Receptor γ Regulates the Expression of Lipid Phosphate Phosphohydrolase 1 in Human Vascular Endothelial Cells." PPAR research vol. 2014 (2014): 740121. doi: https://doi.org/10.1155/2014/740121
Huang Y, Zhao B, Liu Y, Wang N. Peroxisome Proliferator-Activated Receptor γ Regulates the Expression of Lipid Phosphate Phosphohydrolase 1 in Human Vascular Endothelial Cells. PPAR Res. 2014;2014:740121. doi: 10.1155/2014/740121. Epub 2014 May 12. PMID: 24955089; PMCID: PMC4052932.
Copy Download .nbib Format: NLM
Expression and clinical significance of IGF-1, IGFBP-3, and IGFBP-7 in serum and lung cancer tissues from patients with non-small cell lung cancer.

OncoTargets and therapy

Wang Z, Wang Z, Liang Z, Liu J, Shi W, Bai P, Lin X, Magaye R, Zhao J.
PMID: 24204158
Onco Targets Ther. 2013 Oct 16;6:1437-44. doi: 10.2147/OTT.S51997. eCollection 2013.

The expression and clinical significance of insulin-like growth factor 1 (IGF-1), insulin-like growth factor binding protein 3 (IGFBP-3), and insulin-like growth factor binding protein 7 (IGFBP-7) were investigated in serum and lung cancer tissues from 57 patients with non-small...

Cite
Wang Z, Wang Z, Liang Z, et al. Expression and clinical significance of IGF-1, IGFBP-3, and IGFBP-7 in serum and lung cancer tissues from patients with non-small cell lung cancer. Onco Targets Ther. 2013;6:1437-44doi: 10.2147/OTT.S51997.
Wang, Z., Wang, Z., Liang, Z., Liu, J., Shi, W., Bai, P., Lin, X., Magaye, R., & Zhao, J. (2013). Expression and clinical significance of IGF-1, IGFBP-3, and IGFBP-7 in serum and lung cancer tissues from patients with non-small cell lung cancer. OncoTargets and therapy, 61437-44. https://doi.org/10.2147/OTT.S51997
Wang, Zhigang, et al. "Expression and clinical significance of IGF-1, IGFBP-3, and IGFBP-7 in serum and lung cancer tissues from patients with non-small cell lung cancer." OncoTargets and therapy vol. 6 (2013): 1437-44. doi: https://doi.org/10.2147/OTT.S51997
Wang Z, Wang Z, Liang Z, Liu J, Shi W, Bai P, Lin X, Magaye R, Zhao J. Expression and clinical significance of IGF-1, IGFBP-3, and IGFBP-7 in serum and lung cancer tissues from patients with non-small cell lung cancer. Onco Targets Ther. 2013 Oct 16;6:1437-44. doi: 10.2147/OTT.S51997. eCollection 2013. PMID: 24204158; PMCID: PMC3804563.
Copy Download .nbib Format: NLM
Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC.

OncoTargets and therapy

Wu X, Liang W, Hou X, Lin Z, Zhao H, Huang Y, Fang W, Zhao Y, Wu J, Yang Y, Xue C, Hu Z, Zhang J, Zhang J, Ma Y, Zhou T, Qin T, Zhang L.
PMID: 24204163
Onco Targets Ther. 2013 Oct 21;6:1481-91. doi: 10.2147/OTT.S51887. eCollection 2013.

BACKGROUND: Although epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) are widely used for EGFR mutated non-small-cell lung cancer (NSCLC) patients, tumor sample availability and heterogeneity of the tumor remain challenging for physicians' selection of these patients. Here, we...

Cite
Wu X, Liang W, Hou X, et al. Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC. Onco Targets Ther. 2013;6:1481-91doi: 10.2147/OTT.S51887.
Wu, X., Liang, W., Hou, X., Lin, Z., Zhao, H., Huang, Y., Fang, W., Zhao, Y., Wu, J., Yang, Y., Xue, C., Hu, Z., Zhang, J., Zhang, J., Ma, Y., Zhou, T., Qin, T., & Zhang, L. (2013). Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC. OncoTargets and therapy, 61481-91. https://doi.org/10.2147/OTT.S51887
Wu, Xuan, et al. "Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC." OncoTargets and therapy vol. 6 (2013): 1481-91. doi: https://doi.org/10.2147/OTT.S51887
Wu X, Liang W, Hou X, Lin Z, Zhao H, Huang Y, Fang W, Zhao Y, Wu J, Yang Y, Xue C, Hu Z, Zhang J, Zhang J, Ma Y, Zhou T, Qin T, Zhang L. Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC. Onco Targets Ther. 2013 Oct 21;6:1481-91. doi: 10.2147/OTT.S51887. eCollection 2013. PMID: 24204163; PMCID: PMC3818102.
Copy Download .nbib Format: NLM
Hydrogen sulfide intervention in focal cerebral ischemia/reperfusion injury in rats.

Neural regeneration research

Li XJ, Li CK, Wei LY, Lu N, Wang GH, Zhao HG, Li DL.
PMID: 26199610
Neural Regen Res. 2015 Jun;10(6):932-7. doi: 10.4103/1673-5374.158353.

The present study aimed to explore the mechanism underlying the protective effects of hydrogen sulfide against neuronal damage caused by cerebral ischemia/reperfusion. We established the middle cerebral artery occlusion model in rats via the suture method. Ten minutes after...

Cite
Li XJ, Li CK, Wei LY, et al. Hydrogen sulfide intervention in focal cerebral ischemia/reperfusion injury in rats. Neural Regen Res. 2015;10(6):932-7doi: 10.4103/1673-5374.158353.
Li, X. J., Li, C. K., Wei, L. Y., Lu, N., Wang, G. H., Zhao, H. G., & Li, D. L. (2015). Hydrogen sulfide intervention in focal cerebral ischemia/reperfusion injury in rats. Neural regeneration research, 10(6), 932-7. https://doi.org/10.4103/1673-5374.158353
Li, Xin-Juan, et al. "Hydrogen sulfide intervention in focal cerebral ischemia/reperfusion injury in rats." Neural regeneration research vol. 10,6 (2015): 932-7. doi: https://doi.org/10.4103/1673-5374.158353
Li XJ, Li CK, Wei LY, Lu N, Wang GH, Zhao HG, Li DL. Hydrogen sulfide intervention in focal cerebral ischemia/reperfusion injury in rats. Neural Regen Res. 2015 Jun;10(6):932-7. doi: 10.4103/1673-5374.158353. PMID: 26199610; PMCID: PMC4498355.
Copy Download .nbib Format: NLM
Unraveling the Nature of Anomalously Fast Energy Storage in T-Nb.

Journal of the American Chemical Society

Chen D, Wang JH, Chou TF, Zhao B, El-Sayed MA, Liu M.
PMID: 28441872
J Am Chem Soc. 2017 May 24;139(20):7071-7081. doi: 10.1021/jacs.7b03141. Epub 2017 May 12.

While T-Nb

Cite
Chen D, Wang JH, Chou TF, et al. Unraveling the Nature of Anomalously Fast Energy Storage in T-Nb. J Am Chem Soc. 2017;139(20):7071-7081doi: 10.1021/jacs.7b03141.
Chen, D., Wang, J. H., Chou, T. F., Zhao, B., El-Sayed, M. A., & Liu, M. (2017). Unraveling the Nature of Anomalously Fast Energy Storage in T-Nb. Journal of the American Chemical Society, 139(20), 7071-7081. https://doi.org/10.1021/jacs.7b03141
Chen, Dongchang, et al. "Unraveling the Nature of Anomalously Fast Energy Storage in T-Nb." Journal of the American Chemical Society vol. 139,20 (2017): 7071-7081. doi: https://doi.org/10.1021/jacs.7b03141
Chen D, Wang JH, Chou TF, Zhao B, El-Sayed MA, Liu M. Unraveling the Nature of Anomalously Fast Energy Storage in T-Nb. J Am Chem Soc. 2017 May 24;139(20):7071-7081. doi: 10.1021/jacs.7b03141. Epub 2017 May 12. PMID: 28441872.
Copy Download .nbib Format: NLM
Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism.

PloS one

Chen Y, Zhang Y, Zhao G, Chen C, Yang P, Ye S, Tan X.
PMID: 27657912
PLoS One. 2016 Sep 22;11(9):e0162953. doi: 10.1371/journal.pone.0162953. eCollection 2016.

There are sex differences in many inflammatory and immune diseases, and the differences tend to diminish after menopause. The underlying reasons are unclear, but sex hormone levels are likely to be an important factor. Blood leukocyte count and composition...

Cite
Chen Y, Zhang Y, Zhao G, et al. Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism. PLoS One. 2016;11(9):e0162953doi: 10.1371/journal.pone.0162953.
Chen, Y., Zhang, Y., Zhao, G., Chen, C., Yang, P., Ye, S., & Tan, X. (2016). Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism. PloS one, 11(9), e0162953. https://doi.org/10.1371/journal.pone.0162953
Chen, Yequn, et al. "Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism." PloS one vol. 11,9 (2016): e0162953. doi: https://doi.org/10.1371/journal.pone.0162953
Chen Y, Zhang Y, Zhao G, Chen C, Yang P, Ye S, Tan X. Difference in Leukocyte Composition between Women before and after Menopausal Age, and Distinct Sexual Dimorphism. PLoS One. 2016 Sep 22;11(9):e0162953. doi: 10.1371/journal.pone.0162953. eCollection 2016. PMID: 27657912; PMCID: PMC5033487.
Copy Download .nbib Format: NLM
Superior Dielectric Screening in Two-Dimensional MoS.

ACS applied materials & interfaces

Ly TH, Kim H, Thi QH, Lau SP, Zhao J.
PMID: 28967252
ACS Appl Mater Interfaces. 2017 Nov 01;9(43):37941-37946. doi: 10.1021/acsami.7b11468. Epub 2017 Oct 17.

Metals have the best dielectric screening capability among all materials; however, it is usually difficult to fabricate continuous and uniform ultrathin (few-atomic-layer thickness) metal films. Conversely, high-quality atomic-thick semiconductor or semimetal materials (so called two-dimensional materials) such as graphene...

Cite
Ly TH, Kim H, Thi QH, et al. Superior Dielectric Screening in Two-Dimensional MoS. ACS Appl Mater Interfaces. 2017;9(43):37941-37946doi: 10.1021/acsami.7b11468.
Ly, T. H., Kim, H., Thi, Q. H., Lau, S. P., & Zhao, J. (2017). Superior Dielectric Screening in Two-Dimensional MoS. ACS applied materials & interfaces, 9(43), 37941-37946. https://doi.org/10.1021/acsami.7b11468
Ly, Thuc Hue, et al. "Superior Dielectric Screening in Two-Dimensional MoS." ACS applied materials & interfaces vol. 9,43 (2017): 37941-37946. doi: https://doi.org/10.1021/acsami.7b11468
Ly TH, Kim H, Thi QH, Lau SP, Zhao J. Superior Dielectric Screening in Two-Dimensional MoS. ACS Appl Mater Interfaces. 2017 Nov 01;9(43):37941-37946. doi: 10.1021/acsami.7b11468. Epub 2017 Oct 17. PMID: 28967252.
Copy Download .nbib Format: NLM
Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability.

ACS applied materials & interfaces

Xu W, Xie Z, Cui X, Zhao K, Zhang L, Dietrich G, Dooley KM, Wang Y.
PMID: 26389757
ACS Appl Mater Interfaces. 2015 Oct 14;7(40):22533-41. doi: 10.1021/acsami.5b06765. Epub 2015 Sep 30.

Complex hierarchical structures have received tremendous attention due to their superior properties over their constitute components. In this study, hierarchical graphene-encapsulated hollow SnO2@SnS2 nanostructures are successfully prepared by in situ sulfuration on the backbones of hollow SnO2 spheres via...

Cite
Xu W, Xie Z, Cui X, et al. Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability. ACS Appl Mater Interfaces. 2015;7(40):22533-41doi: 10.1021/acsami.5b06765.
Xu, W., Xie, Z., Cui, X., Zhao, K., Zhang, L., Dietrich, G., Dooley, K. M., & Wang, Y. (2015). Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability. ACS applied materials & interfaces, 7(40), 22533-41. https://doi.org/10.1021/acsami.5b06765
Xu, Wangwang, et al. "Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability." ACS applied materials & interfaces vol. 7,40 (2015): 22533-41. doi: https://doi.org/10.1021/acsami.5b06765
Xu W, Xie Z, Cui X, Zhao K, Zhang L, Dietrich G, Dooley KM, Wang Y. Hierarchical Graphene-Encapsulated Hollow SnO2@SnS2 Nanostructures with Enhanced Lithium Storage Capability. ACS Appl Mater Interfaces. 2015 Oct 14;7(40):22533-41. doi: 10.1021/acsami.5b06765. Epub 2015 Sep 30. PMID: 26389757.
Copy Download .nbib Format: NLM
Systematical Evaluation of Mechanically Strong 3D Printed Diluted magnesium Doping Wollastonite Scaffolds on Osteogenic Capacity in Rabbit Calvarial Defects.

Scientific reports

Sun M, Liu A, Shao H, Yang X, Ma C, Yan S, Liu Y, He Y, Gou Z.
PMID: 27658481
Sci Rep. 2016 Sep 23;6:34029. doi: 10.1038/srep34029.

Wollastonite (CaSiO3; CSi) ceramic is a promising bioactive material for bone defect repair due to slightly fast degradation of its porous constructs in vivo. In our previous strategy some key features of CSi ceramic have been significantly improved by...

Cite
Sun M, Liu A, Shao H, et al. Systematical Evaluation of Mechanically Strong 3D Printed Diluted magnesium Doping Wollastonite Scaffolds on Osteogenic Capacity in Rabbit Calvarial Defects. Sci Rep. 2016;6:34029doi: 10.1038/srep34029.
Sun, M., Liu, A., Shao, H., Yang, X., Ma, C., Yan, S., Liu, Y., He, Y., & Gou, Z. (2016). Systematical Evaluation of Mechanically Strong 3D Printed Diluted magnesium Doping Wollastonite Scaffolds on Osteogenic Capacity in Rabbit Calvarial Defects. Scientific reports, 634029. https://doi.org/10.1038/srep34029
Sun, Miao, et al. "Systematical Evaluation of Mechanically Strong 3D Printed Diluted magnesium Doping Wollastonite Scaffolds on Osteogenic Capacity in Rabbit Calvarial Defects." Scientific reports vol. 6 (2016): 34029. doi: https://doi.org/10.1038/srep34029
Sun M, Liu A, Shao H, Yang X, Ma C, Yan S, Liu Y, He Y, Gou Z. Systematical Evaluation of Mechanically Strong 3D Printed Diluted magnesium Doping Wollastonite Scaffolds on Osteogenic Capacity in Rabbit Calvarial Defects. Sci Rep. 2016 Sep 23;6:34029. doi: 10.1038/srep34029. PMID: 27658481; PMCID: PMC5034319.
Copy Download .nbib Format: NLM
Combination curcumin and (-)-epigallocatechin-3-gallate inhibits colorectal carcinoma microenvironment-induced angiogenesis by JAK/STAT3/IL-8 pathway.

Oncogenesis

Jin G, Yang Y, Liu K, Zhao J, Chen X, Liu H, Bai R, Li X, Jiang Y, Zhang X, Lu J, Dong Z.
PMID: 28967875
Oncogenesis. 2017 Oct 02;6(10):e384. doi: 10.1038/oncsis.2017.84.

Tumor microenvironment has a crucial role in cancer development and progression, whereas the mechanism of how it regulates angiogenesis is unclear. In this study, we simulated the colorectal carcinoma microenvironment by conditioned medium (CM) of colorectal carcinoma cell lines...

Cite
Jin G, Yang Y, Liu K, et al. Combination curcumin and (-)-epigallocatechin-3-gallate inhibits colorectal carcinoma microenvironment-induced angiogenesis by JAK/STAT3/IL-8 pathway. Oncogenesis. 2017;6(10):e384doi: 10.1038/oncsis.2017.84.
Jin, G., Yang, Y., Liu, K., Zhao, J., Chen, X., Liu, H., Bai, R., Li, X., Jiang, Y., Zhang, X., Lu, J., & Dong, Z. (2017). Combination curcumin and (-)-epigallocatechin-3-gallate inhibits colorectal carcinoma microenvironment-induced angiogenesis by JAK/STAT3/IL-8 pathway. Oncogenesis, 6(10), e384. https://doi.org/10.1038/oncsis.2017.84
Jin, G, et al. "Combination curcumin and (-)-epigallocatechin-3-gallate inhibits colorectal carcinoma microenvironment-induced angiogenesis by JAK/STAT3/IL-8 pathway." Oncogenesis vol. 6,10 (2017): e384. doi: https://doi.org/10.1038/oncsis.2017.84
Jin G, Yang Y, Liu K, Zhao J, Chen X, Liu H, Bai R, Li X, Jiang Y, Zhang X, Lu J, Dong Z. Combination curcumin and (-)-epigallocatechin-3-gallate inhibits colorectal carcinoma microenvironment-induced angiogenesis by JAK/STAT3/IL-8 pathway. Oncogenesis. 2017 Oct 02;6(10):e384. doi: 10.1038/oncsis.2017.84. PMID: 28967875; PMCID: PMC5668882.
Copy Download .nbib Format: NLM
Transcriptomic Analysis of .

Frontiers in microbiology

Liu L, Zhao H, Peng S, Wang T, Su J, Liang Y, Li H, Wang H.
PMID: 28878748
Front Microbiol. 2017 Aug 22;8:1586. doi: 10.3389/fmicb.2017.01586. eCollection 2017.

No abstract available.

Cite
Liu L, Zhao H, Peng S, et al. Transcriptomic Analysis of . Front Microbiol. 2017;8:1586doi: 10.3389/fmicb.2017.01586.
Liu, L., Zhao, H., Peng, S., Wang, T., Su, J., Liang, Y., Li, H., & Wang, H. (2017). Transcriptomic Analysis of . Frontiers in microbiology, 81586. https://doi.org/10.3389/fmicb.2017.01586
Liu, Longxiang, et al. "Transcriptomic Analysis of ." Frontiers in microbiology vol. 8 (2017): 1586. doi: https://doi.org/10.3389/fmicb.2017.01586
Liu L, Zhao H, Peng S, Wang T, Su J, Liang Y, Li H, Wang H. Transcriptomic Analysis of . Front Microbiol. 2017 Aug 22;8:1586. doi: 10.3389/fmicb.2017.01586. eCollection 2017. PMID: 28878748; PMCID: PMC5572241.
Copy Download .nbib Format: NLM
Showing 25 to 36 of 38035 entries