Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1681 to 1689 of 1689 entries
Sorted by: Best Match Show Resources per page
Antioxidant Enzymes and Heat Shock Protein Genes from .

Insects

Miao ZQ, Tu YQ, Guo PY, He W, Jing TX, Wang JJ, Wei DD.
PMID: 33261171
Insects. 2020 Nov 27;11(12). doi: 10.3390/insects11120839.

Psocids are a new risk for global food security and safety because they are significant worldwide pests of stored products. Among these psocids,

Cite
Miao ZQ, Tu YQ, Guo PY, et al. Antioxidant Enzymes and Heat Shock Protein Genes from . Insects. 2020;11(12)doi: 10.3390/insects11120839.
Miao, Z. Q., Tu, Y. Q., Guo, P. Y., He, W., Jing, T. X., Wang, J. J., & Wei, D. D. (2020). Antioxidant Enzymes and Heat Shock Protein Genes from . Insects, 11(12), . https://doi.org/10.3390/insects11120839
Miao, Ze Qing, et al. "Antioxidant Enzymes and Heat Shock Protein Genes from ." Insects vol. 11,12 (2020). doi: https://doi.org/10.3390/insects11120839
Miao ZQ, Tu YQ, Guo PY, He W, Jing TX, Wang JJ, Wei DD. Antioxidant Enzymes and Heat Shock Protein Genes from . Insects. 2020 Nov 27;11(12). doi: 10.3390/insects11120839. PMID: 33261171; PMCID: PMC7759835.
Copy Download .nbib Format: NLM
Analysis of mRNA Expression and DNA Methylation Datasets According to the Genomic Distribution of CpG Sites in Osteoarthritis.

Frontiers in genetics

Yi P, Xu X, Yao J, Qiu B.
PMID: 33936160
Front Genet. 2021 Apr 15;12:618803. doi: 10.3389/fgene.2021.618803. eCollection 2021.

Objectives Transcriptional changes in cartilage can impact function by causing degradation such as that which occurs during the development of osteoarthritis (OA). Epigenetic regulation may be a key factor leading to transcriptional changes in OA. In this study, we...

Cite
Yi P, Xu X, Yao J, et al. Analysis of mRNA Expression and DNA Methylation Datasets According to the Genomic Distribution of CpG Sites in Osteoarthritis. Front Genet. 2021;12:618803doi: 10.3389/fgene.2021.618803.
Yi, P., Xu, X., Yao, J., & Qiu, B. (2021). Analysis of mRNA Expression and DNA Methylation Datasets According to the Genomic Distribution of CpG Sites in Osteoarthritis. Frontiers in genetics, 12618803. https://doi.org/10.3389/fgene.2021.618803
Yi, Peng, et al. "Analysis of mRNA Expression and DNA Methylation Datasets According to the Genomic Distribution of CpG Sites in Osteoarthritis." Frontiers in genetics vol. 12 (2021): 618803. doi: https://doi.org/10.3389/fgene.2021.618803
Yi P, Xu X, Yao J, Qiu B. Analysis of mRNA Expression and DNA Methylation Datasets According to the Genomic Distribution of CpG Sites in Osteoarthritis. Front Genet. 2021 Apr 15;12:618803. doi: 10.3389/fgene.2021.618803. eCollection 2021. PMID: 33936160; PMCID: PMC8082497.
Copy Download .nbib Format: NLM
LRPPRC regulates redox homeostasis via the circANKHD1/FOXM1 axis to enhance bladder urothelial carcinoma tumorigenesis.

Redox biology

Wei WS, Wang N, Deng MH, Dong P, Liu JY, Xiang Z, Li XD, Li ZY, Liu ZH, Peng YL, Li Z, Jiang LJ, Yao K, Ye YL, Lu WH, Zhang ZL, Zhou FJ, Liu ZW, Xie D, Yu CP.
PMID: 34864630
Redox Biol. 2021 Nov 27;48:102201. doi: 10.1016/j.redox.2021.102201. Epub 2021 Nov 27.

Reactive oxygen species (ROS) which are continuously generated mainly by mitochondria, have been proved to play an important role in the stress signaling of cancer cells. Moreover, pentatricopeptide repeat (PPR) proteins have been suggested to take part in mitochondrial...

Cite
Wei WS, Wang N, Deng MH, et al. LRPPRC regulates redox homeostasis via the circANKHD1/FOXM1 axis to enhance bladder urothelial carcinoma tumorigenesis. Redox Biol. 2021;48:102201doi: 10.1016/j.redox.2021.102201.
Wei, W. S., Wang, N., Deng, M. H., Dong, P., Liu, J. Y., Xiang, Z., Li, X. D., Li, Z. Y., Liu, Z. H., Peng, Y. L., Li, Z., Jiang, L. J., Yao, K., Ye, Y. L., Lu, W. H., Zhang, Z. L., Zhou, F. J., Liu, Z. W., Xie, D., & Yu, C. P. (2021). LRPPRC regulates redox homeostasis via the circANKHD1/FOXM1 axis to enhance bladder urothelial carcinoma tumorigenesis. Redox biology, 48102201. https://doi.org/10.1016/j.redox.2021.102201
Wei, Wen-Su, et al. "LRPPRC regulates redox homeostasis via the circANKHD1/FOXM1 axis to enhance bladder urothelial carcinoma tumorigenesis." Redox biology vol. 48 (2021): 102201. doi: https://doi.org/10.1016/j.redox.2021.102201
Wei WS, Wang N, Deng MH, Dong P, Liu JY, Xiang Z, Li XD, Li ZY, Liu ZH, Peng YL, Li Z, Jiang LJ, Yao K, Ye YL, Lu WH, Zhang ZL, Zhou FJ, Liu ZW, Xie D, Yu CP. LRPPRC regulates redox homeostasis via the circANKHD1/FOXM1 axis to enhance bladder urothelial carcinoma tumorigenesis. Redox Biol. 2021 Nov 27;48:102201. doi: 10.1016/j.redox.2021.102201. Epub 2021 Nov 27. PMID: 34864630; PMCID: PMC8645923.
Copy Download .nbib Format: NLM
Exosome-functionalized polyetheretherketone-based implant with immunomodulatory property for enhancing osseointegration.

Bioactive materials

Fan L, Guan P, Xiao C, Wen H, Wang Q, Liu C, Luo Y, Ma L, Tan G, Yu P, Zhou L, Ning C.
PMID: 33665507
Bioact Mater. 2021 Feb 15;6(9):2754-2766. doi: 10.1016/j.bioactmat.2021.02.005. eCollection 2021 Sep.

The host immune response effecting on biomaterials is critical to determine implant fates and bone regeneration property. Bone marrow stem cells (BMSCs) derived exosomes (Exos) contain multiple biosignal molecules and have been demonstrated to exhibit immunomodulatory functions. Herein, we...

Cite
Fan L, Guan P, Xiao C, et al. Exosome-functionalized polyetheretherketone-based implant with immunomodulatory property for enhancing osseointegration. Bioact Mater. 2021;6(9):2754-2766doi: 10.1016/j.bioactmat.2021.02.005.
Fan, L., Guan, P., Xiao, C., Wen, H., Wang, Q., Liu, C., Luo, Y., Ma, L., Tan, G., Yu, P., Zhou, L., & Ning, C. (2021). Exosome-functionalized polyetheretherketone-based implant with immunomodulatory property for enhancing osseointegration. Bioactive materials, 6(9), 2754-2766. https://doi.org/10.1016/j.bioactmat.2021.02.005
Fan, Lei, et al. "Exosome-functionalized polyetheretherketone-based implant with immunomodulatory property for enhancing osseointegration." Bioactive materials vol. 6,9 (2021): 2754-2766. doi: https://doi.org/10.1016/j.bioactmat.2021.02.005
Fan L, Guan P, Xiao C, Wen H, Wang Q, Liu C, Luo Y, Ma L, Tan G, Yu P, Zhou L, Ning C. Exosome-functionalized polyetheretherketone-based implant with immunomodulatory property for enhancing osseointegration. Bioact Mater. 2021 Feb 15;6(9):2754-2766. doi: 10.1016/j.bioactmat.2021.02.005. eCollection 2021 Sep. PMID: 33665507; PMCID: PMC7897935.
Copy Download .nbib Format: NLM
Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design.

European journal of medicinal chemistry

Yeh TK, Song JS, Chang PW, Yu JC, Chang CH, Liao FY, Tien YW, Kuppusamy R, Li AS, Chen CH, Chen CW, Lin LM, Chang HH, Huang CH, Yao JY, Wu MH, Peng YH, Hsueh CC, Hsiao WC, Chen PH, Lin CY, Hsieh SH, Shih C, Hung MS, Wu SY, Kuo CC, Ueng SH.
PMID: 34929581
Eur J Med Chem. 2021 Dec 08;229:114043. doi: 10.1016/j.ejmech.2021.114043. Epub 2021 Dec 08.

Indoleamine 2,3-dioxygenase-1 (IDO1) is a potential target for the next generation of cancer immunotherapies. We describe the development of two series of IDO1 inhibitors incorporating a N-hydroxy-thiophene-carboximidamide core generated by knowledge-based drug design. Structural modifications to improve the cellular...

Cite
Yeh TK, Song JS, Chang PW, et al. Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design. Eur J Med Chem. 2021;229:114043doi: 10.1016/j.ejmech.2021.114043.
Yeh, T. K., Song, J. S., Chang, P. W., Yu, J. C., Chang, C. H., Liao, F. Y., Tien, Y. W., Kuppusamy, R., Li, A. S., Chen, C. H., Chen, C. W., Lin, L. M., Chang, H. H., Huang, C. H., Yao, J. Y., Wu, M. H., Peng, Y. H., Hsueh, C. C., Hsiao, W. C., Chen, P. H., Lin, C. Y., Hsieh, S. H., Shih, C., Hung, M. S., Wu, S. Y., Kuo, C. C., & Ueng, S. H. (2021). Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design. European journal of medicinal chemistry, 229114043. https://doi.org/10.1016/j.ejmech.2021.114043
Yeh, Teng-Kuang, et al. "Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design." European journal of medicinal chemistry vol. 229 (2021): 114043. doi: https://doi.org/10.1016/j.ejmech.2021.114043
Yeh TK, Song JS, Chang PW, Yu JC, Chang CH, Liao FY, Tien YW, Kuppusamy R, Li AS, Chen CH, Chen CW, Lin LM, Chang HH, Huang CH, Yao JY, Wu MH, Peng YH, Hsueh CC, Hsiao WC, Chen PH, Lin CY, Hsieh SH, Shih C, Hung MS, Wu SY, Kuo CC, Ueng SH. Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design. Eur J Med Chem. 2021 Dec 08;229:114043. doi: 10.1016/j.ejmech.2021.114043. Epub 2021 Dec 08. PMID: 34929581.
Copy Download .nbib Format: NLM
AICAR suppresses cell proliferation and synergizes with decitabine in myelodysplastic syndrome via DNA damage induction.

Biotechnology letters

Liu J, Liang L, Li X, Peng YL, Zhang J, Wang XL, Liu J, Nie L.
PMID: 33788127
Biotechnol Lett. 2021 Jun;43(6):1131-1142. doi: 10.1007/s10529-021-03112-2. Epub 2021 Mar 31.

OBJECTIVE: To investigate the efficacy and safety of the AMPK activator AICAR alone or in combination with decitabine on myelodysplastic syndromes (MDS).RESULTS: p-AMPK (Thr172) expression was lower in MDS samples than in healthy donors. AMPK agonist AICAR inhibited the...

Cite
Liu J, Liang L, Li X, et al. AICAR suppresses cell proliferation and synergizes with decitabine in myelodysplastic syndrome via DNA damage induction. Biotechnol Lett. 2021;43(6):1131-1142doi: 10.1007/s10529-021-03112-2.
Liu, J., Liang, L., Li, X., Peng, Y. L., Zhang, J., Wang, X. L., Liu, J., & Nie, L. (2021). AICAR suppresses cell proliferation and synergizes with decitabine in myelodysplastic syndrome via DNA damage induction. Biotechnology letters, 43(6), 1131-1142. https://doi.org/10.1007/s10529-021-03112-2
Liu, Jin, et al. "AICAR suppresses cell proliferation and synergizes with decitabine in myelodysplastic syndrome via DNA damage induction." Biotechnology letters vol. 43,6 (2021): 1131-1142. doi: https://doi.org/10.1007/s10529-021-03112-2
Liu J, Liang L, Li X, Peng YL, Zhang J, Wang XL, Liu J, Nie L. AICAR suppresses cell proliferation and synergizes with decitabine in myelodysplastic syndrome via DNA damage induction. Biotechnol Lett. 2021 Jun;43(6):1131-1142. doi: 10.1007/s10529-021-03112-2. Epub 2021 Mar 31. PMID: 33788127.
Copy Download .nbib Format: NLM
The clinical significance of transcription factor WD repeat and HMG-box DNA binding protein 1 in laryngeal squamous cell carcinoma and its potential molecular mechanism.

Pathology, research and practice

Wu JY, Lan XL, Yan DM, Fang YY, Peng YX, Liang FF, Jiang L, Huang SN, Mo M, Lin CX, Niu YT, Wu XW, Wei ZX.
PMID: 34999279
Pathol Res Pract. 2021 Dec 23;230:153751. doi: 10.1016/j.prp.2021.153751. Epub 2021 Dec 23.

BACKGROUND: Currently, high expression of WD repeat and HMG-box DNA binding protein 1 (WDHD1) has been found in a variety of tumors; but there is no research has been conducted concerning the expression of WDHD1 in laryngeal squamous cell...

Cite
Wu JY, Lan XL, Yan DM, et al. The clinical significance of transcription factor WD repeat and HMG-box DNA binding protein 1 in laryngeal squamous cell carcinoma and its potential molecular mechanism. Pathol Res Pract. 2021;230:153751doi: 10.1016/j.prp.2021.153751.
Wu, J. Y., Lan, X. L., Yan, D. M., Fang, Y. Y., Peng, Y. X., Liang, F. F., Jiang, L., Huang, S. N., Mo, M., Lin, C. X., Niu, Y. T., Wu, X. W., & Wei, Z. X. (2021). The clinical significance of transcription factor WD repeat and HMG-box DNA binding protein 1 in laryngeal squamous cell carcinoma and its potential molecular mechanism. Pathology, research and practice, 230153751. https://doi.org/10.1016/j.prp.2021.153751
Wu, Ji-Yun, et al. "The clinical significance of transcription factor WD repeat and HMG-box DNA binding protein 1 in laryngeal squamous cell carcinoma and its potential molecular mechanism." Pathology, research and practice vol. 230 (2021): 153751. doi: https://doi.org/10.1016/j.prp.2021.153751
Wu JY, Lan XL, Yan DM, Fang YY, Peng YX, Liang FF, Jiang L, Huang SN, Mo M, Lin CX, Niu YT, Wu XW, Wei ZX. The clinical significance of transcription factor WD repeat and HMG-box DNA binding protein 1 in laryngeal squamous cell carcinoma and its potential molecular mechanism. Pathol Res Pract. 2021 Dec 23;230:153751. doi: 10.1016/j.prp.2021.153751. Epub 2021 Dec 23. PMID: 34999279.
Copy Download .nbib Format: NLM
Intermittent Hypoxia-Induced Activation of Endothelial Cells Is Mediated .

Frontiers in physiology

Cetin-Atalay R, Meliton AY, Wu D, Woods PS, Sun KA, Peng YJ, Nanduri J, Su X, Fang Y, Hamanaka RB, Prabhakar N, Mutlu GM.
PMID: 34322038
Front Physiol. 2021 Jul 12;12:701995. doi: 10.3389/fphys.2021.701995. eCollection 2021.

Obstructive sleep apnea (OSA) is a common breathing disorder affecting a significant percentage of the adult population. OSA is an independent risk factor for cardiovascular disease (CVD); however, the underlying mechanisms are not completely understood. Since the severity of...

Cite
Cetin-Atalay R, Meliton AY, Wu D, et al. Intermittent Hypoxia-Induced Activation of Endothelial Cells Is Mediated . Front Physiol. 2021;12:701995doi: 10.3389/fphys.2021.701995.
Cetin-Atalay, R., Meliton, A. Y., Wu, D., Woods, P. S., Sun, K. A., Peng, Y. J., Nanduri, J., Su, X., Fang, Y., Hamanaka, R. B., Prabhakar, N., & Mutlu, G. M. (2021). Intermittent Hypoxia-Induced Activation of Endothelial Cells Is Mediated . Frontiers in physiology, 12701995. https://doi.org/10.3389/fphys.2021.701995
Cetin-Atalay, Rengul, et al. "Intermittent Hypoxia-Induced Activation of Endothelial Cells Is Mediated ." Frontiers in physiology vol. 12 (2021): 701995. doi: https://doi.org/10.3389/fphys.2021.701995
Cetin-Atalay R, Meliton AY, Wu D, Woods PS, Sun KA, Peng YJ, Nanduri J, Su X, Fang Y, Hamanaka RB, Prabhakar N, Mutlu GM. Intermittent Hypoxia-Induced Activation of Endothelial Cells Is Mediated . Front Physiol. 2021 Jul 12;12:701995. doi: 10.3389/fphys.2021.701995. eCollection 2021. PMID: 34322038; PMCID: PMC8311436.
Copy Download .nbib Format: NLM
Mitochondrial targeted rhodium(III) complexes: Synthesis, characterized and antitumor mechanism investigation.

Journal of inorganic biochemistry

Peng YB, Tao C, Tan CP, Zhao P.
PMID: 33684684
J Inorg Biochem. 2021 May;218:111400. doi: 10.1016/j.jinorgbio.2021.111400. Epub 2021 Feb 25.

Recently, rhodium complexes have received intensive attentions due to their tunable chemical and biological properties as well as attractive antitumor activity. In this work, two imidazole triphenylamino rhodium complexes [Rh(ppy)

Cite
Peng YB, Tao C, Tan CP, et al. Mitochondrial targeted rhodium(III) complexes: Synthesis, characterized and antitumor mechanism investigation. J Inorg Biochem. 2021;218:111400doi: 10.1016/j.jinorgbio.2021.111400.
Peng, Y. B., Tao, C., Tan, C. P., & Zhao, P. (2021). Mitochondrial targeted rhodium(III) complexes: Synthesis, characterized and antitumor mechanism investigation. Journal of inorganic biochemistry, 218111400. https://doi.org/10.1016/j.jinorgbio.2021.111400
Peng, Yan-Bo, et al. "Mitochondrial targeted rhodium(III) complexes: Synthesis, characterized and antitumor mechanism investigation." Journal of inorganic biochemistry vol. 218 (2021): 111400. doi: https://doi.org/10.1016/j.jinorgbio.2021.111400
Peng YB, Tao C, Tan CP, Zhao P. Mitochondrial targeted rhodium(III) complexes: Synthesis, characterized and antitumor mechanism investigation. J Inorg Biochem. 2021 May;218:111400. doi: 10.1016/j.jinorgbio.2021.111400. Epub 2021 Feb 25. PMID: 33684684.
Copy Download .nbib Format: NLM
Showing 1681 to 1689 of 1689 entries