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Showing 1 to 12 of 338 entries
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Serum- and glucocorticoid-inducible kinase sgk2 stimulates the transport activity of human organic anion transporters 1 by enhancing the stability of the transporter.

International journal of biochemistry and molecular biology

Xu D, Huang H, Toh MF, You G.
PMID: 27335683
Int J Biochem Mol Biol. 2016 Jun 01;7(1):19-26. eCollection 2016.

Human organic anion transporter 1 (hOAT1) belongs to a family of organic anion transporters that play critical roles in the body disposition of clinically important drugs, including anti-viral therapeutics, anti-cancer drugs, antibiotics, antihypertensives, and anti-inflammatories. hOAT1 is abundantly expressed...

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Xu D, Huang H, Toh MF, et al. Serum- and glucocorticoid-inducible kinase sgk2 stimulates the transport activity of human organic anion transporters 1 by enhancing the stability of the transporter. Int J Biochem Mol Biol. 2016;7(1):19-26
Xu, D., Huang, H., Toh, M. F., & You, G. (2016). Serum- and glucocorticoid-inducible kinase sgk2 stimulates the transport activity of human organic anion transporters 1 by enhancing the stability of the transporter. International journal of biochemistry and molecular biology, 7(1), 19-26.
Xu, Da, et al. "Serum- and glucocorticoid-inducible kinase sgk2 stimulates the transport activity of human organic anion transporters 1 by enhancing the stability of the transporter." International journal of biochemistry and molecular biology vol. 7,1 (2016): 19-26.
Xu D, Huang H, Toh MF, You G. Serum- and glucocorticoid-inducible kinase sgk2 stimulates the transport activity of human organic anion transporters 1 by enhancing the stability of the transporter. Int J Biochem Mol Biol. 2016 Jun 01;7(1):19-26. eCollection 2016. PMID: 27335683; PMCID: PMC4913228.
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Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment.

International journal of biochemistry and molecular biology

Wang S, Lin C, Liu Y, Shen Z, Jeyaseelan J, Qin W.
PMID: 27335681
Int J Biochem Mol Biol. 2016 Jun 01;7(1):1-10. eCollection 2016.

Aspergillus niger is the most commonly used fungus for commercial amylase production, the increase of amylase activity will be beneficial to the amylase industry. Herein we report a high α-amylase producing (HAP) A. niger WLB42 mutated from A. niger...

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Wang S, Lin C, Liu Y, et al. Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment. Int J Biochem Mol Biol. 2016;7(1):1-10
Wang, S., Lin, C., Liu, Y., Shen, Z., Jeyaseelan, J., & Qin, W. (2016). Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment. International journal of biochemistry and molecular biology, 7(1), 1-10.
Wang, Shihui, et al. "Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment." International journal of biochemistry and molecular biology vol. 7,1 (2016): 1-10.
Wang S, Lin C, Liu Y, Shen Z, Jeyaseelan J, Qin W. Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment. Int J Biochem Mol Biol. 2016 Jun 01;7(1):1-10. eCollection 2016. PMID: 27335681; PMCID: PMC4913226.
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Nanomedicine: Application of nanoparticles in clinical therapies and diagnostics.

The international journal of biochemistry & cell biology

Kargul J, Irminger-Finger I, Laurent GJ.
PMID: 27130962
Int J Biochem Cell Biol. 2016 Jun;75:140. doi: 10.1016/j.biocel.2016.04.011. Epub 2016 Apr 27.

No abstract available.

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Kargul J, Irminger-Finger I, Laurent GJ. Nanomedicine: Application of nanoparticles in clinical therapies and diagnostics. Int J Biochem Cell Biol. 2016;75:140doi: 10.1016/j.biocel.2016.04.011.
Kargul, J., Irminger-Finger, I., & Laurent, G. J. (2016). Nanomedicine: Application of nanoparticles in clinical therapies and diagnostics. The international journal of biochemistry & cell biology, 75140. https://doi.org/10.1016/j.biocel.2016.04.011
Kargul, Joanna, et al. "Nanomedicine: Application of nanoparticles in clinical therapies and diagnostics." The international journal of biochemistry & cell biology vol. 75 (2016): 140. doi: https://doi.org/10.1016/j.biocel.2016.04.011
Kargul J, Irminger-Finger I, Laurent GJ. Nanomedicine: Application of nanoparticles in clinical therapies and diagnostics. Int J Biochem Cell Biol. 2016 Jun;75:140. doi: 10.1016/j.biocel.2016.04.011. Epub 2016 Apr 27. PMID: 27130962.
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Phosphatidylcholine-Mediated Aqueous Diffusion of Cellular Cholesterol Down-Regulates the ABCA1 Transporter in Human Skin Fibroblasts.

International journal of biochemistry research & review

Akopian D, Kawashima RL, Medh JD.
PMID: 26042209
Int J Biochem Res Rev. 2015;5(3):214-224. doi: 10.9734/IJBCRR/2015/14058.

ATP-binding cassette protein A1 (ABCA1) is a cholesterol transporter that contributes to the active transport/removal of excess cellular cholesterol. ABCA1 expression is up-regulated when cells accumulate cholesterol.AIMS: The purpose of this study was to determine any correlation between extracellular...

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Akopian D, Kawashima RL, Medh JD. Phosphatidylcholine-Mediated Aqueous Diffusion of Cellular Cholesterol Down-Regulates the ABCA1 Transporter in Human Skin Fibroblasts. Int J Biochem Res Rev. 2015;5(3):214-224doi: 10.9734/IJBCRR/2015/14058.
Akopian, D., Kawashima, R. L., & Medh, J. D. (2015). Phosphatidylcholine-Mediated Aqueous Diffusion of Cellular Cholesterol Down-Regulates the ABCA1 Transporter in Human Skin Fibroblasts. International journal of biochemistry research & review, 5(3), 214-224. https://doi.org/10.9734/IJBCRR/2015/14058
Akopian, David, et al. "Phosphatidylcholine-Mediated Aqueous Diffusion of Cellular Cholesterol Down-Regulates the ABCA1 Transporter in Human Skin Fibroblasts." International journal of biochemistry research & review vol. 5,3 (2015): 214-224. doi: https://doi.org/10.9734/IJBCRR/2015/14058
Akopian D, Kawashima RL, Medh JD. Phosphatidylcholine-Mediated Aqueous Diffusion of Cellular Cholesterol Down-Regulates the ABCA1 Transporter in Human Skin Fibroblasts. Int J Biochem Res Rev. 2015;5(3):214-224. doi: 10.9734/IJBCRR/2015/14058. PMID: 26042209; PMCID: PMC4450801.
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Interleukin-34 induces monocytic-like differentiation in leukemia cell lines.

International journal of biochemistry and molecular biology

Booker BE, Clark RS, Pellom ST, Adunyah SE.
PMID: 26045972
Int J Biochem Mol Biol. 2015 Mar 20;6(1):1-16. eCollection 2015.

Interleukin-34 (IL-34) is a cytokine consisting of a 39kD homodimer, shown to be a ligand for both the Macrophage Colony Stimulating Factor (M-CSF/CSF-1) receptor and the Receptor-like protein tyrosine phosphatase-zeta (RPTP-ƺ). IL-34 has been shown to promote monocyte viability...

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Booker BE, Clark RS, Pellom ST, et al. Interleukin-34 induces monocytic-like differentiation in leukemia cell lines. Int J Biochem Mol Biol. 2015;6(1):1-16
Booker, B. E., Clark, R. S., Pellom, S. T., & Adunyah, S. E. (2015). Interleukin-34 induces monocytic-like differentiation in leukemia cell lines. International journal of biochemistry and molecular biology, 6(1), 1-16.
Booker, Burthia E, et al. "Interleukin-34 induces monocytic-like differentiation in leukemia cell lines." International journal of biochemistry and molecular biology vol. 6,1 (2015): 1-16.
Booker BE, Clark RS, Pellom ST, Adunyah SE. Interleukin-34 induces monocytic-like differentiation in leukemia cell lines. Int J Biochem Mol Biol. 2015 Mar 20;6(1):1-16. eCollection 2015. PMID: 26045972; PMCID: PMC4443290.
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Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism.

International journal of biochemistry and molecular biology

Tseng SH, Cheng CY, Huang MZ, Chung MY, Su TS.
PMID: 24380022
Int J Biochem Mol Biol. 2013 Dec 15;4(4):179-90. eCollection 2013.

Microsatellites are abundant in the human genome and may acquire context-dependent functions. A highly polymorphic GT microsatellite is located downstream of the poly(A) signal of the human argininosuccinate synthetase (ASS1) gene. The ASS1 participates in urea and nitric oxide...

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Tseng SH, Cheng CY, Huang MZ, et al. Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. Int J Biochem Mol Biol. 2013;4(4):179-90
Tseng, S. H., Cheng, C. Y., Huang, M. Z., Chung, M. Y., & Su, T. S. (2013). Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. International journal of biochemistry and molecular biology, 4(4), 179-90.
Tseng, Shih-Heng, et al. "Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism." International journal of biochemistry and molecular biology vol. 4,4 (2013): 179-90.
Tseng SH, Cheng CY, Huang MZ, Chung MY, Su TS. Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. Int J Biochem Mol Biol. 2013 Dec 15;4(4):179-90. eCollection 2013. PMID: 24380022; PMCID: PMC3867704.
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Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells.

International journal of biochemistry and molecular biology

Park SJ, Bijangi-Vishehsaraei K, Safa AR.
PMID: 20953314
Int J Biochem Mol Biol. 2010;1(1):90-100. Epub 2010 Jul 18.

The death-inducing cytokine, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), holds enormous promise as a cancer therapeutic due to its highly selective apoptosis-inducing action on neoplastic versus normal cells. Our results revealed that TRAIL selectively triggered apoptosis in the P-glycoprotein...

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Park SJ, Bijangi-Vishehsaraei K, Safa AR. Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells. Int J Biochem Mol Biol. 2010;1(1):90-100
Park, S. J., Bijangi-Vishehsaraei, K., & Safa, A. R. (2010). Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells. International journal of biochemistry and molecular biology, 1(1), 90-100.
Park, Soo-Jung, et al. "Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells." International journal of biochemistry and molecular biology vol. 1,1 (2010): 90-100.
Park SJ, Bijangi-Vishehsaraei K, Safa AR. Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells. Int J Biochem Mol Biol. 2010;1(1):90-100. Epub 2010 Jul 18. PMID: 20953314; PMCID: PMC2953951.
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WITHDRAWN: The nonstructural protein-1 of influenza virus A.

The international journal of biochemistry & cell biology

Jiang H, Xu C, Zhang Y, Chen G, Xiao Y.
PMID: 19013254
Int J Biochem Cell Biol. 2008 Nov 01; doi: 10.1016/j.biocel.2008.10.016. Epub 2008 Nov 01.

This article has been retracted; please see Elsevier Policy on Article Withdrawal: http://www.elsevier.com/locate/withdrawalpolicy This article has been retracted at the request of the Editor-in-Chief of The International Journal of Biochemistry and Cell Biology, as the authors have plagiarised sections...

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Jiang H, Xu C, Zhang Y, et al. WITHDRAWN: The nonstructural protein-1 of influenza virus A. Int J Biochem Cell Biol. 2008;doi: 10.1016/j.biocel.2008.10.016.
Jiang, H., Xu, C., Zhang, Y., Chen, G., & Xiao, Y. (2008). WITHDRAWN: The nonstructural protein-1 of influenza virus A. The international journal of biochemistry & cell biology, . https://doi.org/10.1016/j.biocel.2008.10.016
Jiang, Hua, et al. "WITHDRAWN: The nonstructural protein-1 of influenza virus A." The international journal of biochemistry & cell biology vol. (2008). doi: https://doi.org/10.1016/j.biocel.2008.10.016
Jiang H, Xu C, Zhang Y, Chen G, Xiao Y. WITHDRAWN: The nonstructural protein-1 of influenza virus A. Int J Biochem Cell Biol. 2008 Nov 01; doi: 10.1016/j.biocel.2008.10.016. Epub 2008 Nov 01. PMID: 19013254.
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Frontiers in diabetic research.

The international journal of biochemistry & cell biology

Leung PS, Hayek A, de Gasparo M.
PMID: 16481209
Int J Biochem Cell Biol. 2006;38(5):687-8. doi: 10.1016/j.biocel.2006.01.012. Epub 2006 Feb 02.

No abstract available.

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Leung PS, Hayek A, de Gasparo M. Frontiers in diabetic research. Int J Biochem Cell Biol. 2006;38(5):687-8doi: 10.1016/j.biocel.2006.01.012.
Leung, P. S., Hayek, A., & de Gasparo, M. (2006). Frontiers in diabetic research. The international journal of biochemistry & cell biology, 38(5), 687-8. https://doi.org/10.1016/j.biocel.2006.01.012
Leung, Po Sing, et al. "Frontiers in diabetic research." The international journal of biochemistry & cell biology vol. 38,5 (2006): 687-8. doi: https://doi.org/10.1016/j.biocel.2006.01.012
Leung PS, Hayek A, de Gasparo M. Frontiers in diabetic research. Int J Biochem Cell Biol. 2006;38(5):687-8. doi: 10.1016/j.biocel.2006.01.012. Epub 2006 Feb 02. PMID: 16481209.
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A new crystal form of mouse thiamin pyrophosphokinase.

International journal of biochemistry and molecular biology

Liu JY, Hurley TD.
PMID: 21552434
Int J Biochem Mol Biol. 2011;2(2):111-8.

Thiamin pyrophosphokinase (TPK) transfers a pyrophosphate group from ATP to the hydroxyl group of thiamin and produces thiamin pyrophosphate (TPP). TPP is the cofactor of metabolically important enzymes such as pyruvate dehydrogenase, α-ketoglutarate dehydrogenase, branched-chain α-keto acid dehydrogenase, transketolase...

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Liu JY, Hurley TD. A new crystal form of mouse thiamin pyrophosphokinase. Int J Biochem Mol Biol. 2011;2(2):111-8
Liu, J. Y., & Hurley, T. D. (2011). A new crystal form of mouse thiamin pyrophosphokinase. International journal of biochemistry and molecular biology, 2(2), 111-8.
Liu, Jing-Yuan, and Hurley, Thomas D. "A new crystal form of mouse thiamin pyrophosphokinase." International journal of biochemistry and molecular biology vol. 2,2 (2011): 111-8.
Liu JY, Hurley TD. A new crystal form of mouse thiamin pyrophosphokinase. Int J Biochem Mol Biol. 2011;2(2):111-8. PMID: 21552434; PMCID: PMC3088427.
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Rapamycin induces the anti-apoptotic protein survivin in neuroblastoma.

International journal of biochemistry and molecular biology

Samkari A, Cooper ZA, Holloway MP, Liu J, Altura RA.
PMID: 22509478
Int J Biochem Mol Biol. 2012;3(1):28-35. Epub 2012 Feb 10.

Neuroblastoma is the most common solid tumor of infancy, accounting for 15% of all cancer cell deaths in children. Expression of the anti-apoptotic protein survivin in these tumors correlates with poor prognostic features and resistance to therapy. The mammalian...

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Samkari A, Cooper ZA, Holloway MP, et al. Rapamycin induces the anti-apoptotic protein survivin in neuroblastoma. Int J Biochem Mol Biol. 2012;3(1):28-35
Samkari, A., Cooper, Z. A., Holloway, M. P., Liu, J., & Altura, R. A. (2012). Rapamycin induces the anti-apoptotic protein survivin in neuroblastoma. International journal of biochemistry and molecular biology, 3(1), 28-35.
Samkari, Ayman, et al. "Rapamycin induces the anti-apoptotic protein survivin in neuroblastoma." International journal of biochemistry and molecular biology vol. 3,1 (2012): 28-35.
Samkari A, Cooper ZA, Holloway MP, Liu J, Altura RA. Rapamycin induces the anti-apoptotic protein survivin in neuroblastoma. Int J Biochem Mol Biol. 2012;3(1):28-35. Epub 2012 Feb 10. PMID: 22509478; PMCID: PMC3325774.
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Multiple protein-protein interactions within the DNA-PK complex are mediated by the C-terminus of Ku 80.

International journal of biochemistry and molecular biology

Bennett SM, Woods DS, Pawelczak KS, Turchi JJ.
PMID: 22509479
Int J Biochem Mol Biol. 2012;3(1):36-45. Epub 2012 Feb 15.

DNA double strand breaks (DSB) are among the most lethal forms of DNA damage and, in humans, are repaired predominantly by the non-homologous end joining (NHEJ) pathway. NHEJ is initiated by the Ku70/80 heterodimer binding free DNA termini and...

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Bennett SM, Woods DS, Pawelczak KS, et al. Multiple protein-protein interactions within the DNA-PK complex are mediated by the C-terminus of Ku 80. Int J Biochem Mol Biol. 2012;3(1):36-45
Bennett, S. M., Woods, D. S., Pawelczak, K. S., & Turchi, J. J. (2012). Multiple protein-protein interactions within the DNA-PK complex are mediated by the C-terminus of Ku 80. International journal of biochemistry and molecular biology, 3(1), 36-45.
Bennett, Sara M, et al. "Multiple protein-protein interactions within the DNA-PK complex are mediated by the C-terminus of Ku 80." International journal of biochemistry and molecular biology vol. 3,1 (2012): 36-45.
Bennett SM, Woods DS, Pawelczak KS, Turchi JJ. Multiple protein-protein interactions within the DNA-PK complex are mediated by the C-terminus of Ku 80. Int J Biochem Mol Biol. 2012;3(1):36-45. Epub 2012 Feb 15. PMID: 22509479; PMCID: PMC3325771.
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Showing 1 to 12 of 338 entries