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Detection of Cellular Proteins and Viral Core Protein Interacting with the 5' Untranslated Region of Hepatitis C Virus RNA.

Journal of biomedical science

Hwang SB, Lo SY, Ou JH, Lai MM.
PMID: 11725058
J Biomed Sci. 1995 Aug;2(3):227-236. doi: 10.1007/BF02253382.

Hepatitis C virus (HCV) is a pesti- and flavi-like virus, which contains a highly conserved 5'-untranslated region (UTR). This region is implicated in the regulation of both translation and RNA replication. To examine the possible cellular factors involved in...

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Hwang SB, Lo SY, Ou JH, et al. Detection of Cellular Proteins and Viral Core Protein Interacting with the 5' Untranslated Region of Hepatitis C Virus RNA. J Biomed Sci. 1995;2(3):227-236doi: 10.1007/BF02253382.
Hwang, S. B., Lo, S. Y., Ou, J. H., & Lai, M. M. (1995). Detection of Cellular Proteins and Viral Core Protein Interacting with the 5' Untranslated Region of Hepatitis C Virus RNA. Journal of biomedical science, 2(3), 227-236. https://doi.org/10.1007/BF02253382
Hwang, S.B., et al. "Detection of Cellular Proteins and Viral Core Protein Interacting with the 5' Untranslated Region of Hepatitis C Virus RNA." Journal of biomedical science vol. 2,3 (1995): 227-236. doi: https://doi.org/10.1007/BF02253382
Hwang SB, Lo SY, Ou JH, Lai MM. Detection of Cellular Proteins and Viral Core Protein Interacting with the 5' Untranslated Region of Hepatitis C Virus RNA. J Biomed Sci. 1995 Aug;2(3):227-236. doi: 10.1007/BF02253382. PMID: 11725058.
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Long-term administering low anticoagulant activity heparin can lessen rat hepatic fibrosis induced by either CCl(4) or porcine serum injection.

Hepatology research : the official journal of the Japan Society of Hepatology

Li W, Zhang J, Huang Q, Zhu H, Zhang X.
PMID: 16904936
Hepatol Res. 2006 Oct;36(2):115-23. doi: 10.1016/j.hepres.2006.07.004. Epub 2006 Aug 14.

BACKGROUND/AIM: Heparin or heparin-derived molecules have been demonstrated to have a renoprotective activity in a number of experimental nephropathies and anti-fibrotic effect on pulmonary fibrosis induced by Bleomycin. However, the effectiveness of low anticoagulant activity heparin (LAAH) in the...

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Li W, Zhang J, Huang Q, et al. Long-term administering low anticoagulant activity heparin can lessen rat hepatic fibrosis induced by either CCl(4) or porcine serum injection. Hepatol Res. 2006;36(2):115-23doi: 10.1016/j.hepres.2006.07.004.
Li, W., Zhang, J., Huang, Q., Zhu, H., & Zhang, X. (2006). Long-term administering low anticoagulant activity heparin can lessen rat hepatic fibrosis induced by either CCl(4) or porcine serum injection. Hepatology research : the official journal of the Japan Society of Hepatology, 36(2), 115-23. https://doi.org/10.1016/j.hepres.2006.07.004
Li, Wencai, et al. "Long-term administering low anticoagulant activity heparin can lessen rat hepatic fibrosis induced by either CCl(4) or porcine serum injection." Hepatology research : the official journal of the Japan Society of Hepatology vol. 36,2 (2006): 115-23. doi: https://doi.org/10.1016/j.hepres.2006.07.004
Li W, Zhang J, Huang Q, Zhu H, Zhang X. Long-term administering low anticoagulant activity heparin can lessen rat hepatic fibrosis induced by either CCl(4) or porcine serum injection. Hepatol Res. 2006 Oct;36(2):115-23. doi: 10.1016/j.hepres.2006.07.004. Epub 2006 Aug 14. PMID: 16904936.
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Turnover of Nuclear Proteins in Amoeba.

Science (New York, N.Y.)

Prescott DM.
PMID: 17815790
Science. 1963 Apr 26;140(3565):384. doi: 10.1126/science.140.3565.384-a.

No abstract available.

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Prescott DM. Turnover of Nuclear Proteins in Amoeba. Science. 1963;140(3565):384doi: 10.1126/science.140.3565.384-a.
Prescott, D. M. (1963). Turnover of Nuclear Proteins in Amoeba. Science (New York, N.Y.), 140(3565), 384. https://doi.org/10.1126/science.140.3565.384-a
Prescott, D M. "Turnover of Nuclear Proteins in Amoeba." Science (New York, N.Y.) vol. 140,3565 (1963): 384. doi: https://doi.org/10.1126/science.140.3565.384-a
Prescott DM. Turnover of Nuclear Proteins in Amoeba. Science. 1963 Apr 26;140(3565):384. doi: 10.1126/science.140.3565.384-a. PMID: 17815790.
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2,4-Dichlorophenoxyacetic Acid-enhanced Phosphorylation of Soybean Nuclear Proteins.

Plant physiology

Murray MG, Key JL.
PMID: 16660258
Plant Physiol. 1978 Feb;61(2):190-8. doi: 10.1104/pp.61.2.190.

In vitro nuclear protein phosphorylation is enhanced in nuclei isolated from 2,4-dichlorophenoxyacetic acid (2,4-d)-treated mature soybean (Glycine max) hypocotyl relative to nuclei from untreated tissue. Increased nuclear protein phosphorylation correlates with increased levels of nuclear protein kinase activity. These...

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Murray MG, Key JL. 2,4-Dichlorophenoxyacetic Acid-enhanced Phosphorylation of Soybean Nuclear Proteins. Plant Physiol. 1978;61(2):190-8doi: 10.1104/pp.61.2.190.
Murray, M. G., & Key, J. L. (1978). 2,4-Dichlorophenoxyacetic Acid-enhanced Phosphorylation of Soybean Nuclear Proteins. Plant physiology, 61(2), 190-8. https://doi.org/10.1104/pp.61.2.190
Murray, M G, and Key, J L. "2,4-Dichlorophenoxyacetic Acid-enhanced Phosphorylation of Soybean Nuclear Proteins." Plant physiology vol. 61,2 (1978): 190-8. doi: https://doi.org/10.1104/pp.61.2.190
Murray MG, Key JL. 2,4-Dichlorophenoxyacetic Acid-enhanced Phosphorylation of Soybean Nuclear Proteins. Plant Physiol. 1978 Feb;61(2):190-8. doi: 10.1104/pp.61.2.190. PMID: 16660258; PMCID: PMC1091830.
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Initial function analysis of a novel erythroid differentiation related gene EDRF1.

Science in China. Series C, Life sciences

Wang D, Li Y, Shen B.
PMID: 18726394
Sci China C Life Sci. 2001 Oct;44(5):489-96. doi: 10.1007/BF02882391.

Erythroid differentiation depends on the establishment of specific patterns of gene expression. Hypersensitive site 2 (HS2, serving as a major enhancer of globin genes)-binding proteins may be involved in its natural open chromosomal environment formation. Previously we prepared monoclonal...

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Wang D, Li Y, Shen B. Initial function analysis of a novel erythroid differentiation related gene EDRF1. Sci China C Life Sci. 2001;44(5):489-96doi: 10.1007/BF02882391.
Wang, D., Li, Y., & Shen, B. (2001). Initial function analysis of a novel erythroid differentiation related gene EDRF1. Science in China. Series C, Life sciences, 44(5), 489-96. https://doi.org/10.1007/BF02882391
Wang, D, et al. "Initial function analysis of a novel erythroid differentiation related gene EDRF1." Science in China. Series C, Life sciences vol. 44,5 (2001): 489-96. doi: https://doi.org/10.1007/BF02882391
Wang D, Li Y, Shen B. Initial function analysis of a novel erythroid differentiation related gene EDRF1. Sci China C Life Sci. 2001 Oct;44(5):489-96. doi: 10.1007/BF02882391. PMID: 18726394.
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Flow-cytometric assessment of cellular poly(ADP-ribosyl)ation capacity in peripheral blood lymphocytes.

Immunity & ageing : I & A

Kunzmann A, Liu D, Annett K, Malaisé M, Thaa B, Hyland P, Barnett Y, Bürkle A.
PMID: 16854233
Immun Ageing. 2006 Jul 19;3:8. doi: 10.1186/1742-4933-3-8.

BACKGROUND: Poly(ADP-ribosyl)ation is a posttranslational modification of nuclear proteins catalysed by poly(ADP-ribose) polymerases (PARPs), using NAD+ as a substrate. Activation of PARP-1 is in immediate response to DNA damage generated by endogenous and exogenous damaging agents. It has been...

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Kunzmann A, Liu D, Annett K, et al. Flow-cytometric assessment of cellular poly(ADP-ribosyl)ation capacity in peripheral blood lymphocytes. Immun Ageing. 2006;3:8doi: 10.1186/1742-4933-3-8.
Kunzmann, A., Liu, D., Annett, K., Malaisé, M., Thaa, B., Hyland, P., Barnett, Y., & Bürkle, A. (2006). Flow-cytometric assessment of cellular poly(ADP-ribosyl)ation capacity in peripheral blood lymphocytes. Immunity & ageing : I & A, 38. https://doi.org/10.1186/1742-4933-3-8
Kunzmann, Andrea, et al. "Flow-cytometric assessment of cellular poly(ADP-ribosyl)ation capacity in peripheral blood lymphocytes." Immunity & ageing : I & A vol. 3 (2006): 8. doi: https://doi.org/10.1186/1742-4933-3-8
Kunzmann A, Liu D, Annett K, Malaisé M, Thaa B, Hyland P, Barnett Y, Bürkle A. Flow-cytometric assessment of cellular poly(ADP-ribosyl)ation capacity in peripheral blood lymphocytes. Immun Ageing. 2006 Jul 19;3:8. doi: 10.1186/1742-4933-3-8. PMID: 16854233; PMCID: PMC1564410.
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In silico analysis of the cyclophilin repertoire of apicomplexan parasites.

Parasites & vectors

Krücken J, Greif G, von Samson-Himmelstjerna G.
PMID: 19555495
Parasit Vectors. 2009 Jun 25;2(1):27. doi: 10.1186/1756-3305-2-27.

BACKGROUND: Cyclophilins (Cyps) are peptidyl cis/trans isomerases implicated in diverse processes such as protein folding, signal transduction, and RNA processing. They are also candidate drug targets, in particular for the immunosuppressant cyclosporine A. In addition, cyclosporine is known to...

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Krücken J, Greif G, von Samson-Himmelstjerna G. In silico analysis of the cyclophilin repertoire of apicomplexan parasites. Parasit Vectors. 2009;2(1):27doi: 10.1186/1756-3305-2-27.
Krücken, J., Greif, G., & von Samson-Himmelstjerna, G. (2009). In silico analysis of the cyclophilin repertoire of apicomplexan parasites. Parasites & vectors, 2(1), 27. https://doi.org/10.1186/1756-3305-2-27
Krücken, Jürgen, et al. "In silico analysis of the cyclophilin repertoire of apicomplexan parasites." Parasites & vectors vol. 2,1 (2009): 27. doi: https://doi.org/10.1186/1756-3305-2-27
Krücken J, Greif G, von Samson-Himmelstjerna G. In silico analysis of the cyclophilin repertoire of apicomplexan parasites. Parasit Vectors. 2009 Jun 25;2(1):27. doi: 10.1186/1756-3305-2-27. PMID: 19555495; PMCID: PMC2713222.
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A novel phosphoprotein analysis scheme for assessing changes in premalignant and malignant breast cell lines using 2D liquid separations, protein microarrays and tandem mass spectrometry.

Proteomics. Clinical applications

Patwa TH, Wang Y, Miller FR, Goodison S, Pennathur S, Barder TJ, Lubman DM.
PMID: 19194518
Proteomics Clin Appl. 2008;3(1):51-66. doi: 10.1002/prca.200800097.

An analysis of phosphorylation changes that occur during cancer progression would provide insights into the molecular pathways responsible for a malignant phenotype. In this study we employed a novel coupling of 2D-liquid separations and protein microarray technology to reveal...

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Patwa TH, Wang Y, Miller FR, et al. A novel phosphoprotein analysis scheme for assessing changes in premalignant and malignant breast cell lines using 2D liquid separations, protein microarrays and tandem mass spectrometry. Proteomics Clin Appl. 2008;3(1):51-66doi: 10.1002/prca.200800097.
Patwa, T. H., Wang, Y., Miller, F. R., Goodison, S., Pennathur, S., Barder, T. J., & Lubman, D. M. (2008). A novel phosphoprotein analysis scheme for assessing changes in premalignant and malignant breast cell lines using 2D liquid separations, protein microarrays and tandem mass spectrometry. Proteomics. Clinical applications, 3(1), 51-66. https://doi.org/10.1002/prca.200800097
Patwa, Tasneem H, et al. "A novel phosphoprotein analysis scheme for assessing changes in premalignant and malignant breast cell lines using 2D liquid separations, protein microarrays and tandem mass spectrometry." Proteomics. Clinical applications vol. 3,1 (2008): 51-66. doi: https://doi.org/10.1002/prca.200800097
Patwa TH, Wang Y, Miller FR, Goodison S, Pennathur S, Barder TJ, Lubman DM. A novel phosphoprotein analysis scheme for assessing changes in premalignant and malignant breast cell lines using 2D liquid separations, protein microarrays and tandem mass spectrometry. Proteomics Clin Appl. 2008;3(1):51-66. doi: 10.1002/prca.200800097. PMID: 19194518; PMCID: PMC2633720.
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Efficient method for generating nuclear fractions from marrow stromal cells.

Cytotechnology

Woodbury D, Len GW, Reynolds K, McAuliffe WG, Coyne T, Wu K.
PMID: 19052892
Cytotechnology. 2008 Oct;58(2):77-84. doi: 10.1007/s10616-008-9176-6. Epub 2008 Dec 04.

Stem cells have received significant attention for their envisioned potential to treat currently unapproachable diseases. No less important is the utility of stem cells to serve as model systems of differentiation. Analyses at the transcriptome, miRNA and proteome levels...

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Woodbury D, Len GW, Reynolds K, et al. Efficient method for generating nuclear fractions from marrow stromal cells. Cytotechnology. 2008;58(2):77-84doi: 10.1007/s10616-008-9176-6.
Woodbury, D., Len, G. W., Reynolds, K., McAuliffe, W. G., Coyne, T., & Wu, K. (2008). Efficient method for generating nuclear fractions from marrow stromal cells. Cytotechnology, 58(2), 77-84. https://doi.org/10.1007/s10616-008-9176-6
Woodbury, Dale, et al. "Efficient method for generating nuclear fractions from marrow stromal cells." Cytotechnology vol. 58,2 (2008): 77-84. doi: https://doi.org/10.1007/s10616-008-9176-6
Woodbury D, Len GW, Reynolds K, McAuliffe WG, Coyne T, Wu K. Efficient method for generating nuclear fractions from marrow stromal cells. Cytotechnology. 2008 Oct;58(2):77-84. doi: 10.1007/s10616-008-9176-6. Epub 2008 Dec 04. PMID: 19052892; PMCID: PMC2612101.
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Rice bZIP protein, REB, interacts with GCN4 motif in promoter of Waxy gene.

Science in China. Series C, Life sciences

Cheng S, Wang Z, Hong M.
PMID: 18759022
Sci China C Life Sci. 2002 Aug;45(4):352-60. doi: 10.1360/02yc9039.

A bifactorial endosperm box (EB), which contains an endosperm motif (EM) and a GCN4 motif, was found in rice Wx promoter. EB was found in 5' upstream region of many seed storage protein genes accounting for these genes expression...

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Cheng S, Wang Z, Hong M. Rice bZIP protein, REB, interacts with GCN4 motif in promoter of Waxy gene. Sci China C Life Sci. 2002;45(4):352-60doi: 10.1360/02yc9039.
Cheng, S., Wang, Z., & Hong, M. (2002). Rice bZIP protein, REB, interacts with GCN4 motif in promoter of Waxy gene. Science in China. Series C, Life sciences, 45(4), 352-60. https://doi.org/10.1360/02yc9039
Cheng, Shijun, et al. "Rice bZIP protein, REB, interacts with GCN4 motif in promoter of Waxy gene." Science in China. Series C, Life sciences vol. 45,4 (2002): 352-60. doi: https://doi.org/10.1360/02yc9039
Cheng S, Wang Z, Hong M. Rice bZIP protein, REB, interacts with GCN4 motif in promoter of Waxy gene. Sci China C Life Sci. 2002 Aug;45(4):352-60. doi: 10.1360/02yc9039. PMID: 18759022.
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2-D DIGE identification of differentially expressed heterogeneous nuclear ribonucleoproteins and transcription factors during neural differentiation of human embryonic stem cells.

Proteomics. Clinical applications

Barthéléry M, Jaishankar A, Salli U, Freeman WM, Vrana KE.
PMID: 21136975
Proteomics Clin Appl. 2009 Apr;3(4):505-14. doi: 10.1002/prca.200800109.

Neural stem cells (NSC) are progenitors that can give rise to all neural lineages. They are found in specific niches of fetal and adult brains and grow in vitro as non-adherent colonies, the neurospheres. These cells express the intermediate...

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Barthéléry M, Jaishankar A, Salli U, et al. 2-D DIGE identification of differentially expressed heterogeneous nuclear ribonucleoproteins and transcription factors during neural differentiation of human embryonic stem cells. Proteomics Clin Appl. 2009;3(4):505-14doi: 10.1002/prca.200800109.
Barthéléry, M., Jaishankar, A., Salli, U., Freeman, W. M., & Vrana, K. E. (2009). 2-D DIGE identification of differentially expressed heterogeneous nuclear ribonucleoproteins and transcription factors during neural differentiation of human embryonic stem cells. Proteomics. Clinical applications, 3(4), 505-14. https://doi.org/10.1002/prca.200800109
Barthéléry, Miguel, et al. "2-D DIGE identification of differentially expressed heterogeneous nuclear ribonucleoproteins and transcription factors during neural differentiation of human embryonic stem cells." Proteomics. Clinical applications vol. 3,4 (2009): 505-14. doi: https://doi.org/10.1002/prca.200800109
Barthéléry M, Jaishankar A, Salli U, Freeman WM, Vrana KE. 2-D DIGE identification of differentially expressed heterogeneous nuclear ribonucleoproteins and transcription factors during neural differentiation of human embryonic stem cells. Proteomics Clin Appl. 2009 Apr;3(4):505-14. doi: 10.1002/prca.200800109. PMID: 21136975.
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Decoding chromatin goes high tech.

Cell

Levy D, Gozani O.
PMID: 20850007
Cell. 2010 Sep 17;142(6):844-6. doi: 10.1016/j.cell.2010.08.032.

Identifying proteins that recognize histone methylation is critical for understanding chromatin function. Vermeulen et al. (2010) now describe a cutting-edge strategy to identify and characterize several nuclear proteins and complexes that recognize five major histone trimethyl marks.

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Levy D, Gozani O. Decoding chromatin goes high tech. Cell. 2010;142(6):844-6doi: 10.1016/j.cell.2010.08.032.
Levy, D., & Gozani, O. (2010). Decoding chromatin goes high tech. Cell, 142(6), 844-6. https://doi.org/10.1016/j.cell.2010.08.032
Levy, Dan, and Gozani, Or. "Decoding chromatin goes high tech." Cell vol. 142,6 (2010): 844-6. doi: https://doi.org/10.1016/j.cell.2010.08.032
Levy D, Gozani O. Decoding chromatin goes high tech. Cell. 2010 Sep 17;142(6):844-6. doi: 10.1016/j.cell.2010.08.032. PMID: 20850007; PMCID: PMC4557769.
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Showing 13 to 24 of 305 entries