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Showing 1 to 12 of 27 entries
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UDP-glucose: Glucan Synthetase in Developing Cotton Fibers: I. Kinetic and Physiological Properties.

Plant physiology

Delmer DP, Heiniger U, Kulow C.
PMID: 16659924
Plant Physiol. 1977 Apr;59(4):713-8. doi: 10.1104/pp.59.4.713.

A uridine diphosphate(UDP)-glucose:glucan synthetase can be demonstrated in detached cotton fibers (Gossypium hirsutum L.) and in an isolated particulate fraction from such fibers. When assayed with detached fibers, the kinetics of the glucan synthetase activity with respect to variation...

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Delmer DP, Heiniger U, Kulow C. UDP-glucose: Glucan Synthetase in Developing Cotton Fibers: I. Kinetic and Physiological Properties. Plant Physiol. 1977;59(4):713-8doi: 10.1104/pp.59.4.713.
Delmer, D. P., Heiniger, U., & Kulow, C. (1977). UDP-glucose: Glucan Synthetase in Developing Cotton Fibers: I. Kinetic and Physiological Properties. Plant physiology, 59(4), 713-8. https://doi.org/10.1104/pp.59.4.713
Delmer, D P, et al. "UDP-glucose: Glucan Synthetase in Developing Cotton Fibers: I. Kinetic and Physiological Properties." Plant physiology vol. 59,4 (1977): 713-8. doi: https://doi.org/10.1104/pp.59.4.713
Delmer DP, Heiniger U, Kulow C. UDP-glucose: Glucan Synthetase in Developing Cotton Fibers: I. Kinetic and Physiological Properties. Plant Physiol. 1977 Apr;59(4):713-8. doi: 10.1104/pp.59.4.713. PMID: 16659924; PMCID: PMC542479.
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Metabolism of cytidine and uridine in bean leaves.

Plant physiology

Ross C, Cole CV.
PMID: 16656905
Plant Physiol. 1968 Aug;43(8):1227-31. doi: 10.1104/pp.43.8.1227.

The metabolism of cytidine-2-(14)C and uridine-2-(14)C was studied in discs cut from leaflets of bean plants (Phaseolus vulgaris L.). Cytidine was degraded to carbon dioxide and incorporated into RNA at about the same rates as was uridine. Both nucleosides...

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Ross C, Cole CV. Metabolism of cytidine and uridine in bean leaves. Plant Physiol. 1968;43(8):1227-31doi: 10.1104/pp.43.8.1227.
Ross, C., & Cole, C. V. (1968). Metabolism of cytidine and uridine in bean leaves. Plant physiology, 43(8), 1227-31. https://doi.org/10.1104/pp.43.8.1227
Ross, C, and Cole, C V. "Metabolism of cytidine and uridine in bean leaves." Plant physiology vol. 43,8 (1968): 1227-31. doi: https://doi.org/10.1104/pp.43.8.1227
Ross C, Cole CV. Metabolism of cytidine and uridine in bean leaves. Plant Physiol. 1968 Aug;43(8):1227-31. doi: 10.1104/pp.43.8.1227. PMID: 16656905; PMCID: PMC1086998.
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Signaling of the Purinergic System in the Joint.

Frontiers in pharmacology

Corciulo C, Cronstein BN.
PMID: 32038258
Front Pharmacol. 2020 Jan 24;10:1591. doi: 10.3389/fphar.2019.01591. eCollection 2019.

The joint is a complex anatomical structure consisting of different tissues, each with a particular feature, playing together to give mobility and stability at the body. All the joints have a similar composition including cartilage for reducing the friction...

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Corciulo C, Cronstein BN. Signaling of the Purinergic System in the Joint. Front Pharmacol. 2020;10:1591doi: 10.3389/fphar.2019.01591.
Corciulo, C., & Cronstein, B. N. (2019). Signaling of the Purinergic System in the Joint. Frontiers in pharmacology, 101591. https://doi.org/10.3389/fphar.2019.01591
Corciulo, Carmen, and Cronstein, Bruce N. "Signaling of the Purinergic System in the Joint." Frontiers in pharmacology vol. 10 (2019): 1591. doi: https://doi.org/10.3389/fphar.2019.01591
Corciulo C, Cronstein BN. Signaling of the Purinergic System in the Joint. Front Pharmacol. 2020 Jan 24;10:1591. doi: 10.3389/fphar.2019.01591. eCollection 2019. PMID: 32038258; PMCID: PMC6993121.
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Hexose-, inositol-, and nucleoside phosphate esters in germinating seeds of crested wheatgrass.

Plant physiology

Wilson AM, Harris GA.
PMID: 16656416
Plant Physiol. 1966 Nov;41(9):1416-9. doi: 10.1104/pp.41.9.1416.

Net synthesis of phosphate esters was measured in crested wheatgrass seeds [Agropyron desertorum (Fisch.) Schult.] to learn what phosphorylating reactions occur in early stages of germination. Phosphate esters were separated on ion exchange columns and identified by cochromatography and...

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Wilson AM, Harris GA. Hexose-, inositol-, and nucleoside phosphate esters in germinating seeds of crested wheatgrass. Plant Physiol. 1966;41(9):1416-9doi: 10.1104/pp.41.9.1416.
Wilson, A. M., & Harris, G. A. (1966). Hexose-, inositol-, and nucleoside phosphate esters in germinating seeds of crested wheatgrass. Plant physiology, 41(9), 1416-9. https://doi.org/10.1104/pp.41.9.1416
Wilson, A M, and Harris, G A. "Hexose-, inositol-, and nucleoside phosphate esters in germinating seeds of crested wheatgrass." Plant physiology vol. 41,9 (1966): 1416-9. doi: https://doi.org/10.1104/pp.41.9.1416
Wilson AM, Harris GA. Hexose-, inositol-, and nucleoside phosphate esters in germinating seeds of crested wheatgrass. Plant Physiol. 1966 Nov;41(9):1416-9. doi: 10.1104/pp.41.9.1416. PMID: 16656416; PMCID: PMC550546.
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Pyrimidine metabolism in cotyledons of germinating alaska peas.

Plant physiology

Ross C, Coddington RL, Murray MG, Bledsoe CS.
PMID: 16657582
Plant Physiol. 1971 Jan;47(1):71-5. doi: 10.1104/pp.47.1.71.

Cotyledons from Pisum sativum L. cv. Alaska seeds were excised 12, 36, 108, 132, and 156 hours after imbibition in aerated distilled water. They were then incubated under aseptic conditions for 6 hours in solutions containing either uridine-2-(14)C or...

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Ross C, Coddington RL, Murray MG, et al. Pyrimidine metabolism in cotyledons of germinating alaska peas. Plant Physiol. 1971;47(1):71-5doi: 10.1104/pp.47.1.71.
Ross, C., Coddington, R. L., Murray, M. G., & Bledsoe, C. S. (1971). Pyrimidine metabolism in cotyledons of germinating alaska peas. Plant physiology, 47(1), 71-5. https://doi.org/10.1104/pp.47.1.71
Ross, C, et al. "Pyrimidine metabolism in cotyledons of germinating alaska peas." Plant physiology vol. 47,1 (1971): 71-5. doi: https://doi.org/10.1104/pp.47.1.71
Ross C, Coddington RL, Murray MG, Bledsoe CS. Pyrimidine metabolism in cotyledons of germinating alaska peas. Plant Physiol. 1971 Jan;47(1):71-5. doi: 10.1104/pp.47.1.71. PMID: 16657582; PMCID: PMC365814.
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Calcium-dependent release of adenosine and uridine nucleotides from A549 cells.

Purinergic signalling

Tatur S, Kreda S, Lazarowski E, Grygorczyk R.
PMID: 18368524
Purinergic Signal. 2008 Jun;4(2):139-46. doi: 10.1007/s11302-007-9059-x. Epub 2007 Jul 25.

Extracellular nucleotides play an important role in lung defense, but the release mechanism and relative abundance of different nucleotide species secreted by lung epithelia are not well defined. In this study, to minimize cell surface hydrolysis, we used a...

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Tatur S, Kreda S, Lazarowski E, et al. Calcium-dependent release of adenosine and uridine nucleotides from A549 cells. Purinergic Signal. 2007;4(2):139-46doi: 10.1007/s11302-007-9059-x.
Tatur, S., Kreda, S., Lazarowski, E., & Grygorczyk, R. (2008). Calcium-dependent release of adenosine and uridine nucleotides from A549 cells. Purinergic signalling, 4(2), 139-46. https://doi.org/10.1007/s11302-007-9059-x
Tatur, Sabina, et al. "Calcium-dependent release of adenosine and uridine nucleotides from A549 cells." Purinergic signalling vol. 4,2 (2008): 139-46. doi: https://doi.org/10.1007/s11302-007-9059-x
Tatur S, Kreda S, Lazarowski E, Grygorczyk R. Calcium-dependent release of adenosine and uridine nucleotides from A549 cells. Purinergic Signal. 2008 Jun;4(2):139-46. doi: 10.1007/s11302-007-9059-x. Epub 2007 Jul 25. PMID: 18368524; PMCID: PMC2377317.
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Effects of alkaline phosphatase activity on nucleotide measurements in aquatic microbial communities.

Applied and environmental microbiology

Karl DM, Craven DB.
PMID: 16345634
Appl Environ Microbiol. 1980 Sep;40(3):549-61. doi: 10.1128/aem.40.3.549-561.1980.

Alkaline phosphatase (APase) activity was detected in aquatic microbial assemblages from the subtropics to Antarctica. The occurrence of APase in environmental nucleotide extracts was shown to significantly affect the measured concentrations of cellular nucleotides (adenosine triphosphate, adenosine diphosphate, adenosine...

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Karl DM, Craven DB. Effects of alkaline phosphatase activity on nucleotide measurements in aquatic microbial communities. Appl Environ Microbiol. 1980;40(3):549-61doi: 10.1128/aem.40.3.549-561.1980.
Karl, D. M., & Craven, D. B. (1980). Effects of alkaline phosphatase activity on nucleotide measurements in aquatic microbial communities. Applied and environmental microbiology, 40(3), 549-61. https://doi.org/10.1128/aem.40.3.549-561.1980
Karl, D M, and Craven, D B. "Effects of alkaline phosphatase activity on nucleotide measurements in aquatic microbial communities." Applied and environmental microbiology vol. 40,3 (1980): 549-61. doi: https://doi.org/10.1128/aem.40.3.549-561.1980
Karl DM, Craven DB. Effects of alkaline phosphatase activity on nucleotide measurements in aquatic microbial communities. Appl Environ Microbiol. 1980 Sep;40(3):549-61. doi: 10.1128/aem.40.3.549-561.1980. PMID: 16345634; PMCID: PMC291620.
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Purine receptors and Ca(2+) signalling in the human blood-brain barrier endothelial cell line hCMEC/D3.

Purinergic signalling

Bintig W, Begandt D, Schlingmann B, Gerhard L, Pangalos M, Dreyer L, Hohnjec N, Couraud PO, Romero IA, Weksler BB, Ngezahayo A.
PMID: 21956217
Purinergic Signal. 2012 Mar;8(1):71-80. doi: 10.1007/s11302-011-9262-7. Epub 2011 Sep 29.

The expression and physiology of purine receptors of the human blood-brain barrier endothelial cells were characterised by application of molecular biological, gene-silencing and Ca(2+)-imaging techniques to hCMEC/D3 cells. Reverse transcription polymerase chain reaction showed the expression of the G-protein-coupled...

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Bintig W, Begandt D, Schlingmann B, et al. Purine receptors and Ca(2+) signalling in the human blood-brain barrier endothelial cell line hCMEC/D3. Purinergic Signal. 2011;8(1):71-80doi: 10.1007/s11302-011-9262-7.
Bintig, W., Begandt, D., Schlingmann, B., Gerhard, L., Pangalos, M., Dreyer, L., Hohnjec, N., Couraud, P. O., Romero, I. A., Weksler, B. B., & Ngezahayo, A. (2012). Purine receptors and Ca(2+) signalling in the human blood-brain barrier endothelial cell line hCMEC/D3. Purinergic signalling, 8(1), 71-80. https://doi.org/10.1007/s11302-011-9262-7
Bintig, Willem, et al. "Purine receptors and Ca(2+) signalling in the human blood-brain barrier endothelial cell line hCMEC/D3." Purinergic signalling vol. 8,1 (2012): 71-80. doi: https://doi.org/10.1007/s11302-011-9262-7
Bintig W, Begandt D, Schlingmann B, Gerhard L, Pangalos M, Dreyer L, Hohnjec N, Couraud PO, Romero IA, Weksler BB, Ngezahayo A. Purine receptors and Ca(2+) signalling in the human blood-brain barrier endothelial cell line hCMEC/D3. Purinergic Signal. 2012 Mar;8(1):71-80. doi: 10.1007/s11302-011-9262-7. Epub 2011 Sep 29. PMID: 21956217; PMCID: PMC3286539.
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Inhibition of Methamphetamine-Induced Cytotoxicity in the U87-Cell Line by Atorvastatin-Conjugated Carbon Nanotubes.

Applied biochemistry and biotechnology

Nikeafshar S, Khazaei A, Tahvilian R.
PMID: 34611858
Appl Biochem Biotechnol. 2021 Oct 06; doi: 10.1007/s12010-021-03667-w. Epub 2021 Oct 06.

In biological systems, carbon nanotubes can enhance the biological effects of drugs and reduce their side effects. Methamphetamine (METH) is a stimulant drug that induces cell death in various cell types, primarily neural cells. On the other hand, specific...

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Nikeafshar S, Khazaei A, Tahvilian R. Inhibition of Methamphetamine-Induced Cytotoxicity in the U87-Cell Line by Atorvastatin-Conjugated Carbon Nanotubes. Appl Biochem Biotechnol. 2021;doi: 10.1007/s12010-021-03667-w.
Nikeafshar, S., Khazaei, A., & Tahvilian, R. (2021). Inhibition of Methamphetamine-Induced Cytotoxicity in the U87-Cell Line by Atorvastatin-Conjugated Carbon Nanotubes. Applied biochemistry and biotechnology, . https://doi.org/10.1007/s12010-021-03667-w
Nikeafshar, Sara, et al. "Inhibition of Methamphetamine-Induced Cytotoxicity in the U87-Cell Line by Atorvastatin-Conjugated Carbon Nanotubes." Applied biochemistry and biotechnology vol. (2021). doi: https://doi.org/10.1007/s12010-021-03667-w
Nikeafshar S, Khazaei A, Tahvilian R. Inhibition of Methamphetamine-Induced Cytotoxicity in the U87-Cell Line by Atorvastatin-Conjugated Carbon Nanotubes. Appl Biochem Biotechnol. 2021 Oct 06; doi: 10.1007/s12010-021-03667-w. Epub 2021 Oct 06. PMID: 34611858.
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Neuronal apoptosis in herpes simplex virus - 1 encephalitis (HSE).

Indian journal of medical microbiology

Athmanathan S, Vydehi BV, Sundaram C, Vemuganti GK, Murthy JM.
PMID: 17664814
Indian J Med Microbiol. 2001 Jul-Sep;19(3):127-31.

Herpes simplex virus infections are encountered often due to their ubiquitous nature. Common sites involved include skin, mucous membrane, genitalia, eye and the nervous system. HSV infection of the central nervous system can be life threatening. Little is known...

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Athmanathan S, Vydehi BV, Sundaram C, et al. Neuronal apoptosis in herpes simplex virus - 1 encephalitis (HSE). Indian J Med Microbiol. 2001;19(3):127-31
Athmanathan, S., Vydehi, B. V., Sundaram, C., Vemuganti, G. K., & Murthy, J. M. (2001). Neuronal apoptosis in herpes simplex virus - 1 encephalitis (HSE). Indian journal of medical microbiology, 19(3), 127-31.
Athmanathan, S, et al. "Neuronal apoptosis in herpes simplex virus - 1 encephalitis (HSE)." Indian journal of medical microbiology vol. 19,3 (2001): 127-31.
Athmanathan S, Vydehi BV, Sundaram C, Vemuganti GK, Murthy JM. Neuronal apoptosis in herpes simplex virus - 1 encephalitis (HSE). Indian J Med Microbiol. 2001 Jul-Sep;19(3):127-31. PMID: 17664814.
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The levels of soluble nucleotides in wheat aleurone tissue.

Plant physiology

Collins GG, Jenner CF, Paleg LG.
PMID: 16657969
Plant Physiol. 1972 Mar;49(3):398-403. doi: 10.1104/pp.49.3.398.

The content of soluble nucleotides in aleurone layers isolated from mature wheat (Triticum aestivum var. Olympic) grain was investigated. The most abundant nucleotides were adenosine triphosphate, uridine triphosphate, and uridine diphosphoglucose. Smaller amounts of guanosine triphosphate, cytidine triphosphate, adenosine...

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Collins GG, Jenner CF, Paleg LG. The levels of soluble nucleotides in wheat aleurone tissue. Plant Physiol. 1972;49(3):398-403doi: 10.1104/pp.49.3.398.
Collins, G. G., Jenner, C. F., & Paleg, L. G. (1972). The levels of soluble nucleotides in wheat aleurone tissue. Plant physiology, 49(3), 398-403. https://doi.org/10.1104/pp.49.3.398
Collins, G G, et al. "The levels of soluble nucleotides in wheat aleurone tissue." Plant physiology vol. 49,3 (1972): 398-403. doi: https://doi.org/10.1104/pp.49.3.398
Collins GG, Jenner CF, Paleg LG. The levels of soluble nucleotides in wheat aleurone tissue. Plant Physiol. 1972 Mar;49(3):398-403. doi: 10.1104/pp.49.3.398. PMID: 16657969; PMCID: PMC365973.
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Preparation of uridine diphosphate-N-acetylgalactosamine from uridine diphosphate-N-acetylglucosamine by using microbial enzymes.

Applied and environmental microbiology

Yamamoto K, Kawai H, Tochikura T.
PMID: 16345713
Appl Environ Microbiol. 1981 Feb;41(2):392-5. doi: 10.1128/aem.41.2.392-395.1981.

A method was developed for the large scale preparation of uridine diphosphate-N-acetylgalactosamine (UDP-GalNAc) from uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) by means of microbial enzymes. With Bacillus subtilis cell-free extract as a source of UDP-GlcNAc 4-epimerase, about 35% of the UDP-GlcNAc added...

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Yamamoto K, Kawai H, Tochikura T. Preparation of uridine diphosphate-N-acetylgalactosamine from uridine diphosphate-N-acetylglucosamine by using microbial enzymes. Appl Environ Microbiol. 1981;41(2):392-5doi: 10.1128/aem.41.2.392-395.1981.
Yamamoto, K., Kawai, H., & Tochikura, T. (1981). Preparation of uridine diphosphate-N-acetylgalactosamine from uridine diphosphate-N-acetylglucosamine by using microbial enzymes. Applied and environmental microbiology, 41(2), 392-5. https://doi.org/10.1128/aem.41.2.392-395.1981
Yamamoto, K, et al. "Preparation of uridine diphosphate-N-acetylgalactosamine from uridine diphosphate-N-acetylglucosamine by using microbial enzymes." Applied and environmental microbiology vol. 41,2 (1981): 392-5. doi: https://doi.org/10.1128/aem.41.2.392-395.1981
Yamamoto K, Kawai H, Tochikura T. Preparation of uridine diphosphate-N-acetylgalactosamine from uridine diphosphate-N-acetylglucosamine by using microbial enzymes. Appl Environ Microbiol. 1981 Feb;41(2):392-5. doi: 10.1128/aem.41.2.392-395.1981. PMID: 16345713; PMCID: PMC243706.
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Showing 1 to 12 of 27 entries