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Showing 1 to 12 of 802 entries
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Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity.

PloS one

Korrer MJ, Zhang Y, Routes JM.
PMID: 27031640
PLoS One. 2016 Mar 31;11(3):e0153122. doi: 10.1371/journal.pone.0153122. eCollection 2016.

No abstract available.

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Korrer MJ, Zhang Y, Routes JM. Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity. PLoS One. 2016;11(3):e0153122doi: 10.1371/journal.pone.0153122.
Korrer, M. J., Zhang, Y., & Routes, J. M. (2016). Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity. PloS one, 11(3), e0153122. https://doi.org/10.1371/journal.pone.0153122
Korrer, Michael J, et al. "Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity." PloS one vol. 11,3 (2016): e0153122. doi: https://doi.org/10.1371/journal.pone.0153122
Korrer MJ, Zhang Y, Routes JM. Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity. PLoS One. 2016 Mar 31;11(3):e0153122. doi: 10.1371/journal.pone.0153122. eCollection 2016. PMID: 27031640; PMCID: PMC4816400.
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Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients.

Neoplasma

Yuan L, Xu B, Fan H, Yuan P, Zhao P, Suo Z.
PMID: 25591589
Neoplasma. 2015;62(2):239-49. doi: 10.4149/neo_2015_029.

UNLABELLED: This study aims to explore whether pre-operative or post-operative percentages of circulating myeloid-derived suppressor cells (MDSC) have any correlations with clinicopathological parameters in patients with rectal cancer and have any predictive values for local recurrence and disease free...

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Yuan L, Xu B, Fan H, et al. Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma. 2015;62(2):239-49doi: 10.4149/neo_2015_029.
Yuan, L., Xu, B., Fan, H., Yuan, P., Zhao, P., & Suo, Z. (2015). Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma, 62(2), 239-49. https://doi.org/10.4149/neo_2015_029
Yuan, L, et al. "Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients." Neoplasma vol. 62,2 (2015): 239-49. doi: https://doi.org/10.4149/neo_2015_029
Yuan L, Xu B, Fan H, Yuan P, Zhao P, Suo Z. Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma. 2015;62(2):239-49. doi: 10.4149/neo_2015_029. PMID: 25591589.
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Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How.

Frontiers in medicine

Di Tommaso L, Roncalli M.
PMID: 28280721
Front Med (Lausanne). 2017 Feb 23;4:10. doi: 10.3389/fmed.2017.00010. eCollection 2017.

Few tissue markers are currently available to pathologists in the study of hepatocellular tumors. These markers should be used carefully taking into consideration not only morphology but also, and sometimes even more important, the clinical setting where the lesion...

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Di Tommaso L, Roncalli M. Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Front Med (Lausanne). 2017;4:10doi: 10.3389/fmed.2017.00010.
Di Tommaso, L., & Roncalli, M. (2017). Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Frontiers in medicine, 410. https://doi.org/10.3389/fmed.2017.00010
Di Tommaso, Luca, and Roncalli, Massimo. "Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How." Frontiers in medicine vol. 4 (2017): 10. doi: https://doi.org/10.3389/fmed.2017.00010
Di Tommaso L, Roncalli M. Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Front Med (Lausanne). 2017 Feb 23;4:10. doi: 10.3389/fmed.2017.00010. eCollection 2017. PMID: 28280721; PMCID: PMC5322593.
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Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity.

Frontiers in immunology

Rodriguez PC, Ochoa AC, Al-Khami AA.
PMID: 28223985
Front Immunol. 2017 Feb 07;8:93. doi: 10.3389/fimmu.2017.00093. eCollection 2017.

Arginine metabolism has been a key catabolic and anabolic process throughout the evolution of the immune response. Accruing evidence indicates that arginine-catabolizing enzymes, mainly nitric oxide synthases and arginases, are closely integrated with the control of immune response under...

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Rodriguez PC, Ochoa AC, Al-Khami AA. Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity. Front Immunol. 2017;8:93doi: 10.3389/fimmu.2017.00093.
Rodriguez, P. C., Ochoa, A. C., & Al-Khami, A. A. (2017). Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity. Frontiers in immunology, 893. https://doi.org/10.3389/fimmu.2017.00093
Rodriguez, Paulo C, et al. "Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity." Frontiers in immunology vol. 8 (2017): 93. doi: https://doi.org/10.3389/fimmu.2017.00093
Rodriguez PC, Ochoa AC, Al-Khami AA. Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity. Front Immunol. 2017 Feb 07;8:93. doi: 10.3389/fimmu.2017.00093. eCollection 2017. PMID: 28223985; PMCID: PMC5293781.
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Effect of Arginase-1 Inhibition on the Incidence of Autoimmune Diabetes in NOD Mice.

Current research in diabetes & obesity journal

Hernandez LF, Buchwald P, Abdulreda MH.
PMID: 29450408
Curr Res Diabetes Obes J. 2018 Jan;5(3). Epub 2018 Aug 01.

Metabolism of the amino acid L-arginine is implicated in many physiological and pathophysiological processes including autoimmune conditions such as type 1 diabetes (T1D). Alternate arginine metabolism through the citrulline-nitric oxide (NO) or the ornithine pathways can lead to proinflammatory...

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Hernandez LF, Buchwald P, Abdulreda MH. Effect of Arginase-1 Inhibition on the Incidence of Autoimmune Diabetes in NOD Mice. Curr Res Diabetes Obes J. 2018;5(3)
Hernandez, L. F., Buchwald, P., & Abdulreda, M. H. (2018). Effect of Arginase-1 Inhibition on the Incidence of Autoimmune Diabetes in NOD Mice. Current research in diabetes & obesity journal, 5(3), .
Hernandez, Luis F, et al. "Effect of Arginase-1 Inhibition on the Incidence of Autoimmune Diabetes in NOD Mice." Current research in diabetes & obesity journal vol. 5,3 (2018).
Hernandez LF, Buchwald P, Abdulreda MH. Effect of Arginase-1 Inhibition on the Incidence of Autoimmune Diabetes in NOD Mice. Curr Res Diabetes Obes J. 2018 Jan;5(3). Epub 2018 Aug 01. PMID: 29450408; PMCID: PMC5810145.
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Exosomes from NSC-34 Cells Transfected with hSOD1-G93A Are Enriched in miR-124 and Drive Alterations in Microglia Phenotype.

Frontiers in neuroscience

Pinto S, Cunha C, Barbosa M, Vaz AR, Brites D.
PMID: 28567000
Front Neurosci. 2017 May 17;11:273. doi: 10.3389/fnins.2017.00273. eCollection 2017.

Amyotrophic lateral sclerosis (ALS) is a fatal adult-onset neurodegenerative disorder affecting motor neurons (MNs). Evidences indicate that ALS is a non-cell autonomous disease in which glial cells participate in both disease onset and progression. Exosomal transfer of mutant copper-zinc...

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Pinto S, Cunha C, Barbosa M, et al. Exosomes from NSC-34 Cells Transfected with hSOD1-G93A Are Enriched in miR-124 and Drive Alterations in Microglia Phenotype. Front Neurosci. 2017;11:273doi: 10.3389/fnins.2017.00273.
Pinto, S., Cunha, C., Barbosa, M., Vaz, A. R., & Brites, D. (2017). Exosomes from NSC-34 Cells Transfected with hSOD1-G93A Are Enriched in miR-124 and Drive Alterations in Microglia Phenotype. Frontiers in neuroscience, 11273. https://doi.org/10.3389/fnins.2017.00273
Pinto, Sara, et al. "Exosomes from NSC-34 Cells Transfected with hSOD1-G93A Are Enriched in miR-124 and Drive Alterations in Microglia Phenotype." Frontiers in neuroscience vol. 11 (2017): 273. doi: https://doi.org/10.3389/fnins.2017.00273
Pinto S, Cunha C, Barbosa M, Vaz AR, Brites D. Exosomes from NSC-34 Cells Transfected with hSOD1-G93A Are Enriched in miR-124 and Drive Alterations in Microglia Phenotype. Front Neurosci. 2017 May 17;11:273. doi: 10.3389/fnins.2017.00273. eCollection 2017. PMID: 28567000; PMCID: PMC5434170.
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Effects in chicks of arsenic, arginine, and zinc and their interaction on body weight, plasma uric acid, plasma urea, and kidney arginase activity.

Biological trace element research

Uthus EO, Nielsen FH.
PMID: 24258871
Biol Trace Elem Res. 1985 Feb;7(1):11-20. doi: 10.1007/BF02916543.

The interaction among arsenic, zinc, and arginine was studied in chicks using two fully crossed, three-way, two-by-two-by-two experiments. Arsenic at levels of 0 and 2 μg/g zinc at levels of 2.5 (zinc-deficient) and 25 (zinc-adequate) μg/g, and arginine at...

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Uthus EO, Nielsen FH. Effects in chicks of arsenic, arginine, and zinc and their interaction on body weight, plasma uric acid, plasma urea, and kidney arginase activity. Biol Trace Elem Res. 1985;7(1):11-20doi: 10.1007/BF02916543.
Uthus, E. O., & Nielsen, F. H. (1985). Effects in chicks of arsenic, arginine, and zinc and their interaction on body weight, plasma uric acid, plasma urea, and kidney arginase activity. Biological trace element research, 7(1), 11-20. https://doi.org/10.1007/BF02916543
Uthus, E O, and Nielsen, F H. "Effects in chicks of arsenic, arginine, and zinc and their interaction on body weight, plasma uric acid, plasma urea, and kidney arginase activity." Biological trace element research vol. 7,1 (1985): 11-20. doi: https://doi.org/10.1007/BF02916543
Uthus EO, Nielsen FH. Effects in chicks of arsenic, arginine, and zinc and their interaction on body weight, plasma uric acid, plasma urea, and kidney arginase activity. Biol Trace Elem Res. 1985 Feb;7(1):11-20. doi: 10.1007/BF02916543. PMID: 24258871.
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Supplementation with Phycocyanobilin, Citrulline, Taurine, and Supranutritional Doses of Folic Acid and Biotin-Potential for Preventing or Slowing the Progression of Diabetic Complications.

Healthcare (Basel, Switzerland)

McCarty MF.
PMID: 28335416
Healthcare (Basel). 2017 Mar 14;5(1). doi: 10.3390/healthcare5010015.

Oxidative stress, the resulting uncoupling of endothelial nitric oxide synthase (eNOS), and loss of nitric oxide (NO) bioactivity, are key mediators of the vascular and microvascular complications of diabetes. Much of this oxidative stress arises from up-regulated nicotinamide adenine...

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McCarty MF. Supplementation with Phycocyanobilin, Citrulline, Taurine, and Supranutritional Doses of Folic Acid and Biotin-Potential for Preventing or Slowing the Progression of Diabetic Complications. Healthcare (Basel). 2017;5(1)doi: 10.3390/healthcare5010015.
McCarty, M. F. (2017). Supplementation with Phycocyanobilin, Citrulline, Taurine, and Supranutritional Doses of Folic Acid and Biotin-Potential for Preventing or Slowing the Progression of Diabetic Complications. Healthcare (Basel, Switzerland), 5(1), . https://doi.org/10.3390/healthcare5010015
McCarty, Mark F. "Supplementation with Phycocyanobilin, Citrulline, Taurine, and Supranutritional Doses of Folic Acid and Biotin-Potential for Preventing or Slowing the Progression of Diabetic Complications." Healthcare (Basel, Switzerland) vol. 5,1 (2017). doi: https://doi.org/10.3390/healthcare5010015
McCarty MF. Supplementation with Phycocyanobilin, Citrulline, Taurine, and Supranutritional Doses of Folic Acid and Biotin-Potential for Preventing or Slowing the Progression of Diabetic Complications. Healthcare (Basel). 2017 Mar 14;5(1). doi: 10.3390/healthcare5010015. PMID: 28335416; PMCID: PMC5371921.
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Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4.

Frontiers in microbiology

Freitas MS, Oliveira AF, da Silva TA, Fernandes FF, Gonçales RA, Almeida F, Roque-Barreira MC.
PMID: 27458431
Front Microbiol. 2016 Jul 05;7:1003. doi: 10.3389/fmicb.2016.01003. eCollection 2016.

The fungal human pathogen Paracoccidioides brasiliensis contains paracoccin (PCN), a multi-domain protein that has lectin and N-acetyl-glucosaminidase activities, which account for its effects on the growth and morphogenesis of the fungus and on the activation of host macrophages through...

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Freitas MS, Oliveira AF, da Silva TA, et al. Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4. Front Microbiol. 2016;7:1003doi: 10.3389/fmicb.2016.01003.
Freitas, M. S., Oliveira, A. F., da Silva, T. A., Fernandes, F. F., Gonçales, R. A., Almeida, F., & Roque-Barreira, M. C. (2016). Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4. Frontiers in microbiology, 71003. https://doi.org/10.3389/fmicb.2016.01003
Freitas, Mateus S, et al. "Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4." Frontiers in microbiology vol. 7 (2016): 1003. doi: https://doi.org/10.3389/fmicb.2016.01003
Freitas MS, Oliveira AF, da Silva TA, Fernandes FF, Gonçales RA, Almeida F, Roque-Barreira MC. Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4. Front Microbiol. 2016 Jul 05;7:1003. doi: 10.3389/fmicb.2016.01003. eCollection 2016. PMID: 27458431; PMCID: PMC4932198.
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Protective Role of Arginase II in Cerebral Ischemia and Excitotoxicity.

Journal of neurology and neuroscience

Ahmad AS, Shah ZA, Doré S.
PMID: 27308186
J Neurol Neurosci. 2016;7(2). doi: 10.21767/2171-6625.100088. Epub 2016 Apr 29.

BACKGROUND: Arginase (Arg), one of the enzymes involved in the urea cycle, provides an essential route for the disposal of excess nitrogen resulting from amino acid and nucleotide metabolism. Two reported subtypes of Arg (ArgI and II) compete with...

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Ahmad AS, Shah ZA, Doré S. Protective Role of Arginase II in Cerebral Ischemia and Excitotoxicity. J Neurol Neurosci. 2016;7(2)doi: 10.21767/2171-6625.100088.
Ahmad, A. S., Shah, Z. A., & Doré, S. (2016). Protective Role of Arginase II in Cerebral Ischemia and Excitotoxicity. Journal of neurology and neuroscience, 7(2), . https://doi.org/10.21767/2171-6625.100088
Ahmad, Abdullah Shafique, et al. "Protective Role of Arginase II in Cerebral Ischemia and Excitotoxicity." Journal of neurology and neuroscience vol. 7,2 (2016). doi: https://doi.org/10.21767/2171-6625.100088
Ahmad AS, Shah ZA, Doré S. Protective Role of Arginase II in Cerebral Ischemia and Excitotoxicity. J Neurol Neurosci. 2016;7(2). doi: 10.21767/2171-6625.100088. Epub 2016 Apr 29. PMID: 27308186; PMCID: PMC4905713.
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Dietary requirements of rainbow trout for tryptophan, lysine and arginine determined by growth and biochemical measurements.

Fish physiology and biochemistry

Walton MJ, Cowey CB, Coloso RM, Adron JW.
PMID: 24233178
Fish Physiol Biochem. 1986 Oct;2(1):161-9. doi: 10.1007/BF02264084.

Three separate studies were performed to determine the dietary requirements of rainbow troutSalmo gairdneri for tryptophan (Trp), lysine (Lys) and arginine (Arg) from both growth and biochemical data. The growth studies were carried out over a 12 week period....

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Walton MJ, Cowey CB, Coloso RM, et al. Dietary requirements of rainbow trout for tryptophan, lysine and arginine determined by growth and biochemical measurements. Fish Physiol Biochem. 1986;2(1):161-9doi: 10.1007/BF02264084.
Walton, M. J., Cowey, C. B., Coloso, R. M., & Adron, J. W. (1986). Dietary requirements of rainbow trout for tryptophan, lysine and arginine determined by growth and biochemical measurements. Fish physiology and biochemistry, 2(1), 161-9. https://doi.org/10.1007/BF02264084
Walton, M J, et al. "Dietary requirements of rainbow trout for tryptophan, lysine and arginine determined by growth and biochemical measurements." Fish physiology and biochemistry vol. 2,1 (1986): 161-9. doi: https://doi.org/10.1007/BF02264084
Walton MJ, Cowey CB, Coloso RM, Adron JW. Dietary requirements of rainbow trout for tryptophan, lysine and arginine determined by growth and biochemical measurements. Fish Physiol Biochem. 1986 Oct;2(1):161-9. doi: 10.1007/BF02264084. PMID: 24233178.
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L-arginine supplementation does not affect chemically induced carcinogenesis and tumor growth in BALB-c mice.

Hippokratia

Eleftheriadis T, Voyatzi S, Sparopoulou T, Kartsios C, Yiannaki E, Antoniadi G, Liakopoulos V, Galaktidou G.
PMID: 19582209
Hippokratia. 2007 Jul;11(3):142-4.

UNLABELLED: T-cell zeta-chain downregulation is common in various types of cancer and it is proposed as a mechanism of cancer immunosubversion. L-arginine consumption by arginase rich suppressor myeloid cells has been incriminated. The effect of L-arginine supplementation on chemically...

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Eleftheriadis T, Voyatzi S, Sparopoulou T, et al. L-arginine supplementation does not affect chemically induced carcinogenesis and tumor growth in BALB-c mice. Hippokratia. 2007;11(3):142-4
Eleftheriadis, T., Voyatzi, S., Sparopoulou, T., Kartsios, C., Yiannaki, E., Antoniadi, G., Liakopoulos, V., & Galaktidou, G. (2007). L-arginine supplementation does not affect chemically induced carcinogenesis and tumor growth in BALB-c mice. Hippokratia, 11(3), 142-4.
Eleftheriadis, T, et al. "L-arginine supplementation does not affect chemically induced carcinogenesis and tumor growth in BALB-c mice." Hippokratia vol. 11,3 (2007): 142-4.
Eleftheriadis T, Voyatzi S, Sparopoulou T, Kartsios C, Yiannaki E, Antoniadi G, Liakopoulos V, Galaktidou G. L-arginine supplementation does not affect chemically induced carcinogenesis and tumor growth in BALB-c mice. Hippokratia. 2007 Jul;11(3):142-4. PMID: 19582209; PMCID: PMC2658798.
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Showing 1 to 12 of 802 entries