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Showing 1 to 12 of 14 entries
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Comparative genomics of cryptosporidium.

International journal of genomics

Mazurie AJ, Alves JM, Ozaki LS, Zhou S, Schwartz DC, Buck GA.
PMID: 23738321
Int J Genomics. 2013;2013:832756. doi: 10.1155/2013/832756. Epub 2013 May 02.

Until recently, the apicomplexan parasites, Cryptosporidium hominis and C. parvum, were considered the same species. However, the two parasites, now considered distinct species, exhibit significant differences in host range, infectivity, and pathogenicity, and their sequenced genomes exhibit only 95-97%...

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Mazurie AJ, Alves JM, Ozaki LS, et al. Comparative genomics of cryptosporidium. Int J Genomics. 2013;2013:832756doi: 10.1155/2013/832756.
Mazurie, A. J., Alves, J. M., Ozaki, L. S., Zhou, S., Schwartz, D. C., & Buck, G. A. (2013). Comparative genomics of cryptosporidium. International journal of genomics, 2013832756. https://doi.org/10.1155/2013/832756
Mazurie, Aurélien J, et al. "Comparative genomics of cryptosporidium." International journal of genomics vol. 2013 (2013): 832756. doi: https://doi.org/10.1155/2013/832756
Mazurie AJ, Alves JM, Ozaki LS, Zhou S, Schwartz DC, Buck GA. Comparative genomics of cryptosporidium. Int J Genomics. 2013;2013:832756. doi: 10.1155/2013/832756. Epub 2013 May 02. PMID: 23738321; PMCID: PMC3659464.
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Characterization and functional properties of gastric tissue-resident memory T cells from children, adults, and the elderly.

Frontiers in immunology

Booth JS, Toapanta FR, Salerno-Goncalves R, Patil S, Kader HA, Safta AM, Czinn SJ, Greenwald BD, Sztein MB.
PMID: 24995010
Front Immunol. 2014 Jun 19;5:294. doi: 10.3389/fimmu.2014.00294. eCollection 2014.

T cells are the main orchestrators of protective immunity in the stomach; however, limited information on the presence and function of the gastric T subsets is available mainly due to the difficulty in recovering high numbers of viable cells...

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Booth JS, Toapanta FR, Salerno-Goncalves R, et al. Characterization and functional properties of gastric tissue-resident memory T cells from children, adults, and the elderly. Front Immunol. 2014;5:294doi: 10.3389/fimmu.2014.00294.
Booth, J. S., Toapanta, F. R., Salerno-Goncalves, R., Patil, S., Kader, H. A., Safta, A. M., Czinn, S. J., Greenwald, B. D., & Sztein, M. B. (2014). Characterization and functional properties of gastric tissue-resident memory T cells from children, adults, and the elderly. Frontiers in immunology, 5294. https://doi.org/10.3389/fimmu.2014.00294
Booth, Jayaum S, et al. "Characterization and functional properties of gastric tissue-resident memory T cells from children, adults, and the elderly." Frontiers in immunology vol. 5 (2014): 294. doi: https://doi.org/10.3389/fimmu.2014.00294
Booth JS, Toapanta FR, Salerno-Goncalves R, Patil S, Kader HA, Safta AM, Czinn SJ, Greenwald BD, Sztein MB. Characterization and functional properties of gastric tissue-resident memory T cells from children, adults, and the elderly. Front Immunol. 2014 Jun 19;5:294. doi: 10.3389/fimmu.2014.00294. eCollection 2014. PMID: 24995010; PMCID: PMC4062881.
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Metal-Enhanced Fluorescence from Nanoparticulate Zinc Films.

The journal of physical chemistry. C, Nanomaterials and interfaces

Aslan K, Previte MJ, Zhang Y, Geddes CD.
PMID: 19946356
J Phys Chem C Nanomater Interfaces. 2008 Nov 27;112(47):18368-18375. doi: 10.1021/jp806790u.

A detailed study of metal-enhanced fluorescence (MEF) from fluorophores in the blue-to- red spectral region placed in close proximity to thermally evaporated zinc nanostructured films is reported. The zinc nanostructured films were deposited onto glass microscope slides as individual...

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Aslan K, Previte MJ, Zhang Y, et al. Metal-Enhanced Fluorescence from Nanoparticulate Zinc Films. J Phys Chem C Nanomater Interfaces. 2008;112(47):18368-18375doi: 10.1021/jp806790u.
Aslan, K., Previte, M. J., Zhang, Y., & Geddes, C. D. (2008). Metal-Enhanced Fluorescence from Nanoparticulate Zinc Films. The journal of physical chemistry. C, Nanomaterials and interfaces, 112(47), 18368-18375. https://doi.org/10.1021/jp806790u
Aslan, Kadir, et al. "Metal-Enhanced Fluorescence from Nanoparticulate Zinc Films." The journal of physical chemistry. C, Nanomaterials and interfaces vol. 112,47 (2008): 18368-18375. doi: https://doi.org/10.1021/jp806790u
Aslan K, Previte MJ, Zhang Y, Geddes CD. Metal-Enhanced Fluorescence from Nanoparticulate Zinc Films. J Phys Chem C Nanomater Interfaces. 2008 Nov 27;112(47):18368-18375. doi: 10.1021/jp806790u. PMID: 19946356; PMCID: PMC2676115.
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Bioinformatic and mass spectrometry identification of Anaplasma phagocytophilum proteins translocated into host cell nuclei.

Frontiers in microbiology

Sinclair SH, Garcia-Garcia JC, Dumler JS.
PMID: 25705208
Front Microbiol. 2015 Feb 06;6:55. doi: 10.3389/fmicb.2015.00055. eCollection 2015.

Obligate intracellular bacteria have an arsenal of proteins that alter host cells to establish and maintain a hospitable environment for replication. Anaplasma phagocytophilum secrets Ankyrin A (AnkA), via a type IV secretion system, which translocates to the nucleus of...

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Sinclair SH, Garcia-Garcia JC, Dumler JS. Bioinformatic and mass spectrometry identification of Anaplasma phagocytophilum proteins translocated into host cell nuclei. Front Microbiol. 2015;6:55doi: 10.3389/fmicb.2015.00055.
Sinclair, S. H., Garcia-Garcia, J. C., & Dumler, J. S. (2015). Bioinformatic and mass spectrometry identification of Anaplasma phagocytophilum proteins translocated into host cell nuclei. Frontiers in microbiology, 655. https://doi.org/10.3389/fmicb.2015.00055
Sinclair, Sara H G, et al. "Bioinformatic and mass spectrometry identification of Anaplasma phagocytophilum proteins translocated into host cell nuclei." Frontiers in microbiology vol. 6 (2015): 55. doi: https://doi.org/10.3389/fmicb.2015.00055
Sinclair SH, Garcia-Garcia JC, Dumler JS. Bioinformatic and mass spectrometry identification of Anaplasma phagocytophilum proteins translocated into host cell nuclei. Front Microbiol. 2015 Feb 06;6:55. doi: 10.3389/fmicb.2015.00055. eCollection 2015. PMID: 25705208; PMCID: PMC4319465.
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Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection.

Frontiers in immunology

Booth JS, Salerno-Goncalves R, Blanchard TG, Patil SA, Kader HA, Safta AM, Morningstar LM, Czinn SJ, Greenwald BD, Sztein MB.
PMID: 26441971
Front Immunol. 2015 Sep 17;6:466. doi: 10.3389/fimmu.2015.00466. eCollection 2015.

Mucosal-associated invariant T (MAIT) cells represent a class of antimicrobial innate-like T cells that have been characterized in human blood, liver, lungs, and intestine. Here, we investigated, for the first time, the presence of MAIT cells in the stomach...

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Booth JS, Salerno-Goncalves R, Blanchard TG, et al. Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection. Front Immunol. 2015;6:466doi: 10.3389/fimmu.2015.00466.
Booth, J. S., Salerno-Goncalves, R., Blanchard, T. G., Patil, S. A., Kader, H. A., Safta, A. M., Morningstar, L. M., Czinn, S. J., Greenwald, B. D., & Sztein, M. B. (2015). Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection. Frontiers in immunology, 6466. https://doi.org/10.3389/fimmu.2015.00466
Booth, Jayaum S, et al. "Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection." Frontiers in immunology vol. 6 (2015): 466. doi: https://doi.org/10.3389/fimmu.2015.00466
Booth JS, Salerno-Goncalves R, Blanchard TG, Patil SA, Kader HA, Safta AM, Morningstar LM, Czinn SJ, Greenwald BD, Sztein MB. Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection. Front Immunol. 2015 Sep 17;6:466. doi: 10.3389/fimmu.2015.00466. eCollection 2015. PMID: 26441971; PMCID: PMC4585133.
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Conversion of just-continuous metallic films to large particulate substrates for metal-enhanced fluorescence.

Journal of applied physics

Aslan K, Malyn SN, Zhang Y, Geddes CD.
PMID: 19479004
J Appl Phys. 2008 Apr 15;103(8):84307-843077. doi: 10.1063/1.2905319. Epub 2008 Apr 25.

We report the effects of thermally annealing, non-, just-, and thick continuous silver films for their potential applications in metal-enhanced fluorescence, a near-field concept which can alter the free-space absorption and emissive properties of close-proximity fluorophores (excited states). We...

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Aslan K, Malyn SN, Zhang Y, et al. Conversion of just-continuous metallic films to large particulate substrates for metal-enhanced fluorescence. J Appl Phys. 2008;103(8):84307-843077doi: 10.1063/1.2905319.
Aslan, K., Malyn, S. N., Zhang, Y., & Geddes, C. D. (2008). Conversion of just-continuous metallic films to large particulate substrates for metal-enhanced fluorescence. Journal of applied physics, 103(8), 84307-843077. https://doi.org/10.1063/1.2905319
Aslan, Kadir, et al. "Conversion of just-continuous metallic films to large particulate substrates for metal-enhanced fluorescence." Journal of applied physics vol. 103,8 (2008): 84307-843077. doi: https://doi.org/10.1063/1.2905319
Aslan K, Malyn SN, Zhang Y, Geddes CD. Conversion of just-continuous metallic films to large particulate substrates for metal-enhanced fluorescence. J Appl Phys. 2008 Apr 15;103(8):84307-843077. doi: 10.1063/1.2905319. Epub 2008 Apr 25. PMID: 19479004; PMCID: PMC2685214.
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Genomic profiling of host responses to Lassa virus: therapeutic potential from primate to man.

Future virology

Zapata JC, Salvato MS.
PMID: 25844088
Future Virol. 2015 Mar 13;10(3):233-256. doi: 10.2217/fvl.15.1.

Lassa virus infection elicits distinctive changes in host gene expression and metabolism. We focus on changes in host gene expression that may be biomarkers that discriminate individual pathogens or may help to provide a prognosis for disease. In addition...

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Zapata JC, Salvato MS. Genomic profiling of host responses to Lassa virus: therapeutic potential from primate to man. Future Virol. 2015;10(3):233-256doi: 10.2217/fvl.15.1.
Zapata, J. C., & Salvato, M. S. (2015). Genomic profiling of host responses to Lassa virus: therapeutic potential from primate to man. Future virology, 10(3), 233-256. https://doi.org/10.2217/fvl.15.1
Zapata, Juan C, and Salvato, Maria S. "Genomic profiling of host responses to Lassa virus: therapeutic potential from primate to man." Future virology vol. 10,3 (2015): 233-256. doi: https://doi.org/10.2217/fvl.15.1
Zapata JC, Salvato MS. Genomic profiling of host responses to Lassa virus: therapeutic potential from primate to man. Future Virol. 2015 Mar 13;10(3):233-256. doi: 10.2217/fvl.15.1. PMID: 25844088; PMCID: PMC4383259.
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Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, .

Journal of clinical & experimental cardiology

Qureshi AA, Khan DA, Mahjabeen W, Papasian CJ, Qureshi N.
PMID: 24319627
J Clin Exp Cardiolog. 2013 Mar 02;4(3). doi: 10.4172/2155-9880.1000238.

BACKGROUND: Age-associated altered redox imbalances and dysregulated immune function, contribute to the development of a variety of age associated diseases. Inflammatory markers and lipid profiles are useful prognostic indicators of a variety of age-associated and cardiovascular diseases. We have...

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Qureshi AA, Khan DA, Mahjabeen W, et al. Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, . J Clin Exp Cardiolog. 2013;4(3)doi: 10.4172/2155-9880.1000238.
Qureshi, A. A., Khan, D. A., Mahjabeen, W., Papasian, C. J., & Qureshi, N. (2013). Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, . Journal of clinical & experimental cardiology, 4(3), . https://doi.org/10.4172/2155-9880.1000238
Qureshi, Asaf A, et al. "Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, ." Journal of clinical & experimental cardiology vol. 4,3 (2013). doi: https://doi.org/10.4172/2155-9880.1000238
Qureshi AA, Khan DA, Mahjabeen W, Papasian CJ, Qureshi N. Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, . J Clin Exp Cardiolog. 2013 Mar 02;4(3). doi: 10.4172/2155-9880.1000238. PMID: 24319627; PMCID: PMC3851026.
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Directional, Broad, and Fixed Angle Surface Plasmon Coupled Fluorescence from Iron Thin Films.

The journal of physical chemistry. C, Nanomaterials and interfaces

Aslan K, Zhang Y, Geddes CD.
PMID: 20657700
J Phys Chem C Nanomater Interfaces. 2009 Nov 09;113(48):20535-20538. doi: 10.1021/jp907510m.

Fixed angle surface plasmon coupled fluorescence (SPCF) from iron thin films is demonstrated for the first time. The optimum thickness of the iron thin films was determined to be 15 nm using Fresnel calculations. The angles of minimum reflectivity...

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Aslan K, Zhang Y, Geddes CD. Directional, Broad, and Fixed Angle Surface Plasmon Coupled Fluorescence from Iron Thin Films. J Phys Chem C Nanomater Interfaces. 2009;113(48):20535-20538doi: 10.1021/jp907510m.
Aslan, K., Zhang, Y., & Geddes, C. D. (2009). Directional, Broad, and Fixed Angle Surface Plasmon Coupled Fluorescence from Iron Thin Films. The journal of physical chemistry. C, Nanomaterials and interfaces, 113(48), 20535-20538. https://doi.org/10.1021/jp907510m
Aslan, Kadir, et al. "Directional, Broad, and Fixed Angle Surface Plasmon Coupled Fluorescence from Iron Thin Films." The journal of physical chemistry. C, Nanomaterials and interfaces vol. 113,48 (2009): 20535-20538. doi: https://doi.org/10.1021/jp907510m
Aslan K, Zhang Y, Geddes CD. Directional, Broad, and Fixed Angle Surface Plasmon Coupled Fluorescence from Iron Thin Films. J Phys Chem C Nanomater Interfaces. 2009 Nov 09;113(48):20535-20538. doi: 10.1021/jp907510m. PMID: 20657700; PMCID: PMC2908412.
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Clostridium difficile contains plasmalogen species of phospholipids and glycolipids.

Biochimica et biophysica acta

Guan Z, Katzianer D, Zhu J, Goldfine H.
PMID: 24983203
Biochim Biophys Acta. 2014 Oct;1842(10):1353-9. doi: 10.1016/j.bbalip.2014.06.011. Epub 2014 Jun 28.

Analysis of the polar lipids of many pathogenic and non-pathogenic clostridia has revealed the presence of plasmalogens, alk-1'-enyl ether-containing phospholipids and glycolipids. An exception to this finding so far has been Clostridium difficile, an important human pathogen which is...

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Guan Z, Katzianer D, Zhu J, et al. Clostridium difficile contains plasmalogen species of phospholipids and glycolipids. Biochim Biophys Acta. 2014;1842(10):1353-9doi: 10.1016/j.bbalip.2014.06.011.
Guan, Z., Katzianer, D., Zhu, J., & Goldfine, H. (2014). Clostridium difficile contains plasmalogen species of phospholipids and glycolipids. Biochimica et biophysica acta, 1842(10), 1353-9. https://doi.org/10.1016/j.bbalip.2014.06.011
Guan, Ziqiang, et al. "Clostridium difficile contains plasmalogen species of phospholipids and glycolipids." Biochimica et biophysica acta vol. 1842,10 (2014): 1353-9. doi: https://doi.org/10.1016/j.bbalip.2014.06.011
Guan Z, Katzianer D, Zhu J, Goldfine H. Clostridium difficile contains plasmalogen species of phospholipids and glycolipids. Biochim Biophys Acta. 2014 Oct;1842(10):1353-9. doi: 10.1016/j.bbalip.2014.06.011. Epub 2014 Jun 28. PMID: 24983203; PMCID: PMC4169322.
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Bacterial superantigen toxins induce a lethal cytokine storm by enhancing B7-2/CD28 costimulatory receptor engagement, a critical immune checkpoint.

Receptors & clinical investigation

Kaempfer R, Popugailo A, Levy R, Arad G, Hillman D, Rotfogel Z.
PMID: 28286804
Receptors Clin Investig. 2017;4(1). Epub 2017 Jan 30.

Formation of the costimulatory axis between the B7-2 and CD28 coreceptors is critical for T-cell activation. Superantigens, Gram-positive bacterial virulence factors, cause toxic shock and sepsis by hyperinducing inflammatory cytokines. We report a novel role for costimulatory receptors CD28...

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Kaempfer R, Popugailo A, Levy R, et al. Bacterial superantigen toxins induce a lethal cytokine storm by enhancing B7-2/CD28 costimulatory receptor engagement, a critical immune checkpoint. Receptors Clin Investig. 2017;4(1)
Kaempfer, R., Popugailo, A., Levy, R., Arad, G., Hillman, D., & Rotfogel, Z. (2017). Bacterial superantigen toxins induce a lethal cytokine storm by enhancing B7-2/CD28 costimulatory receptor engagement, a critical immune checkpoint. Receptors & clinical investigation, 4(1), .
Kaempfer, Raymond, et al. "Bacterial superantigen toxins induce a lethal cytokine storm by enhancing B7-2/CD28 costimulatory receptor engagement, a critical immune checkpoint." Receptors & clinical investigation vol. 4,1 (2017).
Kaempfer R, Popugailo A, Levy R, Arad G, Hillman D, Rotfogel Z. Bacterial superantigen toxins induce a lethal cytokine storm by enhancing B7-2/CD28 costimulatory receptor engagement, a critical immune checkpoint. Receptors Clin Investig. 2017;4(1). Epub 2017 Jan 30. PMID: 28286804; PMCID: PMC5341606.
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Therapeutic Vaccines and Antibodies for Treatment of Orthopoxvirus Infections.

Viruses

Xiao Y, Isaacs SN.
PMID: 21197387
Viruses. 2010 Oct;2(10):2381-2403. doi: 10.3390/v2102381.

Despite the eradication of smallpox several decades ago, variola and monkeypox viruses still have the potential to become significant threats to public health. The current licensed live vaccinia virus-based smallpox vaccine is extremely effective as a prophylactic vaccine to...

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Xiao Y, Isaacs SN. Therapeutic Vaccines and Antibodies for Treatment of Orthopoxvirus Infections. Viruses. 2010;2(10):2381-2403doi: 10.3390/v2102381.
Xiao, Y., & Isaacs, S. N. (2010). Therapeutic Vaccines and Antibodies for Treatment of Orthopoxvirus Infections. Viruses, 2(10), 2381-2403. https://doi.org/10.3390/v2102381
Xiao, Yuhong, and Isaacs, Stuart N. "Therapeutic Vaccines and Antibodies for Treatment of Orthopoxvirus Infections." Viruses vol. 2,10 (2010): 2381-2403. doi: https://doi.org/10.3390/v2102381
Xiao Y, Isaacs SN. Therapeutic Vaccines and Antibodies for Treatment of Orthopoxvirus Infections. Viruses. 2010 Oct;2(10):2381-2403. doi: 10.3390/v2102381. PMID: 21197387; PMCID: PMC3011862.
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Showing 1 to 12 of 14 entries