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Showing 25 to 36 of 232 entries
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Subcutaneous Immunization with Recombinant .

Reports of biochemistry & molecular biology

Torkashvand A, Bahrami F, Adib M, Ajdary S.
PMID: 30805400
Rep Biochem Mol Biol. 2019 Jan;7(2):196-203.

BACKGROUND: Lactic acid bacteria such as METHODS: The fusion gene composed of sequences encoding the F1S1 and the signal peptide of usp45 fragments (SECF1S1) was codon optimized for protein production in RESULTS: The LL-F1S1-immunized mice produced significant levels of...

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Torkashvand A, Bahrami F, Adib M, et al. Subcutaneous Immunization with Recombinant . Rep Biochem Mol Biol. 2019;7(2):196-203
Torkashvand, A., Bahrami, F., Adib, M., & Ajdary, S. (2019). Subcutaneous Immunization with Recombinant . Reports of biochemistry & molecular biology, 7(2), 196-203.
Torkashvand, Ali, et al. "Subcutaneous Immunization with Recombinant ." Reports of biochemistry & molecular biology vol. 7,2 (2019): 196-203.
Torkashvand A, Bahrami F, Adib M, Ajdary S. Subcutaneous Immunization with Recombinant . Rep Biochem Mol Biol. 2019 Jan;7(2):196-203. PMID: 30805400; PMCID: PMC6374061.
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Differential Susceptibility of Guanine Nucleotide-binding Proteins to Pertussis Toxin-catalyzed ADP-ribosylation in Brain Membranes of Two Congeneric Marine Fishes.

The Biological bulletin

Murray TF, Siebenaller JF.
PMID: 29300622
Biol Bull. 1993 Dec;185(3):346-354. doi: 10.2307/1542475.

Pertussis toxin-catalyzed [32P]ADP-ribosylation was used to probe the guanine nucleotide binding regulatory proteins Gi and Go in brain membranes from two scorpaenid fishes, Sebastolobus alascanus and S. altivelis. The membranes of the two species exhibit a differential sensitivity to...

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Murray TF, Siebenaller JF. Differential Susceptibility of Guanine Nucleotide-binding Proteins to Pertussis Toxin-catalyzed ADP-ribosylation in Brain Membranes of Two Congeneric Marine Fishes. Biol Bull. 1993;185(3):346-354doi: 10.2307/1542475.
Murray, T. F., & Siebenaller, J. F. (1993). Differential Susceptibility of Guanine Nucleotide-binding Proteins to Pertussis Toxin-catalyzed ADP-ribosylation in Brain Membranes of Two Congeneric Marine Fishes. The Biological bulletin, 185(3), 346-354. https://doi.org/10.2307/1542475
Murray, T F, and Siebenaller, J F. "Differential Susceptibility of Guanine Nucleotide-binding Proteins to Pertussis Toxin-catalyzed ADP-ribosylation in Brain Membranes of Two Congeneric Marine Fishes." The Biological bulletin vol. 185,3 (1993): 346-354. doi: https://doi.org/10.2307/1542475
Murray TF, Siebenaller JF. Differential Susceptibility of Guanine Nucleotide-binding Proteins to Pertussis Toxin-catalyzed ADP-ribosylation in Brain Membranes of Two Congeneric Marine Fishes. Biol Bull. 1993 Dec;185(3):346-354. doi: 10.2307/1542475. PMID: 29300622.
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Pertussis Toxin Ameliorates Microglial Activation Associated With Ischemic Stroke.

Frontiers in cellular neuroscience

Zhou F, Liu R, Han P, Zhang X, Li Z, Zhang S, Liu C, Xia Y, Tang Z.
PMID: 32676009
Front Cell Neurosci. 2020 Jun 26;14:152. doi: 10.3389/fncel.2020.00152. eCollection 2020.

No abstract available.

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Zhou F, Liu R, Han P, et al. Pertussis Toxin Ameliorates Microglial Activation Associated With Ischemic Stroke. Front Cell Neurosci. 2020;14:152doi: 10.3389/fncel.2020.00152.
Zhou, F., Liu, R., Han, P., Zhang, X., Li, Z., Zhang, S., Liu, C., Xia, Y., & Tang, Z. (2020). Pertussis Toxin Ameliorates Microglial Activation Associated With Ischemic Stroke. Frontiers in cellular neuroscience, 14152. https://doi.org/10.3389/fncel.2020.00152
Zhou, Feihui, et al. "Pertussis Toxin Ameliorates Microglial Activation Associated With Ischemic Stroke." Frontiers in cellular neuroscience vol. 14 (2020): 152. doi: https://doi.org/10.3389/fncel.2020.00152
Zhou F, Liu R, Han P, Zhang X, Li Z, Zhang S, Liu C, Xia Y, Tang Z. Pertussis Toxin Ameliorates Microglial Activation Associated With Ischemic Stroke. Front Cell Neurosci. 2020 Jun 26;14:152. doi: 10.3389/fncel.2020.00152. eCollection 2020. PMID: 32676009; PMCID: PMC7333375.
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Protective effects of pharmacological therapies in animal models of multiple sclerosis: a review of studies 2014-2019.

Neural regeneration research

Martinez B, Peplow PV.
PMID: 31960801
Neural Regen Res. 2020 Jul;15(7):1220-1234. doi: 10.4103/1673-5374.272572.

Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system. The disability caused by inflammatory demyelination clinically dominates the early stages of relapsing-remitting MS and is reversible. Once there is considerable loss of axons, MS patients...

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Martinez B, Peplow PV. Protective effects of pharmacological therapies in animal models of multiple sclerosis: a review of studies 2014-2019. Neural Regen Res. 2020;15(7):1220-1234doi: 10.4103/1673-5374.272572.
Martinez, B., & Peplow, P. V. (2020). Protective effects of pharmacological therapies in animal models of multiple sclerosis: a review of studies 2014-2019. Neural regeneration research, 15(7), 1220-1234. https://doi.org/10.4103/1673-5374.272572
Martinez, Bridget, and Peplow, Philip V. "Protective effects of pharmacological therapies in animal models of multiple sclerosis: a review of studies 2014-2019." Neural regeneration research vol. 15,7 (2020): 1220-1234. doi: https://doi.org/10.4103/1673-5374.272572
Martinez B, Peplow PV. Protective effects of pharmacological therapies in animal models of multiple sclerosis: a review of studies 2014-2019. Neural Regen Res. 2020 Jul;15(7):1220-1234. doi: 10.4103/1673-5374.272572. PMID: 31960801; PMCID: PMC7047782.
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Dual Transmembrane Signalling Mechanisms in Eosinophils: Evidence for Two Functionally Distinct Receptors for Platelet-Activating Factor.

International archives of allergy and immunology

Kroegel C, Warner JA, Giembycz MA, Matthys H, Lichtenstein LM, Barnes PJ.
PMID: 34167200
Int Arch Allergy Immunol. 1992;99(2):226-229. doi: 10.1159/000236253. Epub 2009 Sep 02.

The effect of PAF on eosinophil activation was investigated. TxB2 release required a lower concentration of PAF (ED50 = 17.2 nM) whereas for superoxide anion (O2) production doses in excess of 1 μM (ED50 = 31.7 μM) were needed....

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Kroegel C, Warner JA, Giembycz MA, et al. Dual Transmembrane Signalling Mechanisms in Eosinophils: Evidence for Two Functionally Distinct Receptors for Platelet-Activating Factor. Int Arch Allergy Immunol. 2009;99(2):226-229doi: 10.1159/000236253.
Kroegel, C., Warner, J. A., Giembycz, M. A., Matthys, H., Lichtenstein, L. M., & Barnes, P. J. (1992). Dual Transmembrane Signalling Mechanisms in Eosinophils: Evidence for Two Functionally Distinct Receptors for Platelet-Activating Factor. International archives of allergy and immunology, 99(2), 226-229. https://doi.org/10.1159/000236253
Kroegel, Claus, et al. "Dual Transmembrane Signalling Mechanisms in Eosinophils: Evidence for Two Functionally Distinct Receptors for Platelet-Activating Factor." International archives of allergy and immunology vol. 99,2 (1992): 226-229. doi: https://doi.org/10.1159/000236253
Kroegel C, Warner JA, Giembycz MA, Matthys H, Lichtenstein LM, Barnes PJ. Dual Transmembrane Signalling Mechanisms in Eosinophils: Evidence for Two Functionally Distinct Receptors for Platelet-Activating Factor. Int Arch Allergy Immunol. 1992;99(2):226-229. doi: 10.1159/000236253. Epub 2009 Sep 02. PMID: 34167200.
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IL-3 Primes and Evokes Histamine Release from Human Basophils but not Mast Cells.

International archives of allergy and immunology

Okayama Y, Church MK.
PMID: 34167220
Int Arch Allergy Immunol. 1992;99(2):343-345. doi: 10.1159/000236280. Epub 2009 Sep 02.

To assess the effect of IL-3 on mediator release from human histamine-containing cells, we have investigated IL-3 induced histamine release (HR) and IL-3 priming of IgE-dependent and IgE-independent HR from human basophils and mast cells dispersed from human skin,...

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Okayama Y, Church MK. IL-3 Primes and Evokes Histamine Release from Human Basophils but not Mast Cells. Int Arch Allergy Immunol. 2009;99(2):343-345doi: 10.1159/000236280.
Okayama, Y., & Church, M. K. (1992). IL-3 Primes and Evokes Histamine Release from Human Basophils but not Mast Cells. International archives of allergy and immunology, 99(2), 343-345. https://doi.org/10.1159/000236280
Okayama, Yoshimichi, and Church, Martin K. "IL-3 Primes and Evokes Histamine Release from Human Basophils but not Mast Cells." International archives of allergy and immunology vol. 99,2 (1992): 343-345. doi: https://doi.org/10.1159/000236280
Okayama Y, Church MK. IL-3 Primes and Evokes Histamine Release from Human Basophils but not Mast Cells. Int Arch Allergy Immunol. 1992;99(2):343-345. doi: 10.1159/000236280. Epub 2009 Sep 02. PMID: 34167220.
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Human Peptides α-Defensin-1 and -5 Inhibit Pertussis Toxin.

Toxins

Kling C, Pulliainen AT, Barth H, Ernst K.
PMID: 34357952
Toxins (Basel). 2021 Jul 11;13(7). doi: 10.3390/toxins13070480.

No abstract available.

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Kling C, Pulliainen AT, Barth H, et al. Human Peptides α-Defensin-1 and -5 Inhibit Pertussis Toxin. Toxins (Basel). 2021;13(7)doi: 10.3390/toxins13070480.
Kling, C., Pulliainen, A. T., Barth, H., & Ernst, K. (2021). Human Peptides α-Defensin-1 and -5 Inhibit Pertussis Toxin. Toxins, 13(7), . https://doi.org/10.3390/toxins13070480
Kling, Carolin, et al. "Human Peptides α-Defensin-1 and -5 Inhibit Pertussis Toxin." Toxins vol. 13,7 (2021). doi: https://doi.org/10.3390/toxins13070480
Kling C, Pulliainen AT, Barth H, Ernst K. Human Peptides α-Defensin-1 and -5 Inhibit Pertussis Toxin. Toxins (Basel). 2021 Jul 11;13(7). doi: 10.3390/toxins13070480. PMID: 34357952; PMCID: PMC8310310.
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Evaluation of Outer Membrane Vesicles Obtained from Predominant Local Isolate of Boredetella pertussis as a Vaccine Candidate.

Iranian biomedical journal

Soltani MS, Noofeli M, Banihashemi SR, Shahcheraghi F, Eftekhar F.
PMID: 34719226
Iran Biomed J. 2021 Nov 01;25(6):399-407. doi: 10.52547/ibj.25.6.399.

BACKGROUND: Pertussis is a current contagious bacterial disease caused by Bordetella pertussis (Bp). Given the prevalence of pertussis, development of new vaccines is important. This study was attempted to evaluate the expression of main virulence factors (pertussis toxin [PTX],...

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Soltani MS, Noofeli M, Banihashemi SR, et al. Evaluation of Outer Membrane Vesicles Obtained from Predominant Local Isolate of Boredetella pertussis as a Vaccine Candidate. Iran Biomed J. 2021;25(6):399-407doi: 10.52547/ibj.25.6.399.
Soltani, M. S., Noofeli, M., Banihashemi, S. R., Shahcheraghi, F., & Eftekhar, F. (2021). Evaluation of Outer Membrane Vesicles Obtained from Predominant Local Isolate of Boredetella pertussis as a Vaccine Candidate. Iranian biomedical journal, 25(6), 399-407. https://doi.org/10.52547/ibj.25.6.399
Soltani, Maryam Sadat, et al. "Evaluation of Outer Membrane Vesicles Obtained from Predominant Local Isolate of Boredetella pertussis as a Vaccine Candidate." Iranian biomedical journal vol. 25,6 (2021): 399-407. doi: https://doi.org/10.52547/ibj.25.6.399
Soltani MS, Noofeli M, Banihashemi SR, Shahcheraghi F, Eftekhar F. Evaluation of Outer Membrane Vesicles Obtained from Predominant Local Isolate of Boredetella pertussis as a Vaccine Candidate. Iran Biomed J. 2021 Nov 01;25(6):399-407. doi: 10.52547/ibj.25.6.399. PMID: 34719226.
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Pharmacological targeting of host chaperones protects from pertussis toxin in vitro and in vivo.

Scientific reports

Ernst K, Mittler AK, Winkelmann V, Kling C, Eberhardt N, Anastasia A, Sonnabend M, Lochbaum R, Wirsching J, Sakari M, Pulliainen AT, Skerry C, Carbonetti NH, Frick M, Barth H.
PMID: 33686161
Sci Rep. 2021 Mar 08;11(1):5429. doi: 10.1038/s41598-021-84817-2.

Whooping cough is caused by Bordetella pertussis that releases pertussis toxin (PT) which comprises enzyme A-subunit PTS1 and binding/transport B-subunit. After receptor-mediated endocytosis, PT reaches the endoplasmic reticulum from where unfolded PTS1 is transported to the cytosol. PTS1 ADP-ribosylates...

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Ernst K, Mittler AK, Winkelmann V, et al. Pharmacological targeting of host chaperones protects from pertussis toxin in vitro and in vivo. Sci Rep. 2021;11(1):5429doi: 10.1038/s41598-021-84817-2.
Ernst, K., Mittler, A. K., Winkelmann, V., Kling, C., Eberhardt, N., Anastasia, A., Sonnabend, M., Lochbaum, R., Wirsching, J., Sakari, M., Pulliainen, A. T., Skerry, C., Carbonetti, N. H., Frick, M., & Barth, H. (2021). Pharmacological targeting of host chaperones protects from pertussis toxin in vitro and in vivo. Scientific reports, 11(1), 5429. https://doi.org/10.1038/s41598-021-84817-2
Ernst, Katharina, et al. "Pharmacological targeting of host chaperones protects from pertussis toxin in vitro and in vivo." Scientific reports vol. 11,1 (2021): 5429. doi: https://doi.org/10.1038/s41598-021-84817-2
Ernst K, Mittler AK, Winkelmann V, Kling C, Eberhardt N, Anastasia A, Sonnabend M, Lochbaum R, Wirsching J, Sakari M, Pulliainen AT, Skerry C, Carbonetti NH, Frick M, Barth H. Pharmacological targeting of host chaperones protects from pertussis toxin in vitro and in vivo. Sci Rep. 2021 Mar 08;11(1):5429. doi: 10.1038/s41598-021-84817-2. PMID: 33686161; PMCID: PMC7940712.
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Pertussis Toxin Promotes Pulmonary Hypertension in an Infant Mouse Model of Bordetella pertussis Infection.

The Journal of infectious diseases

Scanlon KM, Chen L, Carbonetti NH.
PMID: 34145457
J Infect Dis. 2022 Jan 05;225(1):172-176. doi: 10.1093/infdis/jiab325.

Pertussis, caused by Bordetella pertussis, is a reemerging disease that can produce severe disease manifestations in infants, including pulmonary hypertension (PH). B. pertussis-induced PH is a major risk factor for infection-induced death, but the molecular mechanisms promoting PH are...

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Scanlon KM, Chen L, Carbonetti NH. Pertussis Toxin Promotes Pulmonary Hypertension in an Infant Mouse Model of Bordetella pertussis Infection. J Infect Dis. 2022;225(1):172-176doi: 10.1093/infdis/jiab325.
Scanlon, K. M., Chen, L., & Carbonetti, N. H. (2022). Pertussis Toxin Promotes Pulmonary Hypertension in an Infant Mouse Model of Bordetella pertussis Infection. The Journal of infectious diseases, 225(1), 172-176. https://doi.org/10.1093/infdis/jiab325
Scanlon, Karen M, et al. "Pertussis Toxin Promotes Pulmonary Hypertension in an Infant Mouse Model of Bordetella pertussis Infection." The Journal of infectious diseases vol. 225,1 (2022): 172-176. doi: https://doi.org/10.1093/infdis/jiab325
Scanlon KM, Chen L, Carbonetti NH. Pertussis Toxin Promotes Pulmonary Hypertension in an Infant Mouse Model of Bordetella pertussis Infection. J Infect Dis. 2022 Jan 05;225(1):172-176. doi: 10.1093/infdis/jiab325. PMID: 34145457.
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Impact of maternal pertussis antibodies on the infants' cellular immune responses.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

Orije MRP, García-Fogeda I, Van Dyck W, Corbière V, Mascart F, Mahieu L, Hens N, Van Damme P, Cools N, Ogunjimi B, Maertens K, Leuridan E.
PMID: 34849638
Clin Infect Dis. 2021 Nov 24; doi: 10.1093/cid/ciab972. Epub 2021 Nov 24.

INTRODUCTION: Maternal antibody interference of the infant's humoral immune responses raises some concern to the strategy of maternal Tdap (tetanus, diphtheria, acellular pertussis [aP]) vaccination. This study assessed the impact of maternal Tdap antibodies on the infant's pertussis-specific T...

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Orije MRP, García-Fogeda I, Van Dyck W, et al. Impact of maternal pertussis antibodies on the infants' cellular immune responses. Clin Infect Dis. 2021;doi: 10.1093/cid/ciab972.
Orije, M. R. P., García-Fogeda, I., Van Dyck, W., Corbière, V., Mascart, F., Mahieu, L., Hens, N., Van Damme, P., Cools, N., Ogunjimi, B., Maertens, K., & Leuridan, E. (2021). Impact of maternal pertussis antibodies on the infants' cellular immune responses. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, . https://doi.org/10.1093/cid/ciab972
Orije, Marjolein R P, et al. "Impact of maternal pertussis antibodies on the infants' cellular immune responses." Clinical infectious diseases : an official publication of the Infectious Diseases Society of America vol. (2021). doi: https://doi.org/10.1093/cid/ciab972
Orije MRP, García-Fogeda I, Van Dyck W, Corbière V, Mascart F, Mahieu L, Hens N, Van Damme P, Cools N, Ogunjimi B, Maertens K, Leuridan E. Impact of maternal pertussis antibodies on the infants' cellular immune responses. Clin Infect Dis. 2021 Nov 24; doi: 10.1093/cid/ciab972. Epub 2021 Nov 24. PMID: 34849638.
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Nobiletin attenuates inflammation via modulating proinflammatory and antiinflammatory cytokine expressions in an autoimmune encephalomyelitis mouse model.

Fitoterapia

Yarim GF, Yarim M, Sozmen M, Gokceoglu A, Ertekin A, Kabak YB, Karaca E.
PMID: 34896483
Fitoterapia. 2022 Jan;156:105099. doi: 10.1016/j.fitote.2021.105099. Epub 2021 Dec 09.

The aim of this study is to investigate the potential preventive and therapeutic effects of nobiletin by evaluating the expression of cytokines associated with inflammatory reactions in an autoimmune encephalomyelitis mouse model. A total of 60 male C57BL/6 mice...

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Yarim GF, Yarim M, Sozmen M, et al. Nobiletin attenuates inflammation via modulating proinflammatory and antiinflammatory cytokine expressions in an autoimmune encephalomyelitis mouse model. Fitoterapia. 2021;156:105099doi: 10.1016/j.fitote.2021.105099.
Yarim, G. F., Yarim, M., Sozmen, M., Gokceoglu, A., Ertekin, A., Kabak, Y. B., & Karaca, E. (2022). Nobiletin attenuates inflammation via modulating proinflammatory and antiinflammatory cytokine expressions in an autoimmune encephalomyelitis mouse model. Fitoterapia, 156105099. https://doi.org/10.1016/j.fitote.2021.105099
Yarim, Gul Fatma, et al. "Nobiletin attenuates inflammation via modulating proinflammatory and antiinflammatory cytokine expressions in an autoimmune encephalomyelitis mouse model." Fitoterapia vol. 156 (2022): 105099. doi: https://doi.org/10.1016/j.fitote.2021.105099
Yarim GF, Yarim M, Sozmen M, Gokceoglu A, Ertekin A, Kabak YB, Karaca E. Nobiletin attenuates inflammation via modulating proinflammatory and antiinflammatory cytokine expressions in an autoimmune encephalomyelitis mouse model. Fitoterapia. 2022 Jan;156:105099. doi: 10.1016/j.fitote.2021.105099. Epub 2021 Dec 09. PMID: 34896483.
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Showing 25 to 36 of 232 entries