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Largely Accelerated Arterial Aging in Rheumatoid Arthritis Is Associated With Inflammatory Activity and Smoking in the Early Stage of the Disease.

Frontiers in pharmacology

Mong N, Tarjanyi Z, Tothfalusi L, Bartykowszki A, Nagy AI, Szekely A, Becker D, Maurovich-Horvat P, Merkely B, Nagy G.
PMID: 33390933
Front Pharmacol. 2020 Nov 26;11:523962. doi: 10.3389/fphar.2020.601344. eCollection 2020.

No abstract available.

Cite
Mong N, Tarjanyi Z, Tothfalusi L, et al. Largely Accelerated Arterial Aging in Rheumatoid Arthritis Is Associated With Inflammatory Activity and Smoking in the Early Stage of the Disease. Front Pharmacol. 2020;11:523962doi: 10.3389/fphar.2020.601344.
Mong, N., Tarjanyi, Z., Tothfalusi, L., Bartykowszki, A., Nagy, A. I., Szekely, A., Becker, D., Maurovich-Horvat, P., Merkely, B., & Nagy, G. (2020). Largely Accelerated Arterial Aging in Rheumatoid Arthritis Is Associated With Inflammatory Activity and Smoking in the Early Stage of the Disease. Frontiers in pharmacology, 11523962. https://doi.org/10.3389/fphar.2020.601344
Mong, Nikolett, et al. "Largely Accelerated Arterial Aging in Rheumatoid Arthritis Is Associated With Inflammatory Activity and Smoking in the Early Stage of the Disease." Frontiers in pharmacology vol. 11 (2020): 523962. doi: https://doi.org/10.3389/fphar.2020.601344
Mong N, Tarjanyi Z, Tothfalusi L, Bartykowszki A, Nagy AI, Szekely A, Becker D, Maurovich-Horvat P, Merkely B, Nagy G. Largely Accelerated Arterial Aging in Rheumatoid Arthritis Is Associated With Inflammatory Activity and Smoking in the Early Stage of the Disease. Front Pharmacol. 2020 Nov 26;11:523962. doi: 10.3389/fphar.2020.601344. eCollection 2020. PMID: 33390933; PMCID: PMC7774279.
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The complete mitochondrial genome of the lesser sac-winged bat .

Mitochondrial DNA. Part B, Resources

Grau JH, Nagy M, Coraman E, Mayer F.
PMID: 33473781
Mitochondrial DNA B Resour. 2017 Apr 21;2(1):234-235. doi: 10.1080/23802359.2017.1318679.

Here we present the first complete mitochondrial genome of the lesser sac-winged bat

Cite
Grau JH, Nagy M, Coraman E, et al. The complete mitochondrial genome of the lesser sac-winged bat . Mitochondrial DNA B Resour. 2017;2(1):234-235doi: 10.1080/23802359.2017.1318679.
Grau, J. H., Nagy, M., Coraman, E., & Mayer, F. (2017). The complete mitochondrial genome of the lesser sac-winged bat . Mitochondrial DNA. Part B, Resources, 2(1), 234-235. https://doi.org/10.1080/23802359.2017.1318679
Grau, José Horacio, et al. "The complete mitochondrial genome of the lesser sac-winged bat ." Mitochondrial DNA. Part B, Resources vol. 2,1 (2017): 234-235. doi: https://doi.org/10.1080/23802359.2017.1318679
Grau JH, Nagy M, Coraman E, Mayer F. The complete mitochondrial genome of the lesser sac-winged bat . Mitochondrial DNA B Resour. 2017 Apr 21;2(1):234-235. doi: 10.1080/23802359.2017.1318679. PMID: 33473781; PMCID: PMC7800868.
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N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product.

Journal of pharmaceutical and biomedical analysis

Szabo M, Filep C, Nagy M, Sarkozy D, Szigeti M, Sperling E, Csanky E, Guttman A.
PMID: 34864596
J Pharm Biomed Anal. 2021 Nov 25;209:114483. doi: 10.1016/j.jpba.2021.114483. Epub 2021 Nov 25.

Omalizumab, a glycoprotein based biotherapeutics, is one of the most frequently used targeted antibody biopharmaceutical to reduce asthma exacerbations, improve lung function and reduce oral corticosteroid use. The effector function and clearance time of such glycoprotein drugs is affected...

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Szabo M, Filep C, Nagy M, et al. N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product. J Pharm Biomed Anal. 2021;209:114483doi: 10.1016/j.jpba.2021.114483.
Szabo, M., Filep, C., Nagy, M., Sarkozy, D., Szigeti, M., Sperling, E., Csanky, E., & Guttman, A. (2021). N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product. Journal of pharmaceutical and biomedical analysis, 209114483. https://doi.org/10.1016/j.jpba.2021.114483
Szabo, Miklos, et al. "N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product." Journal of pharmaceutical and biomedical analysis vol. 209 (2021): 114483. doi: https://doi.org/10.1016/j.jpba.2021.114483
Szabo M, Filep C, Nagy M, Sarkozy D, Szigeti M, Sperling E, Csanky E, Guttman A. N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product. J Pharm Biomed Anal. 2021 Nov 25;209:114483. doi: 10.1016/j.jpba.2021.114483. Epub 2021 Nov 25. PMID: 34864596.
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Characterization of Nuclear Progesterone Receptor Isoforms in the Term Equine Placenta.

Frontiers in veterinary science

Nagy AM, Sathe SR, Atta AH, Hammam AMM, Hsu WH.
PMID: 33869328
Front Vet Sci. 2021 Apr 01;8:660177. doi: 10.3389/fvets.2021.660177. eCollection 2021.

In equine parturition, the role of progestins along with the nuclear progesterone receptor (nPR) signaling pathway in the placenta is not completely clarified. The progestins play an integral role in maintaining myometrial quiescence during the late stage of pregnancy...

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Nagy AM, Sathe SR, Atta AH, et al. Characterization of Nuclear Progesterone Receptor Isoforms in the Term Equine Placenta. Front Vet Sci. 2021;8:660177doi: 10.3389/fvets.2021.660177.
Nagy, A. M., Sathe, S. R., Atta, A. H., Hammam, A. M. M., & Hsu, W. H. (2021). Characterization of Nuclear Progesterone Receptor Isoforms in the Term Equine Placenta. Frontiers in veterinary science, 8660177. https://doi.org/10.3389/fvets.2021.660177
Nagy, Ahmed M, et al. "Characterization of Nuclear Progesterone Receptor Isoforms in the Term Equine Placenta." Frontiers in veterinary science vol. 8 (2021): 660177. doi: https://doi.org/10.3389/fvets.2021.660177
Nagy AM, Sathe SR, Atta AH, Hammam AMM, Hsu WH. Characterization of Nuclear Progesterone Receptor Isoforms in the Term Equine Placenta. Front Vet Sci. 2021 Apr 01;8:660177. doi: 10.3389/fvets.2021.660177. eCollection 2021. PMID: 33869328; PMCID: PMC8047131.
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Showing 373 to 376 of 376 entries