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Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion.

Oncotarget

Pavo N, Lukovic D, Zlabinger K, Lorant D, Goliasch G, Winkler J, Pils D, Auer K, Ankersmit HJ, Giricz Z, Sárközy M, Jakab A, Garamvölgyi R, Emmert MY, Hoerstrup SP, Hausenloy DJ, Ferdinandy P, Maurer G, Gyöngyösi M.
PMID: 28978029
Oncotarget. 2017 Jun 12;8(40):67227-67240. doi: 10.18632/oncotarget.18438. eCollection 2017 Sep 15.

We have previously shown that distal anterior wall ischemia/reperfusion induces gene expression changes in the proximal anterior myocardial area, involving genes responsible for cardiac remodeling. Here we investigated the molecular signals of the ischemia non-affected remote lateral and posterior...

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Pavo N, Lukovic D, Zlabinger K, et al. Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget. 2017;8(40):67227-67240doi: 10.18632/oncotarget.18438.
Pavo, N., Lukovic, D., Zlabinger, K., Lorant, D., Goliasch, G., Winkler, J., Pils, D., Auer, K., Ankersmit, H. J., Giricz, Z., Sárközy, M., Jakab, A., Garamvölgyi, R., Emmert, M. Y., Hoerstrup, S. P., Hausenloy, D. J., Ferdinandy, P., Maurer, G., & Gyöngyösi, M. (2017). Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget, 8(40), 67227-67240. https://doi.org/10.18632/oncotarget.18438
Pavo, Noemi, et al. "Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion." Oncotarget vol. 8,40 (2017): 67227-67240. doi: https://doi.org/10.18632/oncotarget.18438
Pavo N, Lukovic D, Zlabinger K, Lorant D, Goliasch G, Winkler J, Pils D, Auer K, Ankersmit HJ, Giricz Z, Sárközy M, Jakab A, Garamvölgyi R, Emmert MY, Hoerstrup SP, Hausenloy DJ, Ferdinandy P, Maurer G, Gyöngyösi M. Intrinsic remote conditioning of the myocardium as a comprehensive cardiac response to ischemia and reperfusion. Oncotarget. 2017 Jun 12;8(40):67227-67240. doi: 10.18632/oncotarget.18438. eCollection 2017 Sep 15. PMID: 28978029; PMCID: PMC5620169.
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Isolation of High-Purity Extracellular Vesicles by the Combination of Iodixanol Density Gradient Ultracentrifugation and Bind-Elute Chromatography From Blood Plasma.

Frontiers in physiology

Onódi Z, Pelyhe C, Terézia Nagy C, Brenner GB, Almási L, Kittel Á, Manček-Keber M, Ferdinandy P, Buzás EI, Giricz Z.
PMID: 30405435
Front Physiol. 2018 Oct 23;9:1479. doi: 10.3389/fphys.2018.01479. eCollection 2018.

No abstract available.

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Onódi Z, Pelyhe C, Terézia Nagy C, et al. Isolation of High-Purity Extracellular Vesicles by the Combination of Iodixanol Density Gradient Ultracentrifugation and Bind-Elute Chromatography From Blood Plasma. Front Physiol. 2018;9:1479doi: 10.3389/fphys.2018.01479.
Onódi, Z., Pelyhe, C., Terézia Nagy, C., Brenner, G. B., Almási, L., Kittel, �. �., Manček-Keber, M., Ferdinandy, P., Buzás, E. I., & Giricz, Z. (2018). Isolation of High-Purity Extracellular Vesicles by the Combination of Iodixanol Density Gradient Ultracentrifugation and Bind-Elute Chromatography From Blood Plasma. Frontiers in physiology, 91479. https://doi.org/10.3389/fphys.2018.01479
Onódi, Zsófia, et al. "Isolation of High-Purity Extracellular Vesicles by the Combination of Iodixanol Density Gradient Ultracentrifugation and Bind-Elute Chromatography From Blood Plasma." Frontiers in physiology vol. 9 (2018): 1479. doi: https://doi.org/10.3389/fphys.2018.01479
Onódi Z, Pelyhe C, Terézia Nagy C, Brenner GB, Almási L, Kittel Á, Manček-Keber M, Ferdinandy P, Buzás EI, Giricz Z. Isolation of High-Purity Extracellular Vesicles by the Combination of Iodixanol Density Gradient Ultracentrifugation and Bind-Elute Chromatography From Blood Plasma. Front Physiol. 2018 Oct 23;9:1479. doi: 10.3389/fphys.2018.01479. eCollection 2018. PMID: 30405435; PMCID: PMC6206048.
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Potent Chimeric Antimicrobial Derivatives of the .

Frontiers in microbiology

Jenei S, Tiricz H, Szolomájer J, Tímár E, Klement É, Al Bouni MA, Lima RM, Kata D, Harmati M, Buzás K, Földesi I, Tóth GK, Endre G, Kondorosi É.
PMID: 32153547
Front Microbiol. 2020 Feb 21;11:270. doi: 10.3389/fmicb.2020.00270. eCollection 2020.

In Rhizobium-legume symbiosis, the bacteria are converted into nitrogen-fixing bacteroids. In many legume species, differentiation of the endosymbiotic bacteria is irreversible, culminating in definitive loss of their cell division ability. This terminal differentiation is mediated by plant peptides produced...

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Jenei S, Tiricz H, Szolomájer J, et al. Potent Chimeric Antimicrobial Derivatives of the . Front Microbiol. 2020;11:270doi: 10.3389/fmicb.2020.00270.
Jenei, S., Tiricz, H., Szolomájer, J., Tímár, E., Klement, �. �., Al Bouni, M. A., Lima, R. M., Kata, D., Harmati, M., Buzás, K., Földesi, I., Tóth, G. K., Endre, G., & Kondorosi, �. �. (2020). Potent Chimeric Antimicrobial Derivatives of the . Frontiers in microbiology, 11270. https://doi.org/10.3389/fmicb.2020.00270
Jenei, Sándor, et al. "Potent Chimeric Antimicrobial Derivatives of the ." Frontiers in microbiology vol. 11 (2020): 270. doi: https://doi.org/10.3389/fmicb.2020.00270
Jenei S, Tiricz H, Szolomájer J, Tímár E, Klement É, Al Bouni MA, Lima RM, Kata D, Harmati M, Buzás K, Földesi I, Tóth GK, Endre G, Kondorosi É. Potent Chimeric Antimicrobial Derivatives of the . Front Microbiol. 2020 Feb 21;11:270. doi: 10.3389/fmicb.2020.00270. eCollection 2020. PMID: 32153547; PMCID: PMC7047876.
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Effect of pH in the Hydrothermal Preparation of Bi.

Materials (Basel, Switzerland)

Nagyné-Kovács T, Shahnazarova G, Lukács IE, Szabó A, Hernadi K, Igricz T, László K, Szilágyi IM, Pokol G.
PMID: 31141883
Materials (Basel). 2019 May 28;12(11). doi: 10.3390/ma12111728.

In this study, Bi

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Nagyné-Kovács T, Shahnazarova G, Lukács IE, et al. Effect of pH in the Hydrothermal Preparation of Bi. Materials (Basel). 2019;12(11)doi: 10.3390/ma12111728.
Nagyné-Kovács, T., Shahnazarova, G., Lukács, I. E., Szabó, A., Hernadi, K., Igricz, T., László, K., Szilágyi, I. M., & Pokol, G. (2019). Effect of pH in the Hydrothermal Preparation of Bi. Materials (Basel, Switzerland), 12(11), . https://doi.org/10.3390/ma12111728
Nagyné-Kovács, Teodóra, et al. "Effect of pH in the Hydrothermal Preparation of Bi." Materials (Basel, Switzerland) vol. 12,11 (2019). doi: https://doi.org/10.3390/ma12111728
Nagyné-Kovács T, Shahnazarova G, Lukács IE, Szabó A, Hernadi K, Igricz T, László K, Szilágyi IM, Pokol G. Effect of pH in the Hydrothermal Preparation of Bi. Materials (Basel). 2019 May 28;12(11). doi: 10.3390/ma12111728. PMID: 31141883; PMCID: PMC6600692.
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Author Correction: MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium.

Scientific reports

Ágg B, Baranyai T, Makkos A, Vető B, Faragó N, Zvara Á, Giricz Z, Veres DV, Csermely P, Arányi T, Puskás LG, Varga ZV, Ferdinandy P.
PMID: 30089810
Sci Rep. 2018 Aug 09;8(1):12159. doi: 10.1038/s41598-018-30163-9.

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper.

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Ágg B, Baranyai T, Makkos A, et al. Author Correction: MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium. Sci Rep. 2018;8(1):12159doi: 10.1038/s41598-018-30163-9.
Ágg, B., Baranyai, T., Makkos, A., Vető, B., Faragó, N., Zvara, �. �., Giricz, Z., Veres, D. V., Csermely, P., Arányi, T., Puskás, L. G., Varga, Z. V., & Ferdinandy, P. (2018). Author Correction: MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium. Scientific reports, 8(1), 12159. https://doi.org/10.1038/s41598-018-30163-9
Ágg, Bence, et al. "Author Correction: MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium." Scientific reports vol. 8,1 (2018): 12159. doi: https://doi.org/10.1038/s41598-018-30163-9
Ágg B, Baranyai T, Makkos A, Vető B, Faragó N, Zvara Á, Giricz Z, Veres DV, Csermely P, Arányi T, Puskás LG, Varga ZV, Ferdinandy P. Author Correction: MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium. Sci Rep. 2018 Aug 09;8(1):12159. doi: 10.1038/s41598-018-30163-9. PMID: 30089810; PMCID: PMC6082891.
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Sex Differences in Morphological and Functional Aspects of Exercise-Induced Cardiac Hypertrophy in a Rat Model.

Frontiers in physiology

Oláh A, Mátyás C, Kellermayer D, Ruppert M, Barta BA, Sayour AA, Török M, Koncsos G, Giricz Z, Ferdinandy P, Merkely B, Radovits T.
PMID: 31354526
Front Physiol. 2019 Jul 12;10:889. doi: 10.3389/fphys.2019.00889. eCollection 2019.

No abstract available.

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Oláh A, Mátyás C, Kellermayer D, et al. Sex Differences in Morphological and Functional Aspects of Exercise-Induced Cardiac Hypertrophy in a Rat Model. Front Physiol. 2019;10:889doi: 10.3389/fphys.2019.00889.
Oláh, A., Mátyás, C., Kellermayer, D., Ruppert, M., Barta, B. A., Sayour, A. A., Török, M., Koncsos, G., Giricz, Z., Ferdinandy, P., Merkely, B., & Radovits, T. (2019). Sex Differences in Morphological and Functional Aspects of Exercise-Induced Cardiac Hypertrophy in a Rat Model. Frontiers in physiology, 10889. https://doi.org/10.3389/fphys.2019.00889
Oláh, Attila, et al. "Sex Differences in Morphological and Functional Aspects of Exercise-Induced Cardiac Hypertrophy in a Rat Model." Frontiers in physiology vol. 10 (2019): 889. doi: https://doi.org/10.3389/fphys.2019.00889
Oláh A, Mátyás C, Kellermayer D, Ruppert M, Barta BA, Sayour AA, Török M, Koncsos G, Giricz Z, Ferdinandy P, Merkely B, Radovits T. Sex Differences in Morphological and Functional Aspects of Exercise-Induced Cardiac Hypertrophy in a Rat Model. Front Physiol. 2019 Jul 12;10:889. doi: 10.3389/fphys.2019.00889. eCollection 2019. PMID: 31354526; PMCID: PMC6639783.
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ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine.

Blood cancer journal

Rahmani NE, Ramachandra N, Sahu S, Gitego N, Lopez A, Pradhan K, Bhagat TD, Gordon-Mitchell S, Pena BR, Kazemi M, Rao K, Giricz O, Maqbool SB, Olea R, Zhao Y, Zhang J, Dolatshad H, Tittrea V, Tatwavedi D, Singh S, Lee J, Sun T, Steidl U, Shastri A, Inoue D, Abdel-Wahab O, Pellagatti A, Gavathiotis E, Boultwood J, Verma A.
PMID: 34548471
Blood Cancer J. 2021 Sep 21;11(9):157. doi: 10.1038/s41408-021-00541-0.

The BCL2-inhibitor, Venetoclax (VEN), has shown significant anti-leukemic efficacy in combination with the DNMT-inhibitor, Azacytidine (AZA). To explore the mechanisms underlying the selective sensitivity of mutant leukemia cells to VEN and AZA, we used cell-based isogenic models containing a...

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Rahmani NE, Ramachandra N, Sahu S, et al. ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine. Blood Cancer J. 2021;11(9):157doi: 10.1038/s41408-021-00541-0.
Rahmani, N. E., Ramachandra, N., Sahu, S., Gitego, N., Lopez, A., Pradhan, K., Bhagat, T. D., Gordon-Mitchell, S., Pena, B. R., Kazemi, M., Rao, K., Giricz, O., Maqbool, S. B., Olea, R., Zhao, Y., Zhang, J., Dolatshad, H., Tittrea, V., Tatwavedi, D., Singh, S., Lee, J., Sun, T., Steidl, U., Shastri, A., Inoue, D., Abdel-Wahab, O., Pellagatti, A., Gavathiotis, E., Boultwood, J., & Verma, A. (2021). ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine. Blood cancer journal, 11(9), 157. https://doi.org/10.1038/s41408-021-00541-0
Rahmani, Nora E, et al. "ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine." Blood cancer journal vol. 11,9 (2021): 157. doi: https://doi.org/10.1038/s41408-021-00541-0
Rahmani NE, Ramachandra N, Sahu S, Gitego N, Lopez A, Pradhan K, Bhagat TD, Gordon-Mitchell S, Pena BR, Kazemi M, Rao K, Giricz O, Maqbool SB, Olea R, Zhao Y, Zhang J, Dolatshad H, Tittrea V, Tatwavedi D, Singh S, Lee J, Sun T, Steidl U, Shastri A, Inoue D, Abdel-Wahab O, Pellagatti A, Gavathiotis E, Boultwood J, Verma A. ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine. Blood Cancer J. 2021 Sep 21;11(9):157. doi: 10.1038/s41408-021-00541-0. PMID: 34548471; PMCID: PMC8455571.
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Initial Whole-Genome Sequencing of Plasma Cell Neoplasms in First Responders and Recovery Workers Exposed to the World Trade Center Attack of September 11, 2001.

Clinical cancer research : an official journal of the American Association for Cancer Research

Maura F, Diamond B, Maclachlan KH, Derkach A, Yellapantula VD, Rustad EH, Hultcrantz M, Shah UA, Hong J, Landau HJ, Iacobuzio-Donahue CA, Papaemmanuil E, Irby S, Crowley L, Crane M, Webber MP, Goldfarb DG, Zeig-Owens R, Giricz O, Verma A, Prezant DJ, Dogan A, Shah SP, Zhang Y, Landgren O.
PMID: 33504553
Clin Cancer Res. 2021 Apr 01;27(7):2111-2118. doi: 10.1158/1078-0432.CCR-20-2245. Epub 2021 Jan 27.

PURPOSE: The World Trade Center (WTC) attack of September 11, 2001 created an unprecedented environmental exposure to known and suspected carcinogens. High incidence of multiple myeloma and precursor conditions has been reported among first responders to the WTC disaster....

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Maura F, Diamond B, Maclachlan KH, et al. Initial Whole-Genome Sequencing of Plasma Cell Neoplasms in First Responders and Recovery Workers Exposed to the World Trade Center Attack of September 11, 2001. Clin Cancer Res. 2021;27(7):2111-2118doi: 10.1158/1078-0432.CCR-20-2245.
Maura, F., Diamond, B., Maclachlan, K. H., Derkach, A., Yellapantula, V. D., Rustad, E. H., Hultcrantz, M., Shah, U. A., Hong, J., Landau, H. J., Iacobuzio-Donahue, C. A., Papaemmanuil, E., Irby, S., Crowley, L., Crane, M., Webber, M. P., Goldfarb, D. G., Zeig-Owens, R., Giricz, O., Verma, A., Prezant, D. J., Dogan, A., Shah, S. P., Zhang, Y., & Landgren, O. (2021). Initial Whole-Genome Sequencing of Plasma Cell Neoplasms in First Responders and Recovery Workers Exposed to the World Trade Center Attack of September 11, 2001. Clinical cancer research : an official journal of the American Association for Cancer Research, 27(7), 2111-2118. https://doi.org/10.1158/1078-0432.CCR-20-2245
Maura, Francesco, et al. "Initial Whole-Genome Sequencing of Plasma Cell Neoplasms in First Responders and Recovery Workers Exposed to the World Trade Center Attack of September 11, 2001." Clinical cancer research : an official journal of the American Association for Cancer Research vol. 27,7 (2021): 2111-2118. doi: https://doi.org/10.1158/1078-0432.CCR-20-2245
Maura F, Diamond B, Maclachlan KH, Derkach A, Yellapantula VD, Rustad EH, Hultcrantz M, Shah UA, Hong J, Landau HJ, Iacobuzio-Donahue CA, Papaemmanuil E, Irby S, Crowley L, Crane M, Webber MP, Goldfarb DG, Zeig-Owens R, Giricz O, Verma A, Prezant DJ, Dogan A, Shah SP, Zhang Y, Landgren O. Initial Whole-Genome Sequencing of Plasma Cell Neoplasms in First Responders and Recovery Workers Exposed to the World Trade Center Attack of September 11, 2001. Clin Cancer Res. 2021 Apr 01;27(7):2111-2118. doi: 10.1158/1078-0432.CCR-20-2245. Epub 2021 Jan 27. PMID: 33504553; PMCID: PMC8026670.
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Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype.

Journal of molecular and cellular cardiology

Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV.
PMID: 34959166
J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24.

BACKGROUND: Cardiac cell lines and primary cells are widely used in cardiovascular research. Despite increasing number of publications using these models, comparative characterization of these cell lines has not been performed, therefore, their limitations are undetermined. We aimed to...

Cite
Onódi Z, Visnovitz T, Kiss B, et al. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021;165:19-30doi: 10.1016/j.yjmcc.2021.12.007.
Onódi, Z., Visnovitz, T., Kiss, B., Hambalkó, S., Koncz, A., Ágg, B., Váradi, B., Tóth, V. �. �., Nagy, R. N., Gergely, T. G., Gergő, D., Makkos, A., Pelyhe, C., Varga, N., Reé, D., Apáti, �. �., Leszek, P., Kovács, T., Nagy, N., Ferdinandy, P., Buzás, E. I., Görbe, A., Giricz, Z., & Varga, Z. V. (2021). Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. Journal of molecular and cellular cardiology, 16519-30. https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi, Zsófia, et al. "Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype." Journal of molecular and cellular cardiology vol. 165 (2021): 19-30. doi: https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24. PMID: 34959166.
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Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype.

Journal of molecular and cellular cardiology

Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV.
PMID: 34959166
J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24.

BACKGROUND: Cardiac cell lines and primary cells are widely used in cardiovascular research. Despite increasing number of publications using these models, comparative characterization of these cell lines has not been performed, therefore, their limitations are undetermined. We aimed to...

Cite
Onódi Z, Visnovitz T, Kiss B, et al. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021;165:19-30doi: 10.1016/j.yjmcc.2021.12.007.
Onódi, Z., Visnovitz, T., Kiss, B., Hambalkó, S., Koncz, A., Ágg, B., Váradi, B., Tóth, V. �. �., Nagy, R. N., Gergely, T. G., Gergő, D., Makkos, A., Pelyhe, C., Varga, N., Reé, D., Apáti, �. �., Leszek, P., Kovács, T., Nagy, N., Ferdinandy, P., Buzás, E. I., Görbe, A., Giricz, Z., & Varga, Z. V. (2021). Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. Journal of molecular and cellular cardiology, 16519-30. https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi, Zsófia, et al. "Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype." Journal of molecular and cellular cardiology vol. 165 (2021): 19-30. doi: https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24. PMID: 34959166.
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Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype.

Journal of molecular and cellular cardiology

Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV.
PMID: 34959166
J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24.

BACKGROUND: Cardiac cell lines and primary cells are widely used in cardiovascular research. Despite increasing number of publications using these models, comparative characterization of these cell lines has not been performed, therefore, their limitations are undetermined. We aimed to...

Cite
Onódi Z, Visnovitz T, Kiss B, et al. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021;165:19-30doi: 10.1016/j.yjmcc.2021.12.007.
Onódi, Z., Visnovitz, T., Kiss, B., Hambalkó, S., Koncz, A., Ágg, B., Váradi, B., Tóth, V. �. �., Nagy, R. N., Gergely, T. G., Gergő, D., Makkos, A., Pelyhe, C., Varga, N., Reé, D., Apáti, �. �., Leszek, P., Kovács, T., Nagy, N., Ferdinandy, P., Buzás, E. I., Görbe, A., Giricz, Z., & Varga, Z. V. (2021). Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. Journal of molecular and cellular cardiology, 16519-30. https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi, Zsófia, et al. "Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype." Journal of molecular and cellular cardiology vol. 165 (2021): 19-30. doi: https://doi.org/10.1016/j.yjmcc.2021.12.007
Onódi Z, Visnovitz T, Kiss B, Hambalkó S, Koncz A, Ágg B, Váradi B, Tóth VÉ, Nagy RN, Gergely TG, Gergő D, Makkos A, Pelyhe C, Varga N, Reé D, Apáti Á, Leszek P, Kovács T, Nagy N, Ferdinandy P, Buzás EI, Görbe A, Giricz Z, Varga ZV. Systematic transcriptomic and phenotypic characterization of human and murine cardiac myocyte cell lines and primary cardiomyocytes reveals serious limitations and low resemblances to adult cardiac phenotype. J Mol Cell Cardiol. 2021 Dec 24;165:19-30. doi: 10.1016/j.yjmcc.2021.12.007. Epub 2021 Dec 24. PMID: 34959166.
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Strange bedfellows: anti-abortion and disability rights advocacy.

Journal of law and the biosciences

Giric S.
PMID: 28852553
J Law Biosci. 2016 Dec 07;3(3):736-742. doi: 10.1093/jlb/lsw056. eCollection 2016 Dec.

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Giric S. Strange bedfellows: anti-abortion and disability rights advocacy. J Law Biosci. 2016;3(3):736-742doi: 10.1093/jlb/lsw056.
Giric, S. (2016). Strange bedfellows: anti-abortion and disability rights advocacy. Journal of law and the biosciences, 3(3), 736-742. https://doi.org/10.1093/jlb/lsw056
Giric, Stefanija. "Strange bedfellows: anti-abortion and disability rights advocacy." Journal of law and the biosciences vol. 3,3 (2016): 736-742. doi: https://doi.org/10.1093/jlb/lsw056
Giric S. Strange bedfellows: anti-abortion and disability rights advocacy. J Law Biosci. 2016 Dec 07;3(3):736-742. doi: 10.1093/jlb/lsw056. eCollection 2016 Dec. PMID: 28852553; PMCID: PMC5570694.
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