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Alternative approaches to generating cardiomyocytes are under development.

Nature reviews. Cardiology

Chen IY, Matsa E, Wu JC.
PMID: 27538813
Nat Rev Cardiol. 2016 Oct;13(10):574. doi: 10.1038/nrcardio.2016.130. Epub 2016 Aug 19.

No abstract available.

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Chen IY, Matsa E, Wu JC. Alternative approaches to generating cardiomyocytes are under development. Nat Rev Cardiol. 2016;13(10):574doi: 10.1038/nrcardio.2016.130.
Chen, I. Y., Matsa, E., & Wu, J. C. (2016). Alternative approaches to generating cardiomyocytes are under development. Nature reviews. Cardiology, 13(10), 574. https://doi.org/10.1038/nrcardio.2016.130
Chen, Ian Y, et al. "Alternative approaches to generating cardiomyocytes are under development." Nature reviews. Cardiology vol. 13,10 (2016): 574. doi: https://doi.org/10.1038/nrcardio.2016.130
Chen IY, Matsa E, Wu JC. Alternative approaches to generating cardiomyocytes are under development. Nat Rev Cardiol. 2016 Oct;13(10):574. doi: 10.1038/nrcardio.2016.130. Epub 2016 Aug 19. PMID: 27538813; PMCID: PMC7048237.
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Finding Expandable Induced Cardiovascular Progenitor Cells.

Circulation research

Chen IY, Wu JC.
PMID: 27340267
Circ Res. 2016 Jun 24;119(1):16-20. doi: 10.1161/CIRCRESAHA.116.308679.

No abstract available.

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Chen IY, Wu JC. Finding Expandable Induced Cardiovascular Progenitor Cells. Circ Res. 2016;119(1):16-20doi: 10.1161/CIRCRESAHA.116.308679.
Chen, I. Y., & Wu, J. C. (2016). Finding Expandable Induced Cardiovascular Progenitor Cells. Circulation research, 119(1), 16-20. https://doi.org/10.1161/CIRCRESAHA.116.308679
Chen, Ian Y, and Wu, Joseph C. "Finding Expandable Induced Cardiovascular Progenitor Cells." Circulation research vol. 119,1 (2016): 16-20. doi: https://doi.org/10.1161/CIRCRESAHA.116.308679
Chen IY, Wu JC. Finding Expandable Induced Cardiovascular Progenitor Cells. Circ Res. 2016 Jun 24;119(1):16-20. doi: 10.1161/CIRCRESAHA.116.308679. PMID: 27340267; PMCID: PMC4958376.
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Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix.

Nature biomedical engineering

Lee AS, Inayathullah M, Lijkwan MA, Zhao X, Sun W, Park S, Hong WX, Parekh MB, Malkovskiy AV, Lau E, Qin X, Pothineni VR, Sanchez-Freire V, Zhang WY, Kooreman NG, Ebert AD, Chan CKF, Nguyen PK, Rajadas J, Wu JC.
PMID: 29721363
Nat Biomed Eng. 2018 Feb;2(2):104-113. doi: 10.1038/s41551-018-0191-4. Epub 2018 Feb 06.

Stem-cell-based therapies hold considerable promise for regenerative medicine. However, acute donor-cell death within several weeks after cell delivery remains a critical hurdle for clinical translation. Co-transplantation of stem cells with pro-survival factors can improve cell engraftment, but this strategy...

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Lee AS, Inayathullah M, Lijkwan MA, et al. Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix. Nat Biomed Eng. 2018;2(2):104-113doi: 10.1038/s41551-018-0191-4.
Lee, A. S., Inayathullah, M., Lijkwan, M. A., Zhao, X., Sun, W., Park, S., Hong, W. X., Parekh, M. B., Malkovskiy, A. V., Lau, E., Qin, X., Pothineni, V. R., Sanchez-Freire, V., Zhang, W. Y., Kooreman, N. G., Ebert, A. D., Chan, C. K. F., Nguyen, P. K., Rajadas, J., & Wu, J. C. (2018). Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix. Nature biomedical engineering, 2(2), 104-113. https://doi.org/10.1038/s41551-018-0191-4
Lee, Andrew S, et al. "Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix." Nature biomedical engineering vol. 2,2 (2018): 104-113. doi: https://doi.org/10.1038/s41551-018-0191-4
Lee AS, Inayathullah M, Lijkwan MA, Zhao X, Sun W, Park S, Hong WX, Parekh MB, Malkovskiy AV, Lau E, Qin X, Pothineni VR, Sanchez-Freire V, Zhang WY, Kooreman NG, Ebert AD, Chan CKF, Nguyen PK, Rajadas J, Wu JC. Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix. Nat Biomed Eng. 2018 Feb;2(2):104-113. doi: 10.1038/s41551-018-0191-4. Epub 2018 Feb 06. PMID: 29721363; PMCID: PMC5927627.
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Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy.

Circulation

Ranjbarvaziri S, Kooiker KB, Ellenberger M, Fajardo G, Zhao M, Vander Roest AS, Woldeyes RA, Koyano TT, Fong R, Ma N, Tian L, Traber GM, Chan F, Perrino J, Reddy S, Chiu W, Wu JC, Woo JY, Ruppel KM, Spudich JA, Snyder MP, Contrepois K, Bernstein D.
PMID: 34672721
Circulation. 2021 Nov 23;144(21):1714-1731. doi: 10.1161/CIRCULATIONAHA.121.053575. Epub 2021 Oct 21.

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a complex disease partly explained by the effects of individual gene variants on sarcomeric protein biomechanics. At the cellular level, HCM mutations most commonly enhance force production, leading to higher energy demands. Despite significant...

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Ranjbarvaziri S, Kooiker KB, Ellenberger M, et al. Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation. 2021;144(21):1714-1731doi: 10.1161/CIRCULATIONAHA.121.053575.
Ranjbarvaziri, S., Kooiker, K. B., Ellenberger, M., Fajardo, G., Zhao, M., Vander Roest, A. S., Woldeyes, R. A., Koyano, T. T., Fong, R., Ma, N., Tian, L., Traber, G. M., Chan, F., Perrino, J., Reddy, S., Chiu, W., Wu, J. C., Woo, J. Y., Ruppel, K. M., Spudich, J. A., Snyder, M. P., Contrepois, K., & Bernstein, D. (2021). Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation, 144(21), 1714-1731. https://doi.org/10.1161/CIRCULATIONAHA.121.053575
Ranjbarvaziri, Sara, et al. "Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy." Circulation vol. 144,21 (2021): 1714-1731. doi: https://doi.org/10.1161/CIRCULATIONAHA.121.053575
Ranjbarvaziri S, Kooiker KB, Ellenberger M, Fajardo G, Zhao M, Vander Roest AS, Woldeyes RA, Koyano TT, Fong R, Ma N, Tian L, Traber GM, Chan F, Perrino J, Reddy S, Chiu W, Wu JC, Woo JY, Ruppel KM, Spudich JA, Snyder MP, Contrepois K, Bernstein D. Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation. 2021 Nov 23;144(21):1714-1731. doi: 10.1161/CIRCULATIONAHA.121.053575. Epub 2021 Oct 21. PMID: 34672721; PMCID: PMC8608736.
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Polylactic Acid Piezo-Biopolymers: Chemistry, Structural Evolution, Fabrication Methods, and Tissue Engineering Applications.

Journal of functional biomaterials

Farahani A, Zarei-Hanzaki A, Abedi HR, Tayebi L, Mostafavi E.
PMID: 34940550
J Funct Biomater. 2021 Dec 08;12(4). doi: 10.3390/jfb12040071.

Polylactide acid (PLA), as an FDA-approved biomaterial, has been widely applied due to its unique merits, such as its biocompatibility, biodegradability, and piezoelectricity. Numerous utilizations, including sensors, actuators, and bio-application-its most exciting application to promote cell migration, differentiation, growth,...

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Farahani A, Zarei-Hanzaki A, Abedi HR, et al. Polylactic Acid Piezo-Biopolymers: Chemistry, Structural Evolution, Fabrication Methods, and Tissue Engineering Applications. J Funct Biomater. 2021;12(4)doi: 10.3390/jfb12040071.
Farahani, A., Zarei-Hanzaki, A., Abedi, H. R., Tayebi, L., & Mostafavi, E. (2021). Polylactic Acid Piezo-Biopolymers: Chemistry, Structural Evolution, Fabrication Methods, and Tissue Engineering Applications. Journal of functional biomaterials, 12(4), . https://doi.org/10.3390/jfb12040071
Farahani, Amirhossein, et al. "Polylactic Acid Piezo-Biopolymers: Chemistry, Structural Evolution, Fabrication Methods, and Tissue Engineering Applications." Journal of functional biomaterials vol. 12,4 (2021). doi: https://doi.org/10.3390/jfb12040071
Farahani A, Zarei-Hanzaki A, Abedi HR, Tayebi L, Mostafavi E. Polylactic Acid Piezo-Biopolymers: Chemistry, Structural Evolution, Fabrication Methods, and Tissue Engineering Applications. J Funct Biomater. 2021 Dec 08;12(4). doi: 10.3390/jfb12040071. PMID: 34940550; PMCID: PMC8704870.
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Systems-Wide Approaches in Induced Pluripotent Stem Cell Models.

Annual review of pathology

Lau E, Paik DT, Wu JC.
PMID: 30379619
Annu Rev Pathol. 2019 Jan 24;14:395-419. doi: 10.1146/annurev-pathmechdis-012418-013046. Epub 2018 Oct 31.

Human induced pluripotent stem cells (iPSCs) provide a renewable supply of patient-specific and tissue-specific cells for cellular and molecular studies of disease mechanisms. Combined with advances in various omics technologies, iPSC models can be used to profile the expression...

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Lau E, Paik DT, Wu JC. Systems-Wide Approaches in Induced Pluripotent Stem Cell Models. Annu Rev Pathol. 2018;14:395-419doi: 10.1146/annurev-pathmechdis-012418-013046.
Lau, E., Paik, D. T., & Wu, J. C. (2019). Systems-Wide Approaches in Induced Pluripotent Stem Cell Models. Annual review of pathology, 14395-419. https://doi.org/10.1146/annurev-pathmechdis-012418-013046
Lau, Edward, et al. "Systems-Wide Approaches in Induced Pluripotent Stem Cell Models." Annual review of pathology vol. 14 (2019): 395-419. doi: https://doi.org/10.1146/annurev-pathmechdis-012418-013046
Lau E, Paik DT, Wu JC. Systems-Wide Approaches in Induced Pluripotent Stem Cell Models. Annu Rev Pathol. 2019 Jan 24;14:395-419. doi: 10.1146/annurev-pathmechdis-012418-013046. Epub 2018 Oct 31. PMID: 30379619; PMCID: PMC6450651.
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Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy.

Circulation

Ranjbarvaziri S, Kooiker KB, Ellenberger M, Fajardo G, Zhao M, Vander Roest AS, Woldeyes RA, Koyano TT, Fong R, Ma N, Tian L, Traber GM, Chan F, Perrino J, Reddy S, Chiu W, Wu JC, Woo JY, Ruppel KM, Spudich JA, Snyder MP, Contrepois K, Bernstein D.
PMID: 34672721
Circulation. 2021 Nov 23;144(21):1714-1731. doi: 10.1161/CIRCULATIONAHA.121.053575. Epub 2021 Oct 21.

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a complex disease partly explained by the effects of individual gene variants on sarcomeric protein biomechanics. At the cellular level, HCM mutations most commonly enhance force production, leading to higher energy demands. Despite significant...

Cite
Ranjbarvaziri S, Kooiker KB, Ellenberger M, et al. Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation. 2021;144(21):1714-1731doi: 10.1161/CIRCULATIONAHA.121.053575.
Ranjbarvaziri, S., Kooiker, K. B., Ellenberger, M., Fajardo, G., Zhao, M., Vander Roest, A. S., Woldeyes, R. A., Koyano, T. T., Fong, R., Ma, N., Tian, L., Traber, G. M., Chan, F., Perrino, J., Reddy, S., Chiu, W., Wu, J. C., Woo, J. Y., Ruppel, K. M., Spudich, J. A., Snyder, M. P., Contrepois, K., & Bernstein, D. (2021). Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation, 144(21), 1714-1731. https://doi.org/10.1161/CIRCULATIONAHA.121.053575
Ranjbarvaziri, Sara, et al. "Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy." Circulation vol. 144,21 (2021): 1714-1731. doi: https://doi.org/10.1161/CIRCULATIONAHA.121.053575
Ranjbarvaziri S, Kooiker KB, Ellenberger M, Fajardo G, Zhao M, Vander Roest AS, Woldeyes RA, Koyano TT, Fong R, Ma N, Tian L, Traber GM, Chan F, Perrino J, Reddy S, Chiu W, Wu JC, Woo JY, Ruppel KM, Spudich JA, Snyder MP, Contrepois K, Bernstein D. Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. Circulation. 2021 Nov 23;144(21):1714-1731. doi: 10.1161/CIRCULATIONAHA.121.053575. Epub 2021 Oct 21. PMID: 34672721; PMCID: PMC8608736.
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Spinal Cord Injury Management through the Combination of Stem Cells and Implantable 3D Bioprinted Platforms.

Cells

Zarepour A, Hooshmand S, Gökmen A, Zarrabi A, Mostafavi E.
PMID: 34831412
Cells. 2021 Nov 16;10(11). doi: 10.3390/cells10113189.

Spinal cord injury (SCI) has a major impact on affected patients due to its pathological consequences and absence of capacity for self-repair. Currently available therapies are unable to restore lost neural functions. Thus, there is a pressing need to...

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Zarepour A, Hooshmand S, Gökmen A, et al. Spinal Cord Injury Management through the Combination of Stem Cells and Implantable 3D Bioprinted Platforms. Cells. 2021;10(11)doi: 10.3390/cells10113189.
Zarepour, A., Hooshmand, S., Gökmen, A., Zarrabi, A., & Mostafavi, E. (2021). Spinal Cord Injury Management through the Combination of Stem Cells and Implantable 3D Bioprinted Platforms. Cells, 10(11), . https://doi.org/10.3390/cells10113189
Zarepour, Atefeh, et al. "Spinal Cord Injury Management through the Combination of Stem Cells and Implantable 3D Bioprinted Platforms." Cells vol. 10,11 (2021). doi: https://doi.org/10.3390/cells10113189
Zarepour A, Hooshmand S, Gökmen A, Zarrabi A, Mostafavi E. Spinal Cord Injury Management through the Combination of Stem Cells and Implantable 3D Bioprinted Platforms. Cells. 2021 Nov 16;10(11). doi: 10.3390/cells10113189. PMID: 34831412; PMCID: PMC8620694.
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Preoperative Computed Tomography Angiography Reveals Leaflet-Specific Calcification and Excursion Patterns in Aortic Stenosis.

Circulation. Cardiovascular imaging

Chen IY, Vedula V, Malik SB, Liang T, Chang AY, Chung KS, Sayed N, Tsao PS, Giacomini JC, Marsden AL, Wu JC.
PMID: 34915729
Circ Cardiovasc Imaging. 2021 Dec;14(12):1122-1132. doi: 10.1161/CIRCIMAGING.121.012884. Epub 2021 Dec 17.

BACKGROUND: Computed tomography-based evaluation of aortic stenosis (AS) by calcium scoring does not consider interleaflet differences in leaflet characteristics. Here, we sought to examine the functional implications of these differences.METHODS: We retrospectively reviewed the computed tomography angiograms of 200...

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Chen IY, Vedula V, Malik SB, et al. Preoperative Computed Tomography Angiography Reveals Leaflet-Specific Calcification and Excursion Patterns in Aortic Stenosis. Circ Cardiovasc Imaging. 2021;14(12):1122-1132doi: 10.1161/CIRCIMAGING.121.012884.
Chen, I. Y., Vedula, V., Malik, S. B., Liang, T., Chang, A. Y., Chung, K. S., Sayed, N., Tsao, P. S., Giacomini, J. C., Marsden, A. L., & Wu, J. C. (2021). Preoperative Computed Tomography Angiography Reveals Leaflet-Specific Calcification and Excursion Patterns in Aortic Stenosis. Circulation. Cardiovascular imaging, 14(12), 1122-1132. https://doi.org/10.1161/CIRCIMAGING.121.012884
Chen, Ian Y, et al. "Preoperative Computed Tomography Angiography Reveals Leaflet-Specific Calcification and Excursion Patterns in Aortic Stenosis." Circulation. Cardiovascular imaging vol. 14,12 (2021): 1122-1132. doi: https://doi.org/10.1161/CIRCIMAGING.121.012884
Chen IY, Vedula V, Malik SB, Liang T, Chang AY, Chung KS, Sayed N, Tsao PS, Giacomini JC, Marsden AL, Wu JC. Preoperative Computed Tomography Angiography Reveals Leaflet-Specific Calcification and Excursion Patterns in Aortic Stenosis. Circ Cardiovasc Imaging. 2021 Dec;14(12):1122-1132. doi: 10.1161/CIRCIMAGING.121.012884. Epub 2021 Dec 17. PMID: 34915729.
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Real-time, continuous, fluorescence sensing in a freely-moving subject with an implanted hybrid VCSEL/CMOS biosensor.

Biomedical optics express

O'Sullivan TD, Heitz RT, Parashurama N, Barkin DB, Wooley BA, Gambhir SS, Harris JS, Levi O.
PMID: 24009996
Biomed Opt Express. 2013 Jul 15;4(8):1332-41. doi: 10.1364/BOE.4.001332. eCollection 2013.

Performance improvements in instrumentation for optical imaging have contributed greatly to molecular imaging in living subjects. In order to advance molecular imaging in freely moving, untethered subjects, we designed a miniature vertical-cavity surface-emitting laser (VCSEL)-based biosensor measuring 1cm(3) and...

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O'Sullivan TD, Heitz RT, Parashurama N, et al. Real-time, continuous, fluorescence sensing in a freely-moving subject with an implanted hybrid VCSEL/CMOS biosensor. Biomed Opt Express. 2013;4(8):1332-41doi: 10.1364/BOE.4.001332.
O'Sullivan, T. D., Heitz, R. T., Parashurama, N., Barkin, D. B., Wooley, B. A., Gambhir, S. S., Harris, J. S., & Levi, O. (2013). Real-time, continuous, fluorescence sensing in a freely-moving subject with an implanted hybrid VCSEL/CMOS biosensor. Biomedical optics express, 4(8), 1332-41. https://doi.org/10.1364/BOE.4.001332
O'Sullivan, Thomas D, et al. "Real-time, continuous, fluorescence sensing in a freely-moving subject with an implanted hybrid VCSEL/CMOS biosensor." Biomedical optics express vol. 4,8 (2013): 1332-41. doi: https://doi.org/10.1364/BOE.4.001332
O'Sullivan TD, Heitz RT, Parashurama N, Barkin DB, Wooley BA, Gambhir SS, Harris JS, Levi O. Real-time, continuous, fluorescence sensing in a freely-moving subject with an implanted hybrid VCSEL/CMOS biosensor. Biomed Opt Express. 2013 Jul 15;4(8):1332-41. doi: 10.1364/BOE.4.001332. eCollection 2013. PMID: 24009996; PMCID: PMC3756575.
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Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles.

Advanced functional materials

Qin X, Chen H, Yang H, Wu H, Zhao X, Wang H, Chour T, Neofytou E, Ding D, Daldrup-Link H, Heilshorn SC, Li K, Wu JC.
PMID: 30473658
Adv Funct Mater. 2018 Jan 04;28(1). doi: 10.1002/adfm.201704939. Epub 2017 Nov 08.

The last decade has seen impressive progress in human embryonic stem cell-derived cardiomyocytes (hESC-CMs) that makes them ideal tools to repair injured hearts. To achieve an optimal outcome, advanced molecular imaging methods are essential to accurately track these transplanted...

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Qin X, Chen H, Yang H, et al. Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles. Adv Funct Mater. 2017;28(1)doi: 10.1002/adfm.201704939.
Qin, X., Chen, H., Yang, H., Wu, H., Zhao, X., Wang, H., Chour, T., Neofytou, E., Ding, D., Daldrup-Link, H., Heilshorn, S. C., Li, K., & Wu, J. C. (2018). Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles. Advanced functional materials, 28(1), . https://doi.org/10.1002/adfm.201704939
Qin, Xulei, et al. "Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles." Advanced functional materials vol. 28,1 (2018). doi: https://doi.org/10.1002/adfm.201704939
Qin X, Chen H, Yang H, Wu H, Zhao X, Wang H, Chour T, Neofytou E, Ding D, Daldrup-Link H, Heilshorn SC, Li K, Wu JC. Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles. Adv Funct Mater. 2018 Jan 04;28(1). doi: 10.1002/adfm.201704939. Epub 2017 Nov 08. PMID: 30473658; PMCID: PMC6247950.
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Simply derived epicardial cells.

Nature biomedical engineering

Paik DT, Wu JC.
PMID: 29354320
Nat Biomed Eng. 2017;1. doi: 10.1038/s41551-016-0015. Epub 2017 Jan 10.

A chemically defined protocol requiring no animal-derived components allows for the easier derivation and enduring expansion of epicardial cells from human pluripotent stem cells.

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Paik DT, Wu JC. Simply derived epicardial cells. Nat Biomed Eng. 2017;1doi: 10.1038/s41551-016-0015.
Paik, D. T., & Wu, J. C. (2017). Simply derived epicardial cells. Nature biomedical engineering, 1. https://doi.org/10.1038/s41551-016-0015
Paik, David T, and Wu, Joseph C. "Simply derived epicardial cells." Nature biomedical engineering vol. 1 (2017). doi: https://doi.org/10.1038/s41551-016-0015
Paik DT, Wu JC. Simply derived epicardial cells. Nat Biomed Eng. 2017;1. doi: 10.1038/s41551-016-0015. Epub 2017 Jan 10. PMID: 29354320; PMCID: PMC5772986.
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