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Publications

  • Hope, J. L., Otero, D. C., Bae, E.-A., Stairiker, C. J., Palete, A. B., Faso, H. A., Lin, M., Henriquez, M. L., Roy, S., Seo, H., Lei, X., Wang, E. S., Chow, S., Tinoco, R., Daniels, G. A., Yip, K., Campos, A. R., Yin, J., Adams, P. D., … Bradley, L. M. (2023). PSGL-1 attenuates early TCR signaling to suppress CD8+ T cell progenitor differentiation and elicit terminal CD8+ T cell exhaustion. Cell Reports, 42(5), 112436. https://doi.org/10.1016/j.celrep.2023.112436 — Learn More

  • Lu, M. J., & Lu, Y. (2022). 5-hydroxymethylcytosine (5hmc) at or near cancer mutation hot spots as potential targets for early cancer detection. BMC Research Notes, 15(1). https://doi.org/10.1186/s13104-022-06028-w — Learn More

  • Cui, X., Ma, C., Vasudevaraja, V., Serrano, J., Tong, J., Peng, Y., . . . Chen, W. (2020). Dissecting the immunosuppressive tumor microenvironments in glioblastoma-on-a-chip for optimized pd-1 immunotherapy. ELife, 9. doi:10.7554/elife.52253 — Learn More

  • Demaree, B., Delley, C. L., Vasudevan, H. N., Peretz, C. A., Ruff, D., Smith, C. C., & Abate, A. R. (2020). Joint profiling of dna and proteins in single cells to dissect genotype-phenotype associations in leukemia. BioRxiv. doi:10.1101/2020.02.26.967133 — Learn More

  • Marrero, I., Maricic, I., Morgan, T. R., Stolz, A. A., Schnabl, B., Liu, Z., . . . Kumar, V. (2020). Differential activation of unconventional T cells, including Inkt cells, In Alcohol‐Related liver disease. Alcoholism: Clinical and Experimental Research, 44(5), 1061-1074. doi:10.1111/acer.14323 — Learn More

  • Puniya, B. L., Amin, R., Lichter, B., Moore, R., Ciurej, A., Townsend, S., . . . Helikar, T. (2020). Integrative computational approach identifies new targets in cd4+ t cell-mediated immune disorders. doi:10.1101/2020.01.02.893164 – Learn More

  • Sheng, H., Marrero, I., Maricic, I., Fanchiang, S. S., Zhang, S., Sant’Angelo, D. B., & Kumar, V. (2019). Distinct plzf+cd8αα+ unconventional t cells enriched in liver use a cytotoxic mechanism to limit autoimmunity. The Journal of Immunology, 203(8), 2150-2162. doi:10.4049/jimmunol.1900832 — Learn More

  • Maricic, I., Marrero, I., Eguchi, A., Nakamura, R., Johnson, C. D., Dasgupta, S., . . . Kumar, V. (2018). Differential activation of hepatic invariant nkt cell subsets plays a key role in progression of nonalcoholic steatohepatitis. The Journal of Immunology, 201(10), 3017-3035. doi:10.4049/jimmunol.1800614 — Learn More

  • Cerignoli, F., Abassi, Y. A., Lamarche, B. J., Guenther, G., Santa Ana, D., Guimet, D., . . . Xi, B. (2018). In vitro immunotherapy potency assays using real-time cell analysis. PLOS ONE, 13(3). doi:10.1371/journal.pone.0193498 – Learn More

  • Pryke, K. M., Abraham, J., Sali, T. M., Gall, B. J., Archer, I., Liu, A., . . . DeFilippis, V. R. (2017). A novel agonist of the trif pathway induces a cellular state refractory to replication of zika, chikungunya, and dengue viruses. MBio, 8(3). doi:10.1128/mbio.00452-17 — Learn More

  • Nomanbhoy, T. K. (2017). CHEMOPROTEOMIC evaluation of target engagement in clinical samples. Cancer Chemistry. doi:10.1158/1538-7445.am2017-225 — Learn More
  • Annina Stuber, Anna Cavaccini, Andreea Manole,  Anna Burdina,Yassine Massoud, Tommaso Patriarchi, Theofanis Karayannis, and Nako Nakatsuka 
    (2023). Interfacing Aptamer-Modified Nanopipettes with Neuronal Media and Ex Vivo Brain Tissue — Learn More
  • Wong, J. K., Roselle, A. K., Shue, T. M., Shimshak, S. J., Beaty, J. M., Celestin, N. M., Gao, I., Griffin, R. P., Cudkowicz, M. E., & Sadiq, S. A. (2022). Apolipoprotein B-100-mediated motor neuron degeneration in sporadic amyotrophic lateral sclerosis. Brain Communications, 4(4). https://doi.org/10.1093/braincomms/fcac207 — Learn More
  • Liu B, Li M, Zhang L, Chen Z, Lu P. (2022). Motor neuron replacement therapy for amyotrophic lateral sclerosis. Neural Regen Res;17:1633-9 — Learn More
  • Liu, Y., Dodart, J., Tran, H., Berkovitch, S., Braun, M., Byrne, M., . . . Brown, R. H. (2021). Variant-selective stereopure oligonucleotides protect against pathologies associated with c9orf72-repeat expansion in preclinical models. Nature Communications, 12(1). doi:10.1038/s41467-021-21112-8 — Learn More
  • Shen, X., Beasley, S., Putman, J. N., Li, Y., Prakash, T. P., Rigo, F., . . . Corey, D. R. (2019). Efficient electroporation of neuronal cells using synthetic oligonucleotides: Identifying duplex RNA and antisense oligonucleotide activators of Human frataxin expression. RNA, 25(9), 1118-1129. doi:10.1261/rna.071290.119 — Learn More
  • Gasset-Rosa, F., Lu, S., Yu, H., Chen, C., Melamed, Z., Guo, L., . . . Cleveland, D. W. (2019). Cytoplasmic TDP-43 de-mixing independent of stress granules drives inhibition of nuclear import, loss of nuclear TDP-43, and cell death. Neuron, 102(2). doi:10.1016/j.neuron.2019.02.038 — Learn More
  • Martier, R., Liefhebber, J. M., García-Osta, A., Miniarikova, J., Cuadrado-Tejedor, M., Espelosin, M., . . . Konstantinova, P. (2019). Targeting rna-mediated toxicity in c9orf72 als and/or ftd by rnai-based gene therapy. Molecular Therapy – Nucleic Acids, 16, 26-37. doi:10.1016/j.omtn.2019.02.001 — Learn More
  • Melamed, Z., López-Erauskin, J., Baughn, M. W., Zhang, O., Drenner, K., Lin, N., Wu, D., . . . Cleveland, D. W. (2019). Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of tdp-43-dependent neurodegeneration. Nature Neuroscience, 22(2), 180-190. doi:10.1038/s41593-018-0293-z — Learn More
  • Marei, H. E., Althani, A., Lashen, S., Cenciarelli, C., & Hasan, A. (2017). Genetically unmatched human Ipsc and Esc Exhibit Equivalent gene expression and neuronal differentiation potential. Scientific Reports, 7(1). doi:10.1038/s41598-017-17882-1 — Learn More
  • Danziger, S. A., Miller, L. R., Singh, K., Whitney, G. A., Peskind, E. R., Li, G., . . . Smith, J. J. (2017). An indicator cell assay for blood-based diagnostics. PLOS ONE, 12(6). doi:10.1371/journal.pone.0178608 — Learn More
    • Annina Stuber, Anna Cavaccini, Andreea Manole,  Anna Burdina,Yassine Massoud, Tommaso Patriarchi, Theofanis Karayannis, and Nako Nakatsuka 
      (2023). Interfacing Aptamer-Modified Nanopipettes with Neuronal Media and Ex Vivo Brain Tissue — Learn More

  • Okita K, Matsumura Y, Sato Y, Okada A, Morizane A, Okamoto S, Hong H, Nakagawa M, Tanabe K, Tezuka K, Shibata T, Kunisada T, Takahashi M, Takahashi J, Saji H, Yamanaka S. A more efficient method to generate integration-free human iPS cells. Nature Methods. 2011 May; 8(5):409-12. — Learn More

  • Marei, H. E., Althani, A., Afifi, N., Hasan, A., Caceci, T., Pozzoli, G., & Cenciarelli, C. (2021). Generation of gene edited hipsc from familial alzheimer’s disease patient carrying N141I missense mutation in Presenilin 2. Stem Cell Research, 56, 102552. https://doi.org/10.1016/j.scr.2021.102552 — Learn More

  • Dong, X., Chen, Y., Lu, J., Huang, S., & Pei, G. (2022). Β-arrestin 2 and EPAC2 cooperatively mediate DRD1-stimulated proliferation of human neural stem cells and growth of human cerebral organoids. Stem Cells. https://doi.org/10.1093/stmcls/sxac046 — Learn More

  • Huang, M., Wang, X., Banerjee, M., Mukherji, S. T., Kutz, L. C., Zhao, A., Sepanski, M., Fan, C.-M., Zhu, G.-Z., Tian, J., Wang, D.-Z., Zhu, H., Xie, Z.-J., Pierre, S. V., & Cai, L. (2022). Regulation of myogenesis by a na/K-atpase α1 caveolin binding motif. Stem Cells. https://doi.org/10.1093/stmcls/sxab012 — Learn More

  • Huang, S., Huang, F., Zhang, H., Yang, Y., Lu, J., Chen, J., Shen, L., & Pei, G. (2022). In vivo development and single‐cell transcriptome profiling of human brain organoids. Cell Proliferation. https://doi.org/10.1111/cpr.13201 — Learn More

  • Wang, X., Cai, L., Xie, J. X., Cui, X., Zhang, J., Wang, J., . . . Xie, Z. (2020). A caveolin Binding motif in Na/K-ATPase is required for stem cell differentiation and organogenesis in mammals andc.elegans. Science Advances, 6(22). doi:10.1126/sciadv.aaw5851 — Learn More

  • Hilary Sherman & Hannah J. Gitschier. (2019). A Novel Method for Generating Single, Intestinal Organoids for High Throughput Screening. Corning Application Note — Learn More

  • Gasset-Rosa, F., Lu, S., Yu, H., Chen, C., Melamed, Z., Guo, L., . . . Cleveland, D. W. (2019). Cytoplasmic TDP-43 De-mixing independent of Stress Granules Drives inhibition of NUCLEAR IMPORT, loss of Nuclear TDP-43, and cell death. Neuron, 102(2). doi:10.1016/j.neuron.2019.02.038 — Learn More

  • Gao, X., Sprando, R. L., & Yourick, J. J. (2018). A rapid and highly efficient method for the Isolation, purification, and Passaging of Human-Induced pluripotent stem cells. Cellular Reprogramming, 20(5), 282-288. doi:10.1089/cell.2018.0022 — Learn More

  • Marei, H. E., Althani, A., Lashen, S., Cenciarelli, C., & Hasan, A. (2017). Genetically unmatched human Ipsc and Esc Exhibit Equivalent gene expression and neuronal differentiation potential. Scientific Reports, 7(1). doi:10.1038/s41598-017-17882-1 — Learn More

  • Gao, X., Yourick, J. J., & Sprando, R. L. (2017). Comparative transcriptomic analysis of endothelial progenitor cells derived from umbilical cord blood and adult peripheral blood: Implications for the generation of induced pluripotent stem cells. Stem Cell Research, 25, 202-212. doi:10.1016/j.scr.2017.11.004 — Learn More

  • Ewart, L., Apostolou, A., Briggs, S. A., Carman, C. V., Chaff, J. T., Heng, A. R., Jadalannagari, S., Janardhanan, J., Jang, K.-J., Joshipura, S. R., Kadam, M. M., Kanellias, M., Kujala, V. J., Kulkarni, G., Le, C. Y., Lucchesi, C., Manatakis, D. V., Maniar, K. K., Quinn, M. E., … Levner, D. (2022). Performance assessment and economic analysis of a human liver-chip for predictive toxicology. Communications Medicine, 2(1). doi:10.1038/s43856-022-00209-1 Learn More

  • Zhou, J., Cui, S., He, Q., Guo, Y., Pan, X., Zhang, P., . . . Hao, H. (2020). SUMOylation inhibitors synergize with fxr Agonists in Combating liver fibrosis. Nature Communications, 11(1). doi:10.1038/s41467-019-14138-6 — Learn More

  • Bestion, E., Jilkova, Z. M., Mège, J., Novello, M., Kurma, K., Pour, S. T., . . . Brun, S. (2020). GNS561 acts as a Potent ANTI-FIBROTIC and pro-fibrolytic agent in liver Fibrosis THROUGH tgf-β1 inhibition. Therapeutic Advances in Chronic Disease, 11, 204062232094204. doi:10.1177/2040622320942042 — Learn More

  • Kim, J. H., Lee, C. H., & Lee, S. (2019). Exosomal transmission of microrna from hcv replicating cells stimulates transdifferentiation in hepatic stellate cells. Molecular Therapy – Nucleic Acids, 14, 483-497. doi:10.1016/j.omtn.2019.01.006 — Learn More

  • Pham, T. X., Bae, M., Kim, M., Lee, Y., Hu, S., Kang, H., . . . Lee, J. (2019). Nicotinamide riboside, an nad+ precursor, attenuates the development of liver fibrosis in a diet-induced mouse model of liver fibrosis. Biochimica Et Biophysica Acta (BBA) – Molecular Basis of Disease, 1865(9), 2451-2463. doi:10.1016/j.bbadis.2019.06.009 — Learn More

  • Ehrlich, A., Duche, D., Ouedraogo, G., & Nahmias, Y. (2019). Challenges and opportunities in the design Of LIVER-ON-CHIP Microdevices. Annual Review of Biomedical Engineering, 21(1), 219-239. doi:10.1146/annurev-bioeng-060418-052305 — Learn More

  • Prestigiacomo, V., & Suter-Dick, L. (2018). Nrf2 protects stellate cells FROM SMAD-DEPENDENT cell activation. PLOS ONE, 13(7). doi:10.1371/journal.pone.0201044 — Learn More

  • Kotula-Balak, M., Gorowska-Wojtowicz, E., Milon, A., Pawlicki, P., Tworzydlo, W., Płachno, B. J., . . . Bilinska, B. (2020). Towards understanding leydigioma: Do g protein-coupled estrogen receptor and peroxisome proliferator–activated receptor regulate lipid metabolism and steroidogenesis in leydig cell tumors? Protoplasma, 257(4), 1149-1163. doi:10.1007/s00709-020-01488-y — Learn More

  • Duliban, M., Gorowska-Wojtowicz, E., Tworzydlo, W., Rak, A., Brzoskwinia, M., Krakowska, I., . . . Bilinska, B. (2020). Interstitial leydig cell tumorigenesis—leptin and adiponectin signaling in relation to aromatase expression in the human testis. International Journal of Molecular Sciences, 21(10), 3649. doi:10.3390/ijms21103649 – Learn More

  • Strange, D. P., Jiyarom, B., Pourhabibi Zarandi, N., Xie, X., Baker, C., Sadri-Ardekani, H., . . . Verma, S. (2019). Axl promotes zika virus entry and modulates the antiviral state of human sertoli cells. MBio, 10(4). doi:10.1128/mbio.01372-19 — Learn More

  • Gorowska-Wojtowicz, E., Duliban, M., Kudrycka, M., Dutka, P., Pawlicki, P., Milon, A., . . . Bilinska, B. (2019). Leydig cell tumorigenesis – implication of g-protein coupled membrane estrogen receptor, peroxisome proliferator-activated receptor and xenoestrogen exposure. in vivo and in vitro appraisal. Tissue and Cell, 61, 51-60. doi:10.1016/j.tice.2019.08.001 — Learn More

  • Kotula-Balak, M., Gorowska-Wojtowicz, E., Milon, A., Pawlicki, P., Kaminska, A., Pardyak, L., . . . Wolski, J. K. (2018). Towards understanding biology of leydiogioma. g protein-coupled receptor and peroxisome proliferator-activated receptor crosstalk regulates lipid metabolism and steroidogenesis in leydig cell tumors. BioRxiv. doi:10.1101/477901 — Learn More

  • Alghamri, M. S., Banerjee, K., Mujeeb, A. A., Mauser, A., Taher, A., Thalla, R., McClellan, B. L., Varela, M. L., Stamatovic, S. M., Martinez-Revollar, G., Andjelkovic, A. V., Gregory, J. V., Kadiyala, P., Calinescu, A., Jiménez, J. A., Apfelbaum, A. A., Lawlor, E. R., Carney, S., Comba, A., … Castro, M. G. (2022). Systemic delivery of an adjuvant CXCR4–CXCL12 signaling inhibitor encapsulated in synthetic protein nanoparticles for glioma immunotherapy. ACS Nano, 16(6), 8729–8750. https://doi.org/10.1021/acsnano.1c07492 — Learn More

  • Ranjan, N., Pandey, V., Panigrahi, M. K., Klumpp, L., Naumann, U., & Babu, P. P. (2021). The Tumor Suppressor MTUS1/ATIP1 Modulates Tumor Promotion in Glioma: Association with Epigenetics and DNA Repair. Cancers, 13(6), 1245. — Learn More

  • Shima, A., Nagata, S., & Takeuchi, S. (2020). Three-dimensional co-culture of BLOOD-BRAIN BARRIER-COMPOSING cells in a culture insert with A COLLAGEN Vitrigel membrane. In Vitro Cellular & Developmental Biology – Animal, 56(7), 500-504. doi:10.1007/s11626-020-00486-x — Learn More

  • Cui, X., Ma, C., Vasudevaraja, V., Serrano, J., Tong, J., Peng, Y., . . . Chen, W. (2020). Dissecting the immunosuppressive tumor microenvironments in glioblastoma-on-a-chip for optimized pd-1 immunotherapy. ELife, 9. doi:10.7554/elife.52253 — Learn More

  • Heo, J., Kim, J., Woo, S., Kim, K., Choi, K., Lee, H., & Kim, K. (2019). Stromal Cell-Derived factor 1 PROTECTS Brain vascular endothelial cells FROM radiation-induced brain damage. Cells, 8(10), 1230. doi:10.3390/cells8101230 — Learn More

  • Hunter, L. W., Jayachandran, M., & Miller, V. M. (2019). Sex differences in the expression of cell adhesion molecules on microvesicles derived from cultured human brain microvascular endothelial cells treated with inflammatory and thrombotic stimuli. Biology of Sex Differences, 10(1). doi:10.1186/s13293-019-0241-y — Learn More

  • Ozek, C., Krolewski, R. C., Buchanan, S. M., & Rubin, L. L. (2018). Growth differentiation FACTOR 11 treatment leads to neuronal and Vascular improvements in the hippocampus of aged mice. Scientific Reports, 8(1). doi:10.1038/s41598-018-35716-6 — Learn More

  • Laiva, A. L., O’Brien, F. J., & Keogh, M. B. (2021). SDF-1α Gene-Activated Collagen Scaffold RESTORES pro-angiogenic wound HEALING features in Human Diabetic Adipose-derived stem cells. Biomedicines, 9(2), 160. doi:10.3390/biomedicines9020160 — Learn More

  • Suku, M., Laiva, A. L., O’Brien, F. J., & Keogh, M. B. (2021). Anti-ageing protein β-klotho rejuvenates diabetic stem cells for improved gene-activated scaffold based wound healing. Journal of Personalized Medicine, 11(1), 4. doi:10.3390/jpm11010004 — Learn More

  • Das, R., Curry, E. J., Le, T. T., Awale, G., Liu, Y., Li, S., . . . Nguyen, T. D. (2020). Biodegradable nanofiber bone-tissue scaffold as remotely-controlled and self-powering electrical stimulator. Nano Energy, 76, 105028. doi:10.1016/j.nanoen.2020.105028 — Learn More

  • Srifa, W., Kosaric, N., Amorin, A., Jadi, O., Park, Y., Mantri, S., . . . Porteus, M. (2020). Cas9-aav6-engineered human mesenchymal stromal cells improved cutaneous wound healing in diabetic mice. Nature Communications, 11(1). doi:10.1038/s41467-020-16065-3 — Learn More

  • Li, Y., Zhao, Z., Lin, C., Liu, Y., Staveley-OCarroll, K. F., Li, G., & Cheng, K. (2021). Silencing PCBP2 NORMALIZES Desmoplastic stroma and improves the antitumor activity of chemotherapy in pancreatic cancer. Theranostics, 11(5), 2182-2200. doi:10.7150/thno.53102 — Learn More

  • Li, Y., Zhao, Z., Liu, H., Fetse, J. P., Jain, A., Lin, C., & Cheng, K. (2019). Development of a Tumor-Responsive Nanopolyplex Targeting pancreatic cancer cells and Stroma. ACS Applied Materials & Interfaces, 11(49), 45390-45403. doi:10.1021/acsami.9b15116 — Learn More

  • Lee, S., Park, J., Lee, D., Otsu, K., Kim, P., Mizuno, S., . . . Jung, H. (2020). Mast4 knockout shows the regulation of spermatogonial stem cell self-renewal via the fgf2/erm pathway. Cell Death & Differentiation. doi:10.1038/s41418-020-00670-2 – Learn More

  • Strange, D. P., Jiyarom, B., Pourhabibi Zarandi, N., Xie, X., Baker, C., Sadri-Ardekani, H., . . . Verma, S. (2019). Axl promotes zika virus entry and modulates the antiviral state of human sertoli cells. MBio, 10(4). doi:10.1128/mbio.01372-19 — Learn More

  • Yan, X., Jia, H., & Zhao, J. (2023). LncRNA MEG3 attenuates the malignancy of retinoblastoma cells through inactivating PI3K /AKT/mtor signaling pathway. Experimental Eye Research, 226, 109340. doi:10.1016/j.exer.2022.109340 — Learn More
  • Vidak, M., Jovcevska, I., Samec, N., Zottel, A., Liovic, M., Rozman, D., . . . Komel, R. (2018). Meta-Analysis and experimental VALIDATION Identified Frem2 and SPRY1 as NEW Glioblastoma Marker Candidates. International Journal of Molecular Sciences, 19(5), 1369. doi:10.3390/ijms19051369 — Learn More

  • Al-Serori, H., Ferk, F., Kundi, M., Bileck, A., Gerner, C., Mišík, M., . . . Knasmüller, S. (2018). Mobile phone specific electromagnetic fields induce transient dna damage and nucleotide excision repair in serum-deprived human glioblastoma cells. PLOS ONE, 13(4). doi:10.1371/journal.pone.0193677 — Learn More

  • Hansen, M. H., Cédile, O., Blum, M. K., Hansen, S. V., Ebbesen, L. H., Bentzen, H. H., . . . Nyvold, C. G. (2020). Molecular characterization of sorted malignant b cells from patients clinically identified with mantle cell lymphoma. Experimental Hematology, 84. doi:10.1016/j.exphem.2020.03.001 — Learn More

  • Van Gent, M., Reich, A., Velu, S. E., & Gack, M. U. (2021). Nonsense-mediated decay controls the reactivation of the oncogenic herpesviruses EBV And kshv. PLOS Biology, 19(2). doi:10.1371/journal.pbio.3001097 – Learn More

  • Biswas, S., Shahriar, S., Giangreco, N. P., Arvanitis, P., Winkler, M., Tatonetti, N. P., Brunken, W. J., Cutforth, T., & Agalliu, D. (2022). Mural Norrin/β-catenin signaling regulates Lama2 expression to promote neurovascular unit assembly. https://doi.org/10.1101/2022.02.18.481046 — Learn More

  • Lee, S. J., Kim, S., Jo, D. H., Cho, C. S., Kim, S. R., Kang, D., Chae, J., Yoo, D. K., Ha, S., Chung, J., & Kim, J. H. (2021). Specific ablation of pdgfrβ-overexpressing pericytes with antibody-drug conjugate potently inhibits pathologic ocular neovascularization in mouse models. Communications Medicine, 1(1). https://doi.org/10.1038/s43856-021-00059-3 — Learn More

  • Kaushik, D. K., Bhattacharya, A., Lozinski, B. M., & Wee Yong, V. (2021). Pericytes as mediators of infiltration of macrophages in multiple sclerosis. Journal of Neuroinflammation, 18(1). https://doi.org/10.1186/s12974-021-02358-x — Learn More

  • Bonney, S., Seitz, S., Ryan, C. A., Jones, K. L., Clarke, P., Tyler, K. L., & Siegenthaler, J. A. (2019). Gamma interferon ALTERS Junctional Integrity via Rho Kinase, resulting in blood-brain Barrier leakage in experimental viral encephalitis. MBio, 10(4). doi:10.1128/mbio.01675-19 — Learn More

  • Grant, S., McMillin, M., Frampton, G., Petrescu, A. D., Williams, E., Jaeger, V., . . . DeMorrow, S. (2018). Direct comparison of the Thioacetamide And Azoxymethane models of type A hepatic encephalopathy in mice. Gene Expression, 18(3), 171-185. doi:10.3727/105221618×15287315176503 — Learn More

  • Zhao, Y., Lee, C. K., Lin, C., Gassen, R. B., Xu, X., Huang, Z., . . . Hui, E. (2019). Pd-l1:cd80 cis-heterodimer triggers the co-stimulatory receptor cd28 while repressing the inhibitory pd-1 and ctla-4 pathways. Immunity, 51(6). doi:10.1016/j.immuni.2019.11.003 — Learn More

  • Cho, H., Seo, Y., Loke, K. M., Kim, S., Oh, S., Kim, J., . . . Williams, D. R. (2018). Cancer-Stimulated cafs Enhance MONOCYTE differentiation AND Protumoral TAM activation via IL6 AND GM-CSF SECRETION. Clinical Cancer Research, 24(21), 5407-5421. doi:10.1158/1078-0432.ccr-18-0125 — Learn More

  • Hunt, R. C., Katneni, U., Yalamanoglu, A., Indig, F. E., Ibla, J. C., & Kimchi‐Sarfaty, C. (2022). Contribution of adamts13 ‐independent vwf regulation in sickle cell disease. Journal of Thrombosis and Haemostasis. https://doi.org/10.1111/jth.15804 — Learn More

  • Laiva, A. L., O’Brien, F. J., & Keogh, M. B. (2021). SDF-1α Gene-Activated Collagen Scaffold RESTORES pro-angiogenic wound HEALING features in Human Diabetic Adipose-derived stem cells. Biomedicines, 9(2), 160. doi:10.3390/biomedicines9020160 — Learn More

  • Shen, L., Hu, Y., Lou, J., Yin, S., Wang, W., Wang, Y., . . . Wu, W. (2019). CircRNA‑0044073 is upregulated in atherosclerosis and increases the proliferation and invasion of cells by TARGETING MIR‑107. Molecular Medicine Reports. doi:10.3892/mmr.2019.10011 — Learn More

  • Suku, M., Laiva, A. L., O’Brien, F. J., & Keogh, M. B. (2021). Anti-ageing protein β-klotho rejuvenates diabetic stem cells for improved gene-activated scaffold based wound healing. Journal of Personalized Medicine, 11(1), 4. doi:10.3390/jpm11010004 — Learn More

  • Laiva, A. L., O’Brien, F. J., & Keogh, M. B. (2021). SDF-1α Gene-Activated Collagen Scaffold RESTORES pro-angiogenic wound HEALING features in Human Diabetic Adipose-derived stem cells. Biomedicines, 9(2), 160. doi:10.3390/biomedicines9020160 — Learn More

  • Koo, J., Jang, H., Lee, Y., Moon, Y. J., Bae, E. J., Yun, S., & Park, B. (2019). Myeloid cell-specific sirtuin 6 DEFICIENCY delays wound healing in mice by Modulating inflammation and Macrophage phenotypes. Experimental & Molecular Medicine, 51(4), 1-10. doi:10.1038/s12276-019-0248-9 — Learn More

  • Wang, Z., Mascarenhas, N., Eckmann, L., Miyamoto, Y., Sun, X., Kawakami, T., & Di Nardo, A. (2017). Skin microbiome promotes mast cell maturation by triggering stem cell factor production in keratinocytes. Journal of Allergy and Clinical Immunology, 139(4). doi:10.1016/j.jaci.2016.09.019 — Learn More

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