Publications Acknowledging GEC Support

The UW-Madison Biotechnology Center is currently open and following the university’s COVID-19 Response regarding campus operations.


A visible measure of a core’s impact is made through proper acknowledgement of usage in publications. If you publish data generated via services provided by the GEC, please include a statement acknowledging our contribution.

The following is an incomplete list of publications acknowledging GEC support from 2010 to the present. If you see your publication(s) missing from this list, please notify us at!

  1. Carlson KN et al. Interleukin-10 and Transforming Growth Factor-β cytokines decrease immune activation during normothermic ex vivo machine perfusion of the rat liver. (Liver Transplantation, 2021)
  2. Yang H et al. Single-cell RNA sequencing reveals heterogeneity of vascular cells in early stage murine abdominal aortic aneurysm – brief report. (Arteriosclerosis, Thrombosis, and Vascular Biology, 2021)
  3. Song HW et al. Transcriptomic comparison of human and mouse brain microvessels. (Nature Scientific Reports, 2020)
  4. Simonson L et al. Keratin 13 deficiency causes white sponge nevus in mice. (Developmental Biology, 2020)
  5. Vera JM et al. Genome-Scale Transcription-Translation Mapping Reveals Features of Zymomonas mobilis Transcription Units and Promoters. (mSystems, 2020)
  6. Lee H et al. Beta Cell Dedifferentiation Induced by IRE1α Deletion Prevents Type 1 Diabetes. (Cell Metabolism, 2020)
  7. Stebbins MJ et al. Human Pluripotent Stem Cell-Derived Brain Pericyte-Like Cells Induce Blood-Brain Barrier Properties. (Science Advances, 2019)
  8. Svaren J et al. Schwann cell transcript biomarkers for hereditary neuropathy skin biopsies. (Annals of Neurology, 2019)
  9. Wu MY et al. Systematic Dissection of the Evolutionarily Conserved WetA Developmental Regulator across a Genus of Filamentous Fungi. (mBio, 2018)
  10. Scarborough MJ et al. Metatranscriptomic and Thermodynamic Insights into Medium-Chain Fatty Acid Production Using an Anaerobic Microbiome. (mSystems, 2018)
  11. Rytz TC et al. SUMOylome Profiling Reveals a Diverse Array of Nuclear Targets Modified by the SUMO Ligase SIZ1 during Heat Stress. (The Plant Cell, 2018)
  12. Reinhart JM et al. RNA expression profiling in sulfamethoxazole-treated patients with a range of in vitro lymphocyte cytotoxicity phenotypes. (Pharmacology Research and Perspectives, 2018)
  13. Ma KH et al. Polycomb repression regulates Schwann cell proliferation and axon regeneration after nerve injury. (Glia, 2018)
  14. McCulley DJ et al. PBX transcription factors drive pulmonary vascular adaptation to birth. (The Journal of Clinical Investigation, 2018)
  15. Gladman NP et al. The proteasome stress regulon is controlled by a pair of NAC transcription factors in Arabidopsis. (The Plant Cell, 2016)
  16. Saul MC et al. MicroRNA expression is altered in lateral septum across reproductive stages. (Neuroscience, 2016)
  17. de Sá Rodrigues LC et al. Osteosarcoma tissues and cell lines from patients with differing serum alkaline phosphatase concentrations display minimal differences in gene expression patterns. (Veterinary and Comparative Oncology, 2015)
  18. Driessen TM et al. Genes showing altered expression in the medial preoptic area in the highly social maternal phenotype are related to autism and other disorders with social deficits. (BMC Neuroscience, 2014)
  19. Kim EH et al. Bach2 regulates homeostasis of Foxp3+ regulatory T cells and protects against fatal lung disease in mice. (Journal of Immunology, 2014)
  20. Kawakami-Schulz SV et al. Serum response factor: positive and negative regulation of an epithelial gene expression network in the destrin mutant cornea. (Physiological Genomics, 2014)
  21. Choi YJ et al. Dual RNA-seq of parasite and host reveals gene expression dynamics during filarial worm-mosquito interactions. (PLoS Neglected Tropical Diseases, 2014)
  22. Porras AM et al. Gene expression profiling of valvular interstitial cells in Rapacz familial hypercholesterolemic swine. (Genomics Data, 2014)
  23. Zhao C et al. Addiction and reward-related genes show altered expression in the postpartum nucleus accumbens. (Frontiers in Behavioral Neuroscience, 2014)
  24. Piccinato CA et al. Estradiol and progesterone exhibit similar patterns of hepatic gene expression regulation in the bovine model. (PLoS One, 2013)
  25. Esnault S et al. Identification of genes expressed by human airway eosinophils after an in vivo allergen challenge. (PLoS One, 2013)
  26. Zhan L et al. Identification of genetic modifiers of TDP-43 neurotoxicity in Drosophila. (PLoS One, 2013)
  27. Park JJ et al. Cell-specific gene expression in Anabaena variabilis grown phototrophically, mixotrophically, and heterotrophically. (BMC Genomics, 2013)
  28. Rose CM et al. Rapid phosphoproteomic and transcriptomic changes in the rhizobia-legume symbiosis. (Molecular & Cellular Proteomics, 2012)
  29. Kruzel EK et al. Analysis of Cryptococcus neoformans sexual development reveals rewiring of the pheromone-response network by a change in transcription factor identity. (Genetics, 2012)
  30. Kim EH et alSignal integration by Akt regulates CD8 T cell effector and memory differentiation. (Journal of Immunology, 2012)
  31. Zhao C et al. Gene expression changes in the septum: possible implications for microRNAs in sculpting the maternal brain. (PLoS One, 2012)
  32. Bochkov YA et al. Rhinovirus-induced modulation of gene expression in bronchial epithelial cells from subjects with asthma. (Mucosal Immunology, 2010)
  33. Wagoner MP et al. The transcription factor REST is lost in aggressive breast cancer. (PLoS Genetics, 2010)
  34. Metallo CM et al. Human embryonic stem cell-derived keratinocytes exhibit an epidermal transcription program and undergo epithelial morphogenesis in engineered tissue constructs. (Tissue Engineering Part A, 2010)
  35. Kershner AM and Kimble J. Genome-wide analysis of mRNA targets for Caenorhabditis elegans FBF, a conserved stem cell regulator. (PNAS, 2010)

All data and services provided by the University of Wisconsin Biotechnology Center Gene Expression Center are intended for research purposes only. Services are not intended nor certified for diagnostic or clinical use.