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2. Population screening shows risk of inherited cancer and familial hypercholesterolemia in Oregon

Author

O’Brien, Timothy D., Potter, Amiee B., Driscoll, Catherine C., Goh, Gregory, Letaw, John H., McCabe, Sarah, Thanner, Jane, Kulkarni, Arpita, Wong, Rossana, Medica, Samuel, Week, Tiana, Buitrago, Jacob, Larson, Aaron, Camacho, Katie Johnson, Brown, Kim, Crist, Rachel, Conrad, Casey, Evans-Dutson, Sara, Lutz, Ryan, Mitchell, Asia, Anur, Pavana, Serrato, Vanessa, Shafer, Autumn, Marriott, Lisa K., Hamman, K.J., Mulford, Amelia, Wiszniewski, Wojciech, Sampson, Jone E., Adey, Andrew, O’Roak, Brian J., Harrington, Christina A., Shannon, Jackilen, Spellman, Paul T., and Richards, C. Sue

Published
2023
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3. Clinically available immunosuppression averts rejection but not systemic inflammation after porcine islet xenotransplant in cynomolgus macaques

Author

Graham, Melanie L., Ramachandran, Sabarinathan, Singh, Amar, Moore, Meghan E.G., Flanagan, E. Brian, Azimzadeh, Agnes, Burlak, Christopher, Mueller, Kate R., Martins, Kyra, Anazawa, Takayuki, Appakalai, Balamurugan N., Bansal-Pakala, Pratima, Murtaugh, Michael P., O’Brien, Timothy D., Papas, Klearchos K., Spizzo, Thomas, Schuurman, Henk-J., Hancock, Wayne W., and Hering, Bernhard. J.

Published
2022
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5. FIGURE 5 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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6. FIGURE 2 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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7. Supplementary Figure S2 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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8. FIGURE 3 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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9. Supplementary Table S5 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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10. FIGURE 4 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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11. FIGURE 1 from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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12. Data from Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, primary, Schulte, Ashley J., primary, Sarver, Aaron L., primary, Lee, Donghee, primary, Angelos, Mathew G., primary, Frantz, Aric M., primary, Forster, Colleen L., primary, O'Brien, Timothy D., primary, Cornax, Ingrid, primary, O'Sullivan, M. Gerard, primary, Cheng, Nuojin, primary, Lewellen, Mitzi, primary, Oseth, LeAnn, primary, Kumar, Sunil, primary, Bullman, Susan, primary, Pedamallu, Chandra Sekhar, primary, Goyal, Sagar M., primary, Meyerson, Matthew, primary, Lund, Troy C., primary, Breen, Matthew, primary, Lindblad-Toh, Kerstin, primary, Dickerson, Erin B., primary, Kaufman, Dan S., primary, and Modiano, Jaime F., primary

Published
2024
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13. Development of an exosomal gene signature to detect residual disease in dogs with osteosarcoma using a novel xenograft platform and machine learning

Author

Makielski, Kelly M., Donnelly, Alicia J., Khammanivong, Ali, Scott, Milcah C., Ortiz, Andrea R., Galvan, Dana C., Tomiyasu, Hirotaka, Amaya, Clarissa, Ward, Kristin A., Montoya, Alexa, Garbe, John R., Mills, Lauren J., Cutter, Gary R., Fenger, Joelle M., Kisseberth, William C., O'Brien, Timothy D., Weigel, Brenda J., Spector, Logan G., Bryan, Brad A., Subramanian, Subbaya, and Modiano, Jaime F.

Published
2021
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14. Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion

Author

Kim, Jong Hyuk, Schulte, Ashley J., Sarver, Aaron L., Lee, Donghee, Angelos, Mathew G., Frantz, Aric M., Forster, Colleen L., O'Brien, Timothy D., Cornax, Ingrid, O'Sullivan, M. Gerard, Cheng, Nuojin, Lewellen, Mitzi, Oseth, LeAnn, Kumar, Sunil, Bullman, Susan, Pedamallu, Chandra Sekhar, Goyal, Sagar M., Meyerson, Matthew, Lund, Troy C., Breen, Matthew, Lindblad-Toh, Kerstin, Dickerson, Erin B., Kaufman, Dan S., Modiano, Jaime F., Kim, Jong Hyuk, Schulte, Ashley J., Sarver, Aaron L., Lee, Donghee, Angelos, Mathew G., Frantz, Aric M., Forster, Colleen L., O'Brien, Timothy D., Cornax, Ingrid, O'Sullivan, M. Gerard, Cheng, Nuojin, Lewellen, Mitzi, Oseth, LeAnn, Kumar, Sunil, Bullman, Susan, Pedamallu, Chandra Sekhar, Goyal, Sagar M., Meyerson, Matthew, Lund, Troy C., Breen, Matthew, Lindblad-Toh, Kerstin, Dickerson, Erin B., Kaufman, Dan S., and Modiano, Jaime F.

Abstract

Hemangiosarcoma and angiosarcoma are soft-tissue sarcomas of blood vessel-forming cells in dogs and humans, respectively. These vasoformative sarcomas are aggressive and highly metastatic, with disorganized, irregular blood-filled vascular spaces. Our objective was to define molecular programs which support the niche that enables progression of canine hemangiosarcoma and human angiosarcoma. Dog-in-mouse hemangiosarcoma xenografts recapitulated the vasoformative and highly angiogenic morphology and molecular characteristics of primary tumors. Blood vessels in the tumors were complex and disorganized, and they were lined by both donor and host cells. In a series of xenografts, we observed that the transplanted hemangiosarcoma cells created exuberant myeloid hyperplasia and gave rise to lymphoproliferative tumors of mouse origin. Our functional analyses indicate that hemangiosarcoma cells generate a microenvironment that supports expansion and differentiation of hematopoietic progenitor populations. Furthermore, gene expression profiling data revealed hemangiosarcoma cells expressed a repertoire of hematopoietic cytokines capable of regulating the surrounding stromal cells. We conclude that canine hemangiosarcomas, and possibly human angiosarcomas, maintain molecular properties that provide hematopoietic support and facilitate stromal reactions, suggesting their potential involvement in promoting the growth of hematopoietic tumors.Significance: We demonstrate that hemangiosarcomas regulate molecular programs supporting hematopoietic expansion and differentiation, providing insights into their potential roles in creating a permissive stromal-immune environment for tumor progression.

Published
2024
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15. A bioengineered artificial interstitium supports long-term islet xenograft survival in nonhuman primates without immunosuppression

Author

Oppler, Scott H., primary, Hocum Stone, Laura L., additional, Leishman, David J., additional, Janecek, Jody L., additional, Moore, Meghan E. G., additional, Rangarajan, Parthasarathy, additional, Willenberg, Bradley J., additional, O’Brien, Timothy D., additional, Modiano, Jaime, additional, Pheil, Natan, additional, Dalton, Jordan, additional, Dalton, Michael, additional, Ramachandran, Sabarinathan, additional, and Graham, Melanie L., additional

Published
2024
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16. Proteomic Analysis of Highly Prevalent Amyloid A Amyloidosis Endemic to Endangered Island Foxes

Author

Gaffney, Patricia M, Imai, Denise M, Clifford, Deana L, Ghassemian, Majid, Sasik, Roman, Chang, Aaron N, O’Brien, Timothy D, Coppinger, Judith, Trejo, Margarita, Masliah, Eliezer, Munson, Linda, and Sigurdson, Christina

Subjects
Analytical Chemistry, Biological Sciences, Chemical Sciences, Digestive Diseases, Neurodegenerative, Neurosciences, Amino Acid Sequence, Amyloidosis, Animals, Blood Vessels, California, Endangered Species, Female, Foxes, Islands, Kidney, Male, Molecular Sequence Data, Mouth, Prevalence, Proteomics, Reproductive Isolation, Serum Amyloid A Protein, Spleen, General Science & Technology
Abstract

Amyloid A (AA) amyloidosis is a debilitating, often fatal, systemic amyloid disease associated with chronic inflammation and persistently elevated serum amyloid A (SAA). Elevated SAA is necessary but not sufficient to cause disease and the risk factors for AA amyloidosis remain poorly understood. Here we identify an extraordinarily high prevalence of AA amyloidosis (34%) in a genetically isolated population of island foxes (Urocyon littoralis) with concurrent chronic inflammatory diseases. Amyloid deposits were most common in kidney (76%), spleen (58%), oral cavity (45%), and vasculature (44%) and were composed of unbranching, 10 nm in diameter fibrils. Peptide sequencing by mass spectrometry revealed that SAA peptides were dominant in amyloid-laden kidney, together with high levels of apolipoprotein E, apolipoprotein A-IV, fibrinogen-α chain, and complement C3 and C4 (false discovery rate ≤ 0.05). Reassembled peptide sequences showed island fox SAA as an 111 amino acid protein, most similar to dog and artic fox, with 5 unique amino acid variants among carnivores. SAA peptides extended to the last two C-terminal amino acids in 5 of 9 samples, indicating that near full length SAA was often present in amyloid aggregates. These studies define a remarkably prevalent AA amyloidosis in island foxes with widespread systemic amyloid deposition, a unique SAA sequence, and the co-occurrence of AA with apolipoproteins.

Published
2014

17. Abnormal infant islet morphology precedes insulin resistance in PCOS-like monkeys.

Author

Nicol, Lindsey E, O'Brien, Timothy D, Dumesic, Daniel A, Grogan, Tristan, Tarantal, Alice F, and Abbott, David H

Subjects
Islets of Langerhans, Animals, Macaca mulatta, Humans, Polycystic Ovary Syndrome, Insulin Resistance, Apoptosis, Cell Proliferation, Pregnancy, Infant, Female, Biomarkers, General Science & Technology
Abstract

Polycystic ovary syndrome (PCOS) is prevalent in reproductive-aged women and confounded by metabolic morbidities, including insulin resistance and type 2 diabetes. Although the etiology of PCOS is undefined, contribution of prenatal androgen (PA) exposure has been proposed in a rhesus monkey model as premenopausal PA female adults have PCOS-like phenotypes in addition to insulin resistance and decreased glucose tolerance. PA female infants exhibit relative hyperinsulinemia, suggesting prenatal sequelae of androgen excess on glucose metabolism and an antecedent to future metabolic disease. We assessed consequences of PA exposure on pancreatic islet morphology to identify evidence of programming on islet development. Islet counts and size were quantified and correlated with data from intravenous glucose tolerance tests (ivGTT) obtained from dams and their offspring. Average islet size was decreased in PA female infants along with corresponding increases in islet number, while islet fractional area was preserved. Infants also demonstrated an increase in both the proliferation marker Ki67 within islets and the beta to alpha cell ratio suggestive of enhanced beta cell expansion. PA adult females have reduced proportion of small islets without changes in proliferative or apoptotic markers, or in beta to alpha cell ratios. Together, these data suggest in utero androgen excess combined with mild maternal glucose intolerance alter infant and adult islet morphology, implicating deviant islet development. Marked infant, but subtle adult, morphological differences provide evidence of islet post-natal plasticity in adapting to changing physiologic demands: from insulin sensitivity and relative hypersecretion to insulin resistance and diminished insulin response to glucose in the mature PCOS-like phenotype.

Published
2014

26. Supplementary Figure S3 from Eradication of Canine Diffuse Large B-Cell Lymphoma in a Murine Xenograft Model with CD47 Blockade and Anti-CD20

Author

Weiskopf, Kipp, primary, Anderson, Katie L., primary, Ito, Daisuke, primary, Schnorr, Peter J., primary, Tomiyasu, Hirotaka, primary, Ring, Aaron M., primary, Bloink, Kristin, primary, Efe, Jem, primary, Rue, Sarah, primary, Lowery, David, primary, Barkal, Amira, primary, Prohaska, Susan, primary, McKenna, Kelly M., primary, Cornax, Ingrid, primary, O'Brien, Timothy D., primary, O'Sullivan, M. Gerard, primary, Weissman, Irving L., primary, and Modiano, Jaime F., primary

Published
2023
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27. Data from Eradication of Canine Diffuse Large B-Cell Lymphoma in a Murine Xenograft Model with CD47 Blockade and Anti-CD20

Author

Weiskopf, Kipp, primary, Anderson, Katie L., primary, Ito, Daisuke, primary, Schnorr, Peter J., primary, Tomiyasu, Hirotaka, primary, Ring, Aaron M., primary, Bloink, Kristin, primary, Efe, Jem, primary, Rue, Sarah, primary, Lowery, David, primary, Barkal, Amira, primary, Prohaska, Susan, primary, McKenna, Kelly M., primary, Cornax, Ingrid, primary, O'Brien, Timothy D., primary, O'Sullivan, M. Gerard, primary, Weissman, Irving L., primary, and Modiano, Jaime F., primary

Published
2023
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28. Supplementary Tables 1 through 3, Supplementary Figure Legends, and Supplementary Materials and Methods from Eradication of Canine Diffuse Large B-Cell Lymphoma in a Murine Xenograft Model with CD47 Blockade and Anti-CD20

Author

Weiskopf, Kipp, primary, Anderson, Katie L., primary, Ito, Daisuke, primary, Schnorr, Peter J., primary, Tomiyasu, Hirotaka, primary, Ring, Aaron M., primary, Bloink, Kristin, primary, Efe, Jem, primary, Rue, Sarah, primary, Lowery, David, primary, Barkal, Amira, primary, Prohaska, Susan, primary, McKenna, Kelly M., primary, Cornax, Ingrid, primary, O'Brien, Timothy D., primary, O'Sullivan, M. Gerard, primary, Weissman, Irving L., primary, and Modiano, Jaime F., primary

Published
2023
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29. Supplemental Table 3 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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30. Supplemental Table 6 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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31. Supplementary Data and Figures from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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32. Data from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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33. Supplemental Table 2 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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34. Supplemental Table 5 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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35. Supplemental Table 1 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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36. Supplemental Table 7 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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37. Supplemental Table 4 from Comparative Transcriptome Analysis Quantifies Immune Cell Transcript Levels, Metastatic Progression, and Survival in Osteosarcoma

Author

Scott, Milcah C., primary, Temiz, Nuri A., primary, Sarver, Anne E., primary, LaRue, Rebecca S., primary, Rathe, Susan K., primary, Varshney, Jyotika, primary, Wolf, Natalie K., primary, Moriarity, Branden S., primary, O'Brien, Timothy D., primary, Spector, Logan G., primary, Largaespada, David A., primary, Modiano, Jaime F., primary, Subramanian, Subbaya, primary, and Sarver, Aaron L., primary

Published
2023
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47. Coda

Author

O’Brien, Timothy D. and O’Brien, Timothy D.

Published
2010
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