Department of Pathology and Cell Biology

Displaying 751 - 800 of 1563CSV
Levy, B., Baughn, L. B., Akkari, Y., Chartrand, S., LaBarge, B., Claxton, D., Lennon, P. A., Cujar, C., Kolhe, R., Kroeger, K., Pitel, B., Sahajpal, N., Sathanoori, M., Vlad, G., Zhang, L., Fang, M., Kanagal-Shamanna, R., & Broach, J. R. (2023). Optical genome mapping in acute myeloid leukemia: a multicenter evaluation. Blood Advances, 7(7), 1297–1307. https://doi.org/10.1182/bloodadvances.2022007583
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Prieur, D. S., Francius, C., Gaspar, P., Mason, C. A., & Rebsam, A. (2023). Semaphorin-6D and Plexin-A1 Act in a Non–Cell-Autonomous Manner to Position and Target Retinal Ganglion Cell Axons. The Journal of Neuroscience, 43(32), 5769–5778. https://doi.org/10.1523/jneurosci.0072-22.2023
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Connors, T. J., Matsumoto, R., Verma, S., Szabo, P. A., Guyer, R., Gray, J., Wang, Z., Thapa, P., Dogra, P., Poon, M. M. L., Rybkina, K., Bradley, M. C., Idzikowski, E., McNichols, J., Kubota, M., Pethe, K., Shen, Y., Atkinson, M. A., Brusko, M., … Farber, D. L. (2023). Site-specific development and progressive maturation of human tissue-resident memory T cells over infancy and childhood. Immunity, 56(8), 1894-1909.e5. https://doi.org/10.1016/j.immuni.2023.06.008
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Yang, X., Wang, Z., Zandkarimi, F., Liu, Y., Duan, S., Li, Z., Kon, N., Zhang, Z., Jiang, X., Stockwell, B. R., & Gu, W. (2023). Regulation of VKORC1L1 is critical for p53-mediated tumor suppression through vitamin K metabolism. Cell Metabolism, 35(8), 1474-1490.e8. https://doi.org/10.1016/j.cmet.2023.06.014
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Bridge, J. A., Halling, K. C., Moncur, J. T., Souers, R. J., Hameed, M. R., Fernandes, H., Roy, A., Surrey, L., Tafe, L. J., Vasalos, P., & Lopez-Terrada, D. H. (2023). RNA Sequencing for Solid Tumor Fusion Gene Detection: Proficiency Testing Practice and Performance Comparison. Archives of Pathology & Laboratory Medicine, 148(5), 538–544. https://doi.org/10.5858/arpa.2023-0047-cp
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Jiang, Z., Wu, F., Laise, P., Takayuki, T., Na, F., Kim, W., Kobayashi, H., Chang, W., Takahashi, R., Valenti, G., Sunagawa, M., White, R. A., Macchini, M., Renz, B. W., Middelhoff, M., Hayakawa, Y., Dubeykovskaya, Z. A., Tan, X., Chu, T. H., … Wang, T. C. (2023). Tff2 defines transit-amplifying pancreatic acinar progenitors that lack regenerative potential and are protective against Kras-driven carcinogenesis. Cell Stem Cell, 30(8), 1091-1109.e7. https://doi.org/10.1016/j.stem.2023.07.002
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Pichler Sekulic, S., & Sekulic, M. (2023). Chondromatous metaplasia within native cardiac valves: clinicopathologic characterization with particular focus upon aortic valves. APMIS, 131(8), 410–418. Portico. https://doi.org/10.1111/apm.13340
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Puliatti, G., Li Puma, D. D., Aceto, G., Lazzarino, G., Acquarone, E., Mangione, R., D’Adamio, L., Ripoli, C., Arancio, O., Piacentini, R., & Grassi, C. (2023). Intracellular accumulation of tau oligomers in astrocytes and their synaptotoxic action rely on Amyloid Precursor Protein Intracellular Domain-dependent expression of Glypican-4. Progress in Neurobiology, 227, 102482. https://doi.org/10.1016/j.pneurobio.2023.102482
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Emmons, B. R., Batal, I., Radhakrishnan, J., & Husain, S. A. (2023). Age-related changes in nephrosclerosis in a multiethnic living kidney donor cohort. Kidney International, 104(2), 394–397. https://doi.org/10.1016/j.kint.2023.04.028
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Kudose, S., Cossey, L. N., Canetta, P. A., Sekulic, M., Vanbeek, C. A., Huls, F. B., Gupta, I., Bu, L., Alexander, M. P., Cornell, L. D., Fidler, M. E., Markowitz, G. S., Larsen, C. P., D’Agati, V. D., Nasr, S. H., & Santoriello, D. (2023). Clinicopathologic Spectrum of Lysozyme-Associated Nephropathy. Kidney International Reports, 8(8), 1585–1595. https://doi.org/10.1016/j.ekir.2023.05.007
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Alsaloum, M., Lee, C., Dudorova, E., Szabolcs, M. J., Shetty, M., Navot, B., & Ravalli, S. (2023). A Right Atrial Mass Discovered Postpartum: A Diagnostic Challenge. CASE, 7(8), 325–330. https://doi.org/10.1016/j.case.2023.04.006
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Briese, T., Tokarz, R., Bateman, L., Che, X., Guo, C., Jain, K., Kapoor, V., Levine, S., Hornig, M., Oleynik, A., Quan, P., Wong, W. H., Williams, B. L., Vernon, S. D., Klimas, N. G., Peterson, D. L., Montoya, J. G., & Ian Lipkin, W. (2023). A multicenter virome analysis of blood, feces, and saliva in myalgic encephalomyelitis/chronic fatigue syndrome. Journal of Medical Virology, 95(8). Portico. https://doi.org/10.1002/jmv.28993
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Treml, A., Joshi, S. A., Stephens, L. D., Zantek, N. D., Tanhehco, Y. C., Mason, H. M., Li, Y., Srivaths, P., Mattiazzi, A. D., Schwartz, J., & Wehrli, G. (2023). Apheresis medicine education during the early phase of the COVID‐19 pandemic. Transfusion, 63(8), 1580–1589. Portico. https://doi.org/10.1111/trf.17481
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Martuscello, R. T., Chen, M.-L., Reiken, S., Sittenfeld, L. R., Ruff, D. S., Ni, C.-L., Lin, C.-C., Pan, M.-K., Louis, E. D., Marks, A. R., Kuo, S.-H., & Faust, P. L. (2023). Defective cerebellar ryanodine receptor type 1 and endoplasmic reticulum calcium ‘leak’ in tremor pathophysiology. Acta Neuropathologica, 146(2), 301–318. https://doi.org/10.1007/s00401-023-02602-z
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Agin‐Liebes, J., Hickman, R. A., Vonsattel, J. P., Faust, P. L., Flowers, X., Utkina Sosunova, I., Ntiri, J., Mayeux, R., Surface, M., Marder, K., Fahn, S., Przedborski, S., & Alcalay, R. N. (2023). Patterns of TDP‐43 Deposition in Brains with LRRK2 G2019S Mutations. Movement Disorders, 38(8), 1541–1545. Portico. https://doi.org/10.1002/mds.29449
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Ding, Y. C., Song, H., Adamson, A. W., Schmolze, D., Hu, D., Huntsman, S., Steele, L., Patrick, C. S., Tao, S., Hernandez, N., Adams, C. D., Fejerman, L., Gardner, K., Nápoles, A. M., Pérez-Stable, E. J., Weitzel, J. N., Bengtsson, H., Huang, F. W., Neuhausen, S. L., & Ziv, E. (2023). Profiling the Somatic Mutational Landscape of Breast Tumors from Hispanic/Latina Women Reveals Conserved and Unique Characteristics. Cancer Research, 83(15), 2600–2613. https://doi.org/10.1158/0008-5472.can-22-2510
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Calame, D. G., Guo, T., Wang, C., Garrett, L., Jolly, A., Dawood, M., Kurolap, A., Henig, N. Z., Fatih, J. M., Herman, I., Du, H., Mitani, T., Becker, L., Rathkolb, B., Gerlini, R., Seisenberger, C., Marschall, S., Hunter, J. V., Gerard, A., … Lupski, J. R. (2023). Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease. The American Journal of Human Genetics, 110(8), 1394–1413. https://doi.org/10.1016/j.ajhg.2023.06.013
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Parr, M. F. E., Hidalgo, G., Goldstein, M. J., Batal, I., Lieberman, K. V., Amoruso, M. R., Baer, A. Z., & Jain, N. G. (2023). CMV‐associated collapsing focal segmental glomerulosclerosis after kidney transplant in a pediatric patient. Pediatric Transplantation, 27(5). Portico. https://doi.org/10.1111/petr.14535
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Cortazar, F. B., Cerda, J., Dhanani, R., Roglieri, J., & Santoriello, D. (2023). Avacopan in Patients With Rapidly Progressive Glomerulonephritis Requiring Dialysis. Kidney International Reports, 8(8), 1687–1691. https://doi.org/10.1016/j.ekir.2023.05.017
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Steers, N. J., & Barasch, J. (2023). Their last will and testament: dying immune cells protect the urinary system with extracellular DNA traps. Kidney International, 104(2), 236–238. https://doi.org/10.1016/j.kint.2023.05.021
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Dridi, H., Liu, Y., Reiken, S., Liu, X., Argyrousi, E. K., Yuan, Q., Miotto, M. C., Sittenfeld, L., Meddar, A., Soni, R. K., Arancio, O., Lacampagne, A., & Marks, A. R. (2023). Heart failure-induced cognitive dysfunction is mediated by intracellular Ca2+ leak through ryanodine receptor type 2. Nature Neuroscience, 26(8), 1365–1378. https://doi.org/10.1038/s41593-023-01377-6
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Bonini, K. E., Thomas‐Wilson, A., Marathe, P. N., Sebastin, M., Odgis, J. A., Di Biase, M., Kelly, N. R., Ramos, M. A., Insel, B. J., Scarimbolo, L., Rehman, A. U., Guha, S., Okur, V., Abhyankar, A., Phadke, S., Nava, C., Gallagher, K. M., Elkhoury, L., Edelmann, L., … Jobanputra, V. (2023). Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program. Clinical Genetics, 104(2), 210–225. Portico. https://doi.org/10.1111/cge.14365
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Smithgall, M. C., Liu-Jarin, X., Chen, X., Singh, K., Quddus, M. R., & Cimic, A. (2023). Diagnostic utility of PRAME immunohistochemistry in PEComa family of tumors and morphologic mimics with emphasis on the gynecologic tract. Human Pathology, 138, 12–17. https://doi.org/10.1016/j.humpath.2023.05.006
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Bethamcharla, R., Reddy, H., Teich, A. F., & Sekula, R. F. (2023). Histopathology of the trigeminal ganglion and nerve: A historical review. Journal of Neuroscience Research, 101(8), 1203–1204. Portico. https://doi.org/10.1002/jnr.25192
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Saad-Roy, C. M., Morris, S. E., Baker, R. E., Farrar, J., Graham, A. L., Levin, S. A., Wagner, C. E., Metcalf, C. Jessica. E., & Grenfell, B. T. (2023). Medium-term scenarios of COVID-19 as a function of immune uncertainties and chronic disease. Journal of The Royal Society Interface, 20(205). https://doi.org/10.1098/rsif.2023.0247
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Marasa, M., Ahram, D. F., Rehman, A. U., Mitrotti, A., Abhyankar, A., Jain, N. G., Weng, P. L., Piva, S. E., Fernandez, H. E., Uy, N. S., Chatterjee, D., Kil, B. H., Nestor, J. G., Felice, V., Robinson, D., Whyte, D., Gharavi, A. G., Appel, G. B., Radhakrishnan, J., … Sanna-Cherchi, S. (2023). Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease. Kidney International Reports, 8(8), 1638–1647. https://doi.org/10.1016/j.ekir.2023.05.021
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Shao, Z., Lee, B. J., Zhang, H., Lin, X., Li, C., Jiang, W., Chirathivat, N., Gershik, S., Shen, M. M., Baer, R., & Zha, S. (2023). Inactive PARP1 causes embryonic lethality and genome instability in a dominant-negative manner. Proceedings of the National Academy of Sciences, 120(31). https://doi.org/10.1073/pnas.2301972120
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Lukas, E., Hogan, T., Williams, C., Seddon, B., & Yates, A. J. (2023). Quantifying cellular dynamics in mice using a novel fluorescent division reporter system. Frontiers in Immunology, 14. https://doi.org/10.3389/fimmu.2023.1157705
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Madden, N., Mei, Y. Z. J., Jakubiak, K., Li, J., Hargus, G., Goldman, J. E., & Al-Dalahmah, O. (2023). The link between SARS-CoV-2 related microglial reactivity and astrocyte pathology in the inferior olivary nucleus. Frontiers in Neuroscience, 17. https://doi.org/10.3389/fnins.2023.1198219
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Kornberg, A., Botella, T., Moon, C. S., Rao, S., Gelbs, J., Cheng, L., Miller, J., Bacarella, A. M., García-Vilas, J. A., Vargas, J., Yu, X., Krupska, I., Bush, E., Garcia-Carrasquillo, R., Lebwohl, B., Krishnareddy, S., Lewis, S., Green, P. H. R., Bhagat, G., … Han, A. (2023). Gluten induces rapid reprogramming of natural memory αβ and γδ intraepithelial T cells to induce cytotoxicity in celiac disease. Science Immunology, 8(85). https://doi.org/10.1126/sciimmunol.adf4312
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Min, J., Zhao, J., Zagelbaum, J., Lee, J., Takahashi, S., Cummings, P., Schooley, A., Dekker, J., Gottesman, M. E., Rabadan, R., & Gautier, J. (2023). Mechanisms of insertions at a DNA double-strand break. Molecular Cell, 83(14), 2434-2448.e7. https://doi.org/10.1016/j.molcel.2023.06.016
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Siddiqi, T. J., Usman, M. S., Rashid, A. M., Javaid, S. S., Ahmed, A., Clark, D., Flack, J. M., Shimbo, D., Choi, E., Jones, D. W., & Hall, M. E. (2023). Clinical Outcomes in Hypertensive Emergency: A Systematic Review and Meta‐Analysis. Journal of the American Heart Association, 12(14). https://doi.org/10.1161/jaha.122.029355
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da Costa, B. L., Li, Y., Levi, S. R., Tsang, S. H., & Quinn, P. M. J. (2023). Generation of CRB1 RP Patient-Derived iPSCs and a CRISPR/Cas9-Mediated Homology-Directed Repair Strategy for the CRB1 c.2480G>T Mutation. Retinal Degenerative Diseases XIX, 571–576. https://doi.org/10.1007/978-3-031-27681-1_83
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da Costa, B. L., Jenny, L. A., Maumenee, I. H., Tsang, S. H., & Quinn, P. M. J. (2023). Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing. Retinal Degenerative Diseases XIX, 103–107. https://doi.org/10.1007/978-3-031-27681-1_16
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Nolan, N. D., Jenny, L. A., Tsang, S. H., & Cui, X. (2023). Rod Photoreceptor-Specific Ablation of Metformin Target, AMPK, in a Preclinical Model of Autosomal Recessive Retinitis Pigmentosa. Retinal Degenerative Diseases XIX, 403–408. https://doi.org/10.1007/978-3-031-27681-1_59
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Caruso, S. M., Tsai, Y.-T., da Costa, B. L., Kolesnikova, M., Jenny, L. A., Tsang, S. H., & Quinn, P. M. J. (2023). Prime Editing Strategy to Install the PRPH2 c.828+1G>A Mutation. Retinal Degenerative Diseases XIX, 97–102. https://doi.org/10.1007/978-3-031-27681-1_15
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Tsai, Y.-T., da Costa, B. L., Caruso, S. M., Nolan, N. D., Levi, S. R., Tsang, S. H., & Quinn, P. M. J. (2023). Generation of an Avian Myeloblastosis Virus (AMV) Reverse Transcriptase Prime Editor. Retinal Degenerative Diseases XIX, 109–114. https://doi.org/10.1007/978-3-031-27681-1_17
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Kabir, M., Sun, N., Hu, X., Martin, T. C., Yi, J., Zhong, Y., Xiong, Y., Kaniskan, H. Ü., Gu, W., Parsons, R., & Jin, J. (2023). Acetylation Targeting Chimera Enables Acetylation of the Tumor Suppressor p53. Journal of the American Chemical Society, 145(27), 14932–14944. https://doi.org/10.1021/jacs.3c04640
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Shao, D., Pena, O., Sekulic, M., Valdez Imbert, R., Vegivinti, C. T. R., & Jim, B. (2023). Secondary haemophagocytic lymphohistiocytosis in a patient with new-onset systemic lupus erythematosus: the challenges of timely diagnosis and successful treatment. BMJ Case Reports, 16(7), e252938. https://doi.org/10.1136/bcr-2022-252938
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Montague, T. G., Rieth, I. J., Gjerswold-Selleck, S., Garcia-Rosales, D., Aneja, S., Elkis, D., Zhu, N., Kentis, S., Rubino, F. A., Nemes, A., Wang, K., Hammond, L. A., Emiliano, R., Ober, R. A., Guo, J., & Axel, R. (2023). A brain atlas for the camouflaging dwarf cuttlefish, Sepia bandensis. Current Biology, 33(13), 2794-2801.e3. https://doi.org/10.1016/j.cub.2023.06.007
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Viragova, S., Aparicio, L., Palmerini, P., Zhao, J., Valencia Salazar, L. E., Schurer, A., Dhuri, A., Sahoo, D., Moskaluk, C. A., Rabadan, R., & Dalerba, P. (2023). Inverse agonists of retinoic acid receptor/retinoid X receptor signaling as lineage-specific antitumor agents against human adenoid cystic carcinoma. JNCI: Journal of the National Cancer Institute, 115(7), 838–852. https://doi.org/10.1093/jnci/djad062
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Occelli, L. M., Zobel, L., Stoddard, J., Wagner, J., Pasmanter, N., Querubin, J., Renner, L. M., Reynaga, R., Winkler, P. A., Sun, K., Marinho, L. F. L. P., O’Riordan, C. R., Frederick, A., Lauer, A., Tsang, S. H., Hauswirth, W. W., McGill, T. J., Neuringer, M., Michalakis, S., & Petersen-Jones, S. M. (2023). Development of a translatable gene augmentation therapy for CNGB1-retinitis pigmentosa. Molecular Therapy, 31(7), 2028–2041. https://doi.org/10.1016/j.ymthe.2023.04.005
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Weidmann, M. D., Green, D. A., Berry, G. J., & Wu, F. (2023). Assessing respiratory viral exclusion and affinity interactions through co-infection incidence in a pediatric population during the 2022 resurgence of influenza and RSV. Frontiers in Cellular and Infection Microbiology, 13. https://doi.org/10.3389/fcimb.2023.1208235
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Long, J., Soni, M., Muranski, P., Miller, M. J., Conry-Cantilena, C., & De Giorgi, V. (2023). Case Report: Kinetics and durability of humoral and cellular response of SARS-CoV-2 messenger RNA vaccine in a lung and kidney transplant recipient. Frontiers in Immunology, 14. https://doi.org/10.3389/fimmu.2023.1207638
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Yi, J., Li, H., Chu, B., Kon, N., Hu, X., Hu, J., Xiong, Y., Kaniskan, H. U., Jin, J., & Gu, W. (2023). Inhibition of USP7 induces p53-independent tumor growth suppression in triple-negative breast cancers by destabilizing FOXM1. Cell Death & Differentiation, 30(7), 1799–1810. https://doi.org/10.1038/s41418-023-01180-7
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