Works by Eskandari, Ghazaleh


Results: 24
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    Frequent detection of CBFA2T3::GLIS2 fusion and RAM-phenotype in pediatric non-Down syndrome acute megakaryoblastic leukemia: a possible novel relationship with aberrant cytoplasmic CD3 expression.

    Published in:
    Leukemia & Lymphoma, 2023, v. 64, n. 2, p. 462, doi. 10.1080/10428194.2022.2140285
    By:
    • Chen Wongworawat, Yan;
    • Eskandari, Ghazaleh;
    • Gaikwad, Amos;
    • Marcogliese, Andrea N.;
    • Ferguson, Lizmery S.;
    • Brackett, Julienne;
    • Punia, Jyotinder N.;
    • Elghetany, M. Tarek;
    • Kulkarni, Reshma;
    • Rao, Pulivarthi H.;
    • Ringrose, Jo;
    • Lopez-Terrada, Dolores H.;
    • Roy, Angshumoy;
    • Curry, Choladda V.;
    • Fisher, Kevin E.
    Publication type:
    Article
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    IGF-1R/mTOR Targeted Therapy for Ewing Sarcoma: A Meta-Analysis of Five IGF-1R-Related Trials Matched to Proteomic and Radiologic Predictive Biomarkers.

    Published in:
    Cancers, 2020, v. 12, n. 7, p. 1768, doi. 10.3390/cancers12071768
    By:
    • Amin, Hesham M.;
    • Morani, Ajaykumar C.;
    • Daw, Najat C.;
    • Lamhamedi-Cherradi, Salah-Eddine;
    • Subbiah, Vivek;
    • Menegaz, Brian A.;
    • Vishwamitra, Deeksha;
    • Eskandari, Ghazaleh;
    • George, Bhawana;
    • Benjamin, Robert S.;
    • Patel, Shreyaskumar;
    • Song, Juhee;
    • Lazar, Alexander J.;
    • Wang, Wei-Lien;
    • Kurzrock, Razelle;
    • Pappo, Alberto;
    • Anderson, Peter M.;
    • Schwartz, Gary K.;
    • Araujo, Dejka;
    • Cuglievan, Branko
    Publication type:
    Article
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    Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation.

    Published in:
    2021
    By:
    • Daude, Nathalie;
    • Kim, Chae;
    • Kang, Sang‑Gyun;
    • Eskandari‑Sedighi, Ghazaleh;
    • Haldiman, Tracy;
    • Yang, Jing;
    • Fleck, Shelaine C.;
    • Gomez‑Cardona, Erik;
    • Han, Zhuang Zhuang;
    • Borrego‑Ecija, Sergi;
    • Wohlgemuth, Serene;
    • Julien, Olivier;
    • Wille, Holger;
    • Molina‑Porcel, Laura;
    • Gelpi, Ellen;
    • Safar, Jiri G.;
    • Westaway, David
    Publication type:
    Correction Notice
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    Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 6, p. 1045, doi. 10.1007/s00401-020-02148-4
    By:
    • Daude, Nathalie;
    • Kim, Chae;
    • Kang, Sang-Gyun;
    • Eskandari-Sedighi, Ghazaleh;
    • Haldiman, Tracy;
    • Yang, Jing;
    • Fleck, Shelaine C.;
    • Gomez-Cardona, Erik;
    • Han, Zhuang Zhuang;
    • Borrego-Ecija, Sergi;
    • Wohlgemuth, Serene;
    • Julien, Olivier;
    • Wille, Holger;
    • Molina-Porcel, Laura;
    • Gelpi, Ellen;
    • Safar, Jiri G.;
    • Westaway, David
    Publication type:
    Article
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    Alzheimer's disease associated isoforms of human CD33 distinctively modulate microglial cell responses in 5XFAD mice.

    Published in:
    Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00734-8
    By:
    • Eskandari-Sedighi, Ghazaleh;
    • Crichton, Madeline;
    • Zia, Sameera;
    • Gomez-Cardona, Erik;
    • Cortez, Leonardo M.;
    • Patel, Zain H.;
    • Takahashi-Yamashiro, Kei;
    • St. Laurent, Chris D.;
    • Sidhu, Gaurav;
    • Sarkar, Susmita;
    • Aghanya, Vivian;
    • Sim, Valerie L.;
    • Tan, Qiumin;
    • Julien, Olivier;
    • Plemel, Jason R.;
    • Macauley, Matthew S.
    Publication type:
    Article
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