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Julie M. Vose

Researcher at University of Nebraska Medical Center

Publications -  569
Citations -  51589

Julie M. Vose is an academic researcher from University of Nebraska Medical Center. The author has contributed to research in topics: Transplantation & Lymphoma. The author has an hindex of 97, co-authored 541 publications receiving 46915 citations. Previous affiliations of Julie M. Vose include Memorial Hospital of South Bend.

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The detection of minimal lymphoma by molecular and combined culture-molecular methods.

TL;DR: The substantial frequency of failure of obtaining tumour‐specific IgH CDRIII sequences in paraffin‐embedded B‐NHLs argues for the storage of frozen tumour samples for possible molecular studies.
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Clinical outcome of peripheral blood stem cell support

TL;DR: Patients who receive peripheral stem cell transplantation may experience an improved progression-free survival after high-dose therapy when compared with similar patients who receive autologous bone marrow transplantation.
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A Phase I Dose Expansion Cohort Study of the Safety, Pharmacokinetics and Pharmacodynamics of SAR245409 (S09), An Orally Administered PI3K/mTOR Inhibitor, in Patients with Lymphoma

TL;DR: In this phase 1 dose-expansion cohort study in lymphoma, SAR245409 was generally well tolerated and showed promise in several lymphoma subtypes, with 1 showing robust pharmacodynamic modulation of PI3K and ERK pathway signaling.
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Phase II trial of 131-Iodine tositumomab with high-dose chemotherapy and autologous stem cell transplantation for relapsed diffuse large B cell lymphoma.

TL;DR: The PFS and OS were encouraging in this group of chemotherapy-sensitive persistent, relapsed, or high-risk patients with DLBCL and a follow-up phase III trial with 131-Iodine tositumomab/BEAM vs rituximab /BEAM was planned based on this information.
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Novel therapy for therapy-resistant mantle cell lymphoma: multipronged approach with targeting of hedgehog signaling.

TL;DR: An in vivo model of therapy‐resistant MCL is developed by transplanting a patient‐derived MCL cell line into NOD/SCID mice followed by treatment with combination chemotherapy to reduce tumor burden combined with GLI‐antisense oligonucleotides or bortezomib, a proteosome inhibitor, to target therapy‐ resistant MCL cells that remained after chemotherapy.