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David Wu

Researcher at University of Washington

Publications -  86
Citations -  3753

David Wu is an academic researcher from University of Washington. The author has contributed to research in topics: Minimal residual disease & Population. The author has an hindex of 23, co-authored 82 publications receiving 2814 citations. Previous affiliations of David Wu include Harvard University & University of Washington Medical Center.

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Acquisition of a CD19-negative myeloid phenotype allows immune escape of MLL-rearranged B-ALL from CD19 CAR-T-cell therapy

TL;DR: Administration of lymphodepletion chemotherapy followed by CD19-specific chimeric antigen receptor (CAR)-modified T cells is a remarkably effective approach to treating patients with relapsed and refractory CD19(+) B-cell malignancies.
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Using synthetic templates to design an unbiased multiplex PCR assay

TL;DR: A multiplex PCR with a mixture of primers targeting the rearranged variable and joining segments to capture receptor diversity is applied to a multiplex T cell receptor gamma sequencing assay and can be extended to any adaptive immune locus.
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International, evidence-based consensus diagnostic criteria for HHV-8–negative/idiopathic multicentric Castleman disease

TL;DR: The proposed consensus criteria will facilitate consistent diagnosis, appropriate treatment, and collaborative research and exclude infectious, malignant, and autoimmune disorders that can mimic iMCD.
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Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.

TL;DR: UW-OncoPlex is developed, a clinical molecular diagnostic assay to provide simultaneous deep-sequencing information, based on >500× average coverage, for all classes of mutations in 194 clinically relevant genes, to best guide existing and emerging treatment regimens and facilitate integration of genomic testing with patient care.
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High-Throughput Sequencing Detects Minimal Residual Disease in Acute T Lymphoblastic Leukemia

TL;DR: Next-generation sequencing of lymphoid receptor gene repertoire may improve clinical diagnosis and subsequent MRD monitoring of lymphoproliferative disorders and lower the threshold of detection for MRD and affect treatment decisions.