Comparison of next-generation sequencing (NGS) and next-generation flow (NGF) for minimal residual disease (MRD) assessment in multiple myelomaInvivoscribe Marketing2021-02-11T20:05:42-08:00October 30th, 2020|Read more
Plasticity of the human IgM repertoire in response to long‐term spaceflightInvivoscribe Marketing2021-02-11T20:09:45-08:00October 13th, 2020|Read more
Immune recovery in patients with mantle cell lymphoma receiving long-term ibrutinib and venetoclax combination therapyInvivoscribe Marketing2021-02-11T20:11:02-08:00October 8th, 2020|Read more
Genetic evolution of in situ follicular neoplasia to aggressive B-cell lymphoma of germinal center subtypeInvivoscribe Marketing2021-02-11T20:13:51-08:00August 27th, 2020|Read more
Baseline VDJ clonotype detection using a targeted sequencing NGS assay: allowing for subsequent MRD assessmentInvivoscribe Marketing2021-02-11T20:26:38-08:00July 22nd, 2020|Read more
Invivoscribe® Receives Approval in Japan for its LeukoStrat® CDx FLT3 Mutation Assay to Assess Acute Myeloid Leukemia (AML) Patients Eligible for Treatment with Xospata® (gilteritinib fumarate)Invivoscribe Marketing2021-02-26T19:12:02-08:00September 27th, 2018|Read more
Invivoscribe Announces a Regional “Center of Excellence” Reference Laboratory in Beirut to Offer Specialized Gene PanelsInvivoscribe Marketing2021-02-26T19:12:15-08:00May 9th, 2018|Read more
Invivoscribe Submits Pre-Market Approval Application in Japan and Panel Track Supplement in the US to Screen Acute Myeloid Leukemia (AML) Patients for FLT3 MutationsInvivoscribe Marketing2021-02-26T19:12:23-08:00May 8th, 2018|Read more
Invivoscribe® Releases LymphoTrack® TRB Assay on MiSeq® and LymphoTrack® Minimal Residual Disease (MRD) Softwarewmm2021-02-26T19:12:40-08:00November 7th, 2017|Read more
Invivoscribe® Releases LeukoStrat® CDx FLT3 Mutation Assay as CE-marked IVD Assay Kit.wmm2021-02-26T19:12:46-08:00August 1st, 2017|Read more
AMPNovember 11-15, 2025 Boston, MA Exhibiting and Hosting a Corporate Workshop Visit Conference Website