Molecular profiling of immunoglobulin heavy-chain gene rearrangements unveils new potential prognostic markers for multiple myeloma patientsmarketing2021-02-11T21:58:45+00:00February 6th, 2020|更多详细信息
Monitoring minimal residual disease in the bone marrow using next generation sequencingmarketing2021-02-11T22:00:56+00:00January 17th, 2020|更多详细信息
Plasma Cell Myeloma Residual Disease Quantitation Using a Next-Generation Sequencing-Based IGH Clonal Rearrangement Assay with the Aid of a “Spike-in” Clonal Sequencemarketing2021-02-11T23:36:10+00:00November 13th, 2019|更多详细信息
Clonally-Related CD5+ CLL/SLL and CD10+ high grade B-cell lymphoma suggests common neoplastic progenitor with branched disease evolution, with therapeutic implicationsmarketing2021-02-11T23:40:44+00:00October 15th, 2019|更多详细信息
Stability and uniqueness of clonal immunoglobulin CDR3 sequences for MRD tracking in multiple myelomamarketing2021-02-11T23:43:09+00:00October 1st, 2019|更多详细信息
Invivoscribe Submits the LeukoStrat CDx FLT3 Mutation Assay to Support Daiichi Sankyo Submission for Quizartinib in Japanmarketing2021-02-26T19:11:48+00:00November 19th, 2018|更多详细信息
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)marketing2021-02-26T19:12:02+00:00September 27th, 2018|更多详细信息
Invivoscribe Announces a Regional “Center of Excellence” Reference Laboratory in Beirut to Offer Specialized Gene Panelsmarketing2021-02-26T19:12:15+00:00May 9th, 2018|更多详细信息
Invivoscribe Submits Pre-Market Approval Application in Japan and Panel Track Supplement in the US to Screen Acute Myeloid Leukemia (AML) Patients for FLT3 Mutationsmarketing2021-02-26T19:12:23+00:00May 8th, 2018|更多详细信息
Invivoscribe® Releases LymphoTrack® TRB Assay on MiSeq® and LymphoTrack® Minimal Residual Disease (MRD) Softwarewmm2021-02-26T19:12:40+00:00November 7th, 2017|更多详细信息