Search Results - "Preti, Robert"
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Therapies for rare diseases: therapeutic modalities, progress and challenges ahead
Published in Nature reviews. Drug discovery (01-02-2020)“…Most rare diseases still lack approved treatments despite major advances in research providing the tools to understand their molecular basis, as well as…”
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PreSERVE-AMI: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial of Intracoronary Administration of Autologous CD34+ Cells in Patients With Left Ventricular Dysfunction Post STEMI
Published in Circulation research (20-01-2017)“…RATIONALE:Despite direct immediate intervention and therapy, ST-segment–elevation myocardial infarction (STEMI) victims remain at risk for infarct expansion,…”
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CD34+ cell infusion after ST elevation myocardial infarction is associated with improved perfusion and is dose dependent
Published in The American heart journal (2011)“…Background The objective of the study was to determine whether the effects of infarct-related artery (IRA) infusion of autologous bone marrow–derived CD34+…”
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Multi-site evaluation of the BD Stem Cell Enumeration Kit for CD34+ cell enumeration on the BD FACSCanto II and BD FACSCalibur flow cytometers
Published in Cytotherapy (Oxford, England) (01-11-2014)“…Abstract Background aims Evaluation of the BD Stem Cell Enumeration Kit was conducted at four clinical sites with flow cytometry CD34+ enumeration to assess…”
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Bringing safe and effective cell therapies to the bedside
Published in Nature biotechnology (01-07-2005)Get full text
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Unusual viral infections (progressive multifocal leukoencephalopathy and cytomegalovirus disease) after high-dose chemotherapy with autologous blood stem cell rescue and peritransplantation rituximab
Published in Blood (15-02-2002)“…Efforts to reduce relapse of non-Hodgkin lymphoma after autologous transplantation have included ex vivo stem cell selection and/or peritransplantation…”
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Characterization of mechanical dyssynchrony measured by gated single photon emission computed tomography phase analysis after acute ST-elevation myocardial infarction
Published in Journal of nuclear cardiology (01-10-2011)“…Left ventricular dyssynchrony is an adverse consequence of ST-elevation myocardial infarction (STEMI) and bears an unfavorable prognosis. Mechanical…”
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PreSERVE-AMI
Published in Circulation research (20-01-2017)“…Rationale:Despite direct immediate intervention and therapy, ST-segment–elevation myocardial infarction (STEMI) victims remain at risk for infarct expansion,…”
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Biomanufacturing for clinically advanced cell therapies
Published in Nature biomedical engineering (01-06-2018)“…The achievements of cell-based therapeutics have galvanized efforts to bring cell therapies to the market. To address the demands of the clinical and eventual…”
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Publisher Correction: Therapies for rare diseases: therapeutic modalities, progress and challenges ahead
Published in Nature reviews. Drug discovery (01-04-2020)“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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Abstract 12754: Infused CD34 Cell Dose, not Bone Marrow CD34+ Cell Content, Improves Clinical Outcomes and LVEF in Patients With Left Ventricular Dysfunction post STEMI: Results of the PreSERVE-AMI Trial
Published in Circulation (New York, N.Y.) (10-11-2015)“…BackgroundPrior studies suggest an association between naturally high circulating levels of CD34+ cells (CD34) and better outcomes following ischemic events…”
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ONE YEAR FOLLOW-UP RESULTS FROM PRESERVE-AMI: A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED CLINICAL TRIAL OF INTRACORONARY INFUSION OF AUTOLOGOUS CD34+ CELLS IN PATIENTS WITH LEFT VENTRICULAR DYSFUNCTION POST STEMI
Published in Journal of the American College of Cardiology (17-03-2015)“…Conclusion: PreSERVE-AMI represents the largest study of cell-based therapy for STEMI completed in US and will determine endpoints, sample size and suitability…”
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Reconstitution of T Cell Subset Repertoire Diversity following Multiple Antigen-Mismatched Bone Marrow Transplantation
Published in Biology of blood and marrow transplantation (01-10-2006)Get full text
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CD34+CXCR4+ Cell Therapy (AMR-001) for Myocardial Infarction: Preliminary Processing and Product Results of a Phase I Dose Escalation Study
Published in Blood (16-11-2007)“…Background: Approximately 20% of patients suffering a ST segment elevated acute myocardial infarction (AMI) have progressive peri-infarct zone myocardial cell…”
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Breast cancer cell contamination of blood stem cell products in patients with metastatic breast cancer: Predictors and clinical relevance
Published in Biology of blood and marrow transplantation (01-01-2002)“…The incidence and clinical relevance of tumor cells contaminating the stem cell products of patients with advanced breast cancer treated with high-dose…”
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Bone Marrow Derived CD34+CXCR4+ Cells Maintain Viability, Mobility and Sterility up to 72 Hours and Are Compatible with Balloon Dilatation Catheters Used for Intra Coronary Artery Infusion; Pre-Clinical Development of a Pharmaceutical Grade Cell Therapy for Acute Myocardial Infarction (AMR-001)
Published in Blood (16-11-2007)“…Background: Approximately 20% of patients suffering a ST segment elevated acute myocardial infarction (AMI) have progressive peri-infarct zone myocardial cell…”
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Freezing and Cryostorage of Hematopoietic Progenitor Cells (HPC) Apheresis Using 5% Dimethyl Sulfoxide (DMSO) without Hydroxyethyl Starch (HES) in Cryocyte Freezing Bags and in Cryogenic Vials
Published in Blood (16-11-2006)“…Cryoprotectant formulated with 5% DMSO, 6% HES, 0.2% dextrose and 3.75% human serum albumin (HSA) [DMSO/(+)HES], originally adapted by Stiff et al ( Blood…”
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Cryopreservation of Peripheral Blood Stem Cells (PBSC) with Hydroxyethylstarch (HES) and Dimethylsulfoxide (DMSO) Results in Faster Granulocyte Recovery Than Using Dimethylsulfoxide Alone
Published in Blood (16-11-2007)“…PBSC components are routinely frozen for storage before autologous transplantation in the treatment of malignant diseases. We have used 5% DMSO, 3.75% human…”
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Comprehensive Immune Reconstitution without Development of Graft Versus Host Disease (GvHD) Using Limited T-Cell Add Back at the Time of Unrelated Multi-Antigen Mismatched Pan-T-Cell Depleted Transplant
Published in Blood (16-11-2005)“…Application of unrelated multi-antigen mismatched transplant is limited by a high risk of severe GvHD. Pan-T-Cell depletion successfully limits GvHD in this…”
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