Curt I. Civin

ORCID: 0000-0002-9555-4895
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Acute Myeloid Leukemia Research
  • Hematopoietic Stem Cell Transplantation
  • Chronic Myeloid Leukemia Treatments
  • Immune Cell Function and Interaction
  • Acute Lymphoblastic Leukemia research
  • MicroRNA in disease regulation
  • Chronic Lymphocytic Leukemia Research
  • CAR-T cell therapy research
  • Immunotherapy and Immune Responses
  • RNA Interference and Gene Delivery
  • T-cell and B-cell Immunology
  • Mesenchymal stem cell research
  • Erythrocyte Function and Pathophysiology
  • Protein Degradation and Inhibitors
  • Cancer-related molecular mechanisms research
  • Pluripotent Stem Cells Research
  • Monoclonal and Polyclonal Antibodies Research
  • Virus-based gene therapy research
  • RNA modifications and cancer
  • CRISPR and Genetic Engineering
  • Glycosylation and Glycoproteins Research
  • Immune Response and Inflammation
  • Biomedical Ethics and Regulation
  • Childhood Cancer Survivors' Quality of Life
  • Hematological disorders and diagnostics

University of Maryland, Baltimore
2015-2024

Sidney Kimmel Comprehensive Cancer Center
2001-2023

University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center
1984-2023

Pediatrics and Genetics
2004-2023

Institute for Stem Cell Biology and Regenerative Medicine
2011-2021

U-M Rogel Cancer Center
2012-2020

University of Baltimore
1985-2017

Johns Hopkins University
2000-2010

Johns Hopkins Medicine
1999-2010

University of Maryland, College Park
2010

MicroRNAs (miRNAs) are a recently identified class of epigenetic elements consisting small noncoding RNAs that bind to the 3′ untranslated region mRNAs and down-regulate their translation protein. miRNAs play critical roles in many different cellular processes including metabolism, apoptosis, differentiation, development. We found 33 expressed CD34+ hematopoietic stem-progenitor cells (HSPCs) from normal human bone marrow mobilized peripheral blood stem cell harvests. then combined these...

10.1073/pnas.0610983104 article EN Proceedings of the National Academy of Sciences 2007-02-10

Abstract To facilitate the direct study of molecular events that control development human burst‐forming units‐erythroid (BFU‐E), we have developed a method to purify BFU‐E from peripheral blood. Using density centrifugation, rosetting with mixture neuraminidase‐treated and IgG‐coated sheep erythrocytes, positive panning anti‐My10 monoclonal antibody, overnight adherence plastic dishes, negative antibodies, blood were purified 0.04% 56.6%, 1,400‐fold purification 13% yield. More than 90%...

10.1002/jcp.1041420202 article EN Journal of Cellular Physiology 1990-02-01

Nonadherent marrow mononuclear cells enriched for hematopoietic progenitor were cultured in semisolid medium with recombinant human granulocyte-macrophage colony-stimulating factor 9 days to form colony forming unitgranulocyte macrophage (CFU-GM) colonies. 1,25-Dihydroxyvitamin D was then gently layered over the cultures. After 2 weeks, approximately 30% of colonies that formed composed a unique polygonal morphology. One hundred percent these crossreacted monoclonal antibody 23c6, which...

10.1210/endo-126-5-2733 article EN Endocrinology 1990-05-01

Morphological and biochemical studies of human colony-forming units-erythroid (CFU-E) have been hindered by their extreme rarity. Since burst-forming (BFU-E) develop into CFU-E, we used normal blood BFU-E to generate large numbers highly purified CFU-E in vitro. Using density centrifugation, sheep erythrocyte rosetting, surface immunoglobulin-positive cell depletion, adherence plastic, negative panning with monoclonal antibodies, were from 0.017 0.368%, a 22-fold purification 43% yield. The...

10.1172/jci113080 article EN Journal of Clinical Investigation 1987-08-01

Notch signaling regulates cell fate decisions in a variety of adult and embryonic tissues, represents characteristic feature exocrine pancreatic cancer. In developing mouse pancreas, targeted inactivation pathway components has defined role for regulating early endocrine differentiation, but been less informative with respect to possible subsequent differentiation events. Here, we show that activated target genes actively repress completion an acinar program zebrafish pancreas. the gene Hes1...

10.1242/dev.01280 article EN Development 2004-07-28

Abstract Several members of the Kruppel-like factor (KLF) family transcription factors play important roles in differentiation, survival, and trafficking blood immune cell types. We demonstrate this study that hematopoietic cells from KLF4−/− fetal livers (FL) contained normal numbers functional progenitor cells, were radioprotective, performed as well KLF4+/+ competitive repopulation assays. However, “KLF4−/− chimeras” generated by transplantation into lethally irradiated wild-type mice...

10.4049/jimmunol.180.8.5645 article EN The Journal of Immunology 2008-04-15

Summary A series of 23 monoclonal antibodies reactive with normal lymphoid and myeloid cells at various stages differentiation were used to characterize 96 adult patients acute myelocytic leukaemia (AML), concentrating on the possible role expression these antigens may have in predicting response intensive chemotherapy. Only CD34 ( P = 0·008) HLA‐DR 0·035) was significant therapy; leukaemic expressing (My10) had a complete remission (CR) rate 59% compared 87% for those blasts not antigen. In...

10.1111/j.1365-2141.1990.tb06365.x article EN British Journal of Haematology 1990-11-01

We used a recently developed strategy to analyze patterns of X-chromosome inactivation in human cell populations order study female members families with X-linked agammaglobulinemia — i.e., detect the carrier state and test hypothesis that disorder results from defect intrinsic development B cells. According this strategy, recombinant-DNA probes simultaneously restriction-fragment–length polymorphisms methylation genes. Random X-inactivation were observed isolated peripheral-blood...

10.1056/nejm198702193160802 article EN New England Journal of Medicine 1987-02-19

PURPOSE The objective of this study was to characterize CD34+ cell grafts, obtained using a novel technique, from children undergoing autologous bone marrow transplantation (BMT) for cancer therapy. In particular, we wanted determine if the grafts generated hematopoietic reconstitution, since positive result would motivate further development and use methodology. PATIENTS AND METHODS This pilot feasibility clinical trial involved 13 patients < or = 25 years age with advanced solid tumors,...

10.1200/jco.1996.14.8.2224 article EN Journal of Clinical Oncology 1996-08-01

Lentiviral vectors (LVs) offer several advantages over traditional oncoretroviral vectors. LVs efficiently transduce slowly dividing cells, including hematopoietic stem-progenitor cells (HSCs), resulting in stable gene transfer and expression. Additionally, recently developed self-inactivating (SIN) allow promoter-specific transgene For many applications, transduction of more than one is needed. We obtained inconsistent results our attempts to coexpress two transgenes linked by an internal...

10.1016/s1525-0016(03)00104-7 article EN cc-by-nc-nd Molecular Therapy 2003-04-25

Abstract Highly purified human erythroid colony‐forming cells (ECFC), which consist predominately of units‐erythroid (CFU‐F), were prepared from blood and used to study the binding processing erythropoietin (Ep). When radioiodinated recombinant Ep ( 125 I‐rEp) was incubated with these cells, specific saturable. Specific directly proportional cell concentration did not occur other cells. Saturation at 3°C occurred 1 nM (3.9/U/ml), Scatchard analysis revealed two classes sites on surface. Of a...

10.1002/jcp.1041370218 article EN Journal of Cellular Physiology 1988-11-01

The human CD34(+)/CD38(-)/Lin(-) cell subset, comprising approximately 1-10% of the CD34(+) population, contains few less primitive hematopoietic (lineage-committed) progenitor cells (HPCs) but most in vivo engrafting (lympho-)hematopoietic stem (HSCs). We analyzed gene expression populations isolated from normal adult donor bone marrow, neonatal placental/umbilical cord blood, and mobilized peripheral blood stem-progenitor cells. As measured by Affymetrix microarrays, 4746 genes were...

10.1158/0008-5472.can-03-3247 article EN Cancer Research 2004-07-01

In this paper, we report analysis of differentiation in human hemopoietic colonies derived from a single cell. Cord blood mononulear cells and panned My-10 antigen-positive bone marrow cord were plated methylcellulose medium containing erythropoietin conditioned medium. Initially, performed mapping studies to identify candidate colony-forming cells. Subsequently, using micromanipulator, transferred individually 35-mm dishes for colony formation. Cellular composition the was determined by...

10.1172/jci111645 article EN Journal of Clinical Investigation 1984-12-01
Coming Soon ...