Search Results - "Roberts, Irene A. G"
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Microchimerism in female bone marrow and bone decades after fetal mesenchymal stem-cell trafficking in pregnancy
Published in The Lancet (British edition) (10-07-2004)“…Fetal cells enter maternal blood during pregnancy and persist in women with autoimmune disease. The frequency of subsequent fetomaternal microchimerism in…”
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Activated invariant NKT cells regulate osteoclast development and function
Published in The Journal of immunology (1950) (01-03-2011)“…Invariant NKT (iNKT) cells modulate innate and adaptive immune responses through activation of myeloid dendritic cells and macrophages and via enhanced…”
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3
Chromatin-based, in cis and in trans regulatory rewiring underpins distinct oncogenic transcriptomes in multiple myeloma
Published in Nature communications (14-09-2021)“…Multiple myeloma is a genetically heterogeneous cancer of the bone marrow plasma cells (PC). Distinct myeloma transcriptome profiles are primarily driven by…”
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4
Identification of mesenchymal stem/progenitor cells in human first-trimester fetal blood, liver, and bone marrow
Published in Blood (15-10-2001)“…Human mesenchymal stem/progenitor cells (MSCs) have been identified in adult bone marrow, but little is known about their presence during fetal life. MSCs were…”
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Can routine commercial cord blood banking be scientifically and ethically justified?
Published in PLoS medicine (01-02-2005)“…Umbilical cord blood--the blood that remains in the placenta after birth--can be collected and stored frozen for years. A well-accepted use of cord blood is as…”
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Regulation of hematopoiesis in vitro and in vivo by invariant NKT cells
Published in Blood (15-04-2006)“…Invariant natural killer T cells (iNKT cells) are a small subset of immunoregulatory T cells highly conserved in humans and mice. On activation by glycolipids…”
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The role of hydroxyurea in sickle cell disease
Published in British journal of haematology (01-01-2003)Get full text
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Human Invariant NKT Cells Are Required for Effective In Vitro Alloresponses
Published in The Journal of immunology (1950) (15-10-2005)“…NKT cells are a small subset of regulatory T cells conserved in humans and mice. In humans they express the Valpha24Jalpha18 invariant chain (hence invariant…”
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Human Invariant NKT Cells Display Alloreactivity Instructed by Invariant TCR-CD1d Interaction and Killer Ig Receptors
Published in The Journal of immunology (1950) (01-09-2008)“…Invariant NKT (iNKT) cells are a subset of highly conserved immunoregulatory T cells that modify a variety of immune responses, including alloreactivity…”
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10
Stem cell transplantation for chronic myeloid leukemia in children
Published in Blood (15-08-2003)“…Hematopoietic stem cell transplantation (SCT) is the only proven cure for chronic myeloid leukemia (CML), a rare disease in childhood. We report outcomes of…”
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11
Bone marrow transplantation for β‐thalassaemia major: the UK experience in two paediatric centres
Published in British journal of haematology (01-01-2003)“…Stem cell transplantation (SCT) remains the only cure for thalassaemia major. Recent advances in medical treatment make it even more important that accurate…”
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Systems medicine dissection of chr1q-amp reveals a novel PBX1-FOXM1 axis for targeted therapy in multiple myeloma
Published in Blood (31-03-2022)“…Understanding the biological and clinical impact of copy number aberrations (CNAs) on the development of precision therapies in cancer remains an unmet…”
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13
Therapeutic challenges in childhood sickle cell disease Part 1: current and future treatment options
Published in British journal of haematology (01-03-2003)Get full text
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14
High resolution IgH repertoire analysis reveals fetal liver as the likely origin of life-long, innate B lymphopoiesis in humans
Published in Clinical immunology (Orlando, Fla.) (01-10-2017)“…The ontogeny of the natural, public IgM repertoire remains incompletely explored. Here, high-resolution immunogenetic analysis of B cells from (unrelated)…”
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15
Haemolytic disease of the newborn
Published in Archives of disease in childhood. Fetal and neonatal edition (01-03-2007)“…Table 1 Causes of haemolytic disease of the newborn presenting as early-onset or rapidly progressive hyperbilirubinaemia not predicted by maternal antibody…”
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Targeted Therapy for Inherited GPI Deficiency
Published in The New England journal of medicine (19-04-2007)“…Inherited glycosylphosphatidylinositol (GPI) deficiency, characterized by splanchnic vein thrombosis and epilepsy, is caused by a mutation in the promoter…”
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PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts : implications for the pathogenesis of paroxysmal nocturnal haemoglobinuria
Published in British journal of haematology (01-12-2000)“…The mechanism responsible for the bone marrow failure that is almost invariable in paroxysmal nocturnal haemoglobinuria (PNH) is unknown. Based on the close…”
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Cell-type–specific transcriptional regulation of PIGM underpins the divergent hematologic phenotype in inherited GPl deficiency
Published in Blood (13-11-2014)“…A rare point mutation in the core promoter −270GC-rich box of PIGM, a housekeeping gene, disrupts binding of the generic transcription factor (TF) Sp1 and…”
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The changing face of haemolytic disease of the newborn
Published in Early human development (01-08-2008)“…Abstract The diagnosis, acute management and follow-up of neonates with haemolytic disease of the newborn (HDN) still represents a significant area of activity…”
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Expandability of haemopoietic progenitors in first trimester fetal and maternal blood: implications for non-invasive prenatal diagnosis
Published in Prenatal diagnosis (01-06-2002)“…Objectives Selective amplification of rare fetal cells in maternal blood is a potential strategy for non‐invasive prenatal diagnosis. We assessed the…”
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