Search Results - "Roberts, Irene A. G"

Refine Results
  1. 1

    Microchimerism in female bone marrow and bone decades after fetal mesenchymal stem-cell trafficking in pregnancy by O'Donoghue, Keelin, Chan, Jerry, de la Fuente, Josu, Kennea, Nigel, Sandison, Ann, Anderson, Jonathan R, Roberts, Irene AG, Fisk, Nicholas M

    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…”
    Get full text
    Journal Article
  2. 2

    Activated invariant NKT cells regulate osteoclast development and function by Hu, Ming, Bassett, J H Duncan, Danks, Lynett, Howell, Peter G T, Xu, Ke, Spanoudakis, Emmanouil, Kotsianidis, Ioannis, Boyde, Alan, Williams, Graham R, Horwood, Nikki, Roberts, Irene A G, Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  3. 3
  4. 4

    Identification of mesenchymal stem/progenitor cells in human first-trimester fetal blood, liver, and bone marrow by Campagnoli, Cesare, Roberts, Irene A.G., Kumar, Sailesh, Bennett, Phillip R., Bellantuono, Ilaria, Fisk, Nicholas M.

    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…”
    Get full text
    Journal Article
  5. 5

    Can routine commercial cord blood banking be scientifically and ethically justified? by Fisk, Nicholas M, Roberts, Irene A G, Markwald, Roger, Mironov, Vladimir

    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…”
    Get full text
    Journal Article
  6. 6

    Regulation of hematopoiesis in vitro and in vivo by invariant NKT cells by Kotsianidis, Ioannis, Silk, Jonathan D., Spanoudakis, Emmanouil, Patterson, Scott, Almeida, Antonio, Schmidt, Richard R., Tsatalas, Costas, Bourikas, George, Cerundolo, Vincenzo, Roberts, Irene A.G., Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  7. 7
  8. 8

    Human Invariant NKT Cells Are Required for Effective In Vitro Alloresponses by Patterson, Scott, Kotsianidis, Ioannis, Almeida, Antonio, Politou, Marianna, Rahemtulla, Amin, Matthew, Bini, Schmidt, Richard R, Cerundolo, Vincenzo, Roberts, Irene A. G, Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  9. 9

    Human Invariant NKT Cells Display Alloreactivity Instructed by Invariant TCR-CD1d Interaction and Killer Ig Receptors by Patterson, Scott, Chaidos, Aristeidis, Neville, David C. A, Poggi, Alessandro, Butters, Terry D, Roberts, Irene A. G, Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  10. 10

    Stem cell transplantation for chronic myeloid leukemia in children by Cwynarski, Kate, Roberts, IreneA.G., Iacobelli, Simona, van Biezen, Anja, Brand, Ronald, Devergie, Agnes, Vossen, Jaak M., Aljurf, Mahmoud, Arcese, William, Locatelli, Franco, Dini, Giorgio, Niethammer, Dietrich, Niederwieser, Dietger, Apperley, Jane F.

    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…”
    Get full text
    Journal Article
  11. 11

    Bone marrow transplantation for β‐thalassaemia major: the UK experience in two paediatric centres by Lawson, Sarah E., Roberts, Irene A. G., Amrolia, Persis, Dokal, Inderjeet, Szydlo, Richard, Darbyshire, Philip J.

    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…”
    Get full text
    Journal Article
  12. 12
  13. 13
  14. 14
  15. 15

    Haemolytic disease of the newborn by Murray, Neil A, Roberts, Irene A G

    “…Table 1 Causes of haemolytic disease of the newborn presenting as early-onset or rapidly progressive hyperbilirubinaemia not predicted by maternal antibody…”
    Get full text
    Journal Article
  16. 16

    Targeted Therapy for Inherited GPI Deficiency by Almeida, Antonio M, Murakami, Yoshiko, Baker, Alastair, Maeda, Yusuke, Roberts, Irene A.G, Kinoshita, Taroh, Layton, D. Mark, Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  17. 17

    PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts : implications for the pathogenesis of paroxysmal nocturnal haemoglobinuria by KARADIMITRIS, Anastasios, NOTARO, Rosario, KOEHNE, Gunther, ROBERTS, Irene A. G, LUZZATTO, Lucio

    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…”
    Get full text
    Journal Article
  18. 18

    Cell-type–specific transcriptional regulation of PIGM underpins the divergent hematologic phenotype in inherited GPl deficiency by Costa, Joana R., Caputo, Valentina S., Makarona, Kalliopi, Layton, D. Mark, Irene Roberts, A.G., Almeida, Antonio M., Karadimitris, Anastasios

    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…”
    Get full text
    Journal Article
  19. 19

    The changing face of haemolytic disease of the newborn by Roberts, Irene A.G

    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…”
    Get full text
    Journal Article
  20. 20

    Expandability of haemopoietic progenitors in first trimester fetal and maternal blood: implications for non-invasive prenatal diagnosis by Campagnoli, Cesare, Roberts, Irene A. G., Kumar, Sailesh, Choolani, Mahesh, Bennett, Phillip R., Letsky, Elizabeth, Fisk, Nicholas M.

    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…”
    Get full text
    Journal Article