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Number of items: 74.

A

Adams, S and Veys, P and Hollifield, J and Gaspar, B (2004) Cell lineage specific chimerism in post-haematopoietic stem cell transplant patients. Bone Marrow Transplantation , 33 S101 - S102.

Ahmed, F and Ings, SJ and Pizzey, AR and Blundell, MP and Thrasher, AJ and T Ye, H and Fahey, A and Linch, DC and Yong, KL (2004) Impaired bone marrow homing of cytokine-activated CD34(+) cells in the NOD/SCID model. BLOOD , 103 (6) 2079 - 2087. 10.1182/blood-2003-06-1770.

Ahmed, F and Ings, SJ and Pizzey, AR and Blundell, MP and Thrasher, AJ and Ye, HT and Fahey, A and Linch, DC and Yong, KL (2004) Impaired bone marrow homing of cytokine-activated CD34+ cells in the NOD/SCID model. Blood , 103 (6) 2079 - 2087.
An open access version is available from UCL Discovery
 file

Akgul, C and Moulding, DA and Edwards, SW (2004) Alternative splicing of Bcl-2-related genes: functional consequences and potential therapeutic applications. CELL MOL LIFE SCI , 61 (17) 2189 - 2199. 10.1007/s00018-004-4001-7.

Albuquerque, W and Gaspar, HB (2004) Bilateral sensorineural deafness in adenosine deaminase-deficient severe combined immunodeficiency. J PEDIATR , 144 (2) 278 - 280. 10.1016/j.jpeds.2003.10.055.

Allen, K and Eddaoudi, A and Simpson, C and Warnes, G and Davies, DC (2004) The three E's in a ctyometry core facility: Education, education, education. In: CYTOMETRY PART A. (pp. 157 - 157). WILEY-LISS

Assari, T and Goldblatt, D and Thrasher, A (2004) Investigating mechanisms of inflammatory resolution in chronic gramulomatous disease. In: ESID Versailles, October 2004.

B

Balaggan, KS and Mistry, A and Georgiadis, T and Broderick, C and Bainbridge, J and Thrasher, AJ and Ali, RR (2004) Inhibition of experimental choroidal neovascularisation by lentivirus mediated delivery of pigment epithelium derived factor. Investigative Ophthalmology and Visual Science , 45 3705 - ?.

Beattie, RM and Champion, MP (2004) Essential questions in paediatrics for MRCPCH. PasTest Ltd

Bigger, BW and Siapati, KE and Mistry, A and Waddington, SN and Nivsarkar, MS and Holder, MV and Ridler, C and Kemball-Cook, G and Ali, RR and Forbes, S and Coutelle, C and Alison, M and Wright, N and Thrasher, AJ and Bonnet, D and Themis, M (2004) Induction of immune tolerance and partial phenotypic correction of haermophiliac mice by lentiviral gene transfer of human factor IX to haematopoietic stem cells. The Journal of Gene Medicine , 6 (9) 38 - ?.

Blundell, M and Ancliff, P and Cory, G and Jones, G and de Botton, S and Vainchanker, W and Thrasher, AJ (2004) Unregulated activation of the actin cytoskeleton through WASp promoters cell death and genomic instability. In: ESID Versailles, October 2004. (pp. 127 - ?).

Booth, MJ and Mistry, A and Li, X and Thrasher, A and Coffin, RS (2004) Transfection-free and scalable recombinant AAV vector production using HSV/AAV hybrids. Gene Therapy , 11 (10) 829 - 837.

Booth, MJ and Mistry, A and Li, X and Thrasher, A and Coffin, RS (2004) Transfection-free and scalable recombinant AAV vector production using HSV/AAV hybrids. GENE THER , 11 (10) 829 - 837. 10.1038/sj.gt.3302226.

Bouma, G and Lam-Tse, WK and Wierenga-Wolf, AF and Drexhage, HA and Versnel, MA (2004) Increased serum levels of MRP-8/14 in type 1 diabetes induce an increased expression of CD11b and an enhanced adhesion of circulating monocytes to fibronectin. DIABETES , 53 (8) 1979 - 1986.

Burns, S and Cory, GO and Vainchenker, W and Thrasher, AJ (2004) Mechanisms of WASp-mediated hematologic and immunologic disease. BLOOD , 104 (12) 3454 - 3462. 10.1182/blood-2004-04-1678.

Burns, S and Hardy, SJ and Buddle, J and Yong, KL and Jones, GE and Thrasher, AJ (2004) Maturation of DC is associated with changes in motile characteristics and adherence. CELL MOTIL CYTOSKEL , 57 (2) 118 - 132. 10.1002/cm.10163.

Burns, S and Thrasher, AJ (2004) Dendritic cells: The bare bones of immunity. CURR BIOL , 14 (22) R965 - R967. 10.1016/j.cub.2004.10.044.

C

Calle, Y and Chou, HC and Thrasher, AJ and Jones, GE (2004) Wiskott-Aldrich syndrome protein and the cytoskeletal dynamics of dendritic cells. J PATHOL , 204 (4) 460 - 469. 10.1002/path.1651.

Calle, Y and Jones, GE and Jagger, C and Fuller, K and Blundell, MP and Chow, J and Chambers, T and Thrasher, AJ (2004) WASp deficiency in mice results in failure to form osteoclast sealing zones and defects in bone resorption. BLOOD , 103 (9) 3552 - 3561.

Calle, Y and Jones, GE and Jagger, C and Fuller, K and Blundell, MP and Chow, J and Chambers, T and Thrasher, AJ (2004) WASp deficiency in mice results in failure to form osteoclast sealing zones and defects in bone resorption. Blood , 103 (9) 3552 - 3561. 10.1182/blood-2003-04-1259.

Cavazzana-Calvo, M and Thrasher, A and Mavillo, F (2004) The future of gene therapy. Nature , 427 (6977) 779 - 781.

Couedel, C and Lippert, E and Bernardeau, K and Bonneville, M and Davodeau, F (2004) Allelic exclusion at the TCR delta locus and commitment to gamma delta lineage: Different modalities apply to distinct human gamma delta subsets. J IMMUNOL , 172 (9) 5544 - 5552.

Couedel, C and Mills, KD and Barchi, M and Shen, L and Olshen, A and Johnson, RD and Nussenzweig, A and Essers, J and Kanaar, R and Li, GC and Alt, FW and Jasin, M (2004) Collaboration of homologous recombination and nonhomologous end-joining factors for the survival and integrity of mice and cells. GENE DEV , 18 (11) 1293 - 1304. 10.1101/gad.1209204.

E

Eastwood, D and Gilmour, KC and Gaspar, HB (2004) Molecular diagnosis of congenital immunodeficiency. Methods Mol Med , 91 91 - 108.

Eastwood, D and Gilmour, KC and Nistala, K and Meaney, C and Chapel, H and Sherrell, Z and Webster, AD and Davies, EG and Jones, A and Gaspar, HB (2004) Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency. CLIN EXP IMMUNOL , 137 (3) 584 - 588. 10.1111/j.1365-2249.2004.02581.x.

F

Fischer, A and Abina, SH and Thrasher, A and Von Kalle, C and Cavazzana-Calvo, M (2004) LMO2 and gene therapy for severe combined immunodeficiency. New England Journal of Medicine , 350 (24) 2526 - 2527.

Fischer, A and Hacein-Bey Abina, S and Thrasher, A and Von Kalle, C and Cavazzana-Calvo, M and Stone, BD and Rabbitts, TH and McCormack, MP (2004) LMO2 and gene therapy for severe combined immunodeficiency [7] (multiple letters). New England Journal of Medicine , 350 (24) 2526 - 2527.

G

Gaspar, HB and Bjorkegren, E and Parsley, K and Gilmour, K and Fairbanks, L and King, D and Davies, G and Veys, P and Kinnon, C and Thrasher, A (2004) Somatic gene therapy for ADA SCID following cessation of PEG-ADA and use of a mild conditioning regime. In: ESID Versailles, October 2004. (pp. 96 - ?).

Gaspar, HB and Harwood, C and Leigh, I and Thrasher, A (2004) Chronic cutaneous papillomavirus disease after haematopoietic stem-cell transplantation in patients with severe combined immune deficiency. In: ESID Versailles, October 2004. (pp. 100 - ?).

Gaspar, HB and Harwood, C and Leigh, I and Thrasher, AJ (2004) Severe cutaneous papillomavirus disease after haematopoietic stem-cell transplantation in patients with severe combined immunodeficiency [3]. British Journal of Haematology , 127 (2) 232 - 233.

Gaspar, HB and Parsley, K and Howe, S and Gilmour, K and Sinclair, J and Barington, A and Algonaim, A and Davies, G and Kinnon, C and Thrasher, A (2004) Update on treatment of human SCID-X1 by somatic gene therapy using a pseudotyped gammaretroviral vector. In: ESID Versailles, October 2004. (pp. 100 - ?).

Gaspar, HB and Parsley, KL and Howe, S and King, D and Gilmour, KC and Sinclair, J and Brouns, G and Schmidt, M and Von Kalle, C and Barington, T and Jakobsen, MA and Christensen, HO and Al Ghonaium, A and White, HN and Smith, JL and Levinsky, RJ and Ali, RR and Kinnon, C and Thrasher, AJ (2004) Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector. LANCET , 364 (9452) 2181 - 2187.

Gaspar, HB and Parsley, KL and Howe, S and King, D and Gilmour, KC and Sinclair, J and Brouns, G and Schmidt, M and Von Kalle, C and Barington, T and Jakobsen, MA and Christensen, HO and Al Ghonaium, A and White, HN and Smith, JL and Levinsky, RJ and Ali, RR and Kinnon, C and Thrasher, AJ (2004) Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector. Lancet , 364 (9452) 2181 - 2187. 10.1016/S0140-6736(04)17590-9.

Gennery, AR and Khawaja, K and Veys, P and Bredius, RG and Notarangelo, LD and Mazzolari, E and Fischer, A and Landais, P and Cavazzana-Calvo, M and Friedrich, W and Fasth, A and Wulffraat, NM and Matthes-Martin, S and Bensoussan, D and Bordigoni, P and Lange, A and Pagliuca, A and Andolina, M and Cant, AJ and Davies, EG (2004) Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002. Blood , 103 (3) 1152 - 1157. 10.1182/blood-2003-06-2014.

Gennery, AR and Thrasher, AJ (2004) Gene therapy for severe combined immunodeficiency. Current Anaesthesia and Critical Care , 15 (1) 3 - 9.

Gilmour, K and Eastwood, D and Nistala, C and Meaney, C and Chapel, H and Sherrell, Z and Webster, DA and Davies, EG and Jones, A and Gaspar, HB (2004) Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency. In: ESID Versailles, October 2004. (pp. 125 - ?).

Grosse, S and Aron, Y and Honore, I and Thevenot, G and Danel, C and Roche, AC and Monsigny, M and Fajac, I (2004) Lactosylated polyethylenimine for gene transfer into airway epithelial cells: role of the sugar moiety in cell delivery and intracellular trafficking of the complexes. The Journal of Gene Medicine , 6 (3) 345 - 356. 10.1002/jgm.515.

H

Hart, SL (2004) Synthetic vectors: Prospects and opportunities. The Journal of Gene Medicine , 6 (9) 2 - ?.

Hassan, AS and Elawad, MA and Davies, G and Rao, K and Amrolia, P and Veys, P (2004) Risk factors for graft-versus-host disease of the gut in paediatric haematopoetic stem cell transplant. In: Bone Marrow Transplantation. (pp. S180 - S180).

Hodges, RJ and Jenkins, RG and Wheeler-Jones, CPD and Copeman, DM and Bottoms, SE and Bellingan, GJ and Nanthakumar, CB and Laurent, GJ and Hart, SL and Foster, ML and McAnulty, RJ (2004) Severity of lung injury in cyclooxygenase-2-deficient mice is dependent on reduced prostaglandin E-2 production. AM J PATHOL , 165 (5) 1663 - 1676.
An open access version is available from UCL Discovery
 file

Hubbard, VG and Breuer, J and Leigh, IM and Thrasher, A and Harwood, CA (2004) Viral warts following bone marrow transplantation for severe combined immunodeficiency harbour potentially oncogenic human papillomavirus types. British Journal of Dermatology , 151 19 - 19.

K

Kampmann, B and Cubitt, D and Naik, P and Depala, M and Hassan, A and Rao, K and Gaspar, H and Davies, G and Jones, A and Cale, C and Gilmour, K and Amrolia, P and Real, M and Foo, M and Bennet-Rees, N and Hewitt, N and Veys, P (2004) Which children die from overwhelming adenoviral infection following haematopoietic stem cell transplantation? In: Bone Marrow Transplantation. (pp. S22 - S22).

Kritz, AB and Writer, M and Kinnon, C and Hart, SL (2004) Peptides from phage display libraries for targeted gene delivery via the p75 neurotrophic receptor (p75NTR). In: JOURNAL OF GENE MEDICINE. (pp. S10 - S10). JOHN WILEY & SONS LTD

Kritz, AB and Writer, M and Kinnon, C and Hart, SL (2004) Peptides from phage display libraries for targeted gene delivery via the p75 neurotrophic receptor (p75NTR). The Journal of Gene Medicine , 6 (9) 22 - ?.

M

Martin, F and Toscano, MG and Blundell, M and Frecha, C and Srivastava, G and Santamaria, M and Thrasher, AJ and Molina, IJ (2004) Lentiviral vectors transcriptionally targeted to hematopoietic cells by WAS gene proximal promoter sequences restore Wiskott-Aldrich Syndrome defects. In: ESID Versailles.

Meng, QH and Robinson, D and Jenkins, RG and McAnulty, RJ and Hart, SL (2004) Efficient transfection of non-proliferating human airway epithelial cells with a synthetic vector system. J GENE MED , 6 (2) 210 - 221. 10.1002/jgm.483.

N

Nabarro, S and Thrasher, A and Kempski, H and Anderson, J (2004) The Generation of Immunostimulatory Dendritic Cells from the Malignant Clone in Patients with Juvenile Myelomonocytic Leukemia. Leukemia , 17 1910 - 1912.

P

Philpott, NJ and Gomos, J and Falck-Pedersen, E (2004) Transgene expression after rep-mediated site-specific integration into chromosome 19. Human Gene Therapy , 15 (1) 47 - 61. 10.1089/10430340460732454.

Philpott, NJ and Nociari, M and Falck-Pedersen, E (2004) Adenovirus-induced maturation of dendritic cells through a PI3 kinase-mediated TNF-alpha induction pathway. Proceedings of the National Academy of Sciences of the United States of America , 101 (16) 6200 - 6205. 10.1073/pnas.0308368101.

Q

Qasim, W and Amrolia, PJ (2004) Cellular immunotherapy for viral disease following haematopoietic stem cell transplantation. Blood Therapies in Medicine , 4 (2) 1 - 11.

Qasim, W and Chatziandreou, I and Thrasher, A and Gaspar, H (2004) Lentiviral vector and suicide gene systems for T-cell therapies. BONE MARROW TRANSPLANTATION , 33 S22 - S22.

Qasim, W and Chatziandreou, L and Thrasher, A and Gaspar, H (2004) Lentiviral delivery of suicide gene and selection molecules to non-dividng T cells. In: BLOOD. (pp. 403B - 404B). AMER SOC HEMATOLOGY

Qasim, W and Gaspar, HB and Thrasher, AJ (2004) Gene therapy for severe combined immune deficiency. Expert Rev Mol Med , 6 (13) 1 - 15. 10.1017/S1462399404007884.

Quartier, P and Bustamante, J and Sanal, O and Plebani, A and Debre, M and Deville, A and Litzman, J and Levy, J and Fermand, JP and Lane, P and Horneff, G and Aksu, G and Yalcin, I and Davies, G and Tezcan, I and Ersoy, F and Catalan, N and Imai, K and Fischer, A and Durandy, A (2004) Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation- Induced Cytidine Deaminase deficiency (vol 110, pg 22, 2004). Clinical Immunology , 113 (2) 220 - 220.

R

Raghuram, CP and Wynn, RF and Will, A and Carr, T and Veys, P and Webb, D and Amrolia, P and Rao, K and Barber, S and Cornish, J and Steward, C and Goulden, N (2004) Reduced-intensity conditioning in first and second allograft in children without immunodeficiency: experience of three British transplant centres. In: Bone Marrow Transplantation. (pp. S48 - S49).

Roesler, J and Horwitz, ME and Picard, C and Bordigoni, P and Davies, G and Koscielniak, E and Levin, M and Veys, P and Reuter, U and Schulz, A and Thiede, C and Klingebiel, T and Fischer, A and Holland, SM and Casanova, JL and Friedrich, W (2004) Hematopoietic stem cell transplantation for complete IFN-gamma receptor 1 deficiency: a multi-institutional survey. J Pediatr , 145 (6) 806 - 812. 10.1016/j.jpeds.2004.08.021.

S

Schlichtenbrede, FC and Smith, AJ and Bainbridge, JWB and Thrasher, AJ and Salt, TE and Ali, RR (2004) Improvement of neuronal visual responses in the superior colliculus in Prph2 (Rd2/Rd2) mice following gene therapy. MOL CELL NEUROSCI , 25 (1) 103 - 110. 10.1016/j.mcn.2003.09.020.

Schwarzwaelder, K and Schmidt, M and Howe, S and Prinz, C and Wissler, M and Schmidt, S and Deichmann, A and Glimm, H and Gaspar, HB and Thrasher, A and Von Kalle, C (2004) Sustained polyclonal hematopoietic repopulation after successful SCID-X1 gene therapy by means of a non random integrating pseudotyped gammaretrovector. In: ESGT Finland Nov 2004.

Schwickerath, O and Brouns, G and Thrasher, A and Kinnon, C and Roes, J and Casimir, C (2004) Enhancer-deleted retroviral vectors restore high levels of superoxide generation in a mouse model of CGD. J GENE MED , 6 (6) 603 - 615. 10.1002/jgm.557.

Sebire, NJ and Malone, M and Anderson, G and Shah, N and Gaspar, HB and Cubitt, WD (2004) "Human intestinal astrovirus infection in an immunocompromised child following bone marrow transplantation". In: (pp. 39A - ?).

Sebire, NJ and Malone, M and Anderson, G and Shah, N and Gaspar, HB and Cubitt, WD (2004) Human intestinal astrovirus infection in an immunocomprimised child following bone marrow transplantation. In: JOURNAL OF PATHOLOGY. (pp. 39A - 39A). JOHN WILEY & SONS LTD

Sebire, NJ and Malone, M and Shah, N and Anderson, G and Gaspar, HB and Cubitt, WD (2004) Pathology of astrovirus associated diarrhoea in a paediatric bone marrow transplant recipient. J CLIN PATHOL , 57 (9) 1001 - 1003. 10.1136/jcp.2004.017178.

Seymour, RM and Allan, MJ and Pomiankowski, A and Gustafsson, K (2004) Evolution of the human ABO polymorphism by two complementary selective pressures. P R SOC B , 271 (1543) 1065 - 1072. 10.1098/rspb.2004.2674.

Sharifi, R and Sinclair, JC and Gilmour, KC and Arkwright, PD and Kinnon, C and Thrasher, AJ and Gaspar, HB (2004) SAP mediates specific cytotoxic T-cell functions in X-linked lymphoproliferative disease. BLOOD , 103 (10) 3821 - 3827. 10.1182/blood-2003-09-3359.

Spencer, H and Rampling, D and Aurora, P and Bonnet, D and Hart, SL and Jaffe, A (2004) Evidence for long-term epithelial engraftment in children following sex-mismatched lung transplantation. In: Journal of Cystic Fibrosis. (pp. S28 - ?).

T

Thrasher, AJ (2004) Haematological trials for monogenic disorders; lessons to be learned. The Journal of Gene Medicine , 6 (9) 43 - ?.

Thrasher, AJ and Edwards, RG (2004) Averting abnormal inheritance: potential of gene therapy and preimplantation diagnosis. REPROD BIOMED ONLINE , 8 (1) 99 - 106.

Thrasher, AJ and Edwards, RG (2004) Averting abnormal inheritance: potential of gene therapy and preimplantation diagnosis. Reprod Biomed Online , 8 (1) 99 - 106.

Titman, P and Pink, L and Melvin, D and Gaspar, J and Jones, AM and Davies, EG and Thrasher, AJ and Gaspar, HB (2004) Cognitive and behavioiural outcome following haematopoietic stem cell transplantation for severe congenital immunodeficiencies. In: ESID Versailles, October 2004. (pp. 167 - ?).

W

Waddington, S.N. and Nivsarkar, M.S. and Mistry, A.R. and Buckley, S.M.K. and Kemball-Cook, G. and Mosley, K.L. and Mitrophanous, K. and Radcliffe, P. and Holder, M.V. and Brittan, M. and Georgiadis, A. and Al-Allaf, F. and Bigger, B.W. and Gregory, L.G. and Cook, H.T. and Ali, R.R. and Thrasher, A. and Tuddenham, E.D.G. and Themis, M. and Coutelle, C. (2004) Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy. Blood , 104 (9) pp. 2714-2721. 10.1182/blood-2004-02-0627.

Waddington, SN and Nivsarkar, M and Mistry, A and Buckley, SMK and Kemball-Cook, G and Mosley, KL and Mitrophanous, K and Radcliffe, P and Holder, M and Brittan, M and Georgiadis, T and Al-Allaf, F and Bigger, B and Gregory, L and Cook, HT and Ali, RR and Thrasher, A and Tuddenham, EGD and Themis, M and Coutelle, C (2004) Permanent phenotypic correction of Haemophilia B in immunocompetent mice by prenatal gene therapy. In: JOURNAL OF GENE MEDICINE. (pp. S17 - S17). JOHN WILEY & SONS LTD

Waddington, SN and Nivsarkar, MS and Mistry, AR and Buckley, SMK and Kemball-Cook, G and Mosley, KL and Mitrophanous, K and Radcliffe, P and Holder, MV and Brittan, M and Georgiadis, A and Al-Allaf, F and Bigger, BW and Gregory, LG and Cook, HT and Ali, RR and Thrasher, A and Tuddenham, EGD and Themis, M and Coutelle, C (2004) Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy. BLOOD , 104 (9) 2714 - 2721. 10.1182/blood-2004-02-0627.

Writer, MJ and Marshall, B and Pilkington-Miksa, MA and Barker, SE and Jacobsen, M and Kritz, A and Bell, PC and Lester, DH and Tabor, AB and Hailes, HC and Klein, N and Hart, SL (2004) Targeted gene delivery to human airway epithelial cells with synthetic vectors incorporating novel targeting peptides selected by phage display. J DRUG TARGET , 12 (4) 185 - 193. 10.1080/10611860410001724459.

Y

Yeung, J and O'Sullivan, E and Hubank, M and Brady, HJM (2004) E4BP4 expression is regulated by the t(17;19)-associated oncoprotein E2A-HLF in pro-B cells. BRIT J HAEMATOL , 125 (5) 560 - 567. 10.1111/j.1365-2141.2004.04953.x.

This list was generated on Tue May 21 08:57:51 2013 BST.