Jo Sinclair

发表

Failure of SCID-X1 gene therapy in older patients.

Kathryn L. Parsley, C. von Kalle, A. Fischer, 2005, Blood.

Successful reconstitution of immunity in ADA-SCID by stem cell gene therapy following cessation of PEG-ADA and use of mild preconditioning.

Kathryn L. Parsley, P. Veys, A. Thrasher, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

SAP mediates specific cytotoxic T-cell functions in X-linked lymphoproliferative disease.

A. Thrasher, C. Kinnon, K. Gilmour, 2004, Blood.

Bone morphogenetic protein 4 modulates c-Kit expression and differentiation potential in murine embryonic aorta-gonad-mesonephros haematopoiesis in vitro

A. Thrasher, C. Kinnon, C. Marshall, 2007, British journal of haematology.

Capture and generation of adenovirus specific T cells for adoptive immunotherapy

H. Bobby Gaspar, C. Kinnon, W. Qasim, 2007, British journal of haematology.

Gammaretrovirus-mediated correction of SCID-X1 is associated with skewed vector integration site distribution in vivo.

Christine Kinnon, Christof von Kalle, Dick de Ridder, 2007, The Journal of clinical investigation.

Mutations in TNFRSF13B Encoding TACI Are Associated With Common Variable Immunodeficiency in Humans

Christine Kinnon, Manfred Schmidt, R. Levinsky, 2006, Pediatrics.

Lentiviral vectors containing an enhancer-less ubiquitously acting chromatin opening element (UCOE) provide highly reproducible and stable transgene expression in hematopoietic cells

A. Schambach, A. Thrasher, M. Antoniou, 2007, Blood.

Impaired dendritic-cell homing in vivo in the absence of Wiskott-Aldrich syndrome protein.

Samantha J. Hardy, A. Thrasher, J. Strid, 2005, Blood.

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia.

Christine Kinnon, Austen Worth, A. Worth, 2006, Blood.

Lentiviral vectors for T-cell suicide gene therapy: preservation of T-cell effector function after cytokine-mediated transduction.

A. Thrasher, C. Kinnon, W. Qasim, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Impaired neutrophil migration and phagocytosis in IRAK‐4 deficiency

Smita Y. Patel, S. Burns, A. Thrasher, 2009, British journal of haematology.

Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia

Christine Kinnon, David G. Spiller, Adrian J. Thrasher, 2007, The Journal of experimental medicine.

Immune Reconstitution and Recovery of FOXP3 (Forkhead Box P3)-Expressing T Cells After Transplantation for IPEX (Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked) Syndrome

P. Amrolia, W. Qasim, H. Zhan, 2008, Pediatrics.

Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

K. Laurie, R. Holmdahl, K. Gustafsson, 2007, Gene Therapy.

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

Kathryn L. Parsley, R. Levinsky, R. Ali, 2004, The Lancet.

Update on treatment of human SCID-X1 by somatic gene therapy using a pseudotyped gammaretroviral vector

Kathryn L. Parsley, A. Thrasher, S. Howe, 2004 .

Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia

D. Spiller, M. White, A. Thrasher, 2007, The Journal of experimental medicine.