Gene therapy for severe combined immunodeficiency.
Explore this paper's citation graph
Summary
Recent developments in SCID identification and treatment are discussed, including the possibility of molecular therapy as an alternative to allogeneic hematopoietic stem cell transplantation.
- Type
- article
- Published
- 2005-01-01
- Cited by
- 128
- References
- 70
- OpenAlex
- https://openalex.org/W15660528
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:23245221
Keywords
Humanities, Philosophy, Physics
References
- Restoration of lymphocyte function in Janus Kinase 3-deficient mice by retroviral-mediated gene transfer
- Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease.
- Murine Leukemia Induced by Retroviral Gene Marking
- Bone marrow gene transfer in three patients with adenosine deaminase deficiency.
- Restoration of lymphoid populations in a murine model of X-linked severe combined immunodeficiency by a gene-therapy approach.
- TTG-2, a new gene encoding a cysteine-rich protein with the LIM motif, is overexpressed in acute T-cell leukaemia with the t(11;14)(p13;q11).
- Update on treatment of human SCID-X1 by somatic gene therapy using a pseudotyped gammaretroviral vector
- Stable and functional lymphoid reconstitution of common cytokine receptor gamma chain deficient mice by retroviral-mediated gene transfer.
- T Cell Repertoire Development in Humans with SCID After Nonablative Allogeneic Marrow Transplantation 1
- Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease
- MHC class II deficiency: a disease of gene regulation.
- Gene Therapy Insertional Mutagenesis Insights
- Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency
- Lack of dominant-negative effects of a truncated gamma(c) on retroviral-mediated gene correction of immunodeficient mice.
- Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursor.
- Position-effect protection and enhancer blocking by the chicken β-globin insulator are separable activities
- Purine Nucleoside Phosphorylase Deficiency Associated with a Dysplastic Marrow Morphology
- Immunological reconstitution of sex-linked lymphopenic immunological deficiency.
- Primary immunodeficiency diseases: dissectors of the immune system
- Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells.
Cited by
- Shock wave-induced permeabilization of mammalian cells.
- Gene therapy for Athabascan SCID
- LA NICHE ÉCOLOGIQUE: CONCEPTS, MODÈLES, APPLICATIONS
- Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine.
- Chromosomal integration in vitro and in vivo of high capacity adenoviral vectors
- Développement de vecteurs lentiviraux régulables pour le transfert de gène dans le système nerveux central
- The fetal respiratory system as target for antenatal therapy
- The interdependence between biological and ethical analyses of safety and efficacy in translational gene therapy
- Etude et Développement de Vecteurs Synthétiques pour la Délivrance d'Oligonucléotides à visée thérapeutique.
- Investigation of the effects of virus integration on host gene expression in mouse tumour samples
- The quest for new improved adenovirus gene therapy vectors against glioma tumours
- Estudio inmunológico de las inmunodeficiencias primarias de células T y B
- The use of retroviral vectors for gene transfer into hematopoietic stem cells.
- Use of murine models to test novel gene transfer strategies for the treatment of fanconi anemia
- Treatment of an infant with X‐linked severe combined immunodeficiency (SCID‐X1) by gene therapy in Australia
- Targeted delivery of biological agents.
- Implications for Gene Therapy-Limiting Expression of IL-2Rγc Delineate Differences in Signaling Thresholds Required for Lymphocyte Development and Maintenance
- Strategy of oral vaccination by polymeric nanoparticles : M cell targeting or bioadhesion
- Cell and tissue engineering and clinical applications: An overview
- CUESTIONAMIENTOS ÉTICOS RELACIONADOS CON LA TERAPIA GÉNICA PARA EL TRATAMIENTO DE ENFERMEDADES HEREDITARIAS
Related papers
No related papers recorded.