(Q45874811)

English

Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients

scientific article published on 27 November 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

cell differentiation

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Jean-Pierre de Villartay

9

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

11

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Marina Cavazzana

13

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Salima Hacein-Bey-Abina

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object named as

Salima Hacein-Bey-Abina

0 references

Chantal Lagresle-Peyrou

1

object named as

Chantal Lagresle-Peyrou

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Pierre Charneau

10

object named as

Pierre Charneau

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

12

object named as

Alain Fischer

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Monique Forveille

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object named as

Monique Forveille

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Fatine Benjelloun

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object named as

Fatine Benjelloun

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

author name string

Chantal Lagresle-Peyrou

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Christophe Hue

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Isabelle Andre-Schmutz

4

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Delphine Bonhomme

5

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Kheira Beldjord

7

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

publication date

27 November 2007

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Molecular Therapy

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

16

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Europe PubMed Central

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17 December 2017

http://europepmc.org/abstract/MED/18223550

2

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

396-403

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

Gene therapy for severe combined immunodeficiency

1 reference

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The mechanisms of immune diversification and their disorders

1 reference

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RAG mutations in human B cell-negative SCID.

1 reference

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based on heuristic

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Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

1 reference

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Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99

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Severe combined immunodeficiency. A model disease for molecular immunology and therapy

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Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

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Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning

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

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

1 reference

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Adapted NOD/SCID model supports development of phenotypically and functionally mature T cells from human umbilical cord blood CD34(+) cells.

1 reference

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7 January 2021

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Murine IL-2 receptor beta chain blockade improves human leukocyte engraftment in SCID mice.

1 reference

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7 January 2021

based on heuristic

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The metallo-beta-lactamase/beta-CASP domain of Artemis constitutes the catalytic core for V(D)J recombination

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MT.6300353

7 January 2021

based on heuristic

inferred from DOI database lookup

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MT.6300353

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Leaky Scid phenotype associated with defective V(D)J coding end processing in Artemis-deficient mice

1 reference

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7 January 2021

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Complete correction of murine Artemis immunodeficiency by lentiviral vector-mediated gene transfer

1 reference

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based on heuristic

inferred from DOI database lookup

Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicity

1 reference

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NOD/SCID/gamma(c)(null) mouse: an excellent recipient mouse model for engraftment of human cells

1 reference

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Human lymphoid and myeloid cell development in NOD/LtSz-scid IL2R gamma null mice engrafted with mobilized human hemopoietic stem cells

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Pois(s)on--it's a question of dose...

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https://api.crossref.org/works/10.1038%2FSJ.MT.6300353

7 January 2021

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Similar myeloid recovery despite superior overall engraftment in NOD/SCID mice after transplantation of human CD34(+) cells from umbilical cord blood as compared to adult sources

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MT.6300353

7 January 2021

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Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors.

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7 January 2021

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A lentiviral vector encoding the human Wiskott-Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice.

1 reference

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7 January 2021

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Enhanced transgene expression in cord blood CD34(+)-derived hematopoietic cells, including developing T cells and NOD/SCID mouse repopulating cells, following transduction with modified trip lentiviral vectors

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Selective long-term elimination of natural killer cells in vivo by an anti-interleukin 2 receptor beta chain monoclonal antibody in mice

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Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936.

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Identifiers

10.1038/SJ.MT.6300353

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/18223550

ResearchGate publication ID

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