List of works - Annick Lim

A modified γ-retrovirus vector for X-linked severe combined immunodeficiency

scientific article

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

scientific article

A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR(-) B cells.

scientific article

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

scientific article published on 25 July 2015

Clonal evidence for the transduction of CD34+ cells with lymphomyeloid differentiation potential and self-renewal capacity in the SCID-X1 gene therapy trial

scientific article published on 7 December 2004

EVER2 deficiency is associated with mild T-cell abnormalities

scientific article published on 19 August 2012

Efficacy of gene therapy for X-linked severe combined immunodeficiency

scientific article

Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections

scientific article (publication date: 4 September 2012)

Human TCR alpha/beta+ CD4-CD8- double-negative T cells in patients with autoimmune lymphoproliferative syndrome express restricted Vbeta TCR diversity and are clonally related to CD8+ T cells

scientific article published on July 2008

Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

scientific article

MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival

scientific article published on 14 December 2011

Massive expansion of maternal T cells in response to EBV infection in a patient with SCID-Xl

article

Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome

scientific article published on April 2015

Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")

scientific article

Stable and functional lymphoid reconstitution in artemis-deficient mice following lentiviral artemis gene transfer into hematopoietic stem cells.

scientific article published on 17 June 2008

Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation

scientific article published on 21 March 2013

List of works by Annick Lim

A modified γ-retrovirus vector for X-linked severe combined immunodeficiency

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR(-) B cells.

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

Clonal evidence for the transduction of CD34+ cells with lymphomyeloid differentiation potential and self-renewal capacity in the SCID-X1 gene therapy trial

EVER2 deficiency is associated with mild T-cell abnormalities

Efficacy of gene therapy for X-linked severe combined immunodeficiency

Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections

Human TCR alpha/beta+ CD4-CD8- double-negative T cells in patients with autoimmune lymphoproliferative syndrome express restricted Vbeta TCR diversity and are clonally related to CD8+ T cells

Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival

Massive expansion of maternal T cells in response to EBV infection in a patient with SCID-Xl

Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome

Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")

Stable and functional lymphoid reconstitution in artemis-deficient mice following lentiviral artemis gene transfer into hematopoietic stem cells.

Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation