List of works - Suzanne M Buckley

AAV-mediated gene transfer in the perinatal period results in expression of FVII at levels that protect against fatal spontaneous hemorrhage.

scientific article published on December 2011

Animal models for prenatal gene therapy: rodent models for prenatal gene therapy.

scientific article

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors.

scientific article

Evidence for contribution of CD4+ CD25+ regulatory T cells in maintaining immune tolerance to human factor IX following perinatal adenovirus vector delivery

scientific article published on 31 January 2015

Factors influencing adenovirus-mediated airway transduction in fetal mice.

scientific article

Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease.

scientific article

Gene Therapy with Adeno-associated Virus for Cystic Fibrosis

scientific article

Gene delivery of a mutant TGFβ3 reduces markers of scar tissue formation after cutaneous wounding

scientific article

Genetic aspects and research development in haemostasis.

scientific article published on July 2008

In utero administration of Ad5 and AAV pseudotypes to the fetal brain leads to efficient, widespread and long-term gene expression.

scientific article

In utero gene therapy: current challenges and perspectives.

scientific article

In utero gene transfer to the mouse nervous system.

scientific article published on December 2010

In vivo bioimaging with tissue-specific transcription factor activated luciferase reporters.

scientific article published on 3 July 2015

Intra-amniotic delivery of CFTR-expressing adenovirus does not reverse cystic fibrosis phenotype in inbred CFTR-knockout mice.

scientific article

Intravenous administration of AAV2/9 to the fetal and neonatal mouse leads to differential targeting of CNS cell types and extensive transduction of the nervous system.

scientific article published on 11 July 2011

Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice.

scientific article published in August 2003

Longitudinal in vivo bioimaging of hepatocyte transcription factor activity following cholestatic liver injury in mice

scientific article published on 03 February 2017

Multiple vitamin K-dependent coagulation zymogens promote adenovirus-mediated gene delivery to hepatocytes

scientific article published on 20 June 2006

Perinatal Gene Delivery to the CNS ⬇️

scientific article published on April 1, 2011

Perinatal Gene Transfer to the Liver ⬇️

scientific article published on January 1, 2011

Perinatal systemic gene delivery using adeno-associated viral vectors

scientific article

Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy.

scientific article published in July 2004

Systemic delivery of scAAV9 in fetal macaques facilitates neuronal transduction of the central and peripheral nervous systems.

scientific article published on 26 January 2012

Systemic gene delivery following intravenous administration of AAV9 to fetal and neonatal mice and late-gestation nonhuman primates.

scientific article

Targeting of adenovirus serotype 5 (Ad5) and 5/47 pseudotyped vectors in vivo: fundamental involvement of coagulation factors and redundancy of CAR binding by Ad5.

scientific article

Transduction of fetal mice with a feline lentiviral vector induces liver tumors which exhibit an E2F activation signature.

scientific article published on 28 August 2013

List of works by Suzanne M Buckley

AAV-mediated gene transfer in the perinatal period results in expression of FVII at levels that protect against fatal spontaneous hemorrhage.

Animal models for prenatal gene therapy: rodent models for prenatal gene therapy.

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors.

Evidence for contribution of CD4+ CD25+ regulatory T cells in maintaining immune tolerance to human factor IX following perinatal adenovirus vector delivery

Factors influencing adenovirus-mediated airway transduction in fetal mice.

Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease.

Gene Therapy with Adeno-associated Virus for Cystic Fibrosis

Gene delivery of a mutant TGFβ3 reduces markers of scar tissue formation after cutaneous wounding

Genetic aspects and research development in haemostasis.

In utero administration of Ad5 and AAV pseudotypes to the fetal brain leads to efficient, widespread and long-term gene expression.

In utero gene therapy: current challenges and perspectives.

In utero gene transfer to the mouse nervous system.

In vivo bioimaging with tissue-specific transcription factor activated luciferase reporters.

Intra-amniotic delivery of CFTR-expressing adenovirus does not reverse cystic fibrosis phenotype in inbred CFTR-knockout mice.

Intravenous administration of AAV2/9 to the fetal and neonatal mouse leads to differential targeting of CNS cell types and extensive transduction of the nervous system.

Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice.

Longitudinal in vivo bioimaging of hepatocyte transcription factor activity following cholestatic liver injury in mice

Multiple vitamin K-dependent coagulation zymogens promote adenovirus-mediated gene delivery to hepatocytes

Perinatal Gene Delivery to the CNS ⬇️

Perinatal Gene Transfer to the Liver ⬇️

Perinatal systemic gene delivery using adeno-associated viral vectors

Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy.

Systemic delivery of scAAV9 in fetal macaques facilitates neuronal transduction of the central and peripheral nervous systems.

Systemic gene delivery following intravenous administration of AAV9 to fetal and neonatal mice and late-gestation nonhuman primates.

Targeting of adenovirus serotype 5 (Ad5) and 5/47 pseudotyped vectors in vivo: fundamental involvement of coagulation factors and redundancy of CAR binding by Ad5.

Transduction of fetal mice with a feline lentiviral vector induces liver tumors which exhibit an E2F activation signature.