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Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo

Gene therapy, 2004-05, Vol.11 (10), p.856-864

2004

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Upregulation of the microRNA cluster at the Dlk1-Dio3 locus in lung adenocarcinoma

Oncogene, 2015-01, Vol.34 (1), p.94-103

2015

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A compound methodology to assess the impact of human and organizational factors impact on the risk level of hazardous industrial plants

Reliability engineering & system safety, 2013-11, Vol.119, p.280-289

2013

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From virus evolution to vector revolution: use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapy

Current gene therapy, 2003-08, Vol.3 (4), p.281

2003

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Therapeutic short hairpin RNA expression in the liver: viral targets and vectors

Gene therapy, 2006-03, Vol.13 (6), p.563-575

2006

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What can we learn from wildlife sightings during the COVID‐19 global shutdown?

Ecosphere (Washington, D.C), 2020-08, Vol.11 (8), p.e03215-n/a

2020

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A simplified system for constructing recombinant adenoviral vectors containing heterologous peptides in the HI loop of their fiber knob

Gene therapy, 2001-05, Vol.8 (9), p.730-735

2001

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Sustainable correction of junctional epidermolysis bullosa via transposon-mediated nonviral gene transfer

Gene therapy, 2003-07, Vol.10 (13), p.1099-1104

2003

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Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system

Nature genetics, 2000-05, Vol.25 (1), p.35-41

2000

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Promoterless gene targeting without nucleases ameliorates haemophilia B in mice

Nature (London), 2015-01, Vol.517 (7534), p.360-364

2015

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Extrachromosomal Recombinant Adeno-Associated Virus Vector Genomes Are Primarily Responsible for Stable Liver Transduction In Vivo

Journal of Virology, 2001-08, Vol.75 (15), p.6969-6976

2001

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Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

Nature genetics, 1997-07, Vol.16 (3), p.270-276

1997

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Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector

Nature genetics, 2000-03, Vol.24 (3), p.257-261

2000

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A simple method for constructing E1- and E1/E4-deleted recombinant adenoviral vectors

Human gene therapy, 1999-08, Vol.10 (12), p.2013-2017

1999

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Plurilingual Pedagogies for Multilingual Writing Classrooms: Engaging the Rich Communicative Repertoires of U.S. Students

1, 2022

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Efficient lentiviral transduction of liver requires cell cycling in vivo

Nature genetics, 2000-01, Vol.24 (1), p.49-52

2000

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Barriers to building wildlife‐inclusive cities: Insights from the deliberations of urban ecologists, urban planners and landscape designers

People and nature (Hoboken, N.J.), 2022-02, Vol.4 (1), p.62-70

2022

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Recruitment of Single-Stranded Recombinant Adeno-Associated Virus Vector Genomes and Intermolecular Recombination Are Responsible for Stable Transduction of Liver In Vivo

Journal of Virology, 2000-10, Vol.74 (20), p.9451-9463

2000

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The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors

Journal of Virology, 1997-11, Vol.71 (11), p.8798-8807

1997

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The effect of physical activity on mother-child relationship and parental attitudes: a follow-up study examining the long-term effects of COVID-19

European review for medical and pharmacological sciences, 2023-05, Vol.27 (9), p.4299

2023

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Site-directed transposon integration in human cells

Nucleic acids research, 2007-04, Vol.35 (7), p.e50

2007

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In vivo Hepatic Gene Therapy: Complete Albeit Transient Correction of Factor IX Deficiency in Hemophilia B Dogs

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (6), p.2353-2357

1994

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Peak moments: the experience of coaches

International journal of evidence based coaching and mentoring, 2022-06 (S16), p.159-172

Kay AM Weijers

2022

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Gene Therapy for the Hemophilias

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (18), p.9973-9975

1999

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Recombinant adenoviruses with large deletions generated by Cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo

Journal of Virology, 1996-12, Vol.70 (12), p.8944-8960

1996

Volltextzugriff (PDF)

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