Transient and intensive pharmacological immunosuppression fails to improve AAV-based liver gene transfer in non-human primates

Mycophenolate Mofetil Impairs Transduction of Single-Stranded Adeno-Associated Viral Vectors

(2011) Paula S. Montenegro-Miranda et al.   HUMAN GENE THERAPY

Adenovirus-Associated Virus Vector–Mediated Gene Transfer in Hemophilia B

(2011) Amit C. Nathwani et al.   NEW ENGLAND JOURNAL OF MEDICINE

Intensive Pharmacological Immunosuppression Allows for Repetitive Liver Gene Transfer With Recombinant Adenovirus in Nonhuman Primates

(2010) Antonio Fontanellas et al.   MOLECULAR THERAPY

Adeno-associated Virus Vectors Serotype 2 Induce Prolonged Proliferation of Capsid-Specific CD8+ T Cells in Mice

(2010) Hua Li et al.   MOLECULAR THERAPY

Sustained Enzymatic Correction by rAAV-Mediated Liver Gene Therapy Protects Against Induced Motor Neuropathy in Acute Porphyria Mice

(2010) Carmen Unzu et al.   MOLECULAR THERAPY

AAV as a Gene Transfer Vector for the Treatment of Neurological Disorders: Novel Treatment Thoughts for ALS

(2009) Mark Hester et al.   CURRENT GENE THERAPY

Effect of Adeno-Associated Virus Serotype and Genomic Structure on Liver Transduction and Biodistribution in Mice of Both Genders

(2009) Astrid Pañeda et al.   HUMAN GENE THERAPY

AAV8-mediated Gene Therapy Prevents Induced Biochemical Attacks of Acute Intermittent Porphyria and Improves Neuromotor Function

(2009) Makiko Yasuda et al.   MOLECULAR THERAPY

Mycophenolate mofetil: effects on cellular immune subsets, infectious complications, and antimicrobial activity

(2009) M.L. Ritter et al.   Transplant Infectious Disease

Potential of AAV vectors in the treatment of metabolic disease

(2008) I E Alexander et al.   GENE THERAPY

AAV-mediated gene transfer for the treatment of hemophilia B: problems and prospects

(2008) N C Hasbrouck et al.   GENE THERAPY