Latest papers

MicroRNA-restricted transgene expression in the retina.

Zinc Finger Protein, Multitype 1, Suppresses Human Th2 Development via Downregulation of IL-4

Transduction of SIV-specific TCR genes into rhesus macaque CD8+ T cells conveys the ability to suppress SIV replication.

Genetic modification of chondrocytes using viral vectors.

Hepatocyte growth factor modification promotes the amelioration effects of human umbilical cord mesenchymal stem cells on rat acute kidney injury.

The c-Abl tyrosine kinase controls protein kinase Cδ-induced Fli-1 phosphorylation in human dermal fibroblasts.

HOIL-1L interacting protein (HOIP) is essential for CD40 signaling.

Enhancement of bone formation by BMP-7 transduced MSCs on biomimetic nano-hydroxyapatite/polyamide composite scaffolds in repair of mandibular defects.

The efficacy of combination therapy using adeno-associated virus-TRAIL targeting to telomerase activity and cisplatin in a mice model of hepatocellular carcinoma.

Suppression of metastatic murine ovarian cancer cells by transduced embryonic progenitor cells.

Epidermal growth factor targeting of bacteriophage to the choroid plexus for gene delivery to the central nervous system via cerebrospinal fluid

T cells expressing constitutively active Akt resist multiple tumor-associated inhibitory mechanisms.

Human mesenchymal stem cells infiltrate the spinal cord, reduce demyelination, and localize to white matter lesions in experimental autoimmune encephalomyelitis.

Satellite phage TLCφ enables toxigenic conversion by CTX phage through dif site alteration.

Biodistribution and retargeting of FX-binding ablated adenovirus serotype 5 vectors.

Enhanced receptor expression and in vitro effector function of a murine-human hybrid MART-1-reactive T cell receptor following a rapid expansion.

Site-specific gene insertion mediated by a Cre-loxP-carrying lentiviral vector.

Targeted antitumor effect induced by hTERT promoter mediated ODC antisense adenovirus.

Advances in the field of lentivector-based transduction of T and B lymphocytes for gene therapy.

Effects of recombinant adeno-associated viral vectors on angiopoiesis and osteogenesis in cultured rabbit bone marrow stem cells via co-expressing hVEGF and hBMP genes: A preliminary study in vitro