T. Tabata

发表

Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1‐based vectors carrying the human coagulation factor VIII gene in NOD/SCID mice

A. Ishiwata, S. Madoiwa, J. Mimuro, 2004, The journal of gene medicine.

pag gene-like protein (ABP-25) of the Cynops embryo: regional distribution and gene expression during early embryogenesis

T. Tabata, K. Kamio, T. Tajima, 1995, Roux's archives of developmental biology.

TITLE Towards Gene Therapy for Cystic Fibrosis Using a Lentivirus Pseudotyped With Sendai Virus Envelopes

K. Mitomo, Y. Ueda, M. Hasegawa, 2015 .

Simian lentiviral vector-mediated retinal gene transfer of pigment epithelium-derived factor protects retinal degeneration and electrical defect in Royal College of Surgeons rats

S. Tobimatsu, Y. Goto, Y. Yonemitsu, 2003, Gene Therapy.

Expression of human coagulation factor VIII in adipocytes transduced with the simian immunodeficiency virus agmTYO1-based vector for hemophilia A gene therapy

S. Madoiwa, J. Mimuro, Y. Sakata, 2004, Gene Therapy.

Differences in the mode of cough augmentation by four angiotensin‐converting enzyme inhibitors in guinea‐pigs

T. Miyata, K. Takahama, T. Tabata, 1993, The Journal of pharmacy and pharmacology.

Comparative study of sequential expression of the organizer‐related genes in normal Cynops pyrrhogaster embryos and mesodermalized ectoderm

T. Tabata, T. Tajima, A. Suzuki, 2001, Development, growth & differentiation.

Stable retinal gene expression in nonhuman primates via subretinal injection of SIVagm-based lentiviral vectors.

Y. Yonemitsu, K. Sueishi, Y. Murakami, 2009, Human gene therapy.

Efficient expression of a transgene in platelets using simian immunodeficiency virus‐based vector harboring glycoprotein Ibα promoter: in vivo model for platelet‐targeting gene therapy

T. Ohmori, Y. Kashiwakura, A. Ishiwata, 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Acute toxicity study of a simian immunodeficiency virus-based lentiviral vector for retinal gene transfer in nonhuman primates.

Y. Goto, Y. Yonemitsu, K. Sueishi, 2009, Human gene therapy.

Efficient generation of transgene-free human induced pluripotent stem cells (iPSCs) by temperature-sensitive Sendai virus vectors

Naoki Nishishita, Shin-Ichi Nishikawa, Shin Kawamata, 2011, Proceedings of the National Academy of Sciences.

Toward gene therapy for cystic fibrosis using a lentivirus pseudotyped with Sendai virus envelopes.

Raymond Farley, Uta Griesenbach, Makoto Inoue, 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

High-level in vivo gene marking after gene-modified autologous hematopoietic stem cell transplantation without marrow conditioning in nonhuman primates.

M. Taniwaki, K. Ozawa, S. Ikehara, 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

Pigment epithelium-derived factor gene therapy targeting retinal ganglion cell injuries: neuroprotection against loss of function in two animal models.

S. Tobimatsu, Y. Goto, Y. Yonemitsu, 2011, Human gene therapy.

A useful approach for the screening of active neural-inducing factors

Yoshiyuki Yamamoto, T. Tabata, A. Suzuki, 1994, Roux's archives of developmental biology.

Simian immunodeficiency virus-based lentivirus vector for retinal gene transfer: a preclinical safety study in adult rats

S. Tobimatsu, Y. Goto, Y. Yonemitsu, 2003, Gene Therapy.

Efficient generation of transgene-free human induced pluripotent stem cells (iPSCs) by temperature-sensitive Sendai virus vectors

S. Nishikawa, M. Hasegawa, N. Fusaki, 2011, Proceedings of the National Academy of Sciences.