Kobayashi H - Search Results

1

Efficient engraftment of genetically modified cells is necessary to ameliorate central nervous system involvement of murine model of mucopolysaccharidosis type II by hematopoietic stem cell targeted gene therapy.

Miwa S, Watabe AM, Shimada Y, Higuchi T, Kobayashi H, Fukuda T, Kato F, Ida H, Ohashi T. Miwa S, et al. Among authors: kobayashi h. Mol Genet Metab. 2020 Aug;130(4):262-273. doi: 10.1016/j.ymgme.2020.06.007. Epub 2020 Jun 24. Mol Genet Metab. 2020. PMID: 32631737

2

Reduction of lysosomal storage in murine mucopolysaccharidosis type VII by transplantation of normal and genetically modified macrophages.

Ohashi T, Yokoo T, Iizuka S, Kobayashi H, Sly WS, Eto Y. Ohashi T, et al. Among authors: kobayashi h. Blood. 2000 Jun 1;95(11):3631-3. Blood. 2000. PMID: 10828055 Free article.

3

Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy.

Suzuki Y, Isogai K, Teramoto T, Tashita H, Shimozawa N, Nishimura M, Asano T, Oda M, Kamei A, Ishiguro H, Kato S, Ohashi T, Kobayashi H, Eto Y, Kondo N. Suzuki Y, et al. Among authors: kobayashi h. J Inherit Metab Dis. 2000 Jul;23(5):453-8. doi: 10.1023/a:1005656029200. J Inherit Metab Dis. 2000. PMID: 10947199

4

Neonatal gene transfer using lentiviral vector for murine Pompe disease: long-term expression and glycogen reduction.

Kyosen SO, Iizuka S, Kobayashi H, Kimura T, Fukuda T, Shen J, Shimada Y, Ida H, Eto Y, Ohashi T. Kyosen SO, et al. Among authors: kobayashi h. Gene Ther. 2010 Apr;17(4):521-30. doi: 10.1038/gt.2009.160. Epub 2009 Dec 24. Gene Ther. 2010. PMID: 20033064

5

Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case.

Kobayashi H, Shimada Y, Ikegami M, Kawai T, Sakurai K, Urashima T, Ijima M, Fujiwara M, Kaneshiro E, Ohashi T, Eto Y, Ishigaki K, Osawa M, Kyosen SO, Ida H. Kobayashi H, et al. Mol Genet Metab. 2010 May;100(1):14-9. doi: 10.1016/j.ymgme.2010.01.015. Epub 2010 Feb 4. Mol Genet Metab. 2010. PMID: 20202878

6

Pathology of the first autopsy case diagnosed as mucolipidosis type III α/β suggesting autophagic dysfunction.

Kobayashi H, Takahashi-Fujigasaki J, Fukuda T, Sakurai K, Shimada Y, Nomura K, Ariga M, Ohashi T, Eto Y, Otomo T, Sakai N, Ida H. Kobayashi H, et al. Mol Genet Metab. 2011 Feb;102(2):170-5. doi: 10.1016/j.ymgme.2010.09.014. Epub 2010 Nov 3. Mol Genet Metab. 2011. PMID: 21051253

7

Oral administration of recombinant human acid α-glucosidase reduces specific antibody formation against enzyme in mouse.

Ohashi T, Iizuka S, Shimada Y, Eto Y, Ida H, Hachimura S, Kobayashi H. Ohashi T, et al. Among authors: kobayashi h. Mol Genet Metab. 2011 May;103(1):98-100. doi: 10.1016/j.ymgme.2011.01.009. Epub 2011 Jan 27. Mol Genet Metab. 2011. PMID: 21320791

8

Combination treatment using adenovirus vector-mediated tumor necrosis factor-alpha gene transfer and a NF-κB inhibitor for pancreatic cancer in mice.

Furukawa K, Ohashi T, Haruki K, Fujiwara Y, Iida T, Shiba H, Uwagawa T, Kobayashi H, Yanaga K. Furukawa K, et al. Among authors: kobayashi h. Cancer Lett. 2011 Jul 1;306(1):92-8. doi: 10.1016/j.canlet.2011.02.036. Epub 2011 Apr 8. Cancer Lett. 2011. PMID: 21482023

9

Minimum requirement of donor cells to reduce the glycolipid storage following bone marrow transplantation in a murine model of Fabry disease.

Yokoi T, Kobayashi H, Shimada Y, Eto Y, Ishige N, Kitagawa T, Otsu M, Nakauchi H, Ida H, Ohashi T. Yokoi T, et al. Among authors: kobayashi h. J Gene Med. 2011 May;13(5):262-8. doi: 10.1002/jgm.1566. J Gene Med. 2011. PMID: 21520359

10

Generation of induced pluripotent stem (iPS) cells derived from a murine model of Pompe disease and differentiation of Pompe-iPS cells into skeletal muscle cells.

Kawagoe S, Higuchi T, Meng XL, Shimada Y, Shimizu H, Hirayama R, Fukuda T, Chang H, Nakahata T, Fukada S, Ida H, Kobayashi H, Ohashi T, Eto Y. Kawagoe S, et al. Among authors: kobayashi h. Mol Genet Metab. 2011 Sep-Oct;104(1-2):123-8. doi: 10.1016/j.ymgme.2011.05.020. Epub 2011 Jun 2. Mol Genet Metab. 2011. PMID: 21703893

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