Gieselmann V - Search Results

1

Lysosomal di-N-acetylchitobiase-deficient mouse tissues accumulate Man2GlcNAc2 and Man3GlcNAc2.

Persichetti E, Klein K, Paciotti S, Lecointe K, Balducci C, Franken S, Duvet S, Matzner U, Roberti R, Hartmann D, Gieselmann V, Beccari T. Persichetti E, et al. Among authors: gieselmann v. Biochim Biophys Acta. 2012 Jul;1822(7):1137-46. doi: 10.1016/j.bbadis.2012.03.005. Epub 2012 Mar 20. Biochim Biophys Acta. 2012. PMID: 22465033 Free article.

2

Lysosomal storage diseases.

Gieselmann V. Gieselmann V. Biochim Biophys Acta. 1995 Apr 24;1270(2-3):103-36. doi: 10.1016/0925-4439(94)00075-2. Biochim Biophys Acta. 1995. PMID: 7727535 Free article. Review. No abstract available.

3

Metachromatic leukodystrophy: molecular genetics and an animal model.

Gieselmann V, Matzner U, Hess B, Lüllmann-Rauch R, Coenen R, Hartmann D, D'Hooge R, DeDeyn P, Nagels G. Gieselmann V, et al. J Inherit Metab Dis. 1998 Aug;21(5):564-74. doi: 10.1023/a:1005471106088. J Inherit Metab Dis. 1998. PMID: 9728336 Review.

4

Retrovirally expressed human arylsulfatase A corrects the metabolic defect of arylsulfatase A-deficient mouse cells.

Matzner U, Habetha M, Gieselmann V. Matzner U, et al. Among authors: gieselmann v. Gene Ther. 2000 May;7(9):805-12. doi: 10.1038/sj.gt.3301150. Gene Ther. 2000. PMID: 10822308

5

Bone marrow stem cell gene therapy of arylsulfatase A-deficient mice, using an arylsulfatase A mutant that is hypersecreted from retrovirally transduced donor-type cells.

Matzner U, Schestag F, Hartmann D, Lüllmann-Rauch R, D'Hooge R, De Deyn PP, Gieselmann V. Matzner U, et al. Among authors: gieselmann v. Hum Gene Ther. 2001 Jun 10;12(9):1021-33. doi: 10.1089/104303401750214258. Hum Gene Ther. 2001. PMID: 11399225

6

Sulfatide storage in visceral organs of arylsulfatase A-deficient mice.

Schott I, Hartmann D, Gieselmann V, Lüllmann-Rauch R. Schott I, et al. Among authors: gieselmann v. Virchows Arch. 2001 Jul;439(1):90-6. doi: 10.1007/s004280000360. Virchows Arch. 2001. PMID: 11499846

7

Lysosomal sulfoglycolipid storage in the kidneys of mice deficient for arylsulfatase A (ASA) and of double-knockout mice deficient for ASA and galactosylceramide synthase.

Lüllmann-Rauch R, Matzner U, Franken S, Hartmann D, Gieselmann V. Lüllmann-Rauch R, et al. Among authors: gieselmann v. Histochem Cell Biol. 2001 Aug;116(2):161-9. doi: 10.1007/s004180100286. Histochem Cell Biol. 2001. PMID: 11685544

8

Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestations.

Matzner U, Hartmann D, Lüllmann-Rauch R, Coenen R, Rothert F, Månsson JE, Fredman P, D'Hooge R, De Deyn PP, Gieselmann V. Matzner U, et al. Among authors: gieselmann v. Gene Ther. 2002 Jan;9(1):53-63. doi: 10.1038/sj.gt.3301593. Gene Ther. 2002. PMID: 11850723

9

Secretion of phosphomannosyl-deficient arylsulphatase A and cathepsin D from isolated human macrophages.

Muschol N, Matzner U, Tiede S, Gieselmann V, Ullrich K, Braulke T. Muschol N, et al. Among authors: gieselmann v. Biochem J. 2002 Dec 15;368(Pt 3):845-53. doi: 10.1042/BJ20020249. Biochem J. 2002. PMID: 12296771 Free PMC article.

10

Gene therapy: prospects for glycolipid storage diseases.

Gieselmann V, Matzner U, Klein D, Mansson JE, D'Hooge R, DeDeyn PD, Lüllmann Rauch R, Hartmann D, Harzer K. Gieselmann V, et al. Philos Trans R Soc Lond B Biol Sci. 2003 May 29;358(1433):921-5. doi: 10.1098/rstb.2003.1277. Philos Trans R Soc Lond B Biol Sci. 2003. PMID: 12803926 Free PMC article. Review.

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