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Results:
1-12
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Results: 12
Authors:
Matzner, U
Schestag, F
Hartmann, D
Lullmann-Rauch, R
D'Hooge, R
De Deyn, PP
Gieselmann, V
Citation: U. Matzner et al., 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, HUM GENE TH, 12(9), 2001, pp. 1021-1033
Authors:
Lullmann-Rauch, R
Matzner, U
Franken, S
Hartmann, D
Gieselmann, V
Citation: R. Lullmann-rauch et al., Lysosomal sulfoglycolipid storage in the kidneys of mice deficient for arylsulfatase A (ASA) and of double-knockout mice deficient for ASA and galactosylceramide synthase, HISTOCHEM C, 116(2), 2001, pp. 161-169
Authors:
Schott, I
Hartmann, D
Gieselmann, V
Lullmann-Rauch, R
Citation: I. Schott et al., Sulfatide storage in visceral organs of arylsulfatase A-deficient mice, VIRCHOWS AR, 439(1), 2001, pp. 90-96
Authors:
D'Hooge, R
Van Dam, D
Franck, F
Gieselmann, V
De Deyn, PP
Citation: R. D'Hooge et al., Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy, BRAIN RES, 907(1-2), 2001, pp. 35-43
Authors:
Coenen, R
Gieselmann, V
Lullmann-Rauch, R
Citation: R. Coenen et al., Morphological alterations in the inner ear of the arylsulfatase A-deficient mouse, ACT NEUROP, 101(5), 2001, pp. 491-498
Authors:
Matzner, U
Habetha, M
Gieselmann, V
Citation: U. Matzner et al., Retrovirally expressed human arylsulfatase A corrects the metabolic defectof arylsulfatase A-deficient mouse cells, GENE THER, 7(9), 2000, pp. 805-812
Authors:
Matzner, U
Harzer, K
Learish, RD
Barranger, JA
Gieselmann, V
Citation: U. Matzner et al., Long-term expression and transfer of arylsulfatase A into brain of arylsulfatase A-deficient mice transplanted with bone marrow expressing the arylsulfatase A cDNA from a retroviral vector, GENE THER, 7(14), 2000, pp. 1250-1257
Authors:
Hermann, S
Schestag, F
Polten, A
Kafert, S
Penzien, J
Zlotogora, J
Baumann, N
Gieselmann, V
Citation: S. Hermann et al., Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophy, AM J MED G, 91(1), 2000, pp. 68-73
Authors:
Li, XR
Johnk, C
Hartmann, D
Schestag, F
Kromer, W
Gieselmann, V
Citation: Xr. Li et al., Enzymatic properties, tissue-specific expression, and lysosomal location of two highly homologous rat SULT1C2 sulfotransferases, BIOC BIOP R, 272(1), 2000, pp. 242-250
Authors:
D'Hooge, R
Hartmann, D
Manil, J
Colin, F
Gieselmann, V
De Deyn, PP
Citation: R. D'Hooge et al., Neuromotor alterations and cerebellar deficits in aged arylsulfatase A-deficient transgenic mice, NEUROSCI L, 273(2), 1999, pp. 93-96
Authors:
Schierau, A
Dietz, F
Lange, H
Schestag, F
Parastar, A
Gieselmann, V
Citation: A. Schierau et al., Interaction of arylsulfatase A with UDP-N-acetylglucosamine : lysosomal enzyme-N-acetylglucosamine-1-phosphotransferase, J BIOL CHEM, 274(6), 1999, pp. 3651-3658
Authors:
D'Hooge, R
Coenen, R
Gieselmann, V
Lullmann-Rauch, R
De Deyn, PP
Citation: R. D'Hooge et al., Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice, BRAIN RES, 847(2), 1999, pp. 352-356
Risultati:
1-12
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