ACNP - Italian Periodicals Catalogue

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Results: 1-10 |

Results: 10

Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficientmice

Authors: Tanaka, Y Guhde, G Suter, A Eskelinen, EL Hartmann, D Lullmann-Rauch, R Janssen, PML Blanz, J von Figura, K Saftig, P

Citation: Y. Tanaka et al., Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficientmice, NATURE, 406(6798), 2000, pp. 902-906

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

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

Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice

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

Disease model: LAMP-2 enlightens Danon disease

Authors: Saftig, P Tanaka, Y Lullmann-Rauch, R von Figura, K

Citation: P. Saftig et al., Disease model: LAMP-2 enlightens Danon disease, TRENDS MO M, 7(1), 2001, pp. 37-39

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

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

Morphological alterations in the inner ear of the arylsulfatase A-deficient mouse

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

Morphological and functional changes due to drug-induced lysosomal storageof sulphated glycosaminoglycans in the rat retina

Authors: Bredehorn, T Clausen, M Duncker, G Lullmann-Rauch, R

Citation: T. Bredehorn et al., Morphological and functional changes due to drug-induced lysosomal storageof sulphated glycosaminoglycans in the rat retina, GR ARCH CL, 239(10), 2001, pp. 788-793

Normal lysosomal morphology and function in LAMP-1-deficient mice

Authors: Andrejewski, N Punnonen, EL Guhde, G Tanaka, Y Lullmann-Rauch, R Hartmann, D von Figura, K Saftig, P

Citation: N. Andrejewski et al., Normal lysosomal morphology and function in LAMP-1-deficient mice, J BIOL CHEM, 274(18), 1999, pp. 12692-12701

Sulfatide storage in visceral organs of arylsulfatase A-deficient mice

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

Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis

Authors: Stinchi, S Lullmann-Rauch, R Hartmann, D Coenen, R Beccari, T Orlacchio, A von Figura, K Saftig, P

Citation: S. Stinchi et al., Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis, HUM MOL GEN, 8(8), 1999, pp. 1365-1372

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