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R Lüllmann-Rauch

Showing results (101-110 of 108) with videos related to

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Lipids in Health and Disease|August 9, 2006
Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase geneS Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry|July 25, 1997
Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous systemP Saftig, D Hartmann, R Lüllmann-Rauch, et al.
Gene Therapy|February 19, 2002
Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestationsU Matzner, D Hartmann, R Lüllmann-Rauch, et al.
Nature|September 6, 2000
Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient miceY Tanaka, G Guhde, A Suter, et al.
Development (Cambridge, England)|December 4, 2001
Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient miceA Suter, V Everts, A Boyde, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophyB Hess, P Saftig, D Hartmann, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 3, 2004
Metachromatic leukodystrophy: consequences of sulphatide accumulationV Gieselmann, S Franken, D Klein, et al.
Circulation|February 27, 2008
Biglycan is required for adaptive remodeling after myocardial infarctionD Westermann, J Mersmann, A Melchior, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
Lipids in Health and Disease|August 9, 2006
Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase geneS Franken, D Wittke, J E Mansson, et al.
The Journal of Biological Chemistry|July 25, 1997
Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous systemP Saftig, D Hartmann, R Lüllmann-Rauch, et al.
Gene Therapy|February 19, 2002
Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestationsU Matzner, D Hartmann, R Lüllmann-Rauch, et al.
Nature|September 6, 2000
Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient miceY Tanaka, G Guhde, A Suter, et al.
Development (Cambridge, England)|December 4, 2001
Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient miceA Suter, V Everts, A Boyde, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophyB Hess, P Saftig, D Hartmann, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 3, 2004
Metachromatic leukodystrophy: consequences of sulphatide accumulationV Gieselmann, S Franken, D Klein, et al.
Circulation|February 27, 2008
Biglycan is required for adaptive remodeling after myocardial infarctionD Westermann, J Mersmann, A Melchior, et al.
Pageof 11