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Human Genetics
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March 8, 2006
Gene symbol: ARSA. Disease: metachromatic leukodystrophy
L Berna, V Gieselmann, H Poupetova, et al.
Human Mutation
|
January 1, 1995
Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite Jews
J Zlotogora, G Bach, C Bösenberg, et al.
Developmental Neuroscience
|
January 1, 1991
Molecular genetics of metachromatic leukodystrophy
V Gieselmann, A Polten, J Kreysing, et al.
American Journal of Human Genetics
|
December 1, 1991
Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient
A L Fluharty, C B Fluharty, W Bohne, et al.
Brain Research
|
November 27, 1999
Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice
R D'Hooge, R Coenen, V Gieselmann, et al.
Brain Research
|
June 30, 2001
Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy
R D'Hooge, D Van Dam, F Franck, et al.
Human Mutation
|
January 1, 1996
Characterization of two arylsulfatase A missense mutations D335V and T274M causing late infantile metachromatic leukodystrophy
B Hess, S Kafert, U Heinisch, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Localization of receptors for endocytosis of lysosomal enzymes on different brain cells
P Schluff, B Flott-Rahmel, V Gieselmann, et al.
Biochemical and Biophysical Research Communications
|
October 29, 1979
Primary cultures of rat hepatocytes synthesize fibronectin
B Voss, S Allam, J Rauterberg, et al.
The Journal of Biological Chemistry
|
September 16, 1994
Translational control of arylsulfatase A expression in mouse testis
J Kreysing, A Polten, G Lukatela, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 87) with videos related to
Sort By:
Page
of 9
Human Genetics
|
March 8, 2006
Gene symbol: ARSA. Disease: metachromatic leukodystrophy
L Berna, V Gieselmann, H Poupetova, et al.
Human Mutation
|
January 1, 1995
Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite Jews
J Zlotogora, G Bach, C Bösenberg, et al.
Developmental Neuroscience
|
January 1, 1991
Molecular genetics of metachromatic leukodystrophy
V Gieselmann, A Polten, J Kreysing, et al.
American Journal of Human Genetics
|
December 1, 1991
Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient
A L Fluharty, C B Fluharty, W Bohne, et al.
Brain Research
|
November 27, 1999
Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice
R D'Hooge, R Coenen, V Gieselmann, et al.
Brain Research
|
June 30, 2001
Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy
R D'Hooge, D Van Dam, F Franck, et al.
Human Mutation
|
January 1, 1996
Characterization of two arylsulfatase A missense mutations D335V and T274M causing late infantile metachromatic leukodystrophy
B Hess, S Kafert, U Heinisch, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Localization of receptors for endocytosis of lysosomal enzymes on different brain cells
P Schluff, B Flott-Rahmel, V Gieselmann, et al.
Biochemical and Biophysical Research Communications
|
October 29, 1979
Primary cultures of rat hepatocytes synthesize fibronectin
B Voss, S Allam, J Rauterberg, et al.
The Journal of Biological Chemistry
|
September 16, 1994
Translational control of arylsulfatase A expression in mouse testis
J Kreysing, A Polten, G Lukatela, et al.
Page
of 9