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G A Grabowski

Showing results (91-100 of 126) with videos related to

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Neurology|July 1, 1981
Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine casesJ P Willner, G A Grabowski, R E Gordon, et al.
Biochimica Et Biophysica Acta|September 27, 1976
Evidence for carrier proteins in bile acid synthesis. The effect of squalene and sterol carrier protein and albumin on the activity of 12alpha-hydroxylaseG A Grabowski, K E McCoy, G C Williams, et al.
American Journal of Human Genetics|September 1, 1991
Gaucher disease: heterologous expression of two alleles associated with neuronopathic phenotypesM E Grace, A Berg, G S He, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 1, 1982
Oculomotor abnormalities in chronic GM2 gangliosidosisM A Musarella, E L Raab, S H Rudolph, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Human acid beta-glucosidase: isolation and amino acid sequence of a peptide containing the catalytic siteT Dinur, K M Osiecki, G Legler, et al.
AJR. American Journal of Roentgenology|November 1, 1986
Gaucher's disease type 1: assessment of bone involvement by CT and scintigraphyG Hermann, J Goldblatt, R N Levy, et al.
Pediatric Research|February 1, 1996
Turnover and distribution of intravenously administered mannose-terminated human acid beta-glucosidase in murine and human tissuesY H Xu, E Ponce, Y Sun, et al.
Journal of Cellular Biochemistry|May 16, 2008
Prosaposin is an AR-target gene and its neurotrophic domain upregulates AR expression and activity in prostate stromal cellsS Koochekpour, T-J Lee, Y Sun, et al.
The Journal of Biological Chemistry|April 15, 1994
Identification of Glu340 as the active-site nucleophile in human glucocerebrosidase by use of electrospray tandem mass spectrometryS Miao, J D McCarter, M E Grace, et al.
American Journal of Medical Genetics|July 1, 1985
Genetic heterogeneity in Gaucher disease: physicokinetic and immunologic studies of the residual enzyme in cultured fibroblasts from non-neuronopathic and neuronopathic patientsG A Grabowski, J Goldblatt, T Dinur, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Neurology|July 1, 1981
Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine casesJ P Willner, G A Grabowski, R E Gordon, et al.
Biochimica Et Biophysica Acta|September 27, 1976
Evidence for carrier proteins in bile acid synthesis. The effect of squalene and sterol carrier protein and albumin on the activity of 12alpha-hydroxylaseG A Grabowski, K E McCoy, G C Williams, et al.
American Journal of Human Genetics|September 1, 1991
Gaucher disease: heterologous expression of two alleles associated with neuronopathic phenotypesM E Grace, A Berg, G S He, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 1, 1982
Oculomotor abnormalities in chronic GM2 gangliosidosisM A Musarella, E L Raab, S H Rudolph, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Human acid beta-glucosidase: isolation and amino acid sequence of a peptide containing the catalytic siteT Dinur, K M Osiecki, G Legler, et al.
AJR. American Journal of Roentgenology|November 1, 1986
Gaucher's disease type 1: assessment of bone involvement by CT and scintigraphyG Hermann, J Goldblatt, R N Levy, et al.
Pediatric Research|February 1, 1996
Turnover and distribution of intravenously administered mannose-terminated human acid beta-glucosidase in murine and human tissuesY H Xu, E Ponce, Y Sun, et al.
Journal of Cellular Biochemistry|May 16, 2008
Prosaposin is an AR-target gene and its neurotrophic domain upregulates AR expression and activity in prostate stromal cellsS Koochekpour, T-J Lee, Y Sun, et al.
The Journal of Biological Chemistry|April 15, 1994
Identification of Glu340 as the active-site nucleophile in human glucocerebrosidase by use of electrospray tandem mass spectrometryS Miao, J D McCarter, M E Grace, et al.
American Journal of Medical Genetics|July 1, 1985
Genetic heterogeneity in Gaucher disease: physicokinetic and immunologic studies of the residual enzyme in cultured fibroblasts from non-neuronopathic and neuronopathic patientsG A Grabowski, J Goldblatt, T Dinur, et al.
Pageof 13