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The Biochemical Journal
|
March 1, 1976
Characterization of human liver alpha-D-mannosidase purified by affinity chromatography
N C Phillips, D Robinson, B G Winchester
Journal of Inherited Metabolic Disease
|
January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome
P T Clayton, B G Winchester, G Keir
Haematologia
|
January 1, 1978
New ideas about self-tolerance and auto-immunity
E Clark, P Lake, N A Mitchison, et al.
The Biochemical Journal
|
April 1, 1970
Study of the thermal denaturation of ribonuclease A by differential thermal analysis and susceptibility to proteolysis
B G Winchester, A P Mathias, B R Rabin
Brain Pathology (Zurich, Switzerland)
|
February 11, 1998
Prenatal diagnosis of lysosomal storage diseases
B D Lake, E P Young, B G Winchester
Immunogenetics
|
January 1, 1984
Antigen-presenting cells do not discriminate between self and nonself
G Winchester, G H Sunshine, N Nardi, et al.
The Journal of Gene Medicine
|
October 17, 2001
Non-viral, integrin-mediated gene transfer into fibroblasts from patients with lysosomal storage diseases
E J Estruch, S L Hart, C Kinnon, et al.
Acta Neuropathologica
|
January 1, 1995
A new form of ovine GM1-gangliosidosis
B J Skelly, M Jeffrey, R J Franklin, et al.
The Biochemical Journal
|
July 1, 1976
The nature of the residual alpha-mannosidase in plasma in bovine mannosidosis
B G Winchester, N S Van-de-Water, R D Jolly
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
Pre- and postnatal diagnosis of patients with CLN1 and CLN2 by assay of palmitoyl-protein thioesterase and tripeptidyl-peptidase I activities
E P Young, V C Worthington, M Jackson, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
The Biochemical Journal
|
March 1, 1976
Characterization of human liver alpha-D-mannosidase purified by affinity chromatography
N C Phillips, D Robinson, B G Winchester
Journal of Inherited Metabolic Disease
|
January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome
P T Clayton, B G Winchester, G Keir
Haematologia
|
January 1, 1978
New ideas about self-tolerance and auto-immunity
E Clark, P Lake, N A Mitchison, et al.
The Biochemical Journal
|
April 1, 1970
Study of the thermal denaturation of ribonuclease A by differential thermal analysis and susceptibility to proteolysis
B G Winchester, A P Mathias, B R Rabin
Brain Pathology (Zurich, Switzerland)
|
February 11, 1998
Prenatal diagnosis of lysosomal storage diseases
B D Lake, E P Young, B G Winchester
Immunogenetics
|
January 1, 1984
Antigen-presenting cells do not discriminate between self and nonself
G Winchester, G H Sunshine, N Nardi, et al.
The Journal of Gene Medicine
|
October 17, 2001
Non-viral, integrin-mediated gene transfer into fibroblasts from patients with lysosomal storage diseases
E J Estruch, S L Hart, C Kinnon, et al.
Acta Neuropathologica
|
January 1, 1995
A new form of ovine GM1-gangliosidosis
B J Skelly, M Jeffrey, R J Franklin, et al.
The Biochemical Journal
|
July 1, 1976
The nature of the residual alpha-mannosidase in plasma in bovine mannosidosis
B G Winchester, N S Van-de-Water, R D Jolly
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
Pre- and postnatal diagnosis of patients with CLN1 and CLN2 by assay of palmitoyl-protein thioesterase and tripeptidyl-peptidase I activities
E P Young, V C Worthington, M Jackson, et al.
Page
of 6