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Journal of Inherited Metabolic Disease
|
January 1, 1989
Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations
C J Danpure, P J Cooper, P R Jennings, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Enzymological characterization of a feline analogue of primary hyperoxaluria type 2: a model for the human disease
C J Danpure, P R Jennings, J Mistry, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severity
B Hoppe, C J Danpure, G Rumsby, et al.
The Journal of Cell Biology
|
October 1, 1995
Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1
A Motley, M J Lumb, P B Oatey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism
C J Danpure, P Fryer, S Griffiths, et al.
American Journal of Human Genetics
|
August 1, 1993
Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation
C J Danpure, P E Purdue, P Fryer, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 26) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 26 results.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations
C J Danpure, P J Cooper, P R Jennings, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Enzymological characterization of a feline analogue of primary hyperoxaluria type 2: a model for the human disease
C J Danpure, P R Jennings, J Mistry, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severity
B Hoppe, C J Danpure, G Rumsby, et al.
The Journal of Cell Biology
|
October 1, 1995
Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1
A Motley, M J Lumb, P B Oatey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism
C J Danpure, P Fryer, S Griffiths, et al.
American Journal of Human Genetics
|
August 1, 1993
Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation
C J Danpure, P E Purdue, P Fryer, et al.
Page
of 3