P E Purdue - JoVE Visualize

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Nature Genetics|April 1, 1997

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptorP E Purdue, J W Zhang, M Skoneczny, et al.

The Biochemical Journal|June 1, 1990

Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonY Takada, N Kaneko, H Esumi, et al.

Neurochemical Research|May 5, 1999

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireviewP E Purdue, M Skoneczny, X Yang, et al.

Genomics|May 1, 1992

A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1P E Purdue, M J Lumb, J Allsop, et al.

Journal of Inherited Metabolic Disease|January 1, 1994

Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneityC J Danpure, P R Jennings, P Fryer, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991

Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutationP E Purdue, J Allsop, G Isaya, et al.

The Plant Journal : for Cell and Molecular Biology|September 1, 1992

The adenine nucleotide translocator of higher plants is synthesized as a large precursor that is processed upon import into mitochondriaB M Winning, C J Sarah, P E Purdue, et al.

Journal of Cell Science|December 1, 1990

Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian speciesC J Danpure, K M Guttridge, P Fryer, et al.

Human Genetics|July 1, 1994

Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase geneC J Danpure, G M Birdsey, G Rumsby, et al.

Genomics|May 1, 1991

Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferaseP E Purdue, M J Lumb, M Fox, et al.

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Showing results (11-20 of 25) with videos related to

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Pageof 3

Nature Genetics|April 1, 1997

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptorP E Purdue, J W Zhang, M Skoneczny, et al.

The Biochemical Journal|June 1, 1990

Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonY Takada, N Kaneko, H Esumi, et al.

Neurochemical Research|May 5, 1999

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireviewP E Purdue, M Skoneczny, X Yang, et al.

Genomics|May 1, 1992

A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1P E Purdue, M J Lumb, J Allsop, et al.

Journal of Inherited Metabolic Disease|January 1, 1994

Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneityC J Danpure, P R Jennings, P Fryer, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991

Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutationP E Purdue, J Allsop, G Isaya, et al.

The Plant Journal : for Cell and Molecular Biology|September 1, 1992

The adenine nucleotide translocator of higher plants is synthesized as a large precursor that is processed upon import into mitochondriaB M Winning, C J Sarah, P E Purdue, et al.

Journal of Cell Science|December 1, 1990

Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian speciesC J Danpure, K M Guttridge, P Fryer, et al.

Human Genetics|July 1, 1994

Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase geneC J Danpure, G M Birdsey, G Rumsby, et al.

Genomics|May 1, 1991

Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferaseP E Purdue, M J Lumb, M Fox, et al.

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