X53414[Secondary Source ID] - Search Results

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1990	2
2003	1
2025	0

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Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon.

Takada Y, Kaneko N, Esumi H, Purdue PE, Danpure CJ. Takada Y, et al. Biochem J. 1990 Jun 1;268(2):517-20. doi: 10.1042/bj2680517. Biochem J. 1990. PMID: 2363689 Free PMC article.

The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in Black Africans.

Coulter-Mackie MB, Tung A, Henderson HE, Toone JR, Applegarth DA. Coulter-Mackie MB, et al. Mol Genet Metab. 2003 Jan;78(1):44-50. doi: 10.1016/s1096-7192(02)00204-4. Mol Genet Metab. 2003. PMID: 12559847

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.

Purdue PE, Takada Y, Danpure CJ. Purdue PE, et al. J Cell Biol. 1990 Dec;111(6 Pt 1):2341-51. doi: 10.1083/jcb.111.6.2341. J Cell Biol. 1990. PMID: 1703535 Free PMC article.

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