(Q44297963)

1 December 2017

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

1 reference

1 December 2017

Marion B Coulter-Mackie

1

1 reference

1 December 2017

Andrew Tung

2

1 reference

1 December 2017

Howard E Henderson

3

1 reference

1 December 2017

Jennifer R Toone

4

1 reference

1 December 2017

Derek A Applegarth

5

1 reference

1 December 2017

1 January 2003

1 reference

Molecular Genetics and Metabolism

1 December 2017

1 reference

1 December 2017

78

1 reference

1 December 2017

1

1 reference

1 December 2017

44-50

1 reference

Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity

1 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

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 mistargeti

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Micromethod for the assay of glutamate: glyoxylate aminotransferase and modifications of a micromethod for the assay of alanine: glyoxylate aminotransferase. Implications for the prenatal diagnosis of type I hyperoxaluria by fetal liver biopsy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Primary hyperoxaluria type 1: diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

Molecular genetics of speciation and human origins

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900204-4

7 January 2021

10.1016/S1096-7192(02)00204-4

Identifiers

DOI

1 reference

1 December 2017

1 reference