(Q48081180)

English

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

scientific article published in July 1994

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scholarly article

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

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

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

1 reference

based on heuristic

inferred from title

Graeme M Birdsey

2

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

author name string

C J Danpure

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

G Rumsby

3

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

M J Lumb

4

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

P E Purdue

5

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

J Allsop

6

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

publication date

1 July 1994

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

94

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

55-64

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

https://scigraph.springernature.com/pub.10.1007/bf02272842

0 references

Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1007%2FBF02272842

21 January 2018

Further studies on the activity and subcellular distribution of alanine: Glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1007%2FBF02272842

21 January 2018

Repeat arrays in cellular DNA related to the Epstein-Barr virus IR3 repeat

1 reference

https://api.crossref.org/works/10.1007%2FBF02272842

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF02272842

21 January 2018

Repeat array in Epstein-Barr virus DNA is related to cell DNA sequences interspersed on human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypervariable 'minisatellite' regions in human DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new micro-assay for human liver alanine: glyoxylate aminotransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hyperoxaluria type 1: clinical manifestations in infancy and prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple repeat sequence in Epstein-Barr virus DNA is transcribed in latent and productive infections

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TaqI polymorphism at the alanine:glyoxylate aminotransferase (AGXT) gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable number of tandem repeat (VNTR) markers for human gene mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A serine-to-phenylalanine substitution leads to loss of alanine:glyoxylate aminotransferase catalytic activity and immunoreactivity in a patient with primary hyperoxaluria type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal exclusion of primary hyperoxaluria type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple Repeat Array in Epstein-Barr Virus DNA Encodes Part of the Epstein-Barr Nuclear Antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential PCR amplification of alleles: mechanisms and solutions

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/8034295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02272842

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/8034295

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