Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism (Q72110090)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 January 1994

Language	Label	Description	Also known as
English	Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism	scientific article published on 01 January 1994

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

author name string

C J Danpure

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

P Fryer

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

S Griffiths

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

K M Guttridge

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

P R Jennings

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

J Allsop

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

A B Moser

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

S Naidu

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

H W Moser

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

M MacCollin

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

publication date

1 January 1994

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

17

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

27-40

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zellweger Syndrome Amniocytes: Morphological Appearance and a Simple Sedimentation Method for Prenatal Diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gas-chromatographic method of analysis for urinary organic acids. II. Description of the procedure, and its application to diagnosis of patients with organic acidurias

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear targeting sequences--a consensus?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

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/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

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/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian species

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

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/8051936

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/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytosol-dependent peroxisomal protein import in a permeabilized cell system

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

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/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gas-chromatographic method of analysis for urinary organic acids. I. Retention indices of 155 metabolically important compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/8051936

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/8051936

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00735393

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8051936%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q72110090&oldid=2219577922"