(Q70393071)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

title

Biochemical characterization of propionyl CoA carboxylase deficiency: heterogeneity within a single genetic complementation group (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

1 reference

C McKeon

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

R Z Eanes

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

B Wolf

series ordinal

3

1 reference

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10 October 2019

publication date

1 February 1982

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10 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

volume

20

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10 October 2019

issue

1-2

1 reference

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10 October 2019

page(s)

77-94

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https://scigraph.springernature.com/pub.10.1007/bf00484937

10 October 2019

exact match

0 references

cites work

Purification of human liver propionyl-CoA carboxylase by carbon tetrachloride extraction and monomeric avidin affinity chromatography

1 reference

12 December 2020

Increased thermal stability of proteins in the presence of sugars and polyols

1 reference

12 December 2020

Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups

1 reference

12 December 2020

Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”

1 reference

12 December 2020

Biochemical differences between mutant propionyl-CoA carboxylases from two complementation groups

1 reference

12 December 2020

Propionyl‐CoA‐carboxylase determination: Study of enzyme parameters in cultured skin fibroblasts from enzyme‐deficient and normal subjects

1 reference

12 December 2020

Bovine kidney 3-methylcrotonyl-CoA and propionyl-CoA carboxylases: each enzyme contains nonidentical subunits

1 reference

12 December 2020

Dysautonomia in an infant with secondary hyperammonemia due to propionyl coenzyme A carboxylase deficiency

1 reference

12 December 2020

Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girl

1 reference

12 December 2020

Evidence for two genetic complementation groups in pyruvate carboxylase-deficient human fibroblast cell lines

1 reference

12 December 2020

Biochemical characterization of mutant propionyl CoA carboxylases from two minor genetic complementation groups

1 reference

12 December 2020

Immunological studies of propionyl CoA carboxylase in livers and fibroblasts of patients with propionic acidemia

1 reference

12 December 2020

Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency

1 reference

12 December 2020

Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts

1 reference

12 December 2020

Human Propionyl CoA Carboxylase: Some Properties of the Partially Purified Enzyme in Fibroblasts from Controls and Patients with Propionic Acidemia

1 reference

12 December 2020

Prenatal Diagnosis of Propionic Acidemia

1 reference

12 December 2020

Isolation and characterization of propionyl-CoA carboxylase from normal human liver. Evidence for a protomeric tetramer of nonidentical subunits

1 reference

12 December 2020

Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00484937

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7092804%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

1 reference