(Q35202266)

English

Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

1 reference

based on heuristic

inferred from title

author name string

Saunders ME

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Sherwood WG

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Duthie M

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Surh L

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Gravel RA

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

0 references

publication date

1 July 1982

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

590-601

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

AVIDIN. 1. THE USE OF (14-C)BIOTIN FOR KINETIC STUDIES AND FOR ASSAY

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

"Protein A" from S. aureus. I. Pseudo-immune reaction with human gamma-globulin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Beta-methylcrotonic aciduria associated with lactic acidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685355

13 July 2018

Two types of ribosome in mouse-hamster hybrid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin-responsive beta-methylcrotonylglycinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the urinary acidic metabolites excreted by patients with β-methylcrotonylglycinuria, propionic acidaemia and methylmalonic acidaemia, using gas-liquid chromatography and mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin activation of carboxylase activity in cultured fibroblasts from a child with a combined carboxylase defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatty-acid-responsive alopecia in multiple carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/7102675

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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