(Q24291317)

English

Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression

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Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression (English)

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Methylcrotonoyl-CoA carboxylase 1

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GOA release 2020-03-11

methylcrotonoyl-CoA carboxylase activity

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GOA release 2020-03-11

author name string

K Obata

1

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T Fukuda

2

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R Morishita

3

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S Abe

4

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S Asakawa

5

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S Yamaguchi

6

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M Yoshino

7

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K Ihara

8

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K Murayama

9

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K Shigemoto

10

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N Shimizu

11

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I Kondo

12

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language of work or name

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publication date

1 March 2001

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72

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2

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145-52

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Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness

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Isolated biotin‐resistant deficiency of 3‐methylcrotonyl‐CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome

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Interpreting cDNA sequences: some insights from studies on translation

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An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme: a carboxylase deficiency detected by newborn screening for maple syrup urine disease

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Isolation of 3-methylcrotonyl-coenzyme A carboxylase from bovine kidney

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Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase

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Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency

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Two siblings with biotin-resistant 3-methylcrotonyl-coenzyme A carboxylase deficiency.

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3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children.

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Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 15-year-old girl

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

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Two mitochondrial matrix proteases act sequentially in the processing of mammalian matrix enzymes

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Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: leader peptides cleaved by two matrix proteases share a three-amino acid motif

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Molecular cloning and characterization of the cDNA coding for the biotin-containing subunit of 3-methylcrotonoyl-CoA carboxylase: identification of the biotin carboxylase and biotin-carrier domains

1 reference

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Molecular characterization of the non-biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase

1 reference

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Molecular cloning of the biotinylated subunit of 3-methylcrotonyl-coenzyme A carboxylase of Arabidopsis thaliana

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Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria

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Identifiers

10.1006/GENO.2000.6366

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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