(Q24539565)

English

Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

0 references

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methylmalonic acidemia

1 reference

based on heuristic

inferred from title

object named as

Timothy Wai

2

0 references

Thomas J. Hudson

7

object named as

Thomas Hudson

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

9

object named as

Roy A Gravel

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

6

object named as

Carole Doré

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

author name string

C Melissa Dobson

1

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Daniel Leclerc

3

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Aaron Wilson

4

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Xuchu Wu

5

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

David S Rosenblatt

8

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

language of work or name

0 references

publication date

15 November 2002

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

99

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

24

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

15554-15559

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Identification of the human methylmalonyl-CoA racemase gene based on the analysis of prokaryotic gene arrangements. Implications for decoding the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Basic local alignment search tool

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Biosynthesis of cobalamin (vitamin B12): a bacterial conundrum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Human methionine synthase. cDNA cloning, gene localization, and expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Cloning, mapping and RNA analysis of the human methionine synthase gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

24 March 2017

Classification and evolution of P-loop GTPases and related ATPases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

7 April 2017

Phosphorylation of the periplasmic binding protein in two transport systems for arginine incorporation in Escherichia coli K-12 is unrelated to the function of the transport system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

A third periplasmic transport system for L-arginine in Escherichia coli: molecular characterization of the artPIQMJ genes, arginine binding and transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Two periplasmic transport proteins which interact with a common membrane receptor show extensive homology: complete nucleotide sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

The Natural History of the Inherited Methylmalonic Acidemias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Methylmalonic acidemia controlled with oral administration of vitamin B12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Genetic and biochemical analysis of human cobalamin mutants in cell culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

27 September 2017

Discovering new enzymes and metabolic pathways: conversion of succinate to propionate by Escherichia coli

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

30 May 2018

Purification and some properties of cytosolic cobalamin-binding protein in Euglena gracilis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137755

30 May 2018

Critical role of mitochondria, but not caspases, during glucocorticosteroid-induced human eosinophil apoptosis

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.242614799

21 January 2018

The Mitochondrial Permeability Transition Pore is Modulated by Oxidative Agents Through Both Pyridine Nucleotides and Glutathione at Two Separate Sites

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.242614799

21 January 2018

Methylmalonic aciduria due to a new defect in adenosylcobalamin accumulation by cells

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.242614799

21 January 2018

Purification and characterization of aquacobalamin reductases from mammals

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.242614799

21 January 2018

Synthesis of cobalamin coenzymes by human cells in tissue culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/12438653

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uptake of hydroxocobalamin by rat liver mitochondria. Binding to a mitochondrial protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/12438653

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial NADH- or NADPH-linked aquacobalamin reductase activity is low in human skin fibroblasts with defects in synthesis of cobalamin coenzymes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12438653

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.242614799

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

2002PNAS...9915554D

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

ResearchGate publication ID

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