(Q35202478)

English

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant

scientific article published on January 1, 1978

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant (English)

1 reference

Europe PubMed Central

7 August 2017

recessive genes

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

author name string

H. F. Willard

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

I. S. Mellman

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

L. E. Rosenberg

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

language of work or name

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publication date

1 January 1978

1 reference

Europe PubMed Central

7 August 2017

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23678/?tool=EBI

online access status

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23678/pdf/?tool=EBI

Portable Document Format

online access status

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

https://europepmc.org/articles/PMC1685448

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

https://europepmc.org/articles/PMC1685448?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A23678

25 March 2022

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

30

1 reference

Europe PubMed Central

7 August 2017

1-13

1 reference

Europe PubMed Central

7 August 2017

1

1 reference

Europe PubMed Central

7 August 2017

Absence of an intracellular cobalamin-binding protein in cultured fibroblasts from patients with defective synthesis of 5'-deoxyadenosylcobalamin and methylcobalamin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Homocystinuria with methylmalonic aciduria: Two cases in a sibship

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Deranged B12 metabolism: Effects on sulfur amino acid metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Genetics of somatic mammalian cells. X. Complementation analysis of glycine-requiring mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Congenital methylmalonic acidemia: enzymatic evidence for two forms of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Fluorometric assay of proteins in the nanogram range

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Genetics of somatic mammalian cells: biochemical genetics of Chinese hamster cell mutants with deviant purine metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Five complementation groups in xeroderma pigmentosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

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=1685448

13 July 2018

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=1685448

13 July 2018

Polyethylene glycol-induced mammalian cell hybridization: effect of polyethylene glycol molecular weight and concentration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Mutant alleles for hypoxanthine phosphoriboxyltransferase: codominant expression, complementation, and segregation in hybrid Chinese hamster cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

On the nature of hereditable variation in cultured somatic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Time and mode of fusion of human fibroblasts treated with polyethylene glycol (PEG)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

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=1685448

13 July 2018

Heterogeneity in maple syrup urine disease: Aspects of cofactor requirement and complementation in cultured fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

High in vivo rates of methionine biosynthesis in transformed human and malignant rat cells auxotrophic for methionine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

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=1685448

13 July 2018

Activation of methionine synthase: Further characterization of the flavoprotein system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Cobalamins in Fibroblasts Cultured from Normal Control Subjects and Patients with Methylmalonic Aciduria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

13 July 2018

Mutants of purine metabolism in cultured mouse and hamster cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685448

26 September 2018

Genetic heterogeneity in GM1-gangliosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Production of mammalian somatic cell hybrids by means of polyethylene glycol treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complementation Analysis of Maple Syrup Urine Disease in Heterokaryons derived from Cultured Human Fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective metabolism of vitamin B12 in fibroblasts from children with methylmalonicaciduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deranged B12 metabolism: Studies of fibroblasts grown in tissue culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of cobalamin coenzymes by human cells in tissue culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylmalonic Aciduria: Metabolic Block Localization and Vitamin B 12 Dependency

1 reference

https://pubmed.ncbi.nlm.nih.gov/23678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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