(Q36913777)

17 August 2017

sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis (English)

1 reference

17 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

author name string

C. O. Harding

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

P. Williams

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

D. M. Pflanzer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

R. E. Colwell

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

P. W. Lyne

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

J. A. Wolff

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

19 September 2022

language of work or name

English

0 references

publication date

1 April 1992

1 reference

PMC publication ID

48718

full work available at URL

17 August 2017

https://europepmc.org/articles/PMC48718

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

https://europepmc.org/articles/PMC48718?pdf=render

19 September 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372986

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

19 September 2022

published in

1 reference

17 August 2017

89

1 reference

17 August 2017

7

1 reference

17 August 2017

2644-2648

1 reference

Labile methyl group balances in the human: The role of sarcosine

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Measurement of protein using bicinchoninic acid

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Mapping to molecular resolution in the T to H-2 region of the mouse genome with a nested set of meiotic recombinants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

The new mouse genetics: altering the genome by gene targeting

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Development and applications of a molecular genetic linkage map of the mouse genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Hypersarcosinemia with craniostenosis-syndactylism syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Massachusetts Metabolic Disorders Screening Program: III. Sarcosinemia

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Clinical and cellular studies of sarcosinemia.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

The clinical and biochemical findings in three cases of hypersarcosinemia and one case of transient hypersarcosinuria associated with folic acid deficiency.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

Hypersarcosinemia: an inborn error of metabolism

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48718

THE OXIDATION OF N-METHYLGLYCINES BY PRIMATE LIVER MITOCHONDRIA. ASSAY, PURIFICATION, AND CHARACTERIZATION OF SARCOSINE DEHYDROGENASE

4 September 2018

1 reference

12 December 2020

Quantitative analysis for organic acids in biological samples: batch isolation followed by gas chromatographic-mass spectrometric analysis

1 reference

12 December 2020

Newborn urine screening experience with over one million infants in the Quebec Network of Genetic Medicine

1 reference

12 December 2020

Hyperphenylalaninemia in the hph-1 mouse mutant

1 reference

12 December 2020

Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen

1 reference

12 December 2020

Hypersarcosinemia with sarcosinuria. Study of a new case

1 reference

12 December 2020

Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally

1 reference

12 December 2020

Glutaric aciduria Type II

1 reference

12 December 2020

Phenylalanine hydroxylase activity in dilute and nondilute strains of mice

1 reference

12 December 2020

Folic acid dependent hypersarcosinaemia

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.89.7.2644

1 reference

17 August 2017

0 references

1 reference

PMC publication ID

48718

17 August 2017

1 reference

PMC publication ID

48718