(Q28366367)

4 July 2017

title

Homocysteine metabolism in children with Down syndrome: in vitro modulation (English)

1 reference

4 July 2017

1 reference

M Pogribna

1

1 reference

4 July 2017

S Melnyk

2

1 reference

4 July 2017

I Pogribny

3

1 reference

4 July 2017

A Chango

4

1 reference

4 July 2017

P Yi

5

1 reference

4 July 2017

S J James

6

1 reference

4 July 2017

language of work or name

English

0 references

publication date

5 June 2001

1 reference

American Journal of Human Genetics

4 July 2017

published in

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4 July 2017

volume

69

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4 July 2017

issue

1

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4 July 2017

page(s)

88-95

1 reference

Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

The DNA sequence of human chromosome 21

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Folate nutriture alters choline status of women and men fed low choline diets

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

The human GARS-AIRS-GART gene encodes two proteins which are differentially expressed during human brain development and temporally overexpressed in cerebellum of individuals with Down syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Down syndrome: genetic recombination and the origin of the extra chromosome 21.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Oxidative stress and neural dysfunction in Down 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=1226051

Evidence against the current hypothesis of "gene dosage effects" of trisomy 21: ets-2, encoded on chromosome 21" is not overexpressed in hearts of patients with Down 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=1226051

Gene identification and DNA sequence analysis in the GC-poor 20 megabase region of human chromosome 21

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromosome 21.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Enhanced metabolism of 1-beta-D-arabinofuranosylcytosine in Down syndrome cells: a contributing factor to the superior event free survival of Down syndrome children with acute myeloid leukemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Down syndrome phenotypes: the consequences of chromosomal imbalance

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

People with Down's syndrome can be distinguished on the basis of cholinergic dysfunction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Pathogenesis of mental deficiency in trisomy 21.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Methotrexate sensitivity in Down's syndrome: a hypothesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Pharmacokinetics of Leucovorin Metabolites in Human Plasma as a Function of Dose Administrated Orally and Intravenously

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Leucocyte ultrastructure and folate metabolism in Down's 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=1226051

Homocystinuria--the effects of betaine in the treatment of patients not responsive to pyridoxine.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Postnatal delay of myelin formation in brains from Down syndrome infants and children.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Anomalies in Down syndrome individuals in a large population-based registry

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Alzheimer's disease and Down syndrome: leukocyte membrane fluidity alterations

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226051

Is absence of atheroma in Down syndrome due to decreased homocysteine levels?

27 November 2018

1 reference

12 December 2020

A new HPLC method for the simultaneous determination of oxidized and reduced plasma aminothiols using coulometric electrochemical detection

1 reference

12 December 2020

In vivo folic acid supplementation partially corrects in vitro methotrexate toxicity in patients with Down syndrome

1 reference

12 December 2020

[Amino acids and trisomy 21]

1 reference

12 December 2020

Cystathionine beta synthase: gene dosage effect in trisomy 21

1 reference

12 December 2020

Down syndrome and celiac disease

1 reference

12 December 2020

Differences in purine metabolism in patients with Down's syndrome

1 reference

12 December 2020

Down’s syndrome, ageing and fragile sites

1 reference

12 December 2020

Levels of some purine metabolizing enzymes in lymphocytes from patients with Down's syndrome

1 reference

12 December 2020

Gene expression relevant to Down syndrome: problems and approaches

1 reference

12 December 2020

Metabolic studies of mongoloids

1 reference

12 December 2020

Measurement of plasma and intracellular S-adenosylmethionine and S-adenosylhomocysteine utilizing coulometric electrochemical detection: alterations with plasma homocysteine and pyridoxal 5'-phosphate concentrations

1 reference

12 December 2020

Comparative epidemiology of Down syndrome in two United States population, 1970-1989

1 reference

12 December 2020

A sensitive new method for rapid detection of abnormal methylation patterns in global DNA and within CpG islands

1 reference

12 December 2020

Identifiers

DOI

10.1086/321262

1 reference

release_xqzccgcif5c2ro6cbebk6vqm5u

4 July 2017

Fatcat ID

0 references

PMC publication ID

1226051

1 reference

4 July 2017

1 reference