(Q44454642)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

S-adenosyl-L-homocysteine

4 November 2019

main subject

patient

0 references

1 reference

S-adenosyl-L-homocysteine

ChEBI release 2020-05-28

1 reference

1 reference

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

Diego Ingrosso

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Amelia Cimmino

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Lucia Masella

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Natale G De Santo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Maria Luigia De Bonis

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Marcella Vacca

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Maurizio D'Esposito

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Michele D'Urso

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Patrizia Galletti

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Vincenzo Zappia

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

language of work or name

English

0 references

publication date

1 May 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

361

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

1693-1699

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

issue

9370

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12767735%20AND%20SRC:MED&resulttype=core&format=json

DNA methylation in health and disease

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Homocysteine and vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Hyperhomocysteinemia confers an independent increased risk of atherosclerosis in end-stage renal disease and is closely linked to plasma folate and pyridoxine concentrations.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Enzymatic methyl esterification of erythrocyte membrane proteins is impaired in chronic renal failure. Evidence for high levels of the natural inhibitor S-adenosylhomocysteine.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Membrane protein damage and methylation reactions in chronic renal failure

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

McrBC: a multisubunit GTP-dependent restriction endonuclease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Methylation analysis on individual chromosomes: improved protocol for bisulphite genomic sequencing.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Imprinting and the epigenetic asymmetry between parental genomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Human diseases with underlying defects in chromatin structure and modification.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

X-chromosome inactivation in mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Genomic imprinting: parental influence on the genome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Elevation in S-Adenosylhomocysteine and DNA Hypomethylation: Potential Epigenetic Mechanism for Homocysteine-Related Pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021

Homocyst(e)ine and cardiovascular disease: a critical review of the epidemiologic evidence

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2913372-7

7 January 2021