(Q29614515)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

main subject

phenotypic plasticity

0 references

author name string

Feinberg AP

series ordinal

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

24 May 2007

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

volume

447

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

page(s)

433-40

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

30 April 2017

issue

7143

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome

30 April 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Imprinting defects on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Imprints of disease at GNAS1.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

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/10.1038%2FNATURE05919

7 January 2021

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Molecular-clinical spectrum of the ATR-X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Hypomethylation distinguishes genes of some human cancers from their normal counterparts

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The history of cancer epigenetics

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The human let-7a-3 locus contains an epigenetically regulated microRNA gene with oncogenic function.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Hypomethylation-linked activation of PAX2 mediates tamoxifen-stimulated endometrial carcinogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The fundamental role of epigenetic events in cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Aberrant CpG-island methylation has non-random and tumour-type-specific patterns.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic remodeling in colorectal cancer results in coordinate gene suppression across an entire chromosome band.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Preference of DNA methyltransferases for CpG islands in mouse embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Distinct effects on gene expression of chemical and genetic manipulation of the cancer epigenome revealed by a multimodality approach.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Genomic imprinting and gene activation in cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of imprinting of IGF2 and not H19 in breast cancer, adjacent normal tissue and derived fibroblast cultures

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Frequent IGF2/H19 domain epigenetic alterations and elevated IGF2 expression in epithelial ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The polycomb group protein EZH2 is involved in progression of prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

A histone H3 methyltransferase controls DNA methylation in Neurospora crassa

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Histone and DNA methylation defects at Hox genes in mice expressing a SET domain-truncated form of Mll.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The C-terminal SET domains of ALL-1 and TRITHORAX interact with the INI1 and SNR1 proteins, components of the SWI/SNF complex

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Haploinsufficiency of NSD1 causes Sotos syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Activation of mouse genes in transformed cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Histone modifications and silencing prior to DNA methylation of a tumor suppressor gene.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of IGF2 imprinting: a potential marker of colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of insulin-like growth factor-II imprinting and the presence of screen-detected colorectal adenomas in women.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

CpG island methylator phenotype in colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Opposing effects of DNA hypomethylation on intestinal and liver carcinogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Induction of Tumors in Mice by Genomic Hypomethylation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Chromosomal Instability and Tumors Promoted by DNA Hypomethylation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Suppression of intestinal neoplasia by DNA hypomethylation.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Heterozygous disruption of Hic1 predisposes mice to a gender-dependent spectrum of malignant tumors.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of imprinting of Igf2 alters intestinal maturation and tumorigenesis in mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Global loss of imprinting leads to widespread tumorigenesis in adult mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The epigenetic progenitor origin of human cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Soluble IGF2 receptor rescues Apc(Min/+) intestinal adenoma progression induced by Igf2 loss of imprinting.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Reprogramming of a melanoma genome by nuclear transplantation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Distinct epigenetic changes in the stromal cells of breast cancers

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

A bivalent chromatin structure marks key developmental genes in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Continuous MLL-ENL expression is necessary to establish a "Hox Code" and maintain immortalization of hematopoietic progenitor cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Transformation from committed progenitor to leukaemia stem cell initiated by MLL-AF9.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Polycomb complexes repress developmental regulators in murine embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Identification of a cluster of X-linked imprinted genes in mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetics, disease, and therapeutic interventions

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Treating activated CD4+ T cells with either of two distinct DNA methyltransferase inhibitors, 5-azacytidine or procainamide, is sufficient to cause a lupus-like disease in syngeneic mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

DNA methylation and autoimmune disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetics and the Environment

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic transgenerational actions of endocrine disruptors and male fertility

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Transposable elements: targets for early nutritional effects on epigenetic gene regulation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Alcohol, one-carbon metabolism, and colorectal cancer: recent insights from molecular studies

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic programming by maternal behavior

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetics and assisted reproductive technology: a call for investigation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

An integrated epigenetic and genetic approach to common human disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic differences arise during the lifetime of monozygotic twins

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Hsp90 as a capacitor for morphological evolution

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Systematic mapping of genetic interactions in Caenorhabditis elegans identifies common modifiers of diverse signaling pathways

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

The emerging science of epigenomics

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Epigenetic cancer therapy makes headway

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

Selective HAT inhibitors as mechanistic tools for protein acetylation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

https://api.crossref.org/works/10.1038%2FNATURE05919

1 reference

7 January 2021

Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05919

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

Identifiers

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

422190

1033770262

0 references

422190

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17522677

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017