(Q46571741)

23 December 2017

title

Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3. (English)

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23 December 2017

author

Jian-Hua Mao

9

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23 December 2017

William A Weiss

11

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23 December 2017

author name string

Tsui-Ting Ching

1

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23 December 2017

Alika K Maunakea

2

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23 December 2017

Peter Jun

3

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23 December 2017

Chibo Hong

4

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23 December 2017

Giuseppe Zardo

5

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23 December 2017

Daniel Pinkel

6

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23 December 2017

Donna G Albertson

7

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23 December 2017

Jane Fridlyand

8

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23 December 2017

Ksenya Shchors

10

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23 December 2017

Joseph F Costello

12

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23 December 2017

language of work or name

English

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publication date

15 May 2005

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23 December 2017

published in

Nature Genetics

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23 December 2017

volume

37

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23 December 2017

page(s)

645-651

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23 December 2017

issue

6

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23 December 2017

https://scigraph.springernature.com/pub.10.1038/ng1563

exact match

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cites work

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

DNA hypomethylation leads to elevated mutation rates

21 January 2018

1 reference

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

Asymmetrical distribution of CpG in an 'average' mammalian gene

21 January 2018

1 reference

CpG islands in vertebrate genomes

21 January 2018

1 reference

CpG islands as gene markers in the human genome.

21 January 2018

1 reference

Comprehensive analysis of CpG islands in human chromosomes 21 and 22

21 January 2018

1 reference

Imprinting and the initiation of gene silencing in the germ line.

21 January 2018

1 reference

Methylation of HoxA5 and HoxB5 and its relevance to expression during mouse development.

21 January 2018

1 reference

Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression

21 January 2018

1 reference

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

21 January 2018

1 reference

DNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoter

21 January 2018

1 reference

Role for DNA methylation in the control of cell type specific maspin expression

21 January 2018

1 reference

The Sequence of the Human Genome

21 January 2018

1 reference

Number of CpG islands and genes in human and mouse

21 January 2018

1 reference

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

21 January 2018

1 reference

Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene

21 January 2018

1 reference

Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

21 January 2018

1 reference

Assembly of microarrays for genome-wide measurement of DNA copy number

21 January 2018

1 reference

Mapping segmental and sequence variations among laboratory mice using BAC array CGH.

21 January 2018

1 reference

Use of restriction enzymes to detect potential gene sequences in mammalian DNA.

21 January 2018

1 reference

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

21 January 2018

1 reference

Linkage of the actin cytoskeleton to the postsynaptic density via direct interactions of Abp1 with the ProSAP/Shank family

21 January 2018

1 reference

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

21 January 2018

1 reference

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome

21 January 2018

1 reference

21 January 2018

22q13 deletion syndrome

1 reference

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

21 January 2018

1 reference

Role of transposable elements in heterochromatin and epigenetic control

21 January 2018

1 reference

Genomic maps and comparative analysis of histone modifications in human and mouse

21 January 2018

1 reference

Amount and distribution of 5-methylcytosine in human DNA from different types of tissues of cells

21 January 2018

1 reference

Intragenic DNA methylation alters chromatin structure and elongation efficiency in mammalian cells

21 January 2018

1 reference

The activation of human gene MAGE-1 in tumor cells is correlated with genome-wide demethylation.

21 January 2018

1 reference

Fully automatic quantification of microarray image data

21 January 2018

1 reference

Bisulfite genomic sequencing: systematic investigation of critical experimental parameters

21 January 2018

1 reference

Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG1563

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23 December 2017

Dimensions Publication ID

0 references

1 reference

23 December 2017