Translating dosage compensation to trisomy 21 (Q34037496)

30 July 2017

Translating dosage compensation to trisomy 21 (English)

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30 July 2017

3

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30 July 2017

15

Carolyn J Brown

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30 July 2017

12

Edward J Rebar

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30 July 2017

16

Fyodor D Urnov

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30 July 2017

Jun Jiang

1

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30 July 2017

Yuanchun Jing

2

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30 July 2017

Jen-Chieh Chiang

4

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30 July 2017

Heather J Kolpa

5

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30 July 2017

Allison M Cotton

6

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30 July 2017

Dawn M Carone

7

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30 July 2017

Benjamin R Carone

8

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30 July 2017

David A Shivak

9

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30 July 2017

Dmitry Y Guschin

10

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30 July 2017

Jocelynn R Pearl

11

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30 July 2017

Meg Byron

13

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30 July 2017

Philip D Gregory

14

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30 July 2017

Lisa L Hall

17

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30 July 2017

Jeanne B Lawrence

18

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30 July 2017

language of work or name

English

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publication date

17 July 2013

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30 July 2017

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30 July 2017

500

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30 July 2017

296-300

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30 July 2017

7462

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https://scigraph.springernature.com/pub.10.1038/nature12394

30 July 2017

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cites work

A multifaceted FISH approach to study endogenous RNAs and DNAs in native nuclear and cell structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Trisomy correction in Down syndrome induced pluripotent stem cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Trisomy 21 and early brain development

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

XIST RNA and architecture of the inactive X chromosome: implications for the repeat genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Rapid and efficient clathrin-mediated endocytosis revealed in genome-edited mammalian cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Genome editing with engineered zinc finger nucleases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

A rapid and general assay for monitoring endogenous gene modification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Human embryonic stem cells as models for aneuploid chromosomal syndromes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Molecular basis of pharmacotherapies for cognition in Down syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

The 50th anniversary of the discovery of trisomy 21: the past, present, and future of research and treatment of Down syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Disease-specific induced pluripotent stem cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Derivation of euploid human embryonic stem cells from aneuploid embryos

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

X-inactivation reveals epigenetic anomalies in most hESC but identifies sublines that initiate as expected

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

An improved zinc-finger nuclease architecture for highly specific genome editing

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Delving into the diversity of facultative heterochromatin: the epigenetics of the inactive X chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Highly efficient endogenous human gene correction using designed zinc-finger nucleases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

X-inactivation profile reveals extensive variability in X-linked gene expression in females

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Unbalanced X;autosome translocations provide evidence for sequence specificity in the association of XIST RNA with chromatin

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

A 450 kb transgene displays properties of the mammalian X-inactivation center.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3848249

Gene therapy grows into young adulthood: special review issue

28 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

Recurrent variations in DNA methylation in human pluripotent stem cells and their differentiated derivatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

Targeted gene addition into a specified location in the human genome using designed zinc finger nucleases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

Functional genomics, proteomics, and regulatory DNA analysis in isogenic settings using zinc finger nuclease-driven transgenesis into a safe harbor locus in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

Widespread proliferation impairment and hypocellularity in the cerebellum of fetuses with down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

A human stem cell model of early Alzheimer's disease pathology in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

Summaries of Affymetrix GeneChip probe level data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE12394

21 January 2018

Identifiers

DOI

10.1038/NATURE12394

1 reference

Dimensions Publication ID

30 July 2017

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30 July 2017

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