(Q21563377)

6 February 2023

Amir Gamliel

2

Amir

Gamliel

1 reference

6 February 2023

Robert J Wessells

3

Robert J

Wessells

1 reference

6 February 2023

Ouarda Taghli-Lamallem

4

Ouarda

Taghli-Lamallem

1 reference

6 February 2023

Kristen Jepsen

5

Kristen

Jepsen

1 reference

6 February 2023

Karen Ocorr

6

Karen

Ocorr

1 reference

6 February 2023

Julie R Korenberg

7

Julie R

Korenberg

1 reference

6 February 2023

Kirk L Peterson

8

Kirk L

Peterson

1 reference

6 February 2023

Michael G Rosenfeld

9

Michael G

Rosenfeld

1 reference

6 February 2023

Rolf Bodmer

10

Rolf

Bodmer

1 reference

6 February 2023

Ethan Bier

11

Ethan

Bier

1 reference

Creative Commons Attribution 4.0 International

6 February 2023

language of work or name

English

0 references

publication date

November 2011

0 references

published in

PLOS Genetics

0 references

volume

7

0 references

issue

11

0 references

page(s)

e1002344

0 references

copyright license

start time

3 November 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

TopHat: discovering splice junctions with RNA-Seq

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

KCNQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

DAVID: Database for Annotation, Visualization, and Integrated Discovery

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

S100A1 in cardiovascular health and disease: closing the gap between basic science and clinical therapy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Drosophila, an emerging model for cardiac disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Regulation of cardiac hypertrophy by intracellular signalling pathways

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Structural variation in the human genome and its role in disease

12 September 2017

1 reference

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Copy number variation in human health, disease, and evolution

12 September 2017

1 reference

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The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

12 September 2017

1 reference

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A new method for detection and quantification of heartbeat parameters in Drosophila, zebrafish, and embryonic mouse hearts

12 September 2017

1 reference

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Disrupted cardiac development but normal hematopoiesis in mice deficient in the second CXCL12/SDF-1 receptor, CXCR7

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

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

12 September 2017

1 reference

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The use of contrast echocardiography for the detection of cardiac shunts

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

GATA2 is associated with familial early-onset coronary artery disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Heart morphogenesis is not affected by overexpression of the Sh3bgr gene mapping to the Down syndrome heart critical region

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Developmental anatomy of the heart: a tale of mice and man.

12 September 2017

1 reference

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Hypertrophic cardiomyopathy: a systematic review

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Molecular basis of inherited neuropathies.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Heart development in Drosophila and vertebrates: conservation of molecular mechanisms.

12 September 2017

1 reference

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Tissue-specific regulation of the alpha-myosin heavy chain gene promoter in transgenic mice.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207880

Faithful tissue-specific expression of the human chromosome 21-linked COL6A1 gene in BAC-transgenic mice.

30 May 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Down syndrome congenital heart disease: a narrowed region and a candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Insulin regulation of heart function in aging fruit flies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Protocol for optimal detection and exclusion of a patent foramen ovale using transthoracic echocardiography with agitated saline microbubbles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Early postnatal lethality and cardiovascular defects in CXCR7-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Gene expression profiling in the adult Down syndrome brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Cardiac fibroblasts regulate myocardial proliferation through beta1 integrin signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Functional analysis of cell adhesion: quantitation of cell-matrix attachment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002344

Genomics. The HapMap gold rush: researchers mine a rich deposit

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/22072978

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hypertrophic cardiomyopathy in a patient with Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22072978

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002344

0 references

Fatcat ID

release_5be74ozxzreehnlqgduaybzjpu

0 references

PMC publication ID

3207880

0 references