(Q35101795)

6 August 2017

title

Gene expression analysis of induced pluripotent stem cells from aneuploid chromosomal syndromes (English)

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6 August 2017

0 references

Ruosi Zhang

1

1 reference

6 August 2017

Lili Hao

2

1 reference

6 August 2017

Lingping Wang

3

1 reference

6 August 2017

Meili Chen

4

1 reference

6 August 2017

Wen Li

5

1 reference

6 August 2017

Rujiao Li

6

1 reference

6 August 2017

Jun Yu

7

1 reference

6 August 2017

Jingfa Xiao

8

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6 August 2017

Jiayan Wu

9

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6 August 2017

language of work or name

English

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publication date

16 October 2013

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6 August 2017

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6 August 2017

volume

14 Suppl 5

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6 August 2017

page(s)

S8

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The in vitro survival of human monosomies and trisomies as embryonic stem cells

6 August 2017

cites work

1 reference

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

9 July 2018

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Dysregulation of gene expression in the artificial human trisomy cells of chromosome 8 associated with transformed cell phenotypes

9 July 2018

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Massive-scale RNA-Seq analysis of non ribosomal transcriptome in human trisomy 21.

9 July 2018

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RNA sequencing shows no dosage compensation of the active X-chromosome

9 July 2018

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FAK: dynamic integration of guidance signals at the growth cone

9 July 2018

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Human embryonic stem cells as models for aneuploid chromosomal syndromes

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Genome-wide misexpression of X-linked versus autosomal genes associated with hybrid male sterility

9 July 2018

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Human embryonic stem cells from aneuploid blastocysts identified by pre-implantation genetic screening

9 July 2018

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The SLIT-ROBO pathway: a regulator of cell function with implications for the reproductive system

9 July 2018

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Intracellular calcium signalling in Alzheimer's disease

9 July 2018

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Retinotopic mapping requires focal adhesion kinase-mediated regulation of growth cone adhesion.

9 July 2018

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RNA-seq: from technology to biology

9 July 2018

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DEGseq: an R package for identifying differentially expressed genes from RNA-seq data

9 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Functional genomic analysis of amniotic fluid cell-free mRNA suggests that oxidative stress is significant in Down syndrome fetuses

9 July 2018

1 reference

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Bidirectional modulation of synaptic functions by Eph/ephrin signaling.

9 July 2018

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RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays

9 July 2018

1 reference

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Stem cell transcriptome profiling via massive-scale mRNA sequencing

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Derivation of euploid human embryonic stem cells from aneuploid embryos

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

High blood pressure arising from a defect in vascular function.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Cancer incidence in women with Turner syndrome in Great Britain: a national cohort study

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Histogenesis of retinal dysplasia in trisomy 13

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Microarray data analysis: from disarray to consolidation and consensus

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Transcriptional consequences of autosomal trisomy: primary gene dosage with complex downstream effects

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Chromosome transfer induced aneuploidy results in complex dysregulation of the cellular transcriptome in immortalized and cancer cells

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Guiding neuronal growth cones using Ca2+ signals.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Mongolism; a chromosomal disease (trisomy).

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

DAVID: Database for Annotation, Visualization, and Integrated Discovery

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Neuronal target genes of the neuron-restrictive silencer factor in neurospheres derived from fetuses with Down's syndrome: a gene expression study

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

To err (meiotically) is human: the genesis of human aneuploidy

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Slit2 is a repellent for retinal ganglion cell axons

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

How aneuploidy may cause cancer and genetic instability

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Occurrence of cancer in women with Turner syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Histogenesis of the retina in murine trisomy 19.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Secondary trisomy or mosaic "tetrasomy" 8p.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

The consequences of chromosome imbalance

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Calcium Dependent Regulation of Vascular Smooth Muscle Contraction

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Trisomy 13 as a primary chromosome aberration in acute leukemia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Molecular Mechanisms of Axon Growth and Guidance

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

9 July 2018

Causes of fetal wastage

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Global disruption of the cerebellar transcriptome in a Down syndrome mouse model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Gene expression profiling in the adult Down syndrome brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Gene expression variation increase in trisomy 21 tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Genetic analysis of ephrin-A2 and ephrin-A5 shows their requirement in multiple aspects of retinocollicular mapping.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

Long-range Ca2+ signaling from growth cone to soma mediates reversal of neuronal migration induced by slit-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

An evaluation of early cardiometabolic risk factors in children and adolescents with Turner syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

An association of craniopharyngioma in Turner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2164-14-S5-S8

A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852284

Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics

16 November 2018

1 reference

12 December 2020

[Warkany syndrome associated with agenesis of the corpus callosum]

1 reference

12 December 2020

Transcriptome analysis of human autosomal trisomy

1 reference

12 December 2020

Impact of trisomy 8 on expression of genes located on chromosome 8 in different AML subgroups

1 reference

12 December 2020

10.1186/1471-2164-14-S5-S8

Identifiers

DOI

1 reference

6 August 2017

1 reference

6 August 2017

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