(Q34195138)

31 July 2017

title

Passage number is a major contributor to genomic structural variations in mouse iPSCs (English)

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31 July 2017

4

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31 July 2017

Orly Reiner

6

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James R. Lupski

series ordinal

5

object named as

James R Lupski

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31 July 2017

Pengfei Liu

1

1 reference

31 July 2017

Anna Kaplan

series ordinal

2

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31 July 2017

Bo Yuan

series ordinal

3

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31 July 2017

publication date

1 October 2014

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31 July 2017

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31 July 2017

volume

32

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31 July 2017

issue

10

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31 July 2017

page(s)

2657-2667

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The distribution of genomic variations in human iPSCs is related to replication-timing reorganization during reprogramming.

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Mosaic copy number variation in human neurons

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Genetics. Genome mosaicism--one human, multiple genomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

A genomic view of mosaicism and human disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Genetic instability in neural stem cells: an inconvenient truth?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Hydroxyurea induces de novo copy number variants in human cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Genome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promises

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Large-scale analysis reveals acquisition of lineage-specific chromosomal aberrations in human adult stem cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Copy number variation and selection during reprogramming to pluripotency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Genomic instability in induced stem cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture

5 July 2018

1 reference

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Single-gene transgenic mouse strains for reprogramming adult somatic cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

A microhomology-mediated break-induced replication model for the origin of human copy number variation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Extensive genomic copy number variation in embryonic stem cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Chromosomal variation in neurons of the developing and adult mammalian nervous system

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Origin of murine B cell lineages

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4165691

Identification and Classification of Chromosomal Aberrations in Human Induced Pluripotent Stem Cells

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FSTEM.1779

Karotypic abnormalities in human induced pluripotent stem cells and embryonic stem cells

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FSTEM.1779

Adaptation to culture of human embryonic stem cells and oncogenesis in vivo

21 January 2018

1 reference

12 December 2020

Production of neurons, astrocytes and oligodendrocytes from mammalian CNS stem cells

1 reference

12 December 2020

Recurrent copy number variations in human induced pluripotent stem cells

1 reference

12 December 2020

High prevalence of evolutionarily conserved and species-specific genomic aberrations in mouse pluripotent stem cells

1 reference

12 December 2020

Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novelSHOXenhancer

1 reference

12 December 2020

Identifiers

DOI

10.1002/STEM.1779

1 reference

31 July 2017

1 reference

31 July 2017

1 reference