Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing (Q21131890)

3

Jason J

Corneveaux

1 reference

16 August 2022

Ashley L Siniard

4

Ashley L

Siniard

1 reference

16 August 2022

Ahmet A Kurdoglu

5

Ahmet A

Kurdoglu

1 reference

16 August 2022

Keri M Ramsey

6

Keri M

Ramsey

1 reference

16 August 2022

Matthew J Huentelman

10

Matthew J

Huentelman

1 reference

16 August 2022

David W Craig

11

David W

Creative Commons Attribution 4.0 International

Craig

1 reference

16 August 2022

language of work or name

English

0 references

publication date

2014

0 references

published in

PLOS One

0 references

volume

9

0 references

issue

12

0 references

page(s)

e113036

0 references

copyright license

start time

12 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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12 September 2017

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Genome and transcriptome sequencing in prospective metastatic triple-negative breast cancer uncovers therapeutic vulnerabilities

12 September 2017

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Genome-wide characterization of pancreatic adenocarcinoma patients using next generation sequencing

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12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome

12 September 2017

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Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes disease

12 September 2017

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Genomic imprinting: the influence of differential methylation in the two sexes.

12 September 2017

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12 September 2017

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Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

12 September 2017

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Modulation of neuritogenesis by a protein implicated in X-linked mental retardation

12 September 2017

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X chromosome inactivation in clinical practice

12 September 2017

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Skewing of X-inactivation ratios in blood cells of aging women is confirmed by independent methodologies

12 September 2017

1 reference

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Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain

12 September 2017

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Global survey of genomic imprinting by transcriptome sequencing

12 September 2017

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Hematopoiesis is not clonal in healthy elderly women.

12 September 2017

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Comparison of X-chromosome inactivation patterns in multiple tissues from human females

12 September 2017

1 reference

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X chromosome-inactivation patterns of 1,005 phenotypically unaffected females

12 September 2017

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Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

12 September 2017

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Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease.

12 September 2017

1 reference

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

12 September 2017

1 reference

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X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

12 September 2017

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Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders

12 September 2017

1 reference

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Escapees on the X chromosome

12 September 2017

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Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

12 September 2017

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The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases.

12 September 2017

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Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0113036