(Q34018852)

English

RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders

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Europe PubMed Central

PubMed publication ID

30 July 2017

RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders (English)

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Deyou Zheng

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Mingyan Lin

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Europe PubMed Central

PubMed publication ID

30 July 2017

Erika Pedrosa

2

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Europe PubMed Central

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30 July 2017

Abhishek Shah

3

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Europe PubMed Central

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30 July 2017

Anastasia Hrabovsky

4

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Europe PubMed Central

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30 July 2017

Shahina Maqbool

5

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30 July 2017

Herbert M Lachman

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30 July 2017

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7 September 2011

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Europe PubMed Central

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30 July 2017

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Europe PubMed Central

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30 July 2017

6

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Europe PubMed Central

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30 July 2017

9

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Europe PubMed Central

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30 July 2017

e23356

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Creative Commons Attribution 4.0 International

7 September 2011

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Neurons derived from reprogrammed fibroblasts functionally integrate into the fetal brain and improve symptoms of rats with Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Immune transcriptome alterations in the temporal cortex of subjects with autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

A genome-wide association study in 574 schizophrenia trios using DNA pooling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Specific expression of long noncoding RNAs in the mouse brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Disruption of neurexin 1 associated with autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Induction of GABAergic postsynaptic differentiation by alpha-neurexins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Clinical characterization of the HOXA1 syndrome BSAS variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

CART mRNA expression in rat monkey and human brain: relevance to cocaine abuse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Regulatory factor X4 variant 3: a transcription factor involved in brain development and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

The PVT-1 oncogene is a Myc protein target that is overexpressed in transformed cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Tpt1 activates transcription of oct4 and nanog in transplanted somatic nuclei

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Regulation of CART mRNA by stress and corticosteroids in the hippocampus and amygdala

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Genomewide suggestive linkage of opioid dependence to chromosome 14q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Targeting glycogen synthase kinase-3 in the CNS: implications for the development of new treatments for mood disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Functional genomic methodologies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Positive association of schizophrenia to JARID2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Germ cell nuclear factor is a repressor of CRIPTO-1 and CRIPTO-3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

MALAT-1, a novel noncoding RNA, and thymosin beta4 predict metastasis and survival in early-stage non-small cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Analysis of the human neurexin genes: alternative splicing and the generation of protein diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Isolation and proteomic characterization of the major proteins of the nucleolin-binding ribonucleoprotein complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Lithium inhibits glycogen synthase kinase-3 activity and mimics wingless signalling in intact cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Problem of diagnosis in postmortem brain studies of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Determinator-inhibitor pairs as a mechanism for threshold setting in development: a possible function for pseudogenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

5 July 2018

Critical factors in gene expression in postmortem human brain: Focus on studies in schizophrenia.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Brief report: S6 ribosomal protein phosphorylation in autistic frontal cortex and cerebellum: a tissue array analysis.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Towards understanding the schizophrenia code: an expanded convergent functional genomics approach.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Expression of two novel mouse Iroquois homeobox genes during neurogenesis

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Defects in brain patterning and head morphogenesis in the mouse mutant Fused toes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Meta-analysis of the heterogeneity of X chromosome inactivation in human pluripotent stem cells.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

An integrated genomic analysis of gene-function correlation on schizophrenia susceptibility genes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023356

21 January 2018

Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

29 October 2018

β-catenin promoter ChIP-chip reveals potential schizophrenia and bipolar disorder gene network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168439

29 October 2018

Identifiers

10.1371/JOURNAL.PONE.0023356

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2011PLoSO...623356L

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

0 references

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