Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions (Q42694136)

5 November 2017

Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions (English)

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5 November 2017

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Xiaolu Sturgeon

1

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PubMed ID

21400203

5 November 2017

Katheleen J Gardiner

series ordinal

2

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5 November 2017

13 March 2011

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5 November 2017

11

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inferred from page(s)

published in

Mammalian Genome

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5 November 2017

22

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5 November 2017

5-6

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5 November 2017

261-271

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https://scigraph.springernature.com/pub.10.1007/s00335-011-9321-y

5 November 2017

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cites work

The Down syndrome critical region protein TTC3 inhibits neuronal differentiation via RhoA and Citron kinase

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Vitamin E increases S100B-mediated microglial activation in an S100B-overexpressing mouse model of pathological aging.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Differentiating protein-coding and noncoding RNA: challenges and ambiguities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Regulatory roles of natural antisense transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Molecular basis of pharmacotherapies for cognition in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

The proteins of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Genome-wide transcription and the implications for genomic organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

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/10.1007%2FS00335-011-9321-Y

Cognitive deficits and associated neurological complications in individuals with Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Long non-coding RNAs: insights into functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Inhibition of tumor cell motility by the interferon-inducible GTPase MxA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Transcriptome analysis by strand-specific sequencing of complementary DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Down syndrome and the genes of human chromosome 21: current knowledge and future potentials

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Antisense transcripts are targets for activating small RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Mouse models of cognitive disorders in trisomy 21: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

LINE-1 retrotransposons: mediators of somatic variation in neuronal genomes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Identification and characterization of human BIC, a gene on chromosome 21 that encodes a noncoding RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Most "dark matter" transcripts are associated with known genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

InvAluable junk: the cellular impact and function of Alu and B2 RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

DNA sequence and comparative analysis of chimpanzee chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Emerging pharmacotherapies for neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

The vertebrate genome annotation (Vega) database

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

Down syndrome--recent progress and future prospects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-011-9321-Y

GENCODE: producing a reference annotation for ENCODE

21 January 2018

1 reference

12 December 2020

Restoration of norepinephrine-modulated contextual memory in a mouse model of Down syndrome.

1 reference

12 December 2020

The DNA sequence of human chromosome 21

1 reference

12 December 2020

Improved national prevalence estimates for 18 selected major birth defects--United States, 1999-2001

1 reference

12 December 2020

10.1007/S00335-011-9321-Y

Identifiers

DOI

1 reference

PubMed ID

21400203

Dimensions Publication ID

5 November 2017

0 references

1 reference

PubMed ID

21400203