Human chromosome 21 gene expression atlas in the mouse (Q52111595)

22 April 2018

title

Human chromosome 21 gene expression atlas in the mouse (English)

1 reference

22 April 2018

author

Stilianos Antonarakis

12

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22 April 2018

Valeria Marigo

Valeria Marigo

2

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Sandro Banfi

Sandro Banfi

10

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Andrea Ballabio

Andrea Ballabio

13

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Alexandre Reymond

1

Alexandre Reymond

1 reference

22 April 2018

Emmanouil Dermitzakis

8

Emmanouil T Dermitzakis

1 reference

22 April 2018

Nathalie Scamuffa

6

Nathalie Scamuffa

1 reference

22 April 2018

author name string

Murat B Yaylaoglu

3

1 reference

22 April 2018

Antonio Leoni

4

1 reference

22 April 2018

Catherine Ucla

5

1 reference

22 April 2018

Cristina Caccioppoli

7

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22 April 2018

Robert Lyle

9

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22 April 2018

Gregor Eichele

11

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22 April 2018

language of work or name

English

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publication date

1 December 2002

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22 April 2018

published in

Nature

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22 April 2018

volume

420

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22 April 2018

issue

6915

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22 April 2018

page(s)

582-586

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22 April 2018

A new dimension for the human genome project: towards comprehensive expression maps

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Large-scale screen for genes controlling mammalian embryogenesis, using high-throughput gene expression analysis in mouse embryos.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres): a comparative and topographic approach to predict gene function.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

The tripartite motif family identifies cell compartments

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

The DNA sequence of human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Evolutionary breakpoints on human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Nineteen additional unpredicted transcripts from human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Developmental expression of the SH3BGR gene, mapping to the Down syndrome heart critical region.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Frameshift mutation in the collagen VI gene causes Ullrich's disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Down's syndrome-like skeletal abnormalities in Ets2 transgenic mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

A gene expression map for Caenorhabditis elegans.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Evidence for large domains of similarly expressed genes in the Drosophila genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

The rise and fall of positional cloning?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

Down syndrome congenital heart disease: a narrowed region and a candidate gene

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01178

7 January 2021

https://api.fatcat.wiki/v0/release/enlpsjzrenhdzomkuvbrw23eeq

Identifiers

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30 July 2022

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Dimensions Publication ID

1008701243

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Fatcat ID

release_enlpsjzrenhdzomkuvbrw23eeq

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Fatcat

https://api.fatcat.wiki/v0/release/enlpsjzrenhdzomkuvbrw23eeq

30 July 2022

mapped directly with Wikidata item

https://api.fatcat.wiki/v0/release/enlpsjzrenhdzomkuvbrw23eeq

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30 July 2022