(Q24562781)

English

Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development

scientific article

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scholarly article

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Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development (English)

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author name string

N Dahmane

1

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G Charron

2

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C Lopes

3

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M L Yaspo

4

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C Maunoury

5

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L Decorte

6

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P M Sinet

7

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B Bloch

8

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J M Delabar

9

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language of work or name

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publication date

26 September 1995

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Proceedings of the National Academy of Sciences of the United States of America

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92

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20

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9191-5

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Identification of functional domains of the aryl hydrocarbon receptor nuclear translocator protein (ARNT)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

24 March 2017

Single-minded and Down syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

24 March 2017

Human Ah receptor cDNA: analysis for highly conserved sequences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Development of the superior temporal neocortex is anomalous in trisomy 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Use of restriction enzymes to detect potential gene sequences in mammalian DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

The Drosophila single-minded gene encodes a helix-loop-helix protein that acts as a master regulator of CNS midline development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Expression of the HBNF (heparin-binding neurite-promoting factor) gene in the brain of fetal, neonatal and adult rat: an in situ hybridization study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

27 September 2017

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

Genetic analysis of the Drosophila single-minded gene reveals a central nervous system influence on muscle development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

A male infant with holoprosencephaly, associated with ring chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

The Drosophila single-minded gene encodes a nuclear protein with sequence similarity to the per gene product

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

Molecular genetics of the single-minded locus: a gene involved in the development of the Drosophila nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

30 May 2018

Single-minded regulation of genes in the embryonic midline of the Drosophila central nervous system.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

28 November 2018

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40950

28 November 2018

The development and function of the Drosophila CNS midline cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7568099

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A NotI restriction map of the entire long arm of human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/7568099

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/7568099

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2

1 reference

https://pubmed.ncbi.nlm.nih.gov/7568099

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.92.20.9191

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1995PNAS...92.9191D

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ResearchGate publication ID

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