(Q34447775)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

E A Lindsay

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

V Jurecic

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Baldini

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 December 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

number of pages

6

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

890-895

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9383280%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s003359900606

7 November 2019

exact match

0 references

cites work

Mouse models of human disease. Part I: techniques and resources for genetic analysis in mice

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Characterization of a novel murine testis-specific serine/threonine kinase

21 January 2018

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The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.

21 January 2018

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Human/mouse homology relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.

21 January 2018

1 reference

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A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FS003359900606

21 January 2018

12 December 2020

Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

A human homolog of the S. cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Chromosome engineering in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Alternative expression of platelet glycoprotein Ib(beta) mRNA from an adjacent 5' gene with an imperfect polyadenylation signal sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

Mapping of the Tuple1 Gene to Mouse Chromosome 16A-B1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900606

DiGeorge syndrome and 22q11 rearrangements

21 January 2018

1 reference

12 December 2020

Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta

1 reference

12 December 2020

Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies

1 reference

12 December 2020

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.

1 reference

12 December 2020

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome

1 reference

12 December 2020

Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene

1 reference

12 December 2020

Interphase and metaphase resolution of different distances within the human dystrophin gene

1 reference

12 December 2020

The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development

1 reference

12 December 2020