(Q24322620)

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Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9441739%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11 (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9441739%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

Goosecoid homeobox 2

1 reference

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Bernice E. Morrow

11

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Europe PubMed Central

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8 November 2019

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Funke B

1

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8 November 2019

Saint-Jore B

2

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8 November 2019

Puech A

3

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8 November 2019

Sirotkin H

4

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8 November 2019

Edelmann L

5

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8 November 2019

Carlson C

6

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8 November 2019

Raft S

7

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8 November 2019

Pandita RK

8

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8 November 2019

Kucherlapati R

9

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8 November 2019

Skoultchi A

10

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8 November 2019

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publication date

1 December 1997

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8 November 2019

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8 November 2019

46

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8 November 2019

3

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8 November 2019

364-372

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8 November 2019

The DiGeorge anomaly as a developmental field defect

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

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Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Velo-cardio-facial syndrome: a review of 120 patients.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

DiGeorge anomaly with renal agenesis in infants of mothers with diabetes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Neural crest and normal development: a new perspective

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular characterization of seizure-related genes isolated by differential screening

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Murine homeobox-containing gene, Msx-1: analysis of genomic organization, promoter structure, and potential autoregulatory cis-acting elements

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

The gradient morphogen bicoid is a concentration-dependent transcriptional activator.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Gastrulation in the mouse: the role of the homeobox gene goosecoid

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Homeodomain-DNA recognition

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

A new concept of the cellular basis of immunity

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

The bicoid protein is a positive regulator of hunchback transcription in the early Drosophila embryo.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Conservation and diversification in homeodomain-DNA interactions: a comparative genetic analysis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Organizer-Specific Homeobox Genes in Xenopus laevis Embryos

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

7 January 2021

based on heuristic

inferred from DOI database lookup

Neural crest cells contribute to normal aorticopulmonary septation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

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based on heuristic

inferred from DOI database lookup

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5046

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based on heuristic

inferred from DOI database lookup

Identifiers

10.1006/GENO.1997.5046

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9441739%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9441739%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

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