Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene (Q24324759)

https://api.crossref.org/works/10.1006/GENO.1997.4829

T-box transcription factor 1

12 November 2024

main subject

1 reference

regulation of transcription by RNA polymerase II

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

T-box 1

1 reference

chromosomal deletion syndrome

GOA release 2020-03-11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

T-box

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

C. Chieffo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

N. Garvey

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

W. Gong

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

B. Roe

1 reference

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12 November 2024

G. Zhang

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

L. Silver

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

B. S. Emanuel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

12 November 2024

M. L. Budarf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

full work available at URL

12 November 2024

language of work or name

English

0 references

publication date

1 August 1997

0 references

https://doi.org/10.1006/geno.1997.4829

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9268629

https://api.elsevier.com/content/article/PII:S0888754397948291?httpAccept=text/xml

12 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

https://api.elsevier.com/content/article/PII:S0888754397948291?httpAccept=text/plain

12 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

12 November 2024

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267-77

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cites work

Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

The DiGeorge anomaly as a developmental field defect

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

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.1997.4829

7 January 2021

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.1997.4829

7 January 2021

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

The T protein encoded by Brachyury is a tissue-specific transcription factor

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Skeletal anomalies and deformities in patients with deletions of 22q11

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

DiGeorge syndrome and 22q11 rearrangements

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Plasticity and predetermination of mesencephalic and trunk neural crest transplanted into the region of the cardiac neural crest

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

CpG islands as gene markers in the human genome.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Conservation of the T-box gene family from Mus musculus to Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

A new concept of the cellular basis of immunity

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

The spectrum of the DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Identification of human chromosome 9 specific genes using exon amplification

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Three new point mutations in type II procollagen (COL2A1) and identification of a fourth family with the COL2A1 Arg519-->Cys base substitution using conformation sensitive gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Rapid transfer of DNA from agarose gels to nylon membranes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

An expression-independent catalog of genes from human chromosome 22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Neural crest cells contribute to normal aorticopulmonary septation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Familial heart disease with skeletal malformations

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

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.1997.4829

7 January 2021

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4829

7 January 2021

Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

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

12 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

Genetical studies on the skeleton of the mouse. XXIII. The development of brachyury and anury

12 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

Hairpin-tail: a case of post-reductional gene action in the mouse egg

12 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4829

12 November 2024

Identifiers

0 references