(Q28592076)

22 June 2017

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients (English)

1 reference

22 June 2017

0 references

1 reference

GOA release 2020-03-11

Andrew K Groves

4

0 references

Bernice E. Morrow

object named as

Bernice E Morrow

7

0 references

author name string

Takahiro Ohyama

3

1 reference

22 June 2017

Jelena S Arnold

1

1 reference

22 June 2017

Evan M Braunstein

2

1 reference

22 June 2017

Joe C Adams

5

1 reference

22 June 2017

M Christian Brown

6

1 reference

22 June 2017

6 April 2006

1 reference

22 June 2017

Human Molecular Genetics

1 reference

22 June 2017

15

1 reference

22 June 2017

10

1 reference

22 June 2017

1629-1639

1 reference

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development

22 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Mutation of the POU-domain gene Brn4/Pou3f4 affects middle-ear sound conduction in the mouse

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Suppression of neural fate and control of inner ear morphogenesis by Tbx1

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Role of TBX1 in human del22q11.2 syndrome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

TBX1 is required for inner ear morphogenesis

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

The role of Six1 in mammalian auditory system development

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Six1 is required for the early organogenesis of mammalian kidney

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Specification of the mammalian cochlea is dependent on Sonic hedgehog

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Generalized lacZ expression with the ROSA26 Cre reporter strain

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Revisiting cell fate specification in the inner ear.

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

The 22q11.2 deletion syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Pax3 and vertebrate development

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Regulatory regions from the Brn4 promoter direct LACZ expression to the developing forebrain and neural tube.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Targeting of cre to the Foxg1 (BF-1) locus mediates loxP recombination in the telencephalon and other developing head structures

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

A new concept of the cellular basis of immunity

3 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Temporal bone pathology in DiGeorge's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL084

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Mondini dysplasia; a clinical and pathological study.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

Temporal bone findings in the third and fourth pharyngeal pouch (DiGeorge) syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563157

What defines DiGeorge anomaly?

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16600992

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Interactions between Hox-negative cephalic neural crest cells and the foregut endoderm in patterning the facial skeleton in the vertebrate head

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16600992

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Aural Abnormalities in Partial DiGeorge Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16600992

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDL084

1 reference

22 June 2017

0 references

1 reference