(Q51899691)

17 April 2018

title

TFII-I gene family during tooth development: candidate genes for tooth anomalies in Williams syndrome. (English)

1 reference

17 April 2018

Paul T Sharpe

2

0 references

author name string

Atsushi Ohazama

series ordinal

1

1 reference

17 April 2018

publication date

1 October 2007

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17 April 2018

published in

Developmental Dynamics

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17 April 2018

volume

236

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17 April 2018

issue

10

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17 April 2018

page(s)

2884-2888

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17 April 2018

Identification of a novel slow-muscle-fiber enhancer binding protein, MusTRD1

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

Dental characteristics in Williams syndrome: a clinical and radiographic evaluation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Williams syndrome: from genotype through to the cognitive phenotype

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Dental anomalies in Williams syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Williams syndrome and related disorders

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Cloning of an inr- and E-box-binding protein, TFII-I, that interacts physically and functionally with USF1

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Facial and dental appearance of Williams syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

GTF2IRD1 in craniofacial development of humans and mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Interactions between Bmp-4 and Msx-1 act to restrict gene expression to odontogenic mesenchyme

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21311

7 January 2021

Identifiers

DOI

10.1002/DVDY.21311

1 reference

17 April 2018

1 reference

17 April 2018