(Q24317196)

12 December 2024

1 reference

GOA release 2020-03-11

hearing

1 reference

GOA release 2020-03-11

author name string

A. Watanabe

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9500554

12 December 2024

K. Takeda

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9500554

12 December 2024

B. Ploplis

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9500554

12 December 2024

M. Tachibana

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9500554

full work available at URL

12 December 2024

language of work or name

English

0 references

publication date

March 1998

0 references

http://www.nature.com/articles/ng0398-283

1 reference

http://www.nature.com/articles/ng0398-283.pdf

12 December 2024

1 reference

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

12 December 2024

0 references

18

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issue

3

0 references

page(s)

283-6

0 references

cites work

1 reference

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

20 April 2017

1 reference

Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma

20 April 2017

1 reference

20 April 2017

1 reference

7 January 2021

Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics

1 reference

7 January 2021

Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation

1 reference

7 January 2021

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

1 reference

7 January 2021

Transcription-factor mutations and disease

1 reference

7 January 2021

Transcriptional regulation of gene expression: mechanisms and pathophysiology

1 reference

7 January 2021

The mutational spectrum in Waardenburg syndrome.

1 reference

7 January 2021

Molecular basis of splotch and Waardenburg Pax-3 mutations

1 reference

7 January 2021

Pax3 modulates expression of the c-Met receptor during limb muscle development

1 reference

7 January 2021

Identification of a melanocyte-type promoter of the microphthalmia-associated transcription factor gene

1 reference

7 January 2021

Pax-3-DNA interaction: flexibility in the DNA binding and induction of DNA conformational changes by paired domains.

1 reference

7 January 2021

The thyroid transcription factor-1 gene is a candidate target for regulation by Hox proteins

1 reference

7 January 2021

Rapid detection of octamer binding proteins with 'mini-extracts', prepared from a small number of cells

1 reference

7 January 2021

The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3

1 reference

7 January 2021

Overlapping positive and negative regulatory elements determine lens-specific activity of the delta 1-crystallin enhancer

1 reference

7 January 2021

Development of a highly efficient expression cDNA cloning system: application to oncogene isolation

1 reference

7 January 2021

22

8

178

DH Jones

1990

1 reference

12 December 2024

Identifiers

DOI

10.1038/NG0398-283

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9500554

Dimensions Publication ID

12 December 2024

1020222435

0 references

1 reference

National Center for Biotechnology Information