(Q36728990)

15 August 2017

A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells (English)

1 reference

15 August 2017

1 reference

T Matsuo

1

1 reference

15 August 2017

N Osumi-Yamashita

2

1 reference

15 August 2017

S Noji

3

1 reference

15 August 2017

H Ohuchi

4

1 reference

15 August 2017

E Koyama

5

1 reference

15 August 2017

F Myokai

6

1 reference

15 August 2017

N Matsuo

7

1 reference

15 August 2017

S Taniguchi

8

1 reference

15 August 2017

H Doi

9

1 reference

15 August 2017

S Iseki

10

1 reference

15 August 2017

language of work or name

English

0 references

publication date

1 April 1993

1 reference

15 August 2017

1 reference

15 August 2017

3

1 reference

15 August 2017

299-304

1 reference

15 August 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1038/ng0493-299

15 August 2017

0 references

cites work

Pax: a murine multigene family of paired box-containing genes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0493-299

1 reference

7 January 2021

Mouse small eye results from mutations in a paired-like homeobox-containing gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

The human PAX6 gene is mutated in two patients with aniridia

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

A mouse model of the aniridia-Wilms tumor deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Migration of cranial neural crest cells to the pharyngeal arches and heart in rat embryos

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Abnormal splice in a mutant human beta-globin gene not at the site of a mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Molecular mechanism of growth hormone (GH) deficiency in the spontaneous dwarf rat: detection of abnormal splicing of GH messenger ribonucleic acid by the polymerase chain reaction.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Spatial and temporal expression pattern of retinoic acid receptor genes during mouse bone development

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-299

7 January 2021

Identifiers

DOI

10.1038/NG0493-299

1 reference

15 August 2017

1 reference