Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9 (Q28242005)

1

0 references

A Weith

2

0 references

P Urbánek

3

0 references

Z Kozmik

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

4

0 references

publication date

April 1993

0 references

language of work or name

0 references

0 references

3

0 references

issue

4

0 references

page(s)

292-8

0 references

cites work

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

The human PAX6 gene is mutated in two patients with aniridia

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila.

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

Pax-8, a paired domain-containing protein, binds to a sequence overlapping the recognition site of a homeodomain and activates transcription from two thyroid-specific promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

The promoter of the CD19 gene is a target for the B-cell-specific transcription factor BSAP

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

The murine paired box gene, Pax7, is expressed specifically during the development of the nervous and muscular system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

The paired box encodes a second DNA-binding domain in the paired homeo domain protein.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

The molecular basis of the undulated/Pax-1 mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

A novel B-cell lineage-specific transcription factor present at early but not late stages of differentiation

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

A mouse model of the aniridia-Wilms tumor deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Chromosome 1 deletions in human neuroblastomas: generation and fine mapping of microclones from the distal 1p region

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH)

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Comparative map for mice and humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Neuroblastoma consensus deletion maps to 1p36.1-2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma?

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Alagille syndrome and deletion of 20p.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-292

7 January 2021