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

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A Weith

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P Urbánek

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Z Kozmik

https://scigraph.springernature.com/pub.10.1038/ng0493-292

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language of work or name

English

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publication date

April 1993

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published in

Nature Genetics

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volume

3

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issue

4

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page(s)

292-8

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exact match

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cites work

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

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

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

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

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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

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

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

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

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

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

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The molecular basis of the undulated/Pax-1 mutation

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

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

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

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A mouse model of the aniridia-Wilms tumor deletion syndrome

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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

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

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

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

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

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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)

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Comparative map for mice and humans

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

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

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

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

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Alagille syndrome and deletion of 20p.

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

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