The genomic organization and the full coding region of the human PAX7 gene (Q24319384)

anatomical structure morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1

E Vorobyov

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author name string

I Mertsalov

2

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B Dockhorn-Dworniczak

3

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B Dworniczak

4

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J Horst

Agreement among and within groups of pathologists in the classification of rhabdomyosarcoma and related childhood sarcomas. Report of an international study of four pathology classifications

5

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language of work or name

English

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publication date

1 October 1997

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published in

Genomics

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volume

45

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page(s)

168-74

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issue

1

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cites work

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Two distinct deleted regions on the short arm of chromosome I in neuroblastoma

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The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2

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Analysis of the Pax-3 gene in the mouse mutant splotch

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The splotch-delayed (Spd) mouse mutant carries a point mutation within the paired box of the Pax-3 gene

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The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36

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Cloning and characterization of CpG islands of the human chromosome 1p36 region

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

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

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

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Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma

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

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Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma

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DNA sequencing with chain-terminating inhibitors

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A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

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The mutational spectrum in Waardenburg syndrome.

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Structural characterization of the FKHR gene and its rearrangement in alveolar rhabdomyosarcoma

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Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

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PAX genes: what's new in developmental biology and cancer?

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Molecular cloning and characterization of a human PAX-7 cDNA expressed in normal and neoplastic myocytes

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