(Q24338309)

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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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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) (English)

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GOA release 2020-03-11

transcription by RNA polymerase II

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GOA release 2020-03-11

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ORCID Public Data File 2021

author name string

S Schnittger

1

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V V Rao

2

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U Deutsch

3

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P Gruss

4

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R Balling

5

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I Hansmann

6

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language of work or name

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publication date

November 1992

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14

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740-4

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3

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describes a project that uses

in situ hybridization

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Alagille syndrome and deletion of 20p.

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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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The molecular basis of the undulated/Pax-1 mutation

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A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes

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Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development

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The human protein-tyrosine phosphatase PTPα/LRP gene (PTPA) is assigned to chromosome 20p13

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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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10.1016/S0888-7543(05)80177-6

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release_zxrsdxkdgffh5f4tvkp5hwudiy

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