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Article

Expression of Trps1 during mouse embryonic development.

Mechanisms of development - 1 Dec 2002

Kunath Melanie, Lüdecke Hermann-Josef, Vortkamp Andrea

Abstract excerpt

The Trps1 gene codes for an atypical member of the GATA type family of transcription factors. Mutations in human TRPS1 lead to the tricho-rhino-phalangeal syndrome types I and III, which are characterized by craniofacial and skeletal abnormalities and disturbed hair development. Correspondingly, during mouse embryonic development strong Trps1 expression is found in the cartilage condensations, the developing...

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Source

Identifiers

PMID: 14516672
DOI: 10.1016/s0925-4773(03)00103-5

Genes

TRPS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Expression of Trps1 during mouse embryonic development.PMID 14516672Read ↗

Deletion of the GATA domain of TRPS1 causes an absence of facial hair and provides new insights into the bone disorder in inherited tricho-rhino-phalangeal syndromes.Semantic proximity Read ↗

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Atypical GATA protein TRPS1 plays indispensable roles in mouse two-cell embryoSemantic proximity Read ↗

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Deletion of Trps1 regulatory elements recapitulates postnatal hip joint abnormalities and growth retardation of Trichorhinophalangeal syndrome in mice.Semantic proximity Read ↗

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