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The T-box family

Transcription factors of the T-box family are required both for early cell-fate decisions, such as those necessary for formation of the basic vertebrate body plan, and for differentiation and organogenesis. When mutated, T-box genes give dramatic phenotypes in mouse and zebrafish, and they have been...

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Detalles Bibliográficos
Autores principales: Wilson, Val, Conlon, Frank L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139375/
https://www.ncbi.nlm.nih.gov/pubmed/12093383
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author Wilson, Val
Conlon, Frank L
author_facet Wilson, Val
Conlon, Frank L
author_sort Wilson, Val
collection PubMed
description Transcription factors of the T-box family are required both for early cell-fate decisions, such as those necessary for formation of the basic vertebrate body plan, and for differentiation and organogenesis. When mutated, T-box genes give dramatic phenotypes in mouse and zebrafish, and they have been implicated both in fundamentals of limb patterning and in a number of human congenital malformations such as Holt-Oram, ulnar-mammary and DiGeorge syndromes, as well as being amplified in a subset of cancers. Genes encoding members of the T-box family have recently been shown to comprise approximately 0.1% of genomes as diverse as those of nematodes and humans and have been identified in a wide variety of animals from ctenophores (comb jellies) to mammals; they are, however, completely absent from genomes from other organisms (such as the model plant Arabidopsis thaliana).
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spelling pubmed-1393752003-03-03 The T-box family Wilson, Val Conlon, Frank L Genome Biol Protein Family Review Transcription factors of the T-box family are required both for early cell-fate decisions, such as those necessary for formation of the basic vertebrate body plan, and for differentiation and organogenesis. When mutated, T-box genes give dramatic phenotypes in mouse and zebrafish, and they have been implicated both in fundamentals of limb patterning and in a number of human congenital malformations such as Holt-Oram, ulnar-mammary and DiGeorge syndromes, as well as being amplified in a subset of cancers. Genes encoding members of the T-box family have recently been shown to comprise approximately 0.1% of genomes as diverse as those of nematodes and humans and have been identified in a wide variety of animals from ctenophores (comb jellies) to mammals; they are, however, completely absent from genomes from other organisms (such as the model plant Arabidopsis thaliana). BioMed Central 2002 2002-05-31 /pmc/articles/PMC139375/ /pubmed/12093383 Text en Copyright © 2002 BioMed Central Ltd
spellingShingle Protein Family Review
Wilson, Val
Conlon, Frank L
The T-box family
title The T-box family
title_full The T-box family
title_fullStr The T-box family
title_full_unstemmed The T-box family
title_short The T-box family
title_sort t-box family
topic Protein Family Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139375/
https://www.ncbi.nlm.nih.gov/pubmed/12093383
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