(Q52109672)

22 April 2018

title

The OAR/aristaless domain of the homeodomain protein Cart1 has an attenuating role in vivo. (English)

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22 April 2018

author name string

Antje Brouwer

1

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22 April 2018

Derk ten Berge

2

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22 April 2018

Rob Wiegerinck

3

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22 April 2018

Frits Meijlink

4

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22 April 2018

publication date

1 February 2003

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22 April 2018

Mechanisms of Development

published in

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22 April 2018

volume

120

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22 April 2018

issue

2

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22 April 2018

page(s)

241-252

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22 April 2018

Multifunctional role of the Pitx2 homeodomain protein C-terminal tail

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Expression patterns of group-I aristaless-related genes during craniofacial and limb development.

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Genetics and manifold effects of Strong's luxoid gene in the mouse, including its interactions with Green's luxoid and Carter's luxate genes

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Evolution of homeobox genes: Q50 Paired-like genes founded the Paired class

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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

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Identification of domains mediating transcription activation, repression, and inhibition in the paired-related homeobox protein, Prx2 (S8).

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

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Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

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Mouse Alx3: an aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm

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7 January 2021

Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling

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High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA

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Conservation and diversification in homeodomain-DNA interactions: a comparative genetic analysis

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Cartilage homeoprotein 1, a homeoprotein selectively expressed in chondrocytes

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7 January 2021

Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene

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7 January 2021

10.1016/S0925-4773(02)00416-1

Identifiers

DOI

1 reference

22 April 2018

1 reference

22 April 2018