Genetic control of caudal development (Q34122680)

31 July 2017

1 reference

title

Genetic control of caudal development (English)

1 reference

31 July 2017

Catala M

1

1 reference

31 July 2017

publication date

1 February 2002

1 reference

31 July 2017

1 reference

31 July 2017

volume

61

1 reference

31 July 2017

issue

2

1 reference

31 July 2017

page(s)

89-96

1 reference

Tbx6, a mouse T-Box gene implicated in paraxial mesoderm formation at gastrulation

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Roles of Wnt proteins in neural development and maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Wnt-3a regulates somite and tailbud formation in the mouse embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Wnt3a-/--like phenotype and limb deficiency in Lef1(-/-)Tcf1(-/-) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Rescue of a Wnt mutation by an activated form of LEF-1: regulation of maintenance but not initiation of Brachyury expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

The developmental potentials of the caudalmost part of the neural crest are restricted to melanocytes and glia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Congenital lumbosacral lipomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

Organization and development of the tail bud analyzed with the quail-chick chimaera system

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

Cell fate and morphogenetic movement in the late mouse primitive streak

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

Three neural tubes in mouse embryos with mutations in the T-box gene Tbx6

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

Retinoic acid induces down-regulation of Wnt-3a, apoptosis and diversion of tail bud cells to a neural fate in the mouse embryo

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

Pancreas dorsal lobe agenesis and abnormal islets of Langerhans in Hlxb9-deficient mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610202.X

7 January 2021

10.1034/J.1399-0004.2002.610202.X

Identifiers

DOI

1 reference

31 July 2017

1 reference