(Q39941619)

15 September 2017

title

Sall4 isoforms act during proximal-distal and anterior-posterior axis formation in the mouse embryo (English)

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15 September 2017

author

Martin Hrabě de Angelis

series ordinal

4

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W. Wurst

series ordinal

6

object named as

Wolfgang Wurst

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15 September 2017

7

Thomas Floss

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15 September 2017

5

Ralf Kühn

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15 September 2017

1

Nikolas Uez

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15 September 2017

Heiko Lickert

2

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15 September 2017

Jürgen Kohlhase

series ordinal

3

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15 September 2017

publication date

1 September 2008

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15 September 2017

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15 September 2017

volume

46

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15 September 2017

issue

9

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15 September 2017

page(s)

463-477

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IVIC syndrome is caused by a c.2607delA mutation in the SALL4 locus

15 September 2017

cites work

1 reference

Mixed-Effects Models in Sand S-PLUS

21 January 2018

1 reference

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family

21 January 2018

1 reference

7 January 2021

A gene network establishing polarity in the early mouse embryo

1 reference

7 January 2021

HNF-3 beta is essential for node and notochord formation in mouse development

1 reference

7 January 2021

Multipotent cell lineages in early mouse development depend on SOX2 function

1 reference

7 January 2021

Extraembryonic proteases regulate Nodal signalling during gastrulation

1 reference

7 January 2021

The nodal precursor acting via activin receptors induces mesoderm by maintaining a source of its convertases and BMP4.

1 reference

7 January 2021

SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism

1 reference

7 January 2021

Nodal signalling in the epiblast patterns the early mouse embryo

1 reference

7 January 2021

BMP signalling inhibits premature neural differentiation in the mouse embryo

1 reference

7 January 2021

Murine inner cell mass-derived lineages depend on Sall4 function

1 reference

7 January 2021

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

1 reference

7 January 2021

FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse

1 reference

7 January 2021

Canonical Wnt signaling and its antagonist regulate anterior-posterior axis polarization by guiding cell migration in mouse visceral endoderm

1 reference

7 January 2021

SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders

1 reference

7 January 2021

Cloning and expression analysis of SALL4, the murine homologue of the gene mutated in Okihiro syndrome

1 reference

7 January 2021

Okihiro syndrome is caused by SALL4 mutations

1 reference

7 January 2021

Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy

1 reference

7 January 2021

spalt encodes an evolutionarily conserved zinc finger protein of novel structure which provides homeotic gene function in the head and tail region of the Drosophila embryo

1 reference

7 January 2021

Functional analysis of cis-regulatory elements controlling initiation and maintenance of early Cdx1 gene expression in the mouse

1 reference

7 January 2021

Formation of multiple hearts in mice following deletion of beta-catenin in the embryonic endoderm

1 reference

7 January 2021

From fertilization to gastrulation: axis formation in the mouse embryo.

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7 January 2021

SALL4, a novel oncogene, is constitutively expressed in human acute myeloid leukemia (AML) and induces AML in transgenic mice

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7 January 2021

The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells

1 reference

7 January 2021

Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4

1 reference

7 January 2021

Asymmetric and node-specific nodal expression patterns are controlled by two distinct cis-acting regulatory elements

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7 January 2021

Primitive streak formation in mice is preceded by localized activation of Brachyury and Wnt3

1 reference

7 January 2021

Control of early anterior-posterior patterning in the mouse embryo by TGF-β signalling

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7 January 2021

Emerging asymmetry and embryonic patterning in early mouse development

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7 January 2021

Eomesodermin is required for mouse trophoblast development and mesoderm formation

1 reference

7 January 2021

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development

1 reference

7 January 2021

The vertebrate spalt genes in development and disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells

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7 January 2021

Sall4 interacts with Nanog and co-occupies Nanog genomic sites in embryonic stem cells

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7 January 2021

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

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7 January 2021

The transcription factor FoxH1 (FAST) mediates Nodal signaling during anterior-posterior patterning and node formation in the mouse

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7 January 2021

Nodal antagonists regulate formation of the anteroposterior axis of the mouse embryo

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7 January 2021

Sall4 modulates embryonic stem cell pluripotency and early embryonic development by the transcriptional regulation of Pou5f1

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7 January 2021

Identifiers

DOI

10.1002/DVG.20421

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15 September 2017

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