The vertebrate spalt genes in development and disease (Q28302623)

A novel spalt gene expressed in branchial arches affects the ability of cranial neural crest cells to populate sensory ganglia

Europe PubMed Central

title

The vertebrate spalt genes in development and disease (English)

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author name string

Dylan Sweetman

series ordinal

1

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Andrea Münsterberg

series ordinal

2

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language of work or name

English

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publication date

15 May 2006

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published in

Developmental Biology

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volume

293

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issue

2

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page(s)

285-93

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cites work

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Identification of regulatory regions driving the expression of the Drosophila spalt complex at different developmental stages.

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

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Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum

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SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype

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Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome

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Embryonic expression of the murine homologue of SALL1, the gene mutated in Townes--Brocks syndrome

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Expression of three spalt (sal) gene homologues in zebrafish embryos

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Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin

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Role of cardiac neural crest cells in cardiovascular development

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Function of the spalt/spalt-related gene complex in positioning the veins in the Drosophila wing.

7 January 2021

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The role of the T-box gene optomotor-blind in patterning the Drosophila wing.

7 January 2021

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Regulation of R7 and R8 differentiation by the spalt genes

7 January 2021

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Spalt transcription factors are required for R3/R4 specification and establishment of planar cell polarity in the Drosophila eye.

7 January 2021

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Drosophila spalt/spalt-related mutants exhibit Townes-Brocks' syndrome phenotypes

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csal1 is controlled by a combination of FGF and Wnt signals in developing limb buds.

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A novel role for cardiac neural crest in heart development

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Cloning and expression of CSAL2, a new member of the spalt gene family in chick.

7 January 2021

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sall4 acts downstream of tbx5 and is required for pectoral fin outgrowth

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Xenopus Xsal-1, a vertebrate homolog of the region specific homeotic gene spalt of Drosophila

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Gene and cluster-specific expression of the Iroquois family members during mouse development

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Head and tail development of the Drosophila embryo involves spalt, a novel homeotic gene.

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SALL1 mutations in Townes-Brocks syndrome and related disorders

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Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt

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Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome

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SALL3, a new member of the human spalt-like gene family, maps to 18q23.

7 January 2021

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Genomic cloning, chromosomal mapping, and expression analysis of msal-2.

7 January 2021

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

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Okihiro syndrome is caused by SALL4 mutations

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High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial case

7 January 2021

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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

7 January 2021

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

7 January 2021

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Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart

7 January 2021

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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

7 January 2021

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A tumor host range selection procedure identifies p150(sal2) as a target of polyoma virus large T antigen

7 January 2021

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p150(Sal2) is a p53-independent regulator of p21(WAF1/CIP)

7 January 2021

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Cloning and characterization of two promoters for the human HSAL2 gene and their transcriptional repression by the Wilms tumor suppressor gene product

7 January 2021

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7 January 2021

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Murine Sall1 represses transcription by recruiting a histone deacetylase complex

7 January 2021

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Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects

7 January 2021

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Expression of Xenopus XlSALL4 during limb development and regeneration.

7 January 2021

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Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1

7 January 2021

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SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Xenopus XsalF: anterior neuroectodermal specification by attenuating cellular responsiveness to Wnt signaling

7 January 2021

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Molecular cloning of a novel Xenopus spalt gene (Xsal-3).

7 January 2021

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The mouse homolog of the region specific homeotic gene spalt of Drosophila is expressed in the developing nervous system and in mesoderm-derived structures

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

A new member of the spalt like zinc finger protein family, Msal-3, is expressed in the CNS and sites of epithelial/mesenchymal interaction

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Zinc finger protein sall2 is not essential for embryonic and kidney development

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Sall1, a causative gene for Townes-Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

How to tell a cell where it is.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

The conserved glutamine-rich region of chick csal1 and csal3 mediates protein interactions with other spalt family members. Implications for Townes-Brocks syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Expression of csal1 in pre limb-bud chick embryos.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009

Expression pattern of Irx1 and Irx2 during mouse digit development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.009