Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice (Q28510846)

1

1 reference

25 January 2017

Heidi A. Heilstedt

2

1 reference

25 January 2017

Lisa G. Shaffer

3

1 reference

25 January 2017

Stuart Schwartz

4

1 reference

25 January 2017

Jeffrey C. Murray

6

1 reference

25 January 2017

Ed Stavnezer

Autonomous neural axis formation by ectopic expression of the protooncogene c-ski.

7

1 reference

25 January 2017

language of work or name

English

0 references

publication date

1 January 2002

1 reference

25 January 2017

1 reference

25 January 2017

30

1 reference

25 January 2017

1

1 reference

25 January 2017

106–109

1 reference

25 January 2017

1 reference

7 January 2021

ski can cause selective growth of skeletal muscle in transgenic mice

1 reference

7 January 2021

The ski oncogene induces muscle differentiation in quail embryo cells.

1 reference

7 January 2021

Ectopic expression of c-ski disrupts gastrulation and neural patterning in zebrafish

1 reference

7 January 2021

Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development

1 reference

7 January 2021

Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes

1 reference

7 January 2021

Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome

1 reference

7 January 2021

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome

1 reference

7 January 2021

Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300

1 reference

7 January 2021

Noggin-mediated antagonism of BMP signaling is required for growth and patterning of the neural tube and somite

1 reference

7 January 2021

Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2

1 reference

7 January 2021

Transcription factor AP-2 essential for cranial closure and craniofacial development

1 reference

7 January 2021

Transformation of hematopoietic cells by the Ski oncoprotein involves repression of retinoic acid receptor signaling

1 reference

7 January 2021

Regulation of transcription factor AP-2 by the morphogen retinoic acid and by second messengers.

1 reference

7 January 2021

Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice.

1 reference

7 January 2021

Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells

1 reference

7 January 2021

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

1 reference

7 January 2021

Molecular cloning and expression of the type 1 and type 2 murine receptors for tumor necrosis factor

1 reference

7 January 2021

The cellular homologue of the transforming gene of SKV avian retrovirus maps to human chromosome region 1q22----q24

1 reference

7 January 2021

The v-ski oncogene encodes a truncated set of c-ski coding exons with limited sequence and structural relatedness to v-myc

1 reference

7 January 2021

C-ski cDNAs are encoded by eight exons, six of which are closely linked within the chicken genome

1 reference

7 January 2021

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders

1 reference

7 January 2021

Peroxisome biogenesis disorders: genetics and cell biology

1 reference

7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

7 January 2021

release_jezplxm3gjczvk5s35cj6cdjye

Identifiers

DOI

10.1038/NG770

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jezplxm3gjczvk5s35cj6cdjye

24 November 2022