Mesoderm-specific Stat3 deletion affects expression of Sox9 yielding Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deletion affects expression of Sox9 yielding Sox9-dependent phenotypes.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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Mesoderm-specific Stat3 deleti ...... ing Sox9-dependent phenotypes.

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P1476

Mesoderm-specific Stat3 deleti ...... ding Sox9-dependent phenotypes

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P2093

Alan O Perantoni

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Caroline A Murray

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Michael D Hall

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P2860

A clinical and genetic study of campomelic dysplasia.

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.

Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal

Targeted disruption of the mouse Stat3 gene leads to early embryonic lethality

Generalized lacZ expression with the ROSA26 Cre reporter strain

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

Targeted disruption of gp130, a common signal transducer for the interleukin 6 family of cytokines, leads to myocardial and hematological disorders

Essential role of Stat6 in IL-4 signalling

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e1006610

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scholarly article

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10.1371/JOURNAL.PGEN.1006610

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P433

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P478

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Michael J Valdez

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2017-02-06T00:00:00Z

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28166224

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P932

5319801

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