FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

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FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

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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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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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FGFR2 mutations in bent bone d ...... rturb cell fate determination.

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FGFR2 mutations in bent bone d ...... rturb cell fate determination.

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FGFR2 mutations in bent bone d ...... rturb cell fate determination.

@en

FGFR2 mutations in bent bone d ...... rturb cell fate determination.

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FGFR2 mutations in bent bone d ...... rturb cell fate determination.

@en

FGFR2 mutations in bent bone d ...... rturb cell fate determination.

@nl

P1476

FGFR2 mutations in bent bone d ...... erturb cell fate determination

@en

P2093

Fides D Lay

http://www.w3.org/2001/XMLSchema#string

Xiaojing Mao

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P2860

The balance between rRNA and ribosomal protein synthesis up- and downregulates the tumour suppressor p53 in mammalian cells

PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylation

The chromatin remodelling complex WSTF-SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription

The Williams syndrome transcription factor interacts with PCNA to target chromatin remodelling by ISWI to replication foci

The chromatin remodeling complex NoRC targets HDAC1 to the ribosomal gene promoter and represses RNA polymerase I transcription.

Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition

Ribosomal protein L11 negatively regulates oncoprotein MDM2 and mediates a p53-dependent ribosomal-stress checkpoint pathway

Ribosomal genes in focus: new transcripts label the dense fibrillar components and form clusters indicative of "Christmas trees" in situ

Ribosomopathies: how a common root can cause a tree of pathologies

Fibroblast growth factor signaling in skeletal development and disease

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3253-3270

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scholarly article

P356

10.1093/HMG/DDX209

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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Amy E Merrill

C T Tuzon

Cynthia L Neben

P577

2017-09-01T00:00:00Z

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P698

28595297

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P932

5886181

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