Found: 10
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Nbs1 is required for ATR-dependent phosphorylation events.
- Published in:
- EMBO Journal, 2005, v. 24, n. 1, p. 199, doi. 10.1038/sj.emboj.7600504
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- Publication type:
- Article
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
- Published in:
- Nature Genetics, 2011, v. 43, n. 4, p. 350, doi. 10.1038/ng.776
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- Publication type:
- Article
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 232, doi. 10.1038/ng.2007.80
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- Publication type:
- Article
CRISPR screens in 3D tumourspheres identified miR-4787-3p as a transcriptional start site miRNA essential for breast tumour-initiating cell growth.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06555-1
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- Publication type:
- Article
Chromosome breakage after G2 checkpoint release.
- Published in:
- Journal of Cell Biology, 2007, v. 176, n. 6, p. 749, doi. 10.1083/jcb.200612047
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- Publication type:
- Article
ATR promotes cilia signalling: links to developmental impacts.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 8, p. 1574, doi. 10.1093/hmg/ddw034
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- Publication type:
- Article
Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage.
- Published in:
- Cell Death & Disease, 2024, v. 15, n. 9, p. 1, doi. 10.1038/s41419-024-07042-5
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- Publication type:
- Article
Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003360
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- Publication type:
- Article
Identification of the First ATRIP--Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR--ATRIP Seckel Syndrome.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1002945
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- Publication type:
- Article
Replication independent ATR signalling leads to G2/M arrest requiring Nbs1, 53BP1 and MDC1.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3247, doi. 10.1093/hmg/ddn220
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- Publication type:
- Article