Found: 14
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A thesaurus of genetic variation for interrogation of repetitive genomic regions.
- Published in:
- Nucleic Acids Research, 2015, v. 43, n. 10, p. 1, doi. 10.1093/nar/gkv178
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- 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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- Article
A reversible gene trap collection empowers haploid genetics in human cells.
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- Nature Methods, 2013, v. 10, n. 10, p. 965, doi. 10.1038/nmeth.2609
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- Article
A novel plant gene essential for meiosis is related to the human CtIP and the yeast COM1/SAE2 gene.
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- EMBO Journal, 2007, v. 26, n. 24, p. 5061, doi. 10.1038/sj.emboj.7601913
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- Article
TOPS: a versatile software tool for statistical analysis and visualization of combinatorial genegene and gene-drug interaction screens.
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- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-98
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- Article
Arabidopsis thaliana FANCD2 Promotes Meiotic Crossover Formation.
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- Plant Cell, 2018, v. 30, n. 2, p. 415, doi. 10.1105/tpc.17.00745
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- Article
Targeting a cell state common to triple-negative breast cancers.
- Published in:
- Molecular Systems Biology, 2015, v. 11, n. 2, p. n/a, doi. 10.15252/msb.20145664
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- Article
Expression of the ubiquitin variant ubR48 decreases proteolytic activity in Arabidopsis and induces cell death.
- Published in:
- Planta: An International Journal of Plant Biology, 2006, v. 223, n. 4, p. 684, doi. 10.1007/s00425-005-0121-z
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- Article
MEK inhibitors block growth of lung tumours with mutations in ataxia-telangiectasia mutated.
- Published in:
- Nature Communications, 2016, v. 7, n. 12, p. 13701, doi. 10.1038/ncomms13701
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- Article
UVB and Caffeine: Inhibiting the DNA Damage Response to Protect Against the Adverse Effects of UVB.
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- Journal of Investigative Dermatology, 2009, v. 129, n. 7, p. 1611, doi. 10.1038/jid.2009.99
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- Article
Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf–Hirschhorn syndrome.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 10, p. 2181, doi. 10.1093/hmg/dds033
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- Article
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 7, p. 1324, doi. 10.1093/hmg/ddq008
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- Article
A chemical-genetic screen reveals a mechanism of resistance to PI3K inhibitors in cancer.
- Published in:
- Nature Chemical Biology, 2011, v. 7, n. 11, p. 787, doi. 10.1038/nchembio.695
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- Article
Gain- and Loss-of-Function Mutations in the Breast Cancer Gene GATA3 Result in Differential Drug Sensitivity.
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- PLoS Genetics, 2016, v. 12, n. 9, p. 1, doi. 10.1371/journal.pgen.1006279
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- Article