Found: 12
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Phenotypic complementation of genetic immunodeficiency by chronic herpesvirus infection.
- Published in:
- eLife, 2015, p. 1, doi. 10.7554/eLife.04494
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- Article
Phenotypic complementation of genetic immunodeiciency by chronic herpesvirus infection.
- Published in:
- eLife, 2015, p. 1, doi. 10.7554/eLife.04494.001
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- Publication type:
- Article
A network of transcriptional and signaling events is activated by FGF to induce chondrocyte growth arrest and differentiation.
- Published in:
- Journal of Cell Biology, 2003, v. 161, n. 6, p. 1053, doi. 10.1083/jcb.200302075
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- Article
FGF signaling targets the pRb-related p107 and p130 proteins to induce chondrocyte growth arrest.
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- Journal of Cell Biology, 2002, v. 158, n. 4, p. 741, doi. 10.1083/jcb.200205025
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- Article
Role of Optineurin in the Mitochondrial Dysfunction: Potential Implications in Neurodegenerative Diseases and Cancer.
- Published in:
- Frontiers in Immunology, 2018, p. N.PAG, doi. 10.3389/fimmu.2018.01243
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- Article
PP2A-Mediated Dephosphorylation of p107 Plays a Critical Role in Chondrocyte Cell Cycle Arrest by FGF.
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- PLoS ONE, 2008, v. 3, n. 10, p. 1, doi. 10.1371/journal.pone.0003447
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- Article
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency.
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- Nature Immunology, 2012, v. 13, n. 12, p. 1178, doi. 10.1038/ni.2457
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- Article
NF-κB: At the Borders of Autoimmunity and Inflammation.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.716469
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- Article
Super-resolution microscopy reveals a preformed NEMO lattice structure that is collapsed in incontinentia pigmenti.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12629, doi. 10.1038/ncomms12629
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- Article
Correction: Optineurin Regulates the Interferon Response in a Cell Cycle-Dependent Manner.
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- 2015
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- Correction Notice
Optineurin Regulates the Interferon Response in a Cell Cycle-Dependent Manner.
- Published in:
- PLoS Pathogens, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.ppat.1004877
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- Article
Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 7, p. 1281, doi. 10.1093/hmg/ddw009
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- Article