| 1 | DDX58, RNF135, TRIM25
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| A distinct role of Riplet-mediated K63-Linked polyubiquitination of the RIG-I repressor domain in human antiviral innate immune responses.
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| Oshiumi H, Miyashita M, Matsumoto M, Seya T.
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| PLoS Pathog 9(8):e1003533. doi: 10.1371/journal.ppat.1003533. Epub 2013 Aug 8.
2013
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| 2 | ADAP2, RNF135
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| Identification of genes potentially involved in the increased risk of malignancy in NF1-microdeleted patients.
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| Pasmant E, Masliah-Planchon J, Lévy P, Laurendeau I, Ortonne N, Parfait B, Valeyrie-Allanore L, Leroy K, Wolkenstein P, Vidaud M, Vidaud D, Bièche I.
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| Mol Med 17(1-2):79-87. doi: 10.2119/molmed.2010.00079. Epub 2010 Sep 10.
2011
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| 3 | DDX58, RNF135
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| The ubiquitin ligase Riplet is essential for RIG-I-dependent innate immune responses to RNA virus infection.
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| Oshiumi H, Miyashita M, Inoue N, Okabe M, Matsumoto M, Seya T.
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| Cell Host Microbe 8(6):496-509. doi: 10.1016/j.chom.2010.11.008.
2010
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| 4 | DDX58, RNF135
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| Riplet/RNF135, a RING finger protein, ubiquitinates RIG-I to promote interferon-beta induction during the early phase of viral infection.
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| Oshiumi H, Matsumoto M, Hatakeyama S, Seya T.
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| J Biol Chem 284(2):807-17. doi: 10.1074/jbc.M804259200. Epub 2008 Nov 18.
2009
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| 5 | RNF135
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| REUL is a novel E3 ubiquitin ligase and stimulator of retinoic-acid-inducible gene-I.
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| Gao D, Yang YK, Wang RP, Zhou X, Diao FC, Li MD, Zhai ZH, Jiang ZF, Chen DY.
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| PLoS One 4(6):e5760. doi: 10.1371/journal.pone.0005760.
2009
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| 6 | ADAP2, ATAD5, C17orf79, CRLF3, EVI2A, EVI2B, NF1, NF1DEL, OMG, RNF135, SUZ12, TEFM, UTP6
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| Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.
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| Douglas J, Cilliers D, Coleman K, Tatton-Brown K, Barker K, Bernhard B, Burn J, Huson S, Josifova D, Lacombe D, Malik M, Mansour S, Reid E, Cormier-Daire V, Cole T; Childhood Overgrowth Collaboration, Rahman N.
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| Nat Genet 39(8):963-5. Epub 2007 Jul 15. 2007
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| 7 | ATAD5, LRRC37B, NF1, NF1DEL, RNF135
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| Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.
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| Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H,Kehrer-Sawatzki H.
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| Am J Hum Genet 69(3):516-27. Epub 2001 Jul 20. 2001
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