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Journal Abstract Search

213 related items for PubMed ID: 15885686

  • 1. TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase.
    Kallijärvi J, Lahtinen U, Hämäläinen R, Lipsanen-Nyman M, Palvimo JJ, Lehesjoki AE.
    Exp Cell Res; 2005 Aug 01; 308(1):146-55. PubMed ID: 15885686
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  • 2. Novel mutations in the TRIM37 gene in Mulibrey Nanism.
    Hämäläinen RH, Avela K, Lambert JA, Kallijärvi J, Eyaid W, Gronau J, Ignaszewski AP, McFadden D, Sorge G, Lipsanen-Nyman M, Lehesjoki AE.
    Hum Mutat; 2004 May 01; 23(5):522. PubMed ID: 15108285
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  • 3. TRIMming down to TRIM37: Relevance to Inflammation, Cardiovascular Disorders, and Cancer in MULIBREY Nanism.
    Brigant B, Metzinger-Le Meuth V, Rochette J, Metzinger L.
    Int J Mol Sci; 2018 Dec 24; 20(1):. PubMed ID: 30586926
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  • 7. CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations.
    Bruzzaniti S, Cirillo E, Prencipe R, Giardino G, Lepore MT, Garziano F, Perna F, Procaccini C, Mascolo L, Pagano C, Fattorusso V, Mozzillo E, Bifulco M, Matarese G, Franzese A, Pignata C, Galgani M.
    Front Immunol; 2020 Dec 24; 11():1742. PubMed ID: 33042106
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  • 8. Trim37-deficient mice recapitulate several features of the multi-organ disorder Mulibrey nanism.
    Kettunen KM, Karikoski R, Hämäläinen RH, Toivonen TT, Antonenkov VD, Kulesskaya N, Voikar V, Hölttä-Vuori M, Ikonen E, Sainio K, Jalanko A, Karlberg S, Karlberg N, Lipsanen-Nyman M, Toppari J, Jauhiainen M, Hiltunen JK, Jalanko H, Lehesjoki AE.
    Biol Open; 2016 May 15; 5(5):584-95. PubMed ID: 27044324
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  • 9. A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy.
    Doğancı T, Yüksel Konuk BE, Alpan N, Konuk O, Hämäläinen RH, Lehesjoki AE, Tekin M.
    Clin Dysmorphol; 2007 Jul 15; 16(3):173-176. PubMed ID: 17551331
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  • 10. Tissue expression of the mulibrey nanism-associated Trim37 protein in embryonic and adult mouse tissues.
    Kallijärvi J, Hämäläinen RH, Karlberg N, Sainio K, Lehesjoki AE.
    Histochem Cell Biol; 2006 Sep 15; 126(3):325-34. PubMed ID: 16514549
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  • 11. Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37.
    Karlberg N, Jalanko H, Kallijärvi J, Lehesjoki AE, Lipsanen-Nyman M.
    Diabetes; 2005 Dec 15; 54(12):3577-81. PubMed ID: 16306379
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  • 14. Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing.
    Hämäläinen RH, Joensuu T, Kallijärvi J, Lehesjoki AE.
    Gene; 2006 Jan 17; 366(1):180-8. PubMed ID: 16310976
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  • 16. A proteomic study of the downregulation of TRIM37 on chondrocytes: Implications for the MULIBREY syndrome.
    Brigant B, Metzinger-Le Meuth V, Boyartchuk V, Ouled-Haddou H, Guerrera IC, Rochette J, Metzinger L.
    Bone; 2024 Oct 17; 187():117205. PubMed ID: 39019132
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  • 17. Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis.
    Lehesjoki AE, Reed VA, Mark Gardiner R, Greene ND.
    Mech Dev; 2001 Oct 17; 108(1-2):221-5. PubMed ID: 11578880
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  • 18. TRIM37 employs peptide motif recognition and substrate-dependent oligomerization to prevent ectopic spindle pole assembly.
    Bellaart A, Brambila A, Xu J, Mendez Diaz F, Deep A, Anzola J, Meitinger F, Ohta M, Corbett KD, Desai A, Oegema K.
    bioRxiv; 2024 Oct 09. PubMed ID: 39416052
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  • 19. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.
    Avela K, Lipsanen-Nyman M, Idänheimo N, Seemanová E, Rosengren S, Mäkelä TP, Perheentupa J, Chapelle AD, Lehesjoki AE.
    Nat Genet; 2000 Jul 09; 25(3):298-301. PubMed ID: 10888877
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