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2. 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; 308(1):146-55. PubMed ID: 15885686 [TBL] [Abstract][Full Text] [Related]
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4. Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism. Hämäläinen RH; Mowat D; Gabbett MT; O'brien TA; Kallijärvi J; Lehesjoki AE Clin Genet; 2006 Dec; 70(6):473-9. PubMed ID: 17100991 [TBL] [Abstract][Full Text] [Related]
5. 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; 20(1):. PubMed ID: 30586926 [TBL] [Abstract][Full Text] [Related]
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7. 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; 16(3):173-176. PubMed ID: 17551331 [TBL] [Abstract][Full Text] [Related]
8. A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity. Jagiello P; Hammans C; Wieczorek S; Arning L; Stefanski A; Strehl H; Epplen JT; Gencik M Hum Mutat; 2003 Jun; 21(6):630-5. PubMed ID: 12754710 [TBL] [Abstract][Full Text] [Related]
9. New intragenic rearrangements in non-Finnish mulibrey nanism. Jobic F; Morin G; Vincent-Delorme C; Cadet E; Cabry R; Mathieu-Dramard M; Copin H; Rochette J; Jedraszak G Am J Med Genet A; 2017 Oct; 173(10):2782-2788. PubMed ID: 28815877 [TBL] [Abstract][Full Text] [Related]
10. 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; 366(1):180-8. PubMed ID: 16310976 [TBL] [Abstract][Full Text] [Related]
11. 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; 5(5):584-95. PubMed ID: 27044324 [TBL] [Abstract][Full Text] [Related]
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14. Refractory congestive heart failure following delayed pericardectomy in a 12-year-old child with Mulibrey nanism due to a novel mutation in TRIM37. Kumpf M; Hämäläinen RH; Hofbeck M; Baden W Eur J Pediatr; 2013 Oct; 172(10):1415-8. PubMed ID: 23385855 [TBL] [Abstract][Full Text] [Related]
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17. Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing. Mozzillo E; Cozzolino C; Genesio R; Melis D; Frisso G; Orrico A; Lombardo B; Fattorusso V; Discepolo V; Della Casa R; Simonelli F; Nitsch L; Salvatore F; Franzese A Am J Med Genet A; 2016 Aug; 170(8):2196-9. PubMed ID: 27256967 [TBL] [Abstract][Full Text] [Related]
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