| 1 | FMF, MEFV, MID1, MID2, PML, TRIM10, TRIM11, TRIM13, TRIM15, TRIM17, TRIM2, TRIM21, TRIM22, TRIM23, TRIM24, TRIM25, TRIM26, TRIM27, TRIM28, TRIM3, TRIM31, TRIM32, TRIM33, TRIM34, TRIM35, TRIM36, TRIM37, TRIM38, TRIM39, TRIM4, TRIM40, TRIM41, TRIM42, TRIM43, TRIM45, TRIM46, TRIM47, TRIM48, TRIM49, TRIM5, TRIM50, TRIM52, TRIM53, TRIM54, TRIM55, TRIM56, TRIM58, TRIM59, TRIM6, TRIM60, TRIM61, TRIM62, TRIM63, TRIM64, TRIM65, TRIM67, TRIM68, TRIM69, TRIM7, TRIM71, TRIM72, TRIM73, TRIM74, TRIM75, TRIM8, TRIM9, TRIML1
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| TRIM family proteins and their emerging roles in innate immunity.
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| Ozato K, Shin DM, Chang TH, Morse HC 3rd.
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| Nat Rev Immunol 8(11):849-60. Review. 2008
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| 2 | MUL, TRIM37
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| Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.
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| Hamalainen RH, Mowat D, Gabbett MT, O'brien TA, Kallijarvi J, Lehesjoki AE.
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| Clin Genet 70(6):473-9. 2006
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| 3 | TRIM37, MUL
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| Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing.
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| HŠmŠlŠinen RH, Joensuu T, KallijŠrvi J, Lehesjoki AE.
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| Gene 366(1):180-8. Epub 2005 Nov 28. 2006
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| 4 | TRIM37, MUL
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| TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase.
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| Kallijarvi J, Lahtinen U, Hamalainen R, Lipsanen-Nyman M, Palvimo JJ, Lehesjoki AE.
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| Exp Cell Res 308(1):146-55. 2005
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| 5 | MUL, TRIM37
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| Novel mutations in the TRIM37 gene in Mulibrey Nanism.
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| Hamalainen RH, Avela K, Lambert JA, Kallijarvi J, Eyaid W, Gronau J, Ignaszewski AP, McFadden D, Sorge G, Lipsanen-Nyman M, Lehesjoki AE.
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| Hum Mutat 23(5):522. 2004
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| 6 | MUL, TRIM37
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| The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder.
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| Kallijarvi J, Avela K, Lipsanen-Nyman M, Ulmanen I, Lehesjoki AE.
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| Am J Hum Genet 70(5):1215-28. 2002
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| 7 | APPBP2, TRIM37, RPS6KB1, MED13
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| Comprehensive copy number and gene expression profiling of the 17q23 amplicon in human breast cancer.
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| Monni O, Barlund M, Mousses S, Kononen J, Sauter G, Heiskanen M, Paavola P, Avela K, Chen Y, Bittner ML, Kallioniemi A.
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| Proc Natl Acad Sci U S A 98(10):5711-6. 2001
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| 8 | ATM, TRIM10, TRIM11, TRIM14, TRIM15, TRIM16, TRIM17, TRIM2, TRIM22, TRIM26, TRIM28, TRIM29, TRIM3, TRIM31, TRIM32, TRIM33, TRIM34, TRIM35, TRIM36, TRIM37, TRIM38, TRIM4, TRIM42, TRIM5, TRIM6, TRIM7, TRIM8, TRIM9, TRIMP1
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| The tripartite motif family identifies cell compartments.
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| Reymond A, Meroni G, Fantozzi A, Merla G, Cairo S, Luzi L, Riganelli D, Zanaria E, Messali S, Cainarca S, Guffanti A, Minucci S, Pelicci PG, Ballabio A.
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| EMBO J 20(9):2140-51. 2001
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| 9 | TRIM37
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| Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.
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| Avela K, Lipsanen-Nyman M, Idanheimo N, Seemanova E, Rosengren S, Makela TP, Perheentupa J, Chapelle Ad, Lehesjoki AE.
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| Nat Genet 25(3):298-301. 2000
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| 10 | MKS1, TRIM37, RAD51C
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| High-resolution physical and genetic mapping of the critical region for meckel syndrome and mulibrey nanism on chromosome 17q22-q23.
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| Paavola P, et al.
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| Genome Res 9(3):267-76. 1999
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| 11 | TRIM37
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| Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.
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| Avela K, Lipsanen-Nyman M, Perheentupa J, Wallgren-Pettersson C, Marchand S, Faure S, Sistonen P, de la Chapelle A, Lehesjoki AE.
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| Am J Hum Genet 60 : 896-902. 1997
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