TRIM37: Difference between revisions

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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{Infobox_gene}}
{{PBB_Controls
'''Tripartite motif-containing protein 37''' is a [[protein]] that in humans is encoded by the ''TRIM37'' [[gene]].<ref name="pmid9106536">{{cite journal | vauthors = Avela K, Lipsanen-Nyman M, Perheentupa J, Wallgren-Pettersson C, Marchand S, Fauré S, Sistonen P, de la Chapelle A, Lehesjoki AE | title = Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis | journal = American Journal of Human Genetics | volume = 60 | issue = 4 | pages = 896–902 | date = Apr 1997 | pmid = 9106536 | pmc = 1712467 | doi =  }}</ref><ref name="pmid10888877">{{cite journal | vauthors = Avela K, Lipsanen-Nyman M, Idänheimo N, Seemanová E, Rosengren S, Mäkelä TP, Perheentupa J, Chapelle AD, Lehesjoki AE | title = Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism | journal = Nature Genetics | volume = 25 | issue = 3 | pages = 298–301 | date = Jul 2000 | pmid = 10888877 | pmc = | doi = 10.1038/77053 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TRIM37 tripartite motif-containing 37| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4591| accessdate = }}</ref>
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Tripartite motif-containing 37
| HGNCid = 7523
| Symbol = TRIM37
| AltSymbols =; KIAA0898; MUL; POB1; TEF3
| OMIM = 605073
| ECnumber = 
| Homologene = 9084
| MGIid = 2153072
| GeneAtlas_image1 = PBB_GE_TRIM37_213009_s_at_tn.png
| Function = {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0008270 |text = zinc ion binding}} {{GNF_GO|id=GO:0046872 |text = metal ion binding}}
| Component = {{GNF_GO|id=GO:0005622 |text = intracellular}} {{GNF_GO|id=GO:0005777 |text = peroxisome}}
| Process =
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 4591
    | Hs_Ensembl = ENSG00000108395
    | Hs_RefseqProtein = NP_001005207
    | Hs_RefseqmRNA = NM_001005207
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 17
    | Hs_GenLoc_start = 54430351
    | Hs_GenLoc_end = 54539011
    | Hs_Uniprot = O94972
    | Mm_EntrezGene = 68729
    | Mm_Ensembl = ENSMUSG00000018548
    | Mm_RefseqmRNA = NM_197987
    | Mm_RefseqProtein = NP_932104
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 11
    | Mm_GenLoc_start = 86943272
    | Mm_GenLoc_end = 87036877
    | Mm_Uniprot = Q5SX31
  }}
}}
'''Tripartite motif-containing 37''', also known as '''TRIM37''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: TRIM37 tripartite motif-containing 37| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4591| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein–protein and/or protein–nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. Alternatively spliced transcript variants encoding the same protein have been identified.<ref name="entrez" />
{{PBB_Summary
| section_title =
| summary_text = This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. Alternatively spliced transcript variants encoding the same protein have been identified.<ref name="entrez">{{cite web | title = Entrez Gene: TRIM37 tripartite motif-containing 37| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4591| accessdate = }}</ref>
}}


==References==
== Interactions ==
{{reflist|2}}
 
==Further reading==
TRIM37 has been shown to [[Protein–protein interaction|interact]] with [[PRC1]].<ref name=pmid16189514>{{cite journal|authorlink30=Huda Zoghbi | vauthors = Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M | title = Towards a proteome-scale map of the human protein-protein interaction network | journal = Nature | volume = 437 | issue = 7062 | pages = 1173–8 | date = Oct 2005 | pmid = 16189514 | doi = 10.1038/nature04209 }}</ref>
 
== See also ==
*[[Mulibrey nanism]]
 
== References ==
{{reflist}}
 
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O | title = Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro | journal = DNA Research | volume = 5 | issue = 6 | pages = 355–64 | date = Dec 1998 | pmid = 10048485 | doi = 10.1093/dnares/5.6.355 }}
| citations =
* {{cite journal | vauthors = Zapata JM, Pawlowski K, Haas E, Ware CF, Godzik A, Reed JC | title = A diverse family of proteins containing tumor necrosis factor receptor-associated factor domains | journal = The Journal of Biological Chemistry | volume = 276 | issue = 26 | pages = 24242–52 | date = Jun 2001 | pmid = 11279055 | doi = 10.1074/jbc.M100354200 }}
*{{cite journal | author=Avela K, Lipsanen-Nyman M, Perheentupa J, ''et al.'' |title=Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis. |journal=Am. J. Hum. Genet. |volume=60 |issue= 4 |pages= 896-902 |year= 1997 |pmid= 9106536 |doi=  }}
* {{cite journal | vauthors = 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 | title = The tripartite motif family identifies cell compartments | journal = The EMBO Journal | volume = 20 | issue = 9 | pages = 2140–51 | date = May 2001 | pmid = 11331580 | pmc = 125245 | doi = 10.1093/emboj/20.9.2140 }}
*{{cite journal  | author=Nagase T, Ishikawa K, Suyama M, ''et al.'' |title=Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. |journal=DNA Res. |volume=5 |issue= 6 |pages= 355-64 |year= 1999 |pmid= 10048485 |doi= }}
* {{cite journal | vauthors = Lehesjoki AE, Reed VA, Mark Gardiner R, Greene ND | title = Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis | journal = Mechanisms of Development | volume = 108 | issue = 1-2 | pages = 221–5 | date = Oct 2001 | pmid = 11578880 | doi = 10.1016/S0925-4773(01)00491-9 }}
*{{cite journal  | author=Avela K, Lipsanen-Nyman M, Idänheimo N, ''et al.'' |title=Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism. |journal=Nat. Genet. |volume=25 |issue= 3 |pages= 298-301 |year= 2000 |pmid= 10888877 |doi= 10.1038/77053 }}
* {{cite journal | vauthors = Kallijärvi J, Avela K, Lipsanen-Nyman M, Ulmanen I, Lehesjoki AE | title = The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder | journal = American Journal of Human Genetics | volume = 70 | issue = 5 | pages = 1215–28 | date = May 2002 | pmid = 11938494 | pmc = 447596 | doi = 10.1086/340256 }}
*{{cite journal | author=Zapata JM, Pawlowski K, Haas E, ''et al.'' |title=A diverse family of proteins containing tumor necrosis factor receptor-associated factor domains. |journal=J. Biol. Chem. |volume=276 |issue= 26 |pages= 24242-52 |year= 2001 |pmid= 11279055 |doi= 10.1074/jbc.M100354200 }}
* {{cite journal | vauthors = Jagiello P, Hammans C, Wieczorek S, Arning L, Stefanski A, Strehl H, Epplen JT, Gencik M | title = A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity | journal = Human Mutation | volume = 21 | issue = 6 | pages = 630–5 | date = Jun 2003 | pmid = 12754710 | doi = 10.1002/humu.10220 }}
*{{cite journal | author=Reymond A, Meroni G, Fantozzi A, ''et al.'' |title=The tripartite motif family identifies cell compartments. |journal=EMBO J. |volume=20 |issue= 9 |pages= 2140-51 |year= 2001 |pmid= 11331580 |doi= 10.1093/emboj/20.9.2140 }}
* {{cite journal | vauthors = Hämäläinen RH, Avela K, Lambert JA, Kallijärvi J, Eyaid W, Gronau J, Ignaszewski AP, McFadden D, Sorge G, Lipsanen-Nyman M, Lehesjoki AE | title = Novel mutations in the TRIM37 gene in Mulibrey Nanism | journal = Human Mutation | volume = 23 | issue = 5 | pages = 522 | date = May 2004 | pmid = 15108285 | doi = 10.1002/humu.9233 }}
*{{cite journal | author=Lehesjoki AE, Reed VA, Mark Gardiner R, Greene ND |title=Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis. |journal=Mech. Dev. |volume=108 |issue= 1-2 |pages= 221-5 |year= 2002 |pmid= 11578880 |doi= }}
* {{cite journal | vauthors = Kallijärvi J, Lahtinen U, Hämäläinen R, Lipsanen-Nyman M, Palvimo JJ, Lehesjoki AE | title = TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase | journal = Experimental Cell Research | volume = 308 | issue = 1 | pages = 146–55 | date = Aug 2005 | pmid = 15885686 | doi = 10.1016/j.yexcr.2005.04.001 }}
*{{cite journal | author=Kallijärvi J, Avela K, Lipsanen-Nyman M, ''et al.'' |title=The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder. |journal=Am. J. Hum. Genet. |volume=70 |issue= 5 |pages= 1215-28 |year= 2002 |pmid= 11938494 |doi=  }}
* {{cite journal | vauthors = Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M | title = Towards a proteome-scale map of the human protein-protein interaction network | journal = Nature | volume = 437 | issue = 7062 | pages = 1173–8 | date = Oct 2005 | pmid = 16189514 | doi = 10.1038/nature04209 }}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
* {{cite journal | vauthors = Karlberg N, Jalanko H, Kallijärvi J, Lehesjoki AE, Lipsanen-Nyman M | title = Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37 | journal = Diabetes | volume = 54 | issue = 12 | pages = 3577–81 | date = Dec 2005 | pmid = 16306379 | doi = 10.2337/diabetes.54.12.3577 }}
*{{cite journal | author=Jagiello P, Hammans C, Wieczorek S, ''et al.'' |title=A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity. |journal=Hum. Mutat. |volume=21 |issue= 6 |pages= 630-5 |year= 2003 |pmid= 12754710 |doi= 10.1002/humu.10220 }}
* {{cite journal | vauthors = Hämäläinen RH, Joensuu T, Kallijärvi J, Lehesjoki AE | title = Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing | journal = Gene | volume = 366 | issue = 1 | pages = 180–8 | date = Jan 2006 | pmid = 16310976 | doi = 10.1016/j.gene.2005.08.008 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
* {{cite journal | vauthors = Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY | title = A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration | journal = Cell | volume = 125 | issue = 4 | pages = 801–14 | date = May 2006 | pmid = 16713569 | doi = 10.1016/j.cell.2006.03.032 }}
*{{cite journal  | author=Hämäläinen RH, Avela K, Lambert JA, ''et al.'' |title=Novel mutations in the TRIM37 gene in Mulibrey Nanism. |journal=Hum. Mutat. |volume=23 |issue= 5 |pages= 522 |year= 2004 |pmid= 15108285 |doi= 10.1002/humu.9233 }}
* {{cite journal | vauthors = Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–48 | date = Nov 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
* {{cite journal | vauthors = Hämäläinen RH, Mowat D, Gabbett MT, O'brien TA, Kallijärvi J, Lehesjoki AE | title = Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism | journal = Clinical Genetics | volume = 70 | issue = 6 | pages = 473–9 | date = Dec 2006 | pmid = 17100991 | doi = 10.1111/j.1399-0004.2006.00700.x }}
*{{cite journal  | author=Kallijärvi J, Lahtinen U, Hämäläinen R, ''et al.'' |title=TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase. |journal=Exp. Cell Res. |volume=308 |issue= 1 |pages= 146-55 |year= 2005 |pmid= 15885686 |doi= 10.1016/j.yexcr.2005.04.001 }}
* {{cite journal | vauthors = Doğanc T, Yüksel Konuk BE, Alpan N, Konuk O, Hämäläinen RH, Lehesjoki AE, Tekin M | title = A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy | journal = Clinical Dysmorphology | volume = 16 | issue = 3 | pages = 173–6 | date = Jul 2007 | pmid = 17551331 | doi = 10.1097/MCD.0b013e3280f6d00b }}
*{{cite journal | author=Rual JF, Venkatesan K, Hao T, ''et al.'' |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173-8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal | author=Karlberg N, Jalanko H, Kallijärvi J, ''et al.'' |title=Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37. |journal=Diabetes |volume=54 |issue= 12 |pages= 3577-81 |year= 2006 |pmid= 16306379 |doi= }}
*{{cite journal | author=Hämäläinen RH, Joensuu T, Kallijärvi J, Lehesjoki AE |title=Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing. |journal=Gene |volume=366 |issue= 1 |pages= 180-8 |year= 2006 |pmid= 16310976 |doi= 10.1016/j.gene.2005.08.008 }}
*{{cite journal | author=Lim J, Hao T, Shaw C, ''et al.'' |title=A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. |journal=Cell |volume=125 |issue= 4 |pages= 801-14 |year= 2006 |pmid= 16713569 |doi= 10.1016/j.cell.2006.03.032 }}
*{{cite journal | author=Olsen JV, Blagoev B, Gnad F, ''et al.'' |title=Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. |journal=Cell |volume=127 |issue= 3 |pages= 635-48 |year= 2006 |pmid= 17081983 |doi= 10.1016/j.cell.2006.09.026 }}
*{{cite journal | author=Hämäläinen RH, Mowat D, Gabbett MT, ''et al.'' |title=Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism. |journal=Clin. Genet. |volume=70 |issue= 6 |pages= 473-9 |year= 2007 |pmid= 17100991 |doi= 10.1111/j.1399-0004.2006.00700.x }}
*{{cite journal | author=Doğanc T, Yüksel Konuk BE, Alpan N, ''et al.'' |title=A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy. |journal=Clin. Dysmorphol. |volume=16 |issue= 3 |pages= 173-6 |year= 2007 |pmid= 17551331 |doi= 10.1097/MCD.0b013e3280f6d00b }}
}}
{{refend}}
{{refend}}


{{protein-stub}}
{{gene-17-stub}}
{{WikiDoc Sources}}

Latest revision as of 15:25, 8 October 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Tripartite motif-containing protein 37 is a protein that in humans is encoded by the TRIM37 gene.[1][2][3]

Function

This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein–protein and/or protein–nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. Alternatively spliced transcript variants encoding the same protein have been identified.[3]

Interactions

TRIM37 has been shown to interact with PRC1.[4]

See also

References

  1. ↑ Avela K, Lipsanen-Nyman M, Perheentupa J, Wallgren-Pettersson C, Marchand S, Fauré S, Sistonen P, de la Chapelle A, Lehesjoki AE (Apr 1997). "Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis". American Journal of Human Genetics. 60 (4): 896–902. PMC 1712467. PMID 9106536.
  2. ↑ Avela K, Lipsanen-Nyman M, Idänheimo N, Seemanová E, Rosengren S, Mäkelä TP, Perheentupa J, Chapelle AD, Lehesjoki AE (Jul 2000). "Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism". Nature Genetics. 25 (3): 298–301. doi:10.1038/77053. PMID 10888877.
  3. ↑ 3.0 3.1 "Entrez Gene: TRIM37 tripartite motif-containing 37".
  4. ↑ Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.

Further reading

  • Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Dec 1998). "Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 5 (6): 355–64. doi:10.1093/dnares/5.6.355. PMID 10048485.
  • Zapata JM, Pawlowski K, Haas E, Ware CF, Godzik A, Reed JC (Jun 2001). "A diverse family of proteins containing tumor necrosis factor receptor-associated factor domains". The Journal of Biological Chemistry. 276 (26): 24242–52. doi:10.1074/jbc.M100354200. PMID 11279055.
  • 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 (May 2001). "The tripartite motif family identifies cell compartments". The EMBO Journal. 20 (9): 2140–51. doi:10.1093/emboj/20.9.2140. PMC 125245. PMID 11331580.
  • Lehesjoki AE, Reed VA, Mark Gardiner R, Greene ND (Oct 2001). "Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis". Mechanisms of Development. 108 (1–2): 221–5. doi:10.1016/S0925-4773(01)00491-9. PMID 11578880.
  • Kallijärvi J, Avela K, Lipsanen-Nyman M, Ulmanen I, Lehesjoki AE (May 2002). "The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder". American Journal of Human Genetics. 70 (5): 1215–28. doi:10.1086/340256. PMC 447596. PMID 11938494.
  • Jagiello P, Hammans C, Wieczorek S, Arning L, Stefanski A, Strehl H, Epplen JT, Gencik M (Jun 2003). "A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity". Human Mutation. 21 (6): 630–5. doi:10.1002/humu.10220. PMID 12754710.
  • Hämäläinen RH, Avela K, Lambert JA, Kallijärvi J, Eyaid W, Gronau J, Ignaszewski AP, McFadden D, Sorge G, Lipsanen-Nyman M, Lehesjoki AE (May 2004). "Novel mutations in the TRIM37 gene in Mulibrey Nanism". Human Mutation. 23 (5): 522. doi:10.1002/humu.9233. PMID 15108285.
  • Kallijärvi J, Lahtinen U, Hämäläinen R, Lipsanen-Nyman M, Palvimo JJ, Lehesjoki AE (Aug 2005). "TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase". Experimental Cell Research. 308 (1): 146–55. doi:10.1016/j.yexcr.2005.04.001. PMID 15885686.
  • Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
  • Karlberg N, Jalanko H, Kallijärvi J, Lehesjoki AE, Lipsanen-Nyman M (Dec 2005). "Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37". Diabetes. 54 (12): 3577–81. doi:10.2337/diabetes.54.12.3577. PMID 16306379.
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