PubMed for id: 11043

Year	Number of Results
1999	2
2001	2
2002	2
2003	1
2004	3
2005	3
2006	2
2007	1
2008	3
2009	2
2011	3
2012	1
2013	2
2014	4
2015	5
2016	4
2017	3
2018	2
2020	2
2021	2
2022	4
2024	0

1

Midline2 is overexpressed and a prognostic indicator in human breast cancer and promotes breast cancer cell proliferation in vitro and in vivo.

Wang L, Wu J, Yuan J, Zhu X, Wu H, Li M. Wang L, et al. Front Med. 2016 Mar;10(1):41-51. doi: 10.1007/s11684-016-0429-z. Epub 2016 Jan 20. Front Med. 2016. PMID: 26791755

2

Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.

Geetha TS, Michealraj KA, Kabra M, Kaur G, Juyal RC, Thelma BK. Geetha TS, et al. Hum Mutat. 2014 Jan;35(1):41-4. doi: 10.1002/humu.22453. Epub 2013 Oct 21. Hum Mutat. 2014. PMID: 24115387

3

An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.

Jehee FS, Rosenberg C, Krepischi-Santos AC, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. Jehee FS, et al. Am J Med Genet A. 2005 Dec 15;139(3):221-6. doi: 10.1002/ajmg.a.30991. Am J Med Genet A. 2005. PMID: 16283679

4

Trim5alpha protein restricts both HIV-1 and murine leukemia virus.

Yap MW, Nisole S, Lynch C, Stoye JP. Yap MW, et al. Proc Natl Acad Sci U S A. 2004 Jul 20;101(29):10786-91. doi: 10.1073/pnas.0402876101. Epub 2004 Jul 12. Proc Natl Acad Sci U S A. 2004. PMID: 15249690 Free PMC article.

5

MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation.

Trockenbacher A, Suckow V, Foerster J, Winter J, Krauss S, Ropers HH, Schneider R, Schweiger S. Trockenbacher A, et al. Nat Genet. 2001 Nov;29(3):287-94. doi: 10.1038/ng762. Nat Genet. 2001. PMID: 11685209

6

FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules.

Perry J, Short KM, Romer JT, Swift S, Cox TC, Ashworth A. Perry J, et al. Genomics. 1999 Dec 15;62(3):385-94. doi: 10.1006/geno.1999.6043. Genomics. 1999. PMID: 10644436

7

The E3 ligase TRIM1 ubiquitinates LRRK2 and controls its localization, degradation, and toxicity.

Stormo AED, Shavarebi F, FitzGibbon M, Earley EM, Ahrendt H, Lum LS, Verschueren E, Swaney DL, Skibinski G, Ravisankar A, van Haren J, Davis EJ, Johnson JR, Von Dollen J, Balen C, Porath J, Crosio C, Mirescu C, Iaccarino C, Dauer WT, Nichols RJ, Wittmann T, Cox TC, Finkbeiner S, Krogan NJ, Oakes SA, Hiniker A. Stormo AED, et al. J Cell Biol. 2022 Apr 4;221(4):e202010065. doi: 10.1083/jcb.202010065. Epub 2022 Mar 10. J Cell Biol. 2022. PMID: 35266954 Free PMC article.

8

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Buchner G, Montini E, Andolfi G, Quaderi N, Cainarca S, Messali S, Bassi MT, Ballabio A, Meroni G, Franco B. Buchner G, et al. Hum Mol Genet. 1999 Aug;8(8):1397-407. doi: 10.1093/hmg/8.8.1397. Hum Mol Genet. 1999. PMID: 10400986

9

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders.

Short KM, Hopwood B, Yi Z, Cox TC. Short KM, et al. BMC Cell Biol. 2002;3:1. doi: 10.1186/1471-2121-3-1. Epub 2002 Jan 4. BMC Cell Biol. 2002. PMID: 11806752 Free PMC article.

10

Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding.

Short KM, Cox TC. Short KM, et al. J Biol Chem. 2006 Mar 31;281(13):8970-80. doi: 10.1074/jbc.M512755200. Epub 2006 Jan 23. J Biol Chem. 2006. PMID: 16434393 Free article.

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