Citations for
1MRD41, TBL1XR1
Pierpont syndrome associated with the p.Tyr446Cys missense mutation in TBL1XR1.
Slavotinek A, Pua H, Hodoglugil U, Abadie J, Shieh J, Van Ziffle J, Kvale M, Lee H, Kwok PY, Risch N, Sabbadini M.
Eur J Med Genet 60(10):504-508. doi: 10.1016/j.ejmg.2017.07.003. Epub 2017 Jul 4. 2017
2MRD41, TBL1XR1
A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndrome.
Riehmer V, Erger F, Herkenrath P, Seland S, Jackels M, Wiater A, Heller R, Beck BB, Netzer C.
Am J Med Genet A 173(8):2132-2138. doi: 10.1002/ajmg.a.38285. Epub 2017 Jun 2. 2017
3SASH3, TBL1XR1
SLY regulates genes involved in chromatin remodeling and interacts with TBL1XR1 during sperm differentiation.
Moretti C, Serrentino ME, Ialy-Radio C, Delessard M, Soboleva TA, Tores F, Leduc M, Nitschké P, Drevet JR, Tremethick DJ, Vaiman D, Kocer A, Cocquet J.
Cell Death Differ 24(6):1029-1044. doi: 10.1038/cdd.2017.32. Epub 2017 May 5. 2017
4TBL1XR1
Nuclear TBLR1 as an ER corepressor promotes cell proliferation, migration and invasion in breast and ovarian cancer.
Wu X, Zhan Y, Li X, Wei J, Santiago L, Daniels G, Deng F, Zhong X, Chiriboga L, Basch R, Xiong S, Dong Y, Zhang X, Lee P.
Am J Cancer Res 6(10):2351-2360. eCollection 2016. 2016
5MRD41, TBL1XR1
A new syndrome of intellectual disability with dysmorphism due to TBL1XR1 deletion.
Pons L, Cordier MP, Labalme A, Till M, Louvrier C, Schluth-Bolard C, Lesca G, Edery P, Sanlaville D.
Am J Med Genet A 167A(1):164-8. doi: 10.1002/ajmg.a.36759. Epub 2014 Nov 25. 2015
6TBL1XR1
TBL1XR1 in physiological and pathological states.
Li JY, Daniels G, Wang J, Zhang X.
Am J Clin Exp Urol 3(1):13-23. eCollection 2015. Review. 2015
7MRD41, TBL1XR1
A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation.
Saitsu H, Tohyama J, Walsh T, Kato M, Kobayashi Y, Lee M, Tsurusaki Y, Miyake N, Goto Y, Nishino I, Ohtake A, King MC, Matsumoto N.
J Hum Genet 59(10):581-3. doi: 10.1038/jhg.2014.71. Epub 2014 Aug 7. 2014
8MRD41, TBL1XR1
De novo deletion of TBL1XR1 in a child with non-specific developmental delay supports its implication in intellectual disability.
Tabet AC, Leroy C, Dupont C, Serrano E, Hernandez K, Gallard J, Pouvreau N, Gadisseux JF, Benzacken B, Verloes A.
Am J Med Genet A 164A(9):2335-7. doi: 10.1002/ajmg.a.36619. Epub 2014 May 28. 2014
9TBL1XR1
TBLR1 as an androgen receptor (AR) coactivator selectively activates AR target genes to inhibit prostate cancer growth.
Daniels G, Li Y, Gellert LL, Zhou A, Melamed J, Wu X, Zhang X, Zhang D, Meruelo D, Logan SK, Basch R, Lee P.
Endocr Relat Cancer 21(1):127-42. doi: 10.1530/ERC-13-0293. Print 2014 Feb. 2014
10TBL1XR1
Transcriptional cofactor TBLR1 controls lipid mobilization in white adipose tissue.
Rohm M, Sommerfeld A, Strzoda D, Jones A, Sijmonsma TP, Rudofsky G, Wolfrum C, Sticht C, Gretz N, Zeyda M, Leitner L, Nawroth PP, Stulnig TM, Berriel Diaz M, Vegiopoulos A, Herzig S.
Cell Metab 17(4):575-85. doi: 10.1016/j.cmet.2013.02.010. Epub 2013 Mar 14. 2013
11TBL1XR1, TP63
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma.
Scott DW, Mungall KL, Ben-Neriah S, Rogic S, Morin RD, Slack GW, Tan KL, Chan FC, Lim RS, Connors JM, Marra MA, Mungall AJ, Steidl C, Gascoyne RD.
Blood 119(21):4949-52. doi: 10.1182/blood-2012-02-414441. Epub 2012 Apr 11. 2012
12BCL3, CTBP1, CTBP2, TBL1XR1
The repressing function of the oncoprotein BCL-3 requires CtBP, while its polyubiquitination and degradation involve the E3 ligase TBLR1.
Keutgens A, Shostak K, Close P, Zhang X, Hennuy B, Aussems M, Chapelle JP, Viatour P, Gothot A, Fillet M, Chariot A.
Mol Cell Biol 30(16):4006-21. Epub 2010 Jun 14.PMID: 20547759 2010
13TBL1X, TBL1XR1
TBL1 and TBLR1 phosphorylation on regulated gene promoters overcomes dual CtBP and NCoR/SMRT transcriptional repression checkpoints.
Perissi V, Scafoglio C, Zhang J, Ohgi KA, Rose DW, Glass CK, Rosenfeld MG.
Mol Cell 29(6):755-66. 2008
14TBL1X, TBL1XR1
TBL1-TBLR1 and beta-catenin recruit each other to Wnt target-gene promoter for transcription activation and oncogenesis.
Li J, Wang CY.
Nat Cell Biol 10(2):160-9. Epub 2008 Jan 13. 2008
15TBL1X, TBL1Y, TBL1XR1
Molecular analysis of TBL1Y, a Y-linked homologue of TBL1X related with X-linked late-onset sensorineural deafness.
Yan HT, Shinka T, Kinoshita K, Sato Y, Umeno M, Chen G, Tsuji K, Unemi Y, Yang XJ, Iwamoto T, Nakahori Y.
J Hum Genet 50(4):175-81. Epub 2005 Apr 15. 2005
16TBL1XR1
Identification of four human cDNAs that are differentially expressed by early hematopoietic progenitors.
Zhang X, Dormady SP, Basch RS.
Exp Hematol 28(11):1286-96. 2000