281 related articles for article (PubMed ID: 28334947)
1. Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα).
Pham DH; Tan CC; Homan CC; Kolc KL; Corbett MA; McAninch D; Fox AH; Thomas PQ; Kumar R; Gecz J
Hum Mol Genet; 2017 Jun; 26(11):2042-2052. PubMed ID: 28334947
[TBL] [Abstract][Full Text] [Related]
2. Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.
Kharade SS; Parekh VI; Agarwal SK
Endocrinology; 2018 Feb; 159(2):1199-1212. PubMed ID: 29309627
[TBL] [Abstract][Full Text] [Related]
3. PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder.
Depienne C; LeGuern E
Hum Mutat; 2012 Apr; 33(4):627-34. PubMed ID: 22267240
[TBL] [Abstract][Full Text] [Related]
4. p54nrb/NONO regulates cyclic AMP-dependent glucocorticoid production by modulating phosphodiesterase mRNA splicing and degradation.
Lu JY; Sewer MB
Mol Cell Biol; 2015 Apr; 35(7):1223-37. PubMed ID: 25605330
[TBL] [Abstract][Full Text] [Related]
5. Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing.
Reinstein E; Tzur S; Cohen R; Bormans C; Behar DM
Eur J Hum Genet; 2016 Nov; 24(11):1635-1638. PubMed ID: 27329731
[TBL] [Abstract][Full Text] [Related]
6. Altered stoichiometry and nuclear delocalization of NonO and PSF promote cellular senescence.
Huang CJ; Das U; Xie W; Ducasse M; Tucker HO
Aging (Albany NY); 2016 Dec; 8(12):3356-3374. PubMed ID: 27992859
[TBL] [Abstract][Full Text] [Related]
7. Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.
Hynes K; Tarpey P; Dibbens LM; Bayly MA; Berkovic SF; Smith R; Raisi ZA; Turner SJ; Brown NJ; Desai TD; Haan E; Turner G; Christodoulou J; Leonard H; Gill D; Stratton MR; Gecz J; Scheffer IE
J Med Genet; 2010 Mar; 47(3):211-6. PubMed ID: 19752159
[TBL] [Abstract][Full Text] [Related]
8. IGFBP-3 interacts with NONO and SFPQ in PARP-dependent DNA damage repair in triple-negative breast cancer.
de Silva HC; Lin MZ; Phillips L; Martin JL; Baxter RC
Cell Mol Life Sci; 2019 May; 76(10):2015-2030. PubMed ID: 30725116
[TBL] [Abstract][Full Text] [Related]
9. Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
Tan C; Shard C; Ranieri E; Hynes K; Pham DH; Leach D; Buchanan G; Corbett M; Shoubridge C; Kumar R; Douglas E; Nguyen LS; Mcmahon J; Sadleir L; Specchio N; Marini C; Guerrini R; Moller RS; Depienne C; Haan E; Thomas PQ; Berkovic SF; Scheffer IE; Gecz J
Hum Mol Genet; 2015 Sep; 24(18):5250-9. PubMed ID: 26123493
[TBL] [Abstract][Full Text] [Related]
10. Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations.
Chaoui A; Kavo A; Baral V; Watanabe Y; Lecerf L; Colley A; Mendoza-Londono R; Pingault V; Bondurand N
Hum Mol Genet; 2015 Sep; 24(17):4933-47. PubMed ID: 26060192
[TBL] [Abstract][Full Text] [Related]
11. Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report.
Tan Y; Hou M; Ma S; Liu P; Xia S; Wang Y; Chen L; Chen Z
BMC Med Genet; 2018 Jun; 19(1):92. PubMed ID: 29866057
[TBL] [Abstract][Full Text] [Related]
12. Interaction of SOCS3 with NonO attenuates IL-1beta-dependent MUC8 gene expression.
Song KS; Kim K; Chung KC; Seol JH; Yoon JH
Biochem Biophys Res Commun; 2008 Dec; 377(3):946-51. PubMed ID: 18952062
[TBL] [Abstract][Full Text] [Related]
13. NONO ubiquitination is mediated by FBW7 and GSK3 β via a degron lost upon chromosomal rearrangement in cancer.
Alfano L; Caporaso A; Altieri A; Costa C; Forte IM; Iannuzzi CA; Barone D; Esposito L; Giordano A; Pentimalli F
J Cell Physiol; 2018 May; 233(5):4338-4344. PubMed ID: 29150959
[TBL] [Abstract][Full Text] [Related]
14. Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects.
Mircsof D; Langouët M; Rio M; Moutton S; Siquier-Pernet K; Bole-Feysot C; Cagnard N; Nitschke P; Gaspar L; Žnidarič M; Alibeu O; Fritz AK; Wolfer DP; Schröter A; Bosshard G; Rudin M; Koester C; Crestani F; Seebeck P; Boddaert N; Prescott K; ; Hines R; Moss SJ; Fritschy JM; Munnich A; Amiel J; Brown SA; Tyagarajan SK; Colleaux L
Nat Neurosci; 2015 Dec; 18(12):1731-6. PubMed ID: 26571461
[TBL] [Abstract][Full Text] [Related]
15. p54(nrb)/NONO regulates lipid metabolism and breast cancer growth through SREBP-1A.
Zhu Z; Zhao X; Zhao L; Yang H; Liu L; Li J; Wu J; Yang F; Huang G; Liu J
Oncogene; 2016 Mar; 35(11):1399-410. PubMed ID: 26148231
[TBL] [Abstract][Full Text] [Related]
16. Non-POU Domain-Containing Octamer-Binding Protein Negatively Regulates HIV-1 Infection in CD4(+) T Cells.
St Gelais C; Roger J; Wu L
AIDS Res Hum Retroviruses; 2015 Aug; 31(8):806-16. PubMed ID: 25769457
[TBL] [Abstract][Full Text] [Related]
17. New Noncoding Lytic Transcripts Derived from the Epstein-Barr Virus Latency Origin of Replication, oriP, Are Hyperedited, Bind the Paraspeckle Protein, NONO/p54nrb, and Support Viral Lytic Transcription.
Cao S; Moss W; O'Grady T; Concha M; Strong MJ; Wang X; Yu Y; Baddoo M; Zhang K; Fewell C; Lin Z; Dong Y; Flemington EK
J Virol; 2015 Jul; 89(14):7120-32. PubMed ID: 25926645
[TBL] [Abstract][Full Text] [Related]
18. Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy.
Pederick DT; Richards KL; Piltz SG; Kumar R; Mincheva-Tasheva S; Mandelstam SA; Dale RC; Scheffer IE; Gecz J; Petrou S; Hughes JN; Thomas PQ
Neuron; 2018 Jan; 97(1):59-66.e5. PubMed ID: 29301106
[TBL] [Abstract][Full Text] [Related]
19. Rasd1 modulates the coactivator function of NonO in the cyclic AMP pathway.
Ong SA; Tan JJ; Tew WL; Chen KS
PLoS One; 2011; 6(9):e24401. PubMed ID: 21915321
[TBL] [Abstract][Full Text] [Related]
20. Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO.
Scott DA; Hernandez-Garcia A; Azamian MS; Jordan VK; Kim BJ; Starkovich M; Zhang J; Wong LJ; Darilek SA; Breman AM; Yang Y; Lupski JR; Jiwani AK; Das B; Lalani SR; Iglesias AD; Rosenfeld JA; Xia F
J Med Genet; 2017 Jan; 54(1):47-53. PubMed ID: 27550220
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]