224 related articles for article (PubMed ID: 31067316)
1. A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis.
Goos JAC; Vogel WK; Mlcochova H; Millard CJ; Esfandiari E; Selman WH; Calpena E; Koelling N; Carpenter EL; Swagemakers SMA; van der Spek PJ; Filtz TM; Schwabe JWR; Iwaniec UT; Mathijssen IMJ; Leid M; Twigg SRF
Hum Mol Genet; 2019 Aug; 28(15):2501-2513. PubMed ID: 31067316
[TBL] [Abstract][Full Text] [Related]
2. BCL11B regulates sutural patency in the mouse craniofacial skeleton.
Kyrylkova K; Iwaniec UT; Philbrick KA; Leid M
Dev Biol; 2016 Jul; 415(2):251-260. PubMed ID: 26453795
[TBL] [Abstract][Full Text] [Related]
3. Insight into the architecture of the NuRD complex: structure of the RbAp48-MTA1 subcomplex.
Alqarni SS; Murthy A; Zhang W; Przewloka MR; Silva AP; Watson AA; Lejon S; Pei XY; Smits AH; Kloet SL; Wang H; Shepherd NE; Stokes PH; Blobel GA; Vermeulen M; Glover DM; Mackay JP; Laue ED
J Biol Chem; 2014 Aug; 289(32):21844-55. PubMed ID: 24920672
[TBL] [Abstract][Full Text] [Related]
4. Differential activation of canonical Wnt signaling determines cranial sutures fate: a novel mechanism for sagittal suture craniosynostosis.
Behr B; Longaker MT; Quarto N
Dev Biol; 2010 Aug; 344(2):922-40. PubMed ID: 20547147
[TBL] [Abstract][Full Text] [Related]
5. Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.
Twigg SR; Vorgia E; McGowan SJ; Peraki I; Fenwick AL; Sharma VP; Allegra M; Zaragkoulias A; Sadighi Akha E; Knight SJ; Lord H; Lester T; Izatt L; Lampe AK; Mohammed SN; Stewart FJ; Verloes A; Wilson LC; Healy C; Sharpe PT; Hammond P; Hughes J; Taylor S; Johnson D; Wall SA; Mavrothalassitis G; Wilkie AO
Nat Genet; 2013 Mar; 45(3):308-13. PubMed ID: 23354439
[TBL] [Abstract][Full Text] [Related]
6. BCL11B expression in intramembranous osteogenesis during murine craniofacial suture development.
Holmes G; van Bakel H; Zhou X; Losic B; Jabs EW
Gene Expr Patterns; 2015 Jan; 17(1):16-25. PubMed ID: 25511173
[TBL] [Abstract][Full Text] [Related]
7. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells.
Lessel D; Gehbauer C; Bramswig NC; Schluth-Bolard C; Venkataramanappa S; van Gassen KLI; Hempel M; Haack TB; Baresic A; Genetti CA; Funari MFA; Lessel I; Kuhlmann L; Simon R; Liu P; Denecke J; Kuechler A; de Kruijff I; Shoukier M; Lek M; Mullen T; Lüdecke HJ; Lerario AM; Kobbe R; Krieger T; Demeer B; Lebrun M; Keren B; Nava C; Buratti J; Afenjar A; Shinawi M; Guillen Sacoto MJ; Gauthier J; Hamdan FF; Laberge AM; Campeau PM; Louie RJ; Cathey SS; Prinz I; Jorge AAL; Terhal PA; Lenhard B; Wieczorek D; Strom TM; Agrawal PB; Britsch S; Tolosa E; Kubisch C
Brain; 2018 Aug; 141(8):2299-2311. PubMed ID: 29985992
[TBL] [Abstract][Full Text] [Related]
8. The MTA1 subunit of the nucleosome remodeling and deacetylase complex can recruit two copies of RBBP4/7.
Schmidberger JW; Sharifi Tabar M; Torrado M; Silva AP; Landsberg MJ; Brillault L; AlQarni S; Zeng YC; Parker BL; Low JK; Mackay JP
Protein Sci; 2016 Aug; 25(8):1472-82. PubMed ID: 27144666
[TBL] [Abstract][Full Text] [Related]
9. Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.
Holmes G; Basilico C
Dev Biol; 2012 Aug; 368(2):283-93. PubMed ID: 22664175
[TBL] [Abstract][Full Text] [Related]
10. Protein Kinase C-Mediated Phosphorylation of BCL11B at Serine 2 Negatively Regulates Its Interaction with NuRD Complexes during CD4+ T-Cell Activation.
Dubuissez M; Loison I; Paget S; Vorng H; Ait-Yahia S; Rohr O; Tsicopoulos A; Leprince D
Mol Cell Biol; 2016 Jul; 36(13):1881-98. PubMed ID: 27161321
[TBL] [Abstract][Full Text] [Related]
11. BCL11B functionally associates with the NuRD complex in T lymphocytes to repress targeted promoter.
Cismasiu VB; Adamo K; Gecewicz J; Duque J; Lin Q; Avram D
Oncogene; 2005 Oct; 24(45):6753-64. PubMed ID: 16091750
[TBL] [Abstract][Full Text] [Related]
12. BMP9 induces osteogenesis and adipogenesis in the immortalized human cranial suture progenitors from the patent sutures of craniosynostosis patients.
Song D; Zhang F; Reid RR; Ye J; Wei Q; Liao J; Zou Y; Fan J; Ma C; Hu X; Qu X; Chen L; Li L; Yu Y; Yu X; Zhang Z; Zhao C; Zeng Z; Zhang R; Yan S; Wu T; Wu X; Shu Y; Lei J; Li Y; Zhang W; Wang J; Lee MJ; Wolf JM; Huang D; He TC
J Cell Mol Med; 2017 Nov; 21(11):2782-2795. PubMed ID: 28470873
[TBL] [Abstract][Full Text] [Related]
13. Structural basis of plant homeodomain finger 6 (PHF6) recognition by the retinoblastoma binding protein 4 (RBBP4) component of the nucleosome remodeling and deacetylase (NuRD) complex.
Liu Z; Li F; Zhang B; Li S; Wu J; Shi Y
J Biol Chem; 2015 Mar; 290(10):6630-8. PubMed ID: 25601084
[TBL] [Abstract][Full Text] [Related]
14. Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathy.
Pande S; Mascarenhas S; Venkatraman A; Bhat V; Narayanan DL; Siddiqui S; Bielas S; Girisha KM; Shukla A
Am J Med Genet A; 2023 Aug; 191(8):2175-2180. PubMed ID: 37337996
[TBL] [Abstract][Full Text] [Related]
15. Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis.
Coussens AK; Wilkinson CR; Hughes IP; Morris CP; van Daal A; Anderson PJ; Powell BC
BMC Genomics; 2007 Dec; 8():458. PubMed ID: 18076769
[TBL] [Abstract][Full Text] [Related]
16. The N-Terminal CCHC Zinc Finger Motif Mediates Homodimerization of Transcription Factor BCL11B.
Grabarczyk P; Winkler P; Delin M; Sappa PK; Bekeschus S; Hildebrandt P; Przybylski GK; Völker U; Hammer E; Schmidt CA
Mol Cell Biol; 2018 Mar; 38(5):. PubMed ID: 29203643
[TBL] [Abstract][Full Text] [Related]
17. Increased bone formation and osteoblastic cell phenotype in premature cranial suture ossification (craniosynostosis).
De Pollack C; Renier D; Hott M; Marie PJ
J Bone Miner Res; 1996 Mar; 11(3):401-7. PubMed ID: 8852951
[TBL] [Abstract][Full Text] [Related]
18. A core chromatin remodeling factor instructs global chromatin signaling through multivalent reading of nucleosome codes.
Nair SS; Li DQ; Kumar R
Mol Cell; 2013 Feb; 49(4):704-18. PubMed ID: 23352453
[TBL] [Abstract][Full Text] [Related]
19. Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionarily conserved non-transcribed region.
Tagariello A; Heller R; Greven A; Kalscheuer VM; Molter T; Rauch A; Kress W; Winterpacht A
J Med Genet; 2006 Jun; 43(6):534-40. PubMed ID: 16258006
[TBL] [Abstract][Full Text] [Related]
20. Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo - in vitro approach.
Coussens AK; Hughes IP; Wilkinson CR; Morris CP; Anderson PJ; Powell BC; van Daal A
Differentiation; 2008 May; 76(5):531-45. PubMed ID: 18093228
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
