| Year |
Citation |
Score |
| 2023 |
Djeghloul D, Dimond A, Cheriyamkunnel S, Kramer H, Patel B, Brown K, Montoya A, Whilding C, Wang YF, Futschik ME, Veland N, Montavon T, Jenuwein T, Merkenschlager M, Fisher AG. Loss of H3K9 trimethylation alters chromosome compaction and transcription factor retention during mitosis. Nature Structural & Molecular Biology. PMID 36941433 DOI: 10.1038/s41594-023-00943-7 |
0.311 |
|
| 2021 |
Puri D, Koschorz B, Engist B, Onishi-Seebacher M, Ryan D, Soujanya M, Montavon T. Foxd3 controls heterochromatin-mediated repression of repeat elements and 2-cell state transcription. Embo Reports. e53180. PMID 34605600 DOI: 10.15252/embr.202153180 |
0.357 |
|
| 2021 |
Montavon T, Shukeir N, Erikson G, Engist B, Onishi-Seebacher M, Ryan D, Musa Y, Mittler G, Meyer AG, Genoud C, Jenuwein T. Complete loss of H3K9 methylation dissolves mouse heterochromatin organization. Nature Communications. 12: 4359. PMID 34272378 DOI: 10.1038/s41467-021-24532-8 |
0.323 |
|
| 2021 |
Montavon T, Shukeir N, Erikson G, Engist B, Onishi-Seebacher M, Ryan D, Musa Y, Mittler G, Meyer AG, Genoud C, Jenuwein T. Complete loss of H3K9 methylation dissolves mouse heterochromatin organization. Nature Communications. 12: 4359. PMID 34272378 DOI: 10.1038/s41467-021-24532-8 |
0.323 |
|
| 2019 |
Nicetto D, Donahue G, Jain T, Peng T, Sidoli S, Sheng L, Montavon T, Becker JS, Grindheim JM, Blahnik K, Garcia BA, Tan K, Bonasio R, Jenuwein T, Zaret KS. H3K9me3-heterochromatin loss at protein-coding genes enables developmental lineage specification. Science (New York, N.Y.). PMID 30606806 DOI: 10.1126/Science.Aau0583 |
0.496 |
|
| 2014 |
Lonfat N, Montavon T, Darbellay F, Gitto S, Duboule D. Convergent evolution of complex regulatory landscapes and pleiotropy at Hox loci. Science (New York, N.Y.). 346: 1004-6. PMID 25414315 DOI: 10.1126/Science.1257493 |
0.697 |
|
| 2014 |
Montavon T, Soshnikova N. Hox gene regulation and timing in embryogenesis. Seminars in Cell & Developmental Biology. 34: 76-84. PMID 24930771 DOI: 10.1016/J.Semcdb.2014.06.005 |
0.783 |
|
| 2013 |
Delpretti S, Montavon T, Leleu M, Joye E, Tzika A, Milinkovitch M, Duboule D. Multiple enhancers regulate Hoxd genes and the Hotdog LncRNA during cecum budding. Cell Reports. 5: 137-50. PMID 24075990 DOI: 10.1016/J.Celrep.2013.09.002 |
0.747 |
|
| 2013 |
Lonfat N, Montavon T, Jebb D, Tschopp P, Nguyen Huynh TH, Zakany J, Duboule D. Transgene- and locus-dependent imprinting reveals allele-specific chromosome conformations. Proceedings of the National Academy of Sciences of the United States of America. 110: 11946-51. PMID 23818637 DOI: 10.1073/Pnas.1310704110 |
0.672 |
|
| 2013 |
Andrey G, Montavon T, Mascrez B, Gonzalez F, Noordermeer D, Leleu M, Trono D, Spitz F, Duboule D. A switch between topological domains underlies HoxD genes collinearity in mouse limbs. Science (New York, N.Y.). 340: 1234167. PMID 23744951 DOI: 10.1126/Science.1234167 |
0.732 |
|
| 2013 |
Montavon T, Duboule D. Chromatin organization and global regulation of Hox gene clusters. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 368: 20120367. PMID 23650639 DOI: 10.1098/Rstb.2012.0367 |
0.695 |
|
| 2012 |
Montavon T, Thevenet L, Duboule D. Impact of copy number variations (CNVs) on long-range gene regulation at the HoxD locus. Proceedings of the National Academy of Sciences of the United States of America. 109: 20204-11. PMID 23134724 DOI: 10.1073/Pnas.1217659109 |
0.721 |
|
| 2012 |
Montavon T, Duboule D. Landscapes and archipelagos: spatial organization of gene regulation in vertebrates. Trends in Cell Biology. 22: 347-54. PMID 22560708 DOI: 10.1016/J.Tcb.2012.04.003 |
0.727 |
|
| 2011 |
Montavon T, Soshnikova N, Mascrez B, Joye E, Thevenet L, Splinter E, de Laat W, Spitz F, Duboule D. A regulatory archipelago controls Hox genes transcription in digits. Cell. 147: 1132-45. PMID 22118467 DOI: 10.1016/J.Cell.2011.10.023 |
0.809 |
|
| 2010 |
Soshnikova N, Montavon T, Leleu M, Galjart N, Duboule D. Functional analysis of CTCF during mammalian limb development. Developmental Cell. 19: 819-30. PMID 21145498 DOI: 10.1016/J.Devcel.2010.11.009 |
0.797 |
|
| 2009 |
Montavon T, Mascrez B, Spitz F, de Laat W, Duboule D. 22-P021 Long-range enhancer–promoter interactions in the HoxD complex Mechanisms of Development. 126: S335. DOI: 10.1016/J.Mod.2009.06.1232 |
0.794 |
|
| 2008 |
Montavon T, Le Garrec JF, Kerszberg M, Duboule D. Modeling Hox gene regulation in digits: reverse collinearity and the molecular origin of thumbness. Genes & Development. 22: 346-59. PMID 18245448 DOI: 10.1101/Gad.1631708 |
0.719 |
|
| 2002 |
Spitz F, Montavon T, Monso-Hinard C, Morris M, Ventruto ML, Antonarakis S, Ventruto V, Duboule D. A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects. Genomics. 79: 493-8. PMID 11944980 DOI: 10.1006/Geno.2002.6735 |
0.752 |
|
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