Littérature scientifique sur le sujet « Complexe polycomb »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Sommaire
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Complexe polycomb ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "Complexe polycomb"
Dong, Guan-Jun, Jia-Le Xu, Yu-Ruo Qi, Zi-Qiao Yuan et Wen Zhao. « Critical Roles of Polycomb Repressive Complexes in Transcription and Cancer ». International Journal of Molecular Sciences 23, no 17 (24 août 2022) : 9574. http://dx.doi.org/10.3390/ijms23179574.
Texte intégralStrutt, H., et R. Paro. « The polycomb group protein complex of Drosophila melanogaster has different compositions at different target genes. » Molecular and Cellular Biology 17, no 12 (décembre 1997) : 6773–83. http://dx.doi.org/10.1128/mcb.17.12.6773.
Texte intégralMeseure, D., S. Vacher, M. Trassard, K. Drak Alsibai, C. Le Ray, C. Régnier, F. Lerebours, R. Le Scodan, R. Lidereau et I. Bièche. « Rôles du complexe répresseur Polycomb EZH2/CBX7 et du long ARN non codant ANRIL dans l’induction des mécanismes de silencing épigénétique. Implications thérapeutiques potentielles dans les carcinomes mammaires de type triple négatif ». Annales de Pathologie 31, no 5 (novembre 2011) : S125. http://dx.doi.org/10.1016/j.annpat.2011.09.021.
Texte intégralAli, Janann Y., et Welcome Bender. « Cross-Regulation among the Polycomb Group Genes in Drosophila melanogaster ». Molecular and Cellular Biology 24, no 17 (1 septembre 2004) : 7737–47. http://dx.doi.org/10.1128/mcb.24.17.7737-7747.2004.
Texte intégralZhou, Haining, Chad B. Stein, Tiasha A. Shafiq, Gergana Shipkovenska, Marian Kalocsay, Joao A. Paulo, Jiuchun Zhang et al. « Rixosomal RNA degradation contributes to silencing of Polycomb target genes ». Nature 604, no 7904 (30 mars 2022) : 167–74. http://dx.doi.org/10.1038/s41586-022-04598-0.
Texte intégralMA, Ke-Xue, et Xing-Zi XI. « Polycomb group protein complexes ». Hereditas (Beijing) 31, no 10 (22 décembre 2009) : 977–81. http://dx.doi.org/10.3724/sp.j.1005.2009.00977.
Texte intégralGahan, James M., Fabian Rentzsch et Christine E. Schnitzler. « The genetic basis for PRC1 complex diversity emerged early in animal evolution ». Proceedings of the National Academy of Sciences 117, no 37 (31 août 2020) : 22880–89. http://dx.doi.org/10.1073/pnas.2005136117.
Texte intégralChittock, Emily C., Sebastian Latwiel, Thomas C. R. Miller et Christoph W. Müller. « Molecular architecture of polycomb repressive complexes ». Biochemical Society Transactions 45, no 1 (8 février 2017) : 193–205. http://dx.doi.org/10.1042/bst20160173.
Texte intégralLund, Anders H., et Maarten van Lohuizen. « Polycomb complexes and silencing mechanisms ». Current Opinion in Cell Biology 16, no 3 (juin 2004) : 239–46. http://dx.doi.org/10.1016/j.ceb.2004.03.010.
Texte intégralSchwartz, Yuri B., et Vincenzo Pirrotta. « Polycomb complexes and epigenetic states ». Current Opinion in Cell Biology 20, no 3 (juin 2008) : 266–73. http://dx.doi.org/10.1016/j.ceb.2008.03.002.
Texte intégralThèses sur le sujet "Complexe polycomb"
Campagne, Antoine. « Etude du complexe Polycomb PR-DUB : une approche mécanistique ». Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066624/document.
Texte intégralBAP1 is as a tumor suppressor that associates to a variety of protein partners, thereby limiting the comprehension of its cellular functions. In Drosophila, BAP1 binds ASX to form the Polycomb PR-DUB complex, which deubiquitinates histone H2A on lysine 119 in order to maintain transcriptional repression on its target genes. Describing BAP1 mechanisms of action and defining how BAP1 cooperates with the Polycomb machinery are prerequisites to understand its role during tumorigenesis. Using a biochemical approach, we described the existence of several distinct subcomplexes associated with BAP1. Therefore, ASXL1 seems required for H2A deubiquitination, while ASXL2 forms a ternary complex of unknown function with BAP1 and the histone demethylase KDM1B. In addition, we demonstrated the transcriptional repressor function of BAP1, which possess several repressive domains. In addition, we are currently performing transcriptomic analysis combined with genome-wide mapping of different histone marks. These last analyses are performed in wild type cells or deficient in PR-DUB or other Polycomb components, which will help us to understand how BAP1 fits within the Polycomb machinery. In parallel, we engaged a comprehensive study aiming at the identification of new BAP1 substrates. Our preliminary results suggest that not only H2A but also H2B may be direct substrates of BAP1. In addition, we identified as a potential substrate the HNRNPM-IMP3 complex, which controls cell proliferation via post-transcriptional regulation of several cyclins. These observations pave the way for new projects that may contribute to explain the consequences of BAP1 mutations in cancer development
Campagne, Antoine. « Etude du complexe Polycomb PR-DUB : une approche mécanistique ». Electronic Thesis or Diss., Paris 6, 2015. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2015PA066624.pdf.
Texte intégralBAP1 is as a tumor suppressor that associates to a variety of protein partners, thereby limiting the comprehension of its cellular functions. In Drosophila, BAP1 binds ASX to form the Polycomb PR-DUB complex, which deubiquitinates histone H2A on lysine 119 in order to maintain transcriptional repression on its target genes. Describing BAP1 mechanisms of action and defining how BAP1 cooperates with the Polycomb machinery are prerequisites to understand its role during tumorigenesis. Using a biochemical approach, we described the existence of several distinct subcomplexes associated with BAP1. Therefore, ASXL1 seems required for H2A deubiquitination, while ASXL2 forms a ternary complex of unknown function with BAP1 and the histone demethylase KDM1B. In addition, we demonstrated the transcriptional repressor function of BAP1, which possess several repressive domains. In addition, we are currently performing transcriptomic analysis combined with genome-wide mapping of different histone marks. These last analyses are performed in wild type cells or deficient in PR-DUB or other Polycomb components, which will help us to understand how BAP1 fits within the Polycomb machinery. In parallel, we engaged a comprehensive study aiming at the identification of new BAP1 substrates. Our preliminary results suggest that not only H2A but also H2B may be direct substrates of BAP1. In addition, we identified as a potential substrate the HNRNPM-IMP3 complex, which controls cell proliferation via post-transcriptional regulation of several cyclins. These observations pave the way for new projects that may contribute to explain the consequences of BAP1 mutations in cancer development
Molitor, Anne. « Caractérisation moléculaire et fonctionnelle du complexe PRC1 chez Arabidopsis thaliana ». Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAJ053.
Texte intégralPolycomb group (PcG) proteins are critical epigenetic repressors implicated in various developmental and cellular processes. While the Polycomb Repressive Complex 2 (PRC2) is evolutionary conserved and its functions extensively studied in Arabidopsis, the PRC1 complex composition and function remain still enigmatic in plants. Our work focuses on several Arabidopsis RING-domain proteins to unravel PRC1-like functions in the regulation of various processes during plant development. Based on sequence similarity we identified three homologues of the animal PRC1 core subunit BMI1: AtBMI1a, AtBMI1b and AtBMI1c. These proteins were found to interact with other PRC1-like components, AtRING1a, AtRING1b and LHP1. Genetic and molecular analyses demonstrated that AtBMI1a/b and AtRING1a/b play crucial roles in stable repression of embryonic traits to allow proper somatic growth. Comparative transcriptome analyses were performed to uncover genetic networks underlying seedling growth and the flower development defects of several different PRC1-like and PRC2 Arabidopsis mutants. Our data revealed overlapping and non-overlapping gene categories of misregulated genes in Atring1a/b, Atbmi1a/b and lhp1 mutants. The Atring1a/b mutant showed particular disturbed expression of flower developmental genes. Accordingly, phenotypic and molecular analyses of the mutant flowers confirmed that AtRING1a/b play a critical role in cell fate determination and in different aspects of flower development. To better understand the broad function of AtRING1a/b, we performed yeast two-hybrid screen and identified PHD-domain proteins of the ALFIN-LIKE (AL) family as binding partners. In vitro AL proteins bind the active mark for gene transcription, H3K4me3. By various methods, both in vitro and in planta, we provided strong evidence for the physical interaction between AL and PRC1 RING-domain proteins. We uncovered that al6/7 similar to Atbmi1a/b mutants exhibit seed germination defects, which are associated with the derepression of several seed related genes. Consistently on the corresponding chromatin a delay of the remodeling from active H3K4me3 labeled to a repressive H3K27me3 marked chromatin could be detected. We propose that through binding to H3K4me3 AL6/7 function as scaffold proteins to target PRC1 RING-domain proteins to active chromatin in order to establish gene silencing. Taken together, the presented work contributes significantly to the knowledge of PRC1 complex(es) in Arabidopsis at both biological function and complex composition levels. It opens several exciting perspectives for future research in the field
Netter, Sophie. « Identification d'un nouveau complexe de genes a homeoboite cible des proteines des groupes polycomb et trithorax : le complexe iroquois ». Paris 6, 1998. http://www.theses.fr/1998PA066258.
Texte intégralCedrone, L. « THE ROLE OF ENHANCED POLYCOMB REPRESSIVE COMPLEX 2 ACTIVITY IN TUMORIGENESIS ». Doctoral thesis, Università degli Studi di Milano, 2017. http://hdl.handle.net/2434/468289.
Texte intégralJacobs, Chean Sern. « Role of PRC2-mediated chromatin regulation in fine tuning Arabidopsis root development ». Thesis, Lyon, 2020. http://www.theses.fr/2020LYSEN085.
Texte intégralChromatin-based mechanisms are pivotal regulators of transcriptional patterns that are central to cell fate determination, organogenesis and development in multicellular organisms. The activity of Polycomb Repressive Complex 2 (PRC2) is involved in the maintenance of transcriptional gene repression by catalysing the trimethylation of histone H3 on lysine 27 at specific loci, and is a conserved modulator of developmental programs.To reveal the extent to which PRC2 shapes transcriptional decisions during cell fate specification, I have characterized the epigenome organization of a single cell type from the root stem cell niche (SCN). Quantitative integration of (epi)-genomic data revealed three main chromatin states that correlate with distinct gene expression levels as well as patterns along the differentiation gradient. These results indicate that PRC2 activity over specific genes within the SCN regulates their timing of expression in daughter cells, at successive differentiation stages.In addition, functional studies of PRC2 catalytic subunit homologues support the notion that distinct PRC2 complexes with different compositions cooperate to fine-tune the transcriptional regulation of key regulatory genes during root development. Taken together, this work highlights the importance of PRC2-regulated chromatin states in shaping expression patterns along a differentiation gradient. They also pinpoint the potential of such epigenetic studies in predicting, from an initial chromatin state, the timing of gene transcriptional activation in subsequent differentiation stages
LA, MASTRA FEDERICA. « POLYCOMB GROUP PROTEINS RING1A/RING1B CONTROL PERIPHERAL B CELL HOMEOSTASIS AND TERMINAL DIFFERENTIATION ». Doctoral thesis, Università degli Studi di Milano, 2019. http://hdl.handle.net/2434/609574.
Texte intégralBrule, Baptiste. « Caractérisation et modulation non pharmacologique des dérégulations épigénétiques associées à la maladie de Huntington : vers l’identification de nouvelles cibles thérapeutiques ». Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAJ015.
Texte intégralHuntington's disease (HD) is a neurodegenerative genetic disease characterized by motor, cognitive, and psychiatric disorders caused by primary damage to the striatum. The pathogenic mechanism is complex and involve epigenetic and transcriptional dysregulations leading to a loss of neuronal identity and cell function. This thesis aimed to characterize the striatal epigenetic signature in mouse models with a celltype-specific resolution at different stages of HD. We observed that striatal neurons expressing the HD mutation undergo epigenetic erosion, reflecting accelerated aging in HD, induced by alterations in polycomb complexes. As epigenetic regulations are sensitive to the environment, we characterized the behavioral phenotype and molecular alterations of HD mouse model after housing in an enriched environment (EE) to decipher the epigenetic and transcriptomic effects induced by EE. Our findings thus provide a better understanding of early pathogenic mechanisms in HD, opening new therapeutic perspectives
Schivre, Geoffrey. « Transcriptome augmentation, Polycomb-mediated chromatin dynamics and their links to metabolism during Arabidopsis thaliana photomorphogenesis ». Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASB014.
Texte intégralLight fuels plant photosynthesis providing the energy source for growth. Light intensity and quality also convey essential information on the plant's immediate surroundings, which are integrated through multiple light sensors, the photoreceptors, enabling developmental and physiological adaptations. The photomorphogenic transition, or de-etiolation, occurs when a young germinating plantlet is exposed to light for the first time, and is one of the most spectacular plant developmental adaptations to light. Seedlings germinating underground, protected from light, undergo an etiolated development, or skotomorphogenesis, during which rapid hypocotyl elongation facilitates plant drilling through the soil, while cotyledon maturation is arrested and the plantlet remains non-photosynthetic. In the absence of photosynthesis, skotomorphogenic growth relies entirely on the plant metabolic reserves, predominantly stored in cotyledons. Upon reaching the soil surface, photoreceptor light sensing triggers the expansion and greening of cotyledons, independently from cell divisions. Inducing chloroplast biogenesis and the acquisition of photosynthesis, this developmental switch marks the transition toward photo-autotrophy. At the molecular scale, cotyledon de-etiolation associates with a specialization of the transcriptome and an intensification of RNA polymerase II (RNA Pol II) activity. At the cytological scale, chromatin rearrangements lead to nucleus enlargement and the condensation of pericentromeric regions in conspicuous heterochromatic foci. Considering that much of these metabolic, cellular, molecular and cytological controls are synchronously achieved during the transition, A. thaliana photomorphogenesis is a model of choice to characterize the interplays between light signaling, gene regulation and chromatin dynamics as well as their link to the plant energetic status. During my thesis, I first contributed to develop an RNA-seq normalization methodology to revisit transcriptome changes in light of the global increase in RNA Pol II activity. This identified a 2-fold increase in transcript abundance during cotyledon photomorphogenesis, which most likely results from the increase in RNA Pol II activity. I further explored the role played by the conserved metabolic sensor Target Of Rapamycin (TOR) in defining the transcriptional regime along with chromatin composition and organization during cotyledon photomorphogenesis. This notably shed a new light on the functional links between the TOR pathway and the homeostasis of a specific histone mark, trimethylation of histone H3 at lysine 27 (H3K27me3), mediated by Polycomb Repressive Complex 2 (PRC2). More precisely, this study revealed that H3K27me3 is less abundant at chromatin in etiolated cotyledons as compared to photomorphogenic ones, a global effect that was further shown here to be sensitive to sugar and TOR signaling. Hence, this work points towards unexpected roles of TOR signaling and the PRC2-regulated mark H3K27me3 in the global regulation of transcription and opens new perspectives on TOR-mediated gene regulation. Future studies aimed at deciphering the role of H3K27me3 homeostasis, especially at specific genes induced by light, should provide new insight on how metabolic signaling interplays with Polycomb-mediated chromatin dynamics and transcription with implications beyond plant photomorphogenesis
Lamiable, Olivier. « Identification et caractérisation des partenaires protéiques de DSP1 chez Drosophila melanogaster ». Phd thesis, Université d'Orléans, 2010. http://tel.archives-ouvertes.fr/tel-00558801.
Texte intégralLivres sur le sujet "Complexe polycomb"
Coleman, Rory Tristan. Making Memories : Modes and Mechanisms of Gene Silencing by the Polycomb Repressive Complexes in Drosophila. [New York, N.Y.?] : [publisher not identified], 2017.
Trouver le texte intégralChapitres de livres sur le sujet "Complexe polycomb"
Brahmachari, Vani, et Shruti Jain. « Polycomb Complexes ». Dans Encyclopedia of Systems Biology, 1720. New York, NY : Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_854.
Texte intégralPalacios, Daniela. « The Dynamics of Polycomb Complexes ». Dans Methods in Molecular Biology, 139–42. New York, NY : Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6380-5_12.
Texte intégralGuo, Yiran, Yao Yu et Gang Greg Wang. « Polycomb Repressive Complex 2 in Oncology ». Dans Cancer Treatment and Research, 273–320. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-45654-1_9.
Texte intégralDuarte-Aké, Fátima, Geovanny Nic-Can et Clelia De-la-Peña. « Somatic Embryogenesis : Polycomb Complexes Control Cell-to-Embryo Transition ». Dans Epigenetics in Plants of Agronomic Importance : Fundamentals and Applications, 339–54. Cham : Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-14760-0_13.
Texte intégralVidal, Miguel. « Polycomb Complexes : Chromatin Regulators Required for Cell Diversity and Tissue Homeostasis ». Dans Transcriptional and Epigenetic Mechanisms Regulating Normal and Aberrant Blood Cell Development, 95–139. Berlin, Heidelberg : Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-45198-0_5.
Texte intégralLiu, Xin. « A Structural Perspective on Gene Repression by Polycomb Repressive Complex 2 ». Dans Subcellular Biochemistry, 519–62. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58971-4_17.
Texte intégralParo, Renato, Ueli Grossniklaus, Raffaella Santoro et Anton Wutz. « Cellular Memory ». Dans Introduction to Epigenetics, 49–66. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68670-3_3.
Texte intégralShirai, Manabu, Yoshihiro Takihara et Takayuki Morisaki. « Pcgf5 Contributes to PRC1 (Polycomb Repressive Complex 1) in Developing Cardiac Cells ». Dans Etiology and Morphogenesis of Congenital Heart Disease, 305–12. Tokyo : Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-54628-3_43.
Texte intégralLuo, Ming, Mingzhu Luo, Fred Berger, E. S. Dennis, Jim W. Peacock et Abed Chaudhury. « DNA-METHYLTRANSFERASE 1 is a Member of FIS Polycomb Complex and is Involved in Seed Development in Arabidopsis ». Dans Biotechnology and Sustainable Agriculture 2006 and Beyond, 131–33. Dordrecht : Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6635-1_16.
Texte intégralPirrotta, V. « Global Functions of PRC2 Complexes ». Dans Polycomb Group Proteins, 317–48. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-809737-3.00013-1.
Texte intégralActes de conférences sur le sujet "Complexe polycomb"
Iwata, Shintaro. « Abstract 4898 : Polycomb group molecule PHC3 regulates polycomb complex composition and prognosis of osteosarcoma ». Dans Proceedings : AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010 ; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4898.
Texte intégralCao, Qi, Ram Mani, Bushra Ateeq, Saravana M. Dhanasekaren, Irfan Asangani, Jindan Yu, John Prensner et al. « Abstract 2795 : An onco-protein axis linking polycomb repressive complex 2 and polycomb repressive complex 1 through miRNAs in cancer ». Dans Proceedings : AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011 ; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-2795.
Texte intégralWilson, Boris G., Xi Wang, Xiaohua Shen, Elizabeth S. McKenna, Madeleine E. Lemieux, Yoon-Jae Cho, Edward C. Koelhoffer, Scott L. Pomeroy, Stuart H. Orkin et Charles W. M. Roberts. « Abstract LB-237 : Epigenetic antagonism between Polycomb and SWI/SNF complexes duringoncogenic transformation ». Dans Proceedings : AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011 ; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-lb-237.
Texte intégralWilson, Boris G., Xiaohua Shen, Elizabeth S. McKenna, Xi Wang, Yoon-Jae Cho, Edward C. Koellhoffer, Phuong T. L. Nguyen, Scott L. Pomeroy, Stuart H. Orkin et Charles W. M. Roberts. « Abstract 4799 : Epigenetic antagonism between Polycomb and SWI/SNF complexes during oncogenic transformation ». Dans Proceedings : AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010 ; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4799.
Texte intégralZHU, Junyu, Lili Li, Connie W. Hui, Joanna H. Tong, Raymond Chan, Chi Hang Wong, Qiyong Ai et al. « Abstract 2923 : Targeting the polycomb repressive complex-2 related proteins in nasopharyngeal carcinoma ». Dans Proceedings : AACR Annual Meeting 2020 ; April 27-28, 2020 and June 22-24, 2020 ; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-2923.
Texte intégralChen, Fan, et Christine F. Brainson. « Abstract 5189 : Activity of polycomb repressive complex 2 determines sensitivity to epigenetic therapy ». Dans Proceedings : AACR Annual Meeting 2019 ; March 29-April 3, 2019 ; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-5189.
Texte intégralChen, Fan, et Christine F. Brainson. « Abstract 5189 : Activity of polycomb repressive complex 2 determines sensitivity to epigenetic therapy ». Dans Proceedings : AACR Annual Meeting 2019 ; March 29-April 3, 2019 ; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-5189.
Texte intégralCao, Qi, Xiaoju Wang, Meng Zhao, Rendong Yang, Rohit Malik, Yuanyuan Qiao, Anton Poliakov et al. « Abstract LB-132 : The central role of EED in orchestration of polycomb group complexes ». Dans Proceedings : AACR Annual Meeting 2014 ; April 5-9, 2014 ; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-lb-132.
Texte intégralLi, Yajun, Beth O. Van Emburgh, Bilian Jin et Keith D. Robertson. « Abstract 4868 : Interaction between DNMT3B and polycomb repression complexes and their role in histone modification ». Dans Proceedings : AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010 ; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4868.
Texte intégralJunco, Sarah E., Vivian J. Bardwell, Chongwoo A. Kim, Renjing Wang, Angela Robinson, Udayar Ilangovan, Alex Taylor et al. « Abstract C28 : Binding to BCOR defines a subfamily of Psc ortholog mediated polycomb group complexes ». Dans Abstracts : Second AACR International Conference on Frontiers in Basic Cancer Research--Sep 14-18, 2011 ; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.fbcr11-c28.
Texte intégralRapports d'organisations sur le sujet "Complexe polycomb"
Ohad, Nir, et Robert Fischer. Regulation of plant development by polycomb group proteins. United States Department of Agriculture, janvier 2008. http://dx.doi.org/10.32747/2008.7695858.bard.
Texte intégralOhad, Nir, et Robert Fischer. Regulation of Fertilization-Independent Endosperm Development by Polycomb Proteins. United States Department of Agriculture, janvier 2004. http://dx.doi.org/10.32747/2004.7695869.bard.
Texte intégralOhad, Nir, et Robert Fischer. Control of Fertilization-Independent Development by the FIE1 Gene. United States Department of Agriculture, août 2000. http://dx.doi.org/10.32747/2000.7575290.bard.
Texte intégralOri, Naomi, et Mark Estelle. Specific mediators of auxin activity during tomato leaf and fruit development. United States Department of Agriculture, janvier 2012. http://dx.doi.org/10.32747/2012.7597921.bard.
Texte intégral