Modulation of ATP-Dependent Chromatin-Remodeling Complexes by Inositol Polyphosphates

Inositol trisphosphate and calcium signalling

Berridge, M. J. (1993) · Nature · doi:10.1038/361315a0 · Cited by 6,545 · see citing works

A chromatin remodelling complex involved in transcription and DNA processing

Shen, X., Mizuguchi, G., Hamiche, A., & Wu, C. (2000) · Nature · doi:10.1038/35020123 · Cited by 807 · see citing works

ATP-Dependent Nucleosome Remodeling

Becker, P. B., & Hörz, W. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135400 · Cited by 790 · see citing works

Rapid and Phosphoinositol-Dependent Binding of the SWI/SNF-like BAF Complex to Chromatin after T Lymphocyte Receptor Signaling

Zhao, K., Wang, W., Rando, O. J., Xue, Y., Swiderek, K. M., Kuo, A., & Crabtree, G. R. (1998) · Cell · doi:10.1016/s0092-8674(00)81633-5 · Cited by 718 · see citing works

Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions

Eisen, J. A., Sweder, K., & Hanawalt, P. C. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.14.2715 · Cited by 712 · see citing works

A Phospholipase C-Dependent Inositol Polyphosphate Kinase Pathway Required for Efficient Messenger RNA Export

York, J. D., John, A. R. O., Murphy, R., Ives, E. B., & Wente, S. R. (1999) · Science · doi:10.1126/science.285.5424.96 · Cited by 547 · see citing works

Nuclear Actin and Actin-Related Proteins in Chromatin Remodeling

Olave, I. A., Reck‐Peterson, S. L., & Crabtree, G. R. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135507 · Cited by 395 · see citing works

A Role for Nuclear Inositol 1,4,5-Trisphosphate Kinase in Transcriptional Control

Odom, A. R., Stahlberg, A., Wente, S. R., & York, J. D. (2000) · Science · doi:10.1126/science.287.5460.2026 · Cited by 394 · see citing works

Whole-genome expression analysis of <i>snf/swi</i> mutants of <i>Saccharomyces</i> <i>cerevisiae</i>

Sudarsanam, P., Iyer, V. R., Brown, P. O., & Winston, F. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3364 · Cited by 389 · see citing works

Characterization of the Imitation Switch subfamily of ATP-dependent chromatin-remodeling factors in Saccharomyces cerevisiaePreprint

Tsukiyama, T., Palmer, J. M., Landel, C. C., Shiloach, J., & Wu, C. (1999) · Genes & Development · doi:10.1101/gad.13.6.686 · Cited by 388 · see citing works

Regulation of Chromatin Remodeling by Inositol Polyphosphates

Steger, D. J., Haswell, E. S., Miller, A. L., Wente, S. R., & O'Shea, E. K. (2003) · Science · doi:10.1126/science.1078062 · Cited by 352 · see citing works

ATP-Dependent Histone Octamer Sliding Mediated by the Chromatin Remodeling Complex NURF

Hamiche, A., Sandaltzopoulos, R., Gdula, D. A., & Wu, C. (1999) · Cell · doi:10.1016/s0092-8674(00)80796-5 · Cited by 339 · see citing works

The Isw2 Chromatin Remodeling Complex Represses Early Meiotic Genes upon Recruitment by Ume6p

Goldmark, J. P., Fazzio, T. G., Estep, P. W., Church, G. M., & Tsukiyama, T. (2000) · Cell · doi:10.1016/s0092-8674(00)00134-3 · Cited by 300 · see citing works

Significance of PIP2 hydrolysis and regulation of phospholipase C isozymes

Lee, S. B., & Rhee, S. G. (1995) · Current Opinion in Cell Biology · doi:10.1016/0955-0674(95)80026-3 · Cited by 290 · see citing works

Binding of Inositol Phosphate to DNA-PK and Stimulation of Double-Strand Break Repair

Hanakahi, L. A., Bartlet‐Jones, M., Chappell, C., Pappin, D., & West, S. C. (2000) · Cell · doi:10.1016/s0092-8674(00)00061-1 · Cited by 263 · see citing works

Dual Functions of Largest NURF Subunit NURF301 in Nucleosome Sliding and Transcription Factor Interactions

Xiao, H., Sandaltzopoulos, R., Wang, H.-M., Hamiche, A., Ranallo, R. T., Lee, K.-M., Fu, D., & Wu, C. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00345-8 · Cited by 259 · see citing works

1l-myo-Inositol-1-phosphate synthase

Majumder, A. L., Johnson, M. D., & Henry, S. A. (1997) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/s0005-2760(97)00122-7 · Cited by 200 · see citing works

Modulation of HIV-like particle assembly in vitro by inositol phosphates

Campbell, S., Fisher, R. J., Towler, E. M., Fox, S. D., Issaq, H. J., Wolfe, T. L., Phillips, L. R., & Rein, A. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191224698 · Cited by 199 · see citing works

Assessing the omnipotence of inositol hexakisphosphate

Shears, S. B. (2001) · Cellular Signalling · doi:10.1016/s0898-6568(01)00129-2 · Cited by 188 · see citing works

A functional interaction between the C-terminal domain of RNA polymerase II and the negative regulator SIN1

Peterson, C. L., Kruger, W. D., & Herskowitz, I. (1991) · Cell · doi:10.1016/0092-8674(91)90268-4 · Cited by 174 · see citing works

The product of the SNF2/SWI2 paralogue INO80 of Saccharomyces cerevisiae required for efficient expression of various yeast structural genes is part of a high‐molecular‐weight protein complex

Ebbert, R., Birkmann, A., & Schüller, H. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01390.x · Cited by 159 · see citing works

Inositol polyphosphate multikinase (ArgRIII) determines nuclear mRNA export in<i>Saccharomyces cerevisiae</i>

Saiardi, A., Caffrey, J. J., Snyder, S. H., & Shears, S. B. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01194-7 · Cited by 139 · see citing works

The Many Faces of Chromatin Remodeling

Fyodorov, D. V., & Kadonaga, J. T. (2001) · Cell · doi:10.1016/s0092-8674(01)00478-0 · Cited by 137 · see citing works

Observation of inositol pentakis- and hexakis-phosphates in mammalian tissues by 31P NMR

Szwergold, B. S., Graham, R. A., & Brown, T. R. (1987) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(87)90489-x · Cited by 130 · see citing works

Specific interaction of IP6 with human Ku70/80, the DNA‐binding subunit of DNA‐PK

Hanakahi, L. A., & West, S. C. (2002) · The EMBO Journal · doi:10.1093/emboj/21.8.2038 · Cited by 109 · see citing works

Comparison of the levels of inositol metabolites in transformed haemopoietic cells and their normal counterparts

Bunce, C. M., French, P. J., Allen, P., Mountford, J. C., Moor, B., Greaves, M. F., Michell, R. H., & Brown, G. (1993) · Biochemical Journal · doi:10.1042/bj2890667 · Cited by 84 · see citing works

Changes in the levels of inositol lipids and phosphates during the differentiation of HL60 promyelocytic cells towards neutrophils or monocytes

French, P. J., Bunce, C. M., Stephens, L. R., Lord, J. M., McConnell, F. M., Brown, G., Creba, J. A., & Michell, R. H. (1991) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1991.0109 · Cited by 66 · see citing works

Transcriptional regulation: a new dominion for inositol phosphate signaling?

Shears, S. B. (2000) · BioEssays · doi:10.1002/1521-1878(200009)22:9 · Cited by 28 · see citing works

New hypotheses for the health-protective mechanisms of whole-grain cereals: what is beyond fibre?

Fardet, A. (2010) · Nutrition Research Reviews · doi:10.1017/s0954422410000041 · Cited by 1,030 · see citing works

Molecular views of recombination proteins and their control

West, S. C. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1127 · Cited by 947 · see citing works

Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics

Kadoch, C., & Crabtree, G. R. (2015) · Science Advances · doi:10.1126/sciadv.1500447 · Cited by 843 · see citing works

The Nucleosome

Khorasanizadeh, S. (2004) · Cell · doi:10.1016/s0092-8674(04)00044-3 · Cited by 672 · see citing works

INO80 and γ-H2AX Interaction Links ATP-Dependent Chromatin Remodeling to DNA Damage Repair

Morrison, A. J., Highland, J., Krogan, N. J., Arbel‐Eden, A., Greenblatt, J., Haber, J. E., & Shen, X. (2004) · Cell · doi:10.1016/j.cell.2004.11.037 · Cited by 567 · see citing works

Structure of Hdac3 Bound to Co-Repressor and Inositol Tetraphosphate

Watson, P. J., Fairall, L., Santos, G. M., & Schwabe, J. W. R. (2012) · Nature · doi:10.1038/nature10728 · Cited by 505 · see citing works

The macro domain is an ADP‐ribose binding module

Karras, G. I., Kustatscher, G., Buhecha, H. R., Allen, M. D., Pugieux, C., Sait, F., Bycroft, M., & Ladurner, A. G. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600664 · Cited by 502 · see citing works

Molecular Evidence for Mitochondrial Dysfunction in Bipolar Disorder

Konradi, C. L., Eaton, M. E., MacDonald, M. L., Walsh, J. P., Benes, F. M., & Heckers, S. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.3.300 · Cited by 499 · see citing works

Control of aldosterone secretion: a model for convergence in cellular signaling pathways

SPÄT, A., & HUNYADY, L. (2004) · Physiological Reviews · doi:10.1152/physrev.00030.2003 · Cited by 494 · see citing works

The PHD Finger of the Chromatin-Associated Protein ING2 Functions as a Nuclear Phosphoinositide Receptor

Gozani, O., Karuman, P., Jones, D. R., Ivanov, D., Cha, J., Lugovskoy, A. A., Baird, C. L., Zhu, H., Field, S. J., Lessnick, S. L., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00480-x · Cited by 487 · see citing works

myo-Inositol-1,2,3,4,5,6-hexakisphosphate

Raboy, V. (2003) · Phytochemistry · doi:10.1016/s0031-9422(03)00446-1 · Cited by 475 · see citing works

Molecular signature of human embryonic stem cells and its comparison with the mouse

Sato, N., Muñoz-Sanjuán, I., Heke, M., Uchida, M., Naef, F., & Brivanlou, A. H. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00256-2 · Cited by 469 · see citing works

Trithorax group proteins: switching genes on and keeping them active

Schuettengruber, B., Martinez, A., Iovino, N., & Cavalli, G. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3230 · Cited by 454 · see citing works

Inositol Hexakisphosphate Is Bound in the ADAR2 Core and Required for RNA Editing

Macbeth, M. R., Schubert, H., VanDemark, A. P., Lingam, A. T., Hill, C. P., & Bass, B. (2005) · Science · doi:10.1126/science.1113150 · Cited by 428 · see citing works

Regulated nucleosome mobility and the histone code

Cosgrove, M. S., Boeke, J. D., & Wolberger, C. (2004) · Nature Structural & Molecular Biology · doi:10.1038/nsmb851 · Cited by 421 · see citing works

An epigenetic view of helper T cell differentiation

Ansel, K. M., Lee, D. U., & Rao, A. (2003) · Nature Immunology · doi:10.1038/ni0703-616 · Cited by 419 · see citing works

Nuclear lipid signalling

Irvine, R. F. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1100 · Cited by 403 · see citing works

Gene Recruitment of the Activated INO1 Locus to the Nuclear Membrane

Brickner, J. H., & Walter, P. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020342 · Cited by 401 · see citing works

H2A.Z-Mediated Localization of Genes at the Nuclear Periphery Confers Epigenetic Memory of Previous Transcriptional State

Brickner, D. G., Cajigas, I., Fondufe‐Mittendorf, Y. N., Ahmed, S. A. A., Lee, P., Widom, J., & Brickner, J. H. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050081 · Cited by 390 · see citing works

Approaches and challenges to engineering seed phytate and total phosphorus

Raboy, V. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.06.012 · Cited by 385 · see citing works

Repair of DNA double strand breaks by non-homologous end joining

Lees‐Miller, S. P. (2003) · Biochimie · doi:10.1016/j.biochi.2003.10.011 · Cited by 367 · see citing works

Myo-inositol and beyond – Emerging networks under stress

Valluru, R., & den Ende, W. V. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.07.009 · Cited by 353 · see citing works

Regulation of Chromatin Remodeling by Inositol Polyphosphates

Steger, D. J., Haswell, E. S., Miller, A. L., Wente, S. R., & O'Shea, E. K. (2003) · Science · doi:10.1126/science.1078062 · Cited by 352 · see citing works

Recent advances in understanding chromatin remodeling by Swi/Snf complexes

Martens, J. A., & Winston, F. (2003) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(03)00022-4 · Cited by 352 · see citing works

Chromatin remodelling beyond transcription: the INO80 and SWR1 complexes

Morrison, A. J., & Shen, X. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2693 · Cited by 311 · see citing works

Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export

Weirich, C. S., Erzberger, J. P., Flick, J. S., Berger, J. M., Thorner, J. W., & Weis, K. (2006) · Nature Cell Biology · doi:10.1038/ncb1424 · Cited by 285 · see citing works

Chromatin dynamics at DNA replication, transcription and repair

Ehrenhofer‐Murray, A. E. (2004) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.2004.04162.x · Cited by 275 · see citing works

Insights into the activation mechanism of class I HDAC complexes by inositol phosphates

Watson, P. J., Millard, C. J., Riley, A. M., Robertson, N. S., Wright, L. C., Godage, H. Y., Cowley, S. M., Jamieson, A. G., Potter, B. V. L., & Schwabe, J. W. R. (2016) · Nature Communications · doi:10.1038/ncomms11262 · Cited by 244 · see citing works

A Mammalian Chromatin Remodeling Complex with Similarities to the Yeast INO80 Complex

Jin, J., Cai, Y., Yao, T., Gottschalk, A. J., Florens, L. A., Swanson, S. K., Gutiérrez, J. L., Coleman, M. K., Workman, J. L., Mushegian, A. R., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509128200 · Cited by 235 · see citing works

The maize low‐phytic acid 3 encodes a myo‐inositol kinase that plays a role in phytic acid biosynthesis in developing seeds

Shi, J., Wang, H., Hazebroek, J. P., Ertl, D., & Harp, T. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02412.x · Cited by 216 · see citing works

Lithium and bipolar mood disorder: the inositol-depletion hypothesis revisited

Harwood, A. J. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001618 · Cited by 208 · see citing works

The nucleoskeleton: lamins and actin are major players in essential nuclear functions

Shumaker, D. K. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(03)00050-4 · Cited by 195 · see citing works

The INO80 chromatin remodeling complex in transcription, replication and repair

Conaway, R. C., & Conaway, J. W. (2008) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2008.10.010 · Cited by 194 · see citing works

Myo-Inositol and Its Derivatives: Their Emerging Role in the Treatment of Human Diseases

Chhetri, D. R. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01172 · Cited by 189 · see citing works

Pharmacodynamics and pharmacokinetics of inositol(s) in health and disease

Bizzarri, M., Fuso, A., Dinicola, S., Cucina, A., & Bevilacqua, A. (2016) · Expert Opinion on Drug Metabolism & Toxicology · doi:10.1080/17425255.2016.1206887 · Cited by 185 · see citing works

How versatile are inositol phosphate kinases?

Shears, S. B. (2004) · Biochemical Journal · doi:10.1042/bj20031428 · Cited by 173 · see citing works

RNAi-mediated silencing of the myo-inositol-1-phosphate synthase gene (GmMIPS1) in transgenic soybean inhibited seed development and reduced phytate content

Nunes, A. C. S., Vianna, G. R., Cúneo, F., Amaya‐Farfán, J., de Capdeville, G., Rech, E. L., & Aragão, F. J. L. (2006) · Planta · doi:10.1007/s00425-005-0201-0 · Cited by 169 · see citing works

Regulation of nuclear processes by inositol polyphosphates

York, J. D. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.04.014 · Cited by 168 · see citing works

A role for inositol hexakisphosphate in the maintenance of basal resistance to plant pathogens

Murphy, A. M., Otto, B., Brearley, C. A., Carr, J. P., & Hanke, D. E. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03629.x · Cited by 165 · see citing works

Roles of inositol phosphates and inositol pyrophosphates in development, cell signaling and nuclear processes

Tsui, M. M. K., & York, J. D. (2009) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2009.12.002 · Cited by 162 · see citing works

The Arabidopsis homolog of trithorax, ATX1, binds phosphatidylinositol 5-phosphate, and the two regulate a common set of target genes

Álvarez-Venegas, R., Sadder, M. T., Hlavačka, A., Baluška, F., Xia, Y., Lu, G., Firsov, A., Sarath, G., Moriyama, H., DUBROVSKY, J. G., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600944103 · Cited by 161 · see citing works

Nuclear bodies and compartments: functional roles and cellular signalling in health and disease

Zimber, A., Nguyen, Q., & Gespach, C. P. (2004) · Cellular Signalling · doi:10.1016/j.cellsig.2004.03.020 · Cited by 159 · see citing works

Unwinding chromatin for development and growth: a few genes at a time

Kwon, C. S., & Wagner, D. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.05.010 · Cited by 155 · see citing works

Sequential Roles of Brg, the ATPase Subunit of BAF Chromatin Remodeling Complexes, in Thymocyte Development

Chi, T. H., Wan, M., Lee, P. P., Akashi, K., METZGER, D., Chambon, P., Wilson, C. B., & Crabtree, G. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00199-7 · Cited by 155 · see citing works

Inositol Diphosphate Signaling Regulates Telomere Length

York, S. J., Armbruster, B. N., Greenwell, P. W., Petes, T. D., & York, J. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m412070200 · Cited by 153 · see citing works

Ca2+-Operated Transcriptional Networks: Molecular Mechanisms and In Vivo Models

Mellström, B., Savignac, M., Gómez‐Villafuertes, R., & Naranjo, J. R. (2008) · Physiological Reviews · doi:10.1152/physrev.00041.2005 · Cited by 152 · see citing works

Mechanisms for ATP-dependent chromatin remodelling: farewell to the tuna-can octamer?

Flaus, A., & Owen‐Hughes, T. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.01.007 · Cited by 152 · see citing works

Nuclear phosphoinositides: a signaling enigma wrapped in a compartmental conundrum

Barlow, C. A., Laishram, R. S., & Anderson, R. A. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.09.009 · Cited by 140 · see citing works

An Essential Role for an Inositol Polyphosphate Multikinase, Ipk2, in Mouse Embryogenesis and Second Messenger Production

Frederick, J. P., Mattiske, D., Wofford, J. A., Megosh, L. C., Drake, L. Y., Chiou, S.-T., Hogan, B. L. M., & York, J. D. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503706102 · Cited by 139 · see citing works

Arabidopsis inositol pentakisphosphate 2‐kinase, A t IPK 1, is required for growth and modulates phosphate homeostasis at the transcriptional level

Kuo, H., Chang, T., Chiang, S., Wang, W., Charng, Y., & Chiou, T. (2014) · The Plant Journal · doi:10.1111/tpj.12650 · Cited by 138 · see citing works

Seed Biofortification and Phytic Acid Reduction: A Conflict of Interest for the Plant?

Sparvoli, F., & Cominelli, E. (2015) · Plants · doi:10.3390/plants4040728 · Cited by 135 · see citing works

Yeast phosphatidylinositol 4-kinase, Pik1, has essential roles at the Golgi and in the nucleus

Strahl, T., Hama, H., DeWald, D. B., & Thorner, J. W. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200504104 · Cited by 130 · see citing works

Regulation of HIV-1 latency by T-cell activation

Williams, S. A., & Greene, W. C. (2007) · Cytokine · doi:10.1016/j.cyto.2007.05.017 · Cited by 122 · see citing works

A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase

Sei, Y., Zhao, X., Forbes, J., Szymczak, S., Li, Q., Trivedi, A., Voellinger, M., Joy, G., Feng, J., Whatley, M., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.04.008 · Cited by 119 · see citing works

The response to inositol: Regulation of glycerolipid metabolism and stress response signaling in yeast

Henry, S. A., Gaspar, M. L., & Jesch, S. A. (2014) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2013.12.013 · Cited by 118 · see citing works

CD4/CD8-lineage differentiation in the thymus: from nuclear effectors to membrane signals

Bosselut, R. (2004) · Nature reviews. Immunology · doi:10.1038/nri1392 · Cited by 118 · see citing works

Characterization of a Selective Inhibitor of Inositol Hexakisphosphate Kinases

Padmanabhan, U., Dollins, D. E., Fridy, P. C., York, J. D., & Downes, C. P. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900752200 · Cited by 117 · see citing works

Inositol Polyphosphates Regulate Zebrafish Left-Right Asymmetry

Sarmah, B., Latimer, A. J., Appel, B., & Wente, S. R. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.05.002 · Cited by 117 · see citing works

Phosphoinositide Signaling

Prestwich, G. D. (2004) · Chemistry & Biology · doi:10.1016/j.chembiol.2004.03.025 · Cited by 117 · see citing works

Direct Modification and Activation of a Nuclear Receptor–PIP ₂ Complex by the Inositol Lipid Kinase IPMK

Blind, R. D., Suzawa, M., & Ingraham, H. A. (2012) · Science Signaling · doi:10.1126/scisignal.2003111 · Cited by 117 · see citing works

INO80 chromatin remodeling complex promotes the removal of UV lesions by the nucleotide excision repair pathway

Jiang, Y., Wang, X., Bao, S., Guo, R., Johnson, D. G., Shen, X., & Li, L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008388107 · Cited by 113 · see citing works

Diverse role of phytic acid in plants and approaches to develop low-phytate grains to enhance bioavailability of micronutrients

Pramitha, L., Rana, S., Aggarwal, P., Ravikesavan, R., Joel, A. J., & Muthamilarasan, M. (2020) · Advances in genetics · doi:10.1016/bs.adgen.2020.11.003 · Cited by 112 · see citing works

Grow-ING, Age-ING and Die-ING: ING proteins link cancer, senescence and apoptosis

Russell, M., Berardi, P., Gong, W., & Riabowol, K. T. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.01.020 · Cited by 107 · see citing works

DNA damage responses in neural cells: Focus on the telomere

Zhang, P., Dilley, C. M., & Mattson, M. P. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.11.052 · Cited by 103 · see citing works

Stress-induced chromatin changes in plants: of memories, metabolites and crop improvement

Vriet, C., Hennig, L., & Laloi, C. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1792-z · Cited by 101 · see citing works

An evolving understanding of nuclear receptor coregulator proteins

Millard, C. J., Watson, P. J., Fairall, L., & Schwabe, J. W. R. (2013) · Journal of Molecular Endocrinology · doi:10.1530/jme-13-0227 · Cited by 101 · see citing works

Inositol phosphate synthesis and the nuclear processes they affect

Monserrate, J. P., & York, J. D. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.03.006 · Cited by 101 · see citing works

Inositol polyphosphates: a new frontier for regulating gene expression

Alcázar-Román, A. R., & Wente, S. R. (2007) · Chromosoma · doi:10.1007/s00412-007-0126-4 · Cited by 99 · see citing works

Broad Spectrum Anticancer Activity of Myo-Inositol and Inositol Hexakisphosphate

Bizzarri, M., Dinicola, S., Bevilacqua, A., & Cucina, A. (2016) · International Journal of Endocrinology · doi:10.1155/2016/5616807 · Cited by 99 · see citing works

The Glycine max Xylem Sap and Apoplast Proteome

Djordjevic, M. A., Oakes, M. P., Li, D. X., Hwang, C. H., Hocart, C. H., & Gresshoff, P. M. (2007) · Journal of Proteome Research · doi:10.1021/pr0606833 · Cited by 96 · see citing works

Rheostat Control of Gene Expression by Metabolites

Ladurner, A. G. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.09.002 · Cited by 95 · see citing works

Phospholipid metabolism and nuclear function: Roles of the lipin family of phosphatidic acid phosphatases

Siniossoglou, S. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2012.09.014 · Cited by 95 · see citing works

A Molecular Basis for Inositol Polyphosphate Synthesis in Drosophila melanogaster

Seeds, A. M., Sandquist, J. C., Spana, E. P., & York, J. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408295200 · Cited by 89 · see citing works

Gas chromatographic–mass spectrometric characterisation of plant gums in samples from painted works of art

Bonaduce, I., Brécoulaki, H., Colombini, M. P., Lluveras‐Tenorio, A., Restivo, V., & Ribechini, E. (2007) · Journal of Chromatography A · doi:10.1016/j.chroma.2007.10.056 · Cited by 89 · see citing works

Phosphatidylinositol biosynthesis: Biochemistry and regulation

Gardocki, M. E., Jani, N. M., & Lopes, J. M. (2005) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2005.05.006 · Cited by 89 · see citing works

Variable Reprogramming of the Pluripotent Stem Cell Marker Oct4 in Mouse Clones: Distinct Developmental Potentials in Different Culture Environments

Boiani, M., Gentile, L., Gambles, V., Cavaleri, F. M., Redi, C. A., & Schöler, H. R. (2005) · Stem Cells · doi:10.1634/stemcells.2004-0352 · Cited by 88 · see citing works

Metabolic intermediates selectively stimulate transcription factor interaction and modulate phosphate and purine pathwaysPreprint

Pinson, B., Vaur, S., Sagot, I., Coulpier, F., Lemoine, S., & Daignan‐Fornier, B. (2009) · Genes & Development · doi:10.1101/gad.521809 · Cited by 86 · see citing works

The Nucleosome Remodeling Factor

Alkhatib, S. G., & Landry, J. W. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.09.003 · Cited by 85 · see citing works

Enhanced Agrobacterium-mediated transformation efficiencies in monocot cells is associated with attenuated defense responses

Zhang, W., Dewey, R. E., Boss, W. F., Phillippy, B. Q., & Rongda Qu, A. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9997-8 · Cited by 84 · see citing works

A BAF-centred view of the immune system

Chi, T. H. (2004) · Nature reviews. Immunology · doi:10.1038/nri1501 · Cited by 84 · see citing works

Novel functions of the phosphatidylinositol metabolic pathway discovered by a chemical genomics screen with wortmannin

Zewail, A., Xie, M. W., Xing, Y., Lin, L., Zhang, P. F., Zou, W., Saxe, J. P., & Huang, J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0530118100 · Cited by 84 · see citing works

Transcriptional regulation of yeast phospholipid biosynthetic genes

Chen, M., Hancock, L. C., & Lopes, J. M. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.05.017 · Cited by 82 · see citing works

Nuclear phosphoinositides and their impact on nuclear functions

Shah, Z. H., Jones, D. R., Sommer, L., Foulger, R., Bultsma, Y., D’Santos, C. S., & Divecha, N. (2013) · FEBS Journal · doi:10.1111/febs.12543 · Cited by 81 · see citing works

Regulation of immune cell development through soluble inositol-1,3,4,5-tetrakisphosphate

Sauer, K., & Cooke, M. P. (2010) · Nature reviews. Immunology · doi:10.1038/nri2745 · Cited by 80 · see citing works

Diabetes-Induced Birth Defects: What Do We Know? What Can We Do?

Reece, E. A. (2011) · Current Diabetes Reports · doi:10.1007/s11892-011-0251-6 · Cited by 80 · see citing works

Chromatin remodeling by the SWI/SNF‐like BAF complex and STAT4 activation synergistically induce IL‐12Rβ2 expression during human Th1 cell differentiation

Letimier, F. A., Passini, N., Gasparian, S., Bianchi, E., & Rogge, L. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601586 · Cited by 79 · see citing works

Nuclear inositides: facts and perspectives

Martelli, A. M., Manzoli, L., & Cocco, L. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2003.10.003 · Cited by 79 · see citing works

Cellular regulators of protein kinase CK2

Montenarh, M. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1068-3 · Cited by 77 · see citing works

Nuclear lipids: key signaling effectors in the nervous system and other tissues

Ledeen, R. W., & Wu, G. (2004) · Journal of Lipid Research · doi:10.1194/jlr.r300015-jlr200 · Cited by 77 · see citing works

How to Achieve High-Quality Oocytes? The Key Role of Myo-Inositol and Melatonin

Vitale, S. G., Rossetti, P., Corrado, F., Rapisarda, A. M. C., Vignera, S. L., Condorelli, R. A., Valenti, G., Sapia, F., Laganà, A. S., & Buscema, M. (2016) · International Journal of Endocrinology · doi:10.1155/2016/4987436 · Cited by 74 · see citing works

Complex changes in cellular inositol phosphate complement accompany transit through the cell cycle

Barker, C. J., WRIGHT, J., Hughes, P., Kirk, C. J., & Michell, R. H. (2004) · Biochemical Journal · doi:10.1042/bj20031872 · Cited by 73 · see citing works

Inositol (1,4,5) trisphosphate 3 kinase B controls positive selection of T cells and modulates Erk activity

Wen, B. G., Pletcher, M. T., Warashina, M., Choe, S. H., Ziaee, N., Wiltshire, T., Sauer, K., & Cooke, M. P. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306907101 · Cited by 73 · see citing works

Linking lipids to chromatin

Jones, D. R., & Divecha, N. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.02.003 · Cited by 72 · see citing works

Differential Roles of the ChiB Chitinase in Autolysis and Cell Death of Aspergillus nidulans

Shin, K.-S., Kwon, N., Kim, Y. H., Park, H.-S., Kwon, G.-S., & Yu, J. (2009) · Eukaryotic Cell · doi:10.1128/ec.00368-08 · Cited by 72 · see citing works

Impact of Tat Genetic Variation on HIV-1 Disease

Li, L., Dahiya, S., Kortagere, S., Aiamkitsumrit, B., Cunningham, D., Pirrone, V., Nonnemacher, M. R., & Wigdahl, B. L. (2012) · Advances in Virology · doi:10.1155/2012/123605 · Cited by 72 · see citing works

Repression of Transcription by WT1-BASP1 Requires the Myristoylation of BASP1 and the PIP2-Dependent Recruitment of Histone Deacetylase

Toska, E., Campbell, H. A., Shandilya, J., Goodfellow, S. J., Shore, P., Medler, K. F., & Roberts, S. G. E. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.08.005 · Cited by 71 · see citing works

MYST opportunities for growth control: yeast genes illuminate human cancer gene functions

Lafon, A., Chang, C., Scott, E. M., Jacobson, S. J., & Pillus, L. (2007) · Oncogene · doi:10.1038/sj.onc.1210606 · Cited by 70 · see citing works

Specificity Determinants in Inositol Polyphosphate Synthesis: Crystal Structure of Inositol 1,3,4-Trisphosphate 5/6-Kinase

Miller, G. J., Wilson, M. P., Majerus, P. W., & Hurley, J. H. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.03.016 · Cited by 69 · see citing works

Structure of chromatin remodeler Swi2/Snf2 in the resting state

Xia, X., Liu, X., Li, T., Fang, X., & Chen, Z. (2016) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3259 · Cited by 67 · see citing works

Inositol Pyrophosphate Synthesis by Inositol Hexakisphosphate Kinase 1 Is Required for Homologous Recombination Repair

Jadav, R. S., Chanduri, M. V. L., Sengupta, S., & Bhandari, R. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.396556 · Cited by 66 · see citing works

Regulation of Chromatin Remodeling by Inositol Polyphosphates

Steger, D. J., Haswell, E. S., Miller, A. L., Wente, S. R., & O'Shea, E. K. (2003) · Science · doi:10.1126/science.1078062 · Cited by 352 · see citing works

Signal to reshape

Heinrichs, A. A. J. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1011 · Cited by 10 · see citing works

Inositol polyphosphates: a new frontier for regulating gene expression

Alcázar-Román, A. R., & Wente, S. R. (2007) · Chromosoma · doi:10.1007/s00412-007-0126-4 · Cited by 99 · see citing works

Inositol phosphate synthesis and the nuclear processes they affect

Monserrate, J. P., & York, J. D. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.03.006 · Cited by 101 · see citing works

The regulation of ATP-dependent nucleosome remodelling factors

Hogan, C., & Varga‐Weisz, P. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.07.010 · Cited by 46 · see citing works