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

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

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

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

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

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

Integrating the MAP kinase signal into the G1 phase cell cycle machinery

Roovers, K., & Assoian, R. K. (2000) · BioEssays · doi:10.1002/1521-1878(200009)22:9 · Cited by 475

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

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

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

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

Coupling Phosphate Homeostasis to Cell Cycle-Specific Transcription: Mitotic Activation of Saccharomyces cerevisiae PHO5 by Mcm1 and Forkhead Proteins

Pondugula, S., Neef, D. W., Voth, W. P., Darst, R. P., Dhasarathy, A., Reynolds, M., Takahata, S., Stillman, D. J., & Kladde, M. P. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00222-09 · Cited by 21

Structural analysis of the carboxy terminal PH domain of pleckstrin bound to D-myo-inositol 1,2,3,5,6-pentakisphosphate

Jackson, S. G., Zhang, Y. Q., Haslam, R. J., & Junop, M. S. (2007) · BMC Structural Biology · doi:10.1186/1472-6807-7-80 · Cited by 21

Toward understanding the role of the neuron-specific BAF chromatin remodeling complex in memory formation

Choi, K., Yoo, M., & Han, J. (2015) · Experimental & Molecular Medicine · doi:10.1038/emm.2014.129 · Cited by 20

Genome-wide transcriptome analyses of developing seeds from low and normal phytic acid soybean lines

Redekar, N. R., Biyashev, R. M., Jensen, R. V., Helm, R. F., Grabau, E. A., & Maroof, M. A. S. (2015) · BMC Genomics · doi:10.1186/s12864-015-2283-9 · Cited by 20

A Low Phytic Acid Barley Mutation Alters Seed Gene Expression

Bowen, D. E., Souza, E. J., Guttieri, M. J., Raboy, V., & Fu, J. (2007) · Crop Science · doi:10.2135/cropsci2006.07.0456tpg · Cited by 20

Phosphoinositides as Regulators of Protein-Chromatin Interactions

Viiri, K. M., Mäki, M., & Lohi, O. (2012) · Science Signaling · doi:10.1126/scisignal.2002917 · Cited by 19

Prolyl Oligopeptidase, Inositol Phosphate Signalling and Lithium Sensitivity

Harwood, A. J. (2011) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152711794653779 · Cited by 19

Yeast Phospholipase C Is Required for Normal Acetyl-CoA Homeostasis and Global Histone Acetylation

Galdieri, L. C., Chang, J. S., Mehrotra, S., & Vančura, A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.492348 · Cited by 19

Acid Phosphatases of Budding Yeast as a Model of Choice for Transcription Regulation Research

Sambuk, E. V., Fizikova, A., Александрович, С. В., & Padkina, M. V. (2011) · Enzyme Research · doi:10.4061/2011/356093 · Cited by 19

Myo-Inositol Safety in Pregnancy: From Preimplantation Development to Newborn Animals

Kuşçu, N., Bizzarri, M., & Bevilacqua, A. (2016) · International Journal of Endocrinology · doi:10.1155/2016/2413857 · Cited by 19

Unconventional metabolites in chromatin regulation

Gapa, L., Alfardus, H., & Fischle, W. (2022) · Bioscience Reports · doi:10.1042/bsr20211558 · Cited by 21

An essential role for the Ino80 chromatin remodeling complex in regulation of gene expression during cellular quiescence

Zahedi, Y., Zeng, S., & Ekwall, K. (2023) · Chromosome Research · doi:10.1007/s10577-023-09723-x · Cited by 18

Inositol synthesis regulates the activation of GSK ‐3α in neuronal cells

Ye, C., & Greenberg, M. L. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12978 · Cited by 18

Myo–inositol and d-chiro–inositol oral supplementation ameliorate cardiac dysfunction and remodeling in a mouse model of diet-induced obesity

L’Abbate, S., Nicolini, G., Forini, F., Marchetti, S., Lascio, N. D., Faita, F., & Kusmic, C. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105047 · Cited by 18

E2F1 regulation of the human myo-inositol 1-phosphate synthase (ISYNA1) gene promoter

Seelan, R. S., Parthasarathy, L. K., & Parthasarathy, R. N. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.08.002 · Cited by 18

Co-suppression of AtMIPS demonstrates cooperation of MIPS1, MIPS2 and MIPS3 in maintaining myo-inositol synthesis

Fleet, C. M., Yen, J. Y., Hill, E. A., & Gillaspy, G. E. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0737-6 · Cited by 17

1D-myo-inositol 3-phosphate synthase: conservation, regulation, and putative target of mood stabilizers

Ju, S., & Greenberg, M. L. (2004) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2004.09.010 · Cited by 17

Aldo-keto reductase 1B: Much learned, much more to do

Zhao, Y., Zhang, M., Li, H., Yang, Y., Lu, X., Yu, J., & Pan, L. (2023) · hLife · doi:10.1016/j.hlife.2023.12.002 · Cited by 16

From farm-scale to lab-scale: The characterization of engineered irrigation water distribution system biofilm models using an artificial freshwater source

Ngan, W. Y., & Habimana, O. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.134025 · Cited by 16

An In Vivo Fluorescent Sensor Reveals Intracellular Ins(1,3,4,5)P4Dynamics in Single Cells

Sakaguchi, R., Tainaka, K., Shimada, N., Nakano, S., Inoue, M., Kiyonaka, S., Mori, Y., & Morii, T. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200903951 · Cited by 16

Molecular characterization, modeling, and docking analysis of late phytic acid biosynthesis pathway gene, inositol polyphosphate 6-/3-/5-kinase, a potential candidate for developing low phytate crops

Punjabi, M., Bharadvaja, N., Sachdev, A., & Krishnan, V. (2018) · 3 Biotech · doi:10.1007/s13205-018-1343-7 · Cited by 16

Are postnatal hemangioblasts generated by dedifferentiation from committed hematopoietic stem cells?

Prindull, G., & Fibach, E. (2007) · Experimental Hematology · doi:10.1016/j.exphem.2007.01.047 · Cited by 16

Inositol polyphosphate–protein interactions: Implications for microbial pathogenicity

Lev, S., Bowring, B. G., Desmarini, D., & Djordjevic, J. T. (2021) · Cellular Microbiology · doi:10.1111/cmi.13325 · Cited by 15

Conformational Changes in Inositol 1,3,4,5,6-Pentakisphosphate 2-Kinase upon Substrate Binding

Baños-Sanz, J. I., Sanz‐Aparicio, J., Whitfield, H. L., Hamilton, C. J., Brearley, C. A., & González, B. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.363671 · Cited by 15

Plc1p is required for proper chromatin structure and activity of the kinetochore in Saccharomyces cerevisiae by facilitating recruitment of the RSC complex

Desai, P., Guha, N., Galdieri, L. C., Hadi, S., & Vančura, A. (2009) · Molecular Genetics and Genomics · doi:10.1007/s00438-009-0427-9 · Cited by 15

MHO1, an Evolutionarily Conserved Gene, Is Synthetic Lethal with PLC1; Mho1p Has a Role in Invasive Growth

Schlatter, I., Meira, M., Ueberschlag-Pitiot, V., Hoepfner, D., Movva, R., & Hynes, N. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032501 · Cited by 15

Regulated transcription of theSaccharomyces cerevisiaephosphatidylinositol biosynthetic gene,PIS1, yields pleiotropic effects on phospholipid synthesis

Jani, N. M., & Lopes, J. M. (2009) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2009.00514.x · Cited by 15

ATP-dependent chromatin remodeling in T cells1This article is part of Special Issue entitled Asilomar Chromatin and has undergone the Journal’s usual peer review process.

Wurster, A. L., & Pazin, M. J. (2012) · Biochemistry and Cell Biology · doi:10.1139/o11-042 · Cited by 15

Inositol Polyphosphate Multikinase Physically Binds to the SWI/SNF Complex and Modulates BRG1 Occupancy in Mouse Embryonic Stem Cells

Beon, J., Han, S., Yang, H., Park, S. E., Hyun, K., Lee, S.-Y., Rhee, H.-W., Seo, J. K., Kim, J., Kim, S., et al. (2022) · eLife · doi:10.7554/elife.73523 · Cited by 15

Dual Functions for the Schizosaccharomyces pombe Inositol Kinase Ipk1 in Nuclear mRNA Export and Polarized Cell Growth

Sarmah, B., & Wente, S. R. (2008) · Eukaryotic Cell · doi:10.1128/ec.00279-08 · Cited by 14

γTub23CInteracts Genetically With Brahma Chromatin-Remodeling Complexes inDrosophila melanogaster

Vâzquez, M., Cooper, M. T., Zurita, M., & Kennison, J. A. (2008) · Genetics · doi:10.1534/genetics.108.093492 · Cited by 14

CHIP and BAP1 Act in Concert to Regulate INO80 Ubiquitination and Stability for DNA Replication

Seo, H.-R., Jeong, D., Lee, S., Lee, H.-S., Lee, S.-A., Kang, S. W., & Kwon, J. (2021) · Molecules and Cells · doi:10.14348/molcells.2021.2258 · Cited by 14

A Class II Histone Deacetylase Acts on Newly Synthesized Histones in Tetrahymena

Smith, J. J., Torigoe, S. E., Maxson, J. E., Fish, L., & Wiley, E. A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00409-07 · Cited by 13

Protocols for Regulation and Study of Diphosphoinositol Polyphosphates

Safrany, S. T. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.002667 · Cited by 13

Fungal Kinases With a Sweet Tooth: Pleiotropic Roles of Their Phosphorylated Inositol Sugar Products in the Pathogenicity of Cryptococcus neoformans Present Novel Drug Targeting Opportunities

Lev, S., Li, C., Desmarini, D., Sorrell, T. C., Saiardi, A., & Djordjevic, J. T. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00248 · Cited by 12

Synthesis of three enantiomeric pairs of scyllo-Inositol phosphate and molecular interactions between all possible regioisomers of scyllo-Inositol phosphate and inositol 1,4,5-Trisphosphate 3-Kinase

Kwon, Y.-U., Im, J., Choi, G., Kim, Y. S., Choi, K. Y., & Chung, S. K. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00629-2 · Cited by 12

Subcellular localisation of human inositol 1,4,5-trisphosphate 3-kinase C: species-specific use of alternative export sites for nucleo-cytoplasmic shuttling indicates divergent roles of the catalytic and N-terminal domains

Nalaskowski, M. M., Windhorst, S., Stockebrand, M. C., & Mayr, G. W. (2006) · Biological Chemistry · doi:10.1515/bc.2006.075 · Cited by 12

Cytoplasmic Protein Serine/Threonine Kinases

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_5 · Cited by 11

Facilitated Assembly of the Preinitiation Complex by Separated Tail and Head/Middle Modules of the Mediator

Galdieri, L. C., Desai, P., & Vančura, A. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.11.020 · Cited by 11

Synthesis of Biotinylated Inositol Hexakisphosphate To Study DNA Double-Strand Break Repair and Affinity Capture of IP6-Binding Proteins

Jiao, C., Summerlin, M., Bruzik, K. S., & Hanakahi, L. A. (2015) · Biochemistry · doi:10.1021/acs.biochem.5b00642 · Cited by 11

Oxidation of the diphosphoinositol polyphosphate phosphohydrolase-like Nudix hydrolase Aps from Drosophila melanogaster induces thermolability—A possible regulatory switch?

Winward, L., Whitfield, W. G. F., McLennan, A. G., & Safrany, S. T. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2010.04.003 · Cited by 11

Comparative modeling and virtual screening for the identification of novel inhibitors for myo-inositol-1-phosphate synthase

Azam, S. S., Sarfaraz, S., & Abro, A. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3370-8 · Cited by 10

Chemo-Genetic Interactions Between Histone Modification and the Antiproliferation Drug AICAR Are Conserved in Yeast and Humans

Albrecht, D., Ceschin, J., Dompierre, J., Gueniot, F., Pinson, B., & Daignan‐Fornier, B. (2016) · Genetics · doi:10.1534/genetics.116.192518 · Cited by 10

Identification of Genes inSaccharomyces cerevisiaethat Are Haploinsufficient for Overcoming Amino Acid Starvation

Bae, N. S., Seberg, A. P., Carroll, L. P., & Swanson, M. J. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.037416 · Cited by 10

Gastric mucosal cell homeostatic physiome. Critical role of ER-initiated membranes restitution in the fidelity of cell function renewal.

Slomiany, A., Sano, S., Grabska, M., Yamaki, K., & Slomiany, B. L. (2004) · PubMed · Cited by 10

Inositol based non-viral vectors for transgene expression in human cervical carcinoma and hepatoma cell lines

Zhang, L., Fan, Y., & Wu, Y. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.11.034 · Cited by 10

Signal to reshape

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

6 Nutrient control of dimorphic growth in Saccharomyces cerevisiae

Harashima, T., & Heitman, J. (2004) · Topics in current genetics · doi:10.1007/978-3-540-39898-1_7 · Cited by 10

Signaling Lipids

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_2 · Cited by 9

Final checkup of neoplastic DNA replication: Evidence for failure in decision-making at the mitotic cell cycle checkpoint G1/S

Prindull, G. (2008) · Experimental Hematology · doi:10.1016/j.exphem.2008.07.009 · Cited by 9

Homeostatic restitution of cell membranes. Nuclear membrane lipid biogenesis and transport of protein from cytosol to intranuclear spaces.

Slomiany, A., Grabska, M., & Slomiany, B. L. (2006) · International Journal of Biological Sciences · doi:10.7150/ijbs.2.216 · Cited by 9

Regulation of lipid biosynthesis by phosphatidylinositol‐specific phospholipase C through the transcriptional repression of upstream activating sequence inositol containing genes

Rupwate, S. D., Rupwate, P. S., & Rajasekharan, R. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.04.022 · Cited by 9

Lipidomic processes in homeostatic and LPS-modified cell renewal cycle. Role of phosphatidylinositol 3-kinase pathway in biomembrane synthesis and restitution of apical epithelial membrane.

Slomiany, A., & Slomiany, B. L. (2003) · PubMed · Cited by 9

Inositol hexakisphosphate increases the size of platelet aggregates

Brehm, M. A., Klemm, U., Rehbach, C., Erdmann, N., Kolšek, K., Lin, H., Aponte-Santamaria, C. A., Gräter, F., Rauch, B. H., Riley, A. M., et al. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.12.011 · Cited by 9

Expression of FLR1 Transporter Requires Phospholipase C and Is Repressed by Mediator

Romero, C., Desai, P., DeLillo, N., & Vančura, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506728200 · Cited by 9

Cytoplasmic Protein Tyrosine Kinases

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_4 · Cited by 8

Phosphorylation-Dependent Enhancement of Rad53 Kinase Activity through the INO80 Chromatin Remodeling Complex

Kapoor, P., Bao, Y., Xiao, J., Espejo, A. B., Yang, L., Bedford, M. T., Peng, G., & Shen, X. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.03.032 · Cited by 8

Regulation of 1D-myo-Inositol-3-Phosphate Synthase in Yeast

Nunez, L. R., & Henry, S. A. (2006) · Springer eBooks · doi:10.1007/0-387-27600-9_6 · Cited by 8

An In Vivo Fluorescent Sensor Reveals Intracellular Ins(1,3,4,5)P4Dynamics in Single Cells

Sakaguchi, R., Tainaka, K., Shimada, N., Nakano, S., Inoue, M., Kiyonaka, S., Mori, Y., & Morii, T. (2009) · Angewandte Chemie · doi:10.1002/ange.200903951 · Cited by 8

Identification of the Antidepressant Vilazodone as an Inhibitor of Inositol Polyphosphate Multikinase by Structure-Based Drug Repositioning.

Lee, B., Park, S. J., Lee, S., Park, S. E., Lee, E., Song, J., Byun, Y., & Kim, S. (2020) · Europe PMC (PubMed Central) · doi:10.14348/molcells.2020.0051 · Cited by 8

Design, Synthesis, and Cellular Characterization of a New Class of IPMK Kinase Inhibitors

Zhou, Y., Chapagain, P., Desmarini, D., Uredi, D., Stashko, M. A., Huluka, H., Rameh, L. E., Djordjevic, J. T., Blind, R. D., & Wang, X. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c00015 · Cited by 7

Guanosine Triphosphatases and Their Regulators

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_9 · Cited by 7

Myo‐Inositol in Fermented Sugar Matrix Improves Human Macrophage Function

Ghosh, N., Das, A., Biswas, N., Mahajan, S. P., Madeshiya, A. K., Khanna, S., Sen, C. K., & Roy, S. (2022) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100852 · Cited by 9

Effect of the Inositol Polyphosphate InsP6 on DNA-PK–Dependent Phosphorylation

Hanakahi, L. A. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-11-0230 · Cited by 7

The inositol polyphosphate kinase Ipk1 transcriptionally regulates mitochondrial functions in Candida albicans

Zhu, H., Zhu, N., Peng, L., Zhang, B., Yu, Q., & Li, M. (2020) · FEMS Yeast Research · doi:10.1093/femsyr/foaa050 · Cited by 7

Dengue and metabolomics in humans

Romagnolo, A. G., & Carvalho, K. I. (2021) · Metabolomics · doi:10.1007/s11306-021-01783-6 · Cited by 7

ATP levels in clone mouse embryos

Boiani, M., Gambles, V., & Schöler, H. R. (2004) · Cytogenetic and Genome Research · doi:10.1159/000078198 · Cited by 7

Dietary Supplementation with Methylsulfonylmethane and Myo-Inosito Supports Hair Quality and Fecal Microbiome in Poodles

Zhang, J., Guo, D., Zhang, L., Li, D., & Deng, B. (2024) · Animals · doi:10.3390/ani14243643 · Cited by 6

Inositol phosphate kinase Vip1p interacts with histone chaperone Asf1p in Saccharomyces cerevisiae

Osada, S., Kageyama, K., Ohnishi, Y., Nishikawa, J., Nishihara, T., & Imagawa, M. (2011) · Molecular Biology Reports · doi:10.1007/s11033-011-1295-z · Cited by 6

Reptin physically interacts with p65 and represses NF‐κB activation

Qiu, H., Gao, Y., & Mao, D. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.04.028 · Cited by 6

IPMK regulates HDAC3 activity and histone H4 acetylation in human cells

Sowd, G. A., Stivison, E. A., Chapagain, P., Hale, A. T., Poland, J. C., Rameh, L. E., & Blind, R. D. (2024) · doi:10.1101/2024.04.29.591660 · Cited by 6

A hypothetical model: Chromatin remodelers couple with acetyltransferases to trigger the elongation of RNA polymerase II (pol II)

Zhang, G. (2024) · Frontiers in Epigenetics and Epigenomics · doi:10.3389/freae.2024.1439973 · Cited by 8

IP4 is an epigenetic coregulator

Kutateladze, T. G. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.795 · Cited by 5

Conformational Stability of Inositol 1,3,4,5,6-Pentakisphosphate 2-Kinase (IPK1) Dictates Its Substrate Selectivity

Gosein, V., & Miller, G. J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.512731 · Cited by 5

A Plasmodium multi-domain protein possesses multiple inositol phosphate kinase activities

Stritzke, C., Nalaskowski, M. M., Fanick, W., Lin, H., & Mayr, G. W. (2012) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2012.10.005 · Cited by 5

Mitogen-Activated Protein Kinase Module

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_6 · Cited by 5

When extreme negativity is a positive thing

Scadden, D. (2005) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1105-940 · Cited by 5

Crystallization and preliminary X-ray diffraction analysis of inositol 1,3,4,5,6-pentakisphosphate kinase fromArabidopsis thaliana

Baños-Sanz, J. I., Villate, M., Sanz‐Aparicio, J., Brearley, C. A., & González, B. (2009) · Acta Crystallographica Section F Structural Biology and Crystallization Communications · doi:10.1107/s1744309109051057 · Cited by 4

Two-way communication between cell cycle and metabolism in budding yeast: what do we know?

Zhang, Y., van der Zee, L., & Barberis, M. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1187304 · Cited by 4

Nuclear Lipids and Their Metabolic and Signaling Properties

Ledeen, R. W., & Wu, G. (2009) · Springer eBooks · doi:10.1007/978-0-387-30378-9_7 · Cited by 4

Zebrafish inositol polyphosphate kinases: New effectors of cilia and developmental signaling

Sarmah, B., & Wente, S. R. (2009) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2009.10.018 · Cited by 4

Development Rapid Analytical Methods for Inositol as a Trace Component by HPLC and LC-MS/MS in Infant Formula

Shin, J., Park, J., Kim, H., Ahn, J., Kwak, B., & Kim, J. (2015) · Korean Journal for Food Science of Animal Resources · doi:10.5851/kosfa.2015.35.4.466 · Cited by 4

Role of Calcium Signaling in Stem and Cancer Cell Proliferation

Amaya, M. J., Goulart, V. A. M., Santos, A. K., Kihara, A. H., Guatimosim, S., & Resende, R. R. (2013) · Springer eBooks · doi:10.1007/978-94-007-6211-4_5 · Cited by 4

Prion propagation and inositol polyphosphates

Wickner, R. B., Edskes, H. K., Bezsonov, E. E., Son, M., & Ducatez, M. (2017) · Current Genetics · doi:10.1007/s00294-017-0788-2 · Cited by 4

Chromatin remodeling complexes: architects influencing breast cancer progression

Giovani, O., Eckersley, G. S., Jones, H. R., & Nagarajan, S. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1690350 · Cited by 3

Crystallization and Preliminary X-Ray Diffraction Analysis of a Mammal Inositol 1,3,4,5,6-Pentakisphosphate 2-Kinase

Franco-Echevarría, E., Sanz‐Aparicio, J., Troffer-Charlier, N., Poterszman, A., & González, B. (2017) · The Protein Journal · doi:10.1007/s10930-017-9717-y · Cited by 3

Role of Plc1p in regulation of Mcm1p-dependent genes

Guzinska, K., Varghese, R., & Vančura, A. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01602.x · Cited by 3

Transcription Through Chromatin

Smolle, M., & Venkatesh, S. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8624-4_11 · Cited by 3

Chemokine Receptors and NeuroAIDS

Meucci, O. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0793-6 · Cited by 3

Inositol Polyphosphates

Resnick, A. C., & Saiardi, A. (2008) · Wiley eBooks · doi:10.1002/9780470048672.wecb252 · Cited by 3

Algorithms for handling arbitrary lineshape distortions in Magnetic Resonance Spectroscopy and Spectroscopic Imaging

Popa, E. (2010) · doi:10.70675/f7c7da1bz166fz4ecbzb4bazf7f111247b20 · Cited by 3

Anti‐Inflammatory Role of Myo‐Inositol in Obesity: Suppression of TNF‐α‐Induced Inflammation and Monocyte Adhesion in Hypertrophic Human Adipocytes

Quarta, S., Calabriso, N., Carluccio, M. A., Rizzo, M. L., Wabitsch, M., Verri, T., Maffia, M., Damiano, F., Siculella, L., Santarpino, G., et al. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70962 · Cited by 2

l-myo-Inositol-1-Phosphate Synthase Expressed in Developing Organ: Isolation and Characterisation of the Enzyme from Human Fetal Liver

Chhetri, D. R., Gupta, S., Mukherjee, A. K., & Adhikari, J. (2012) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-012-9767-8 · Cited by 2

Analysis of SUC2 Promoter Structure by Nucleosome Scanning

Chang, J. S., & Vančura, A. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-376-9_22 · Cited by 2

Chromatin Remodeling in DNA Repair and Replication

Kapoor, P., & Shen, X. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8624-4_12 · Cited by 2

Cell Signaling Properties of Inositol Hexaphosphate (IP6)

Shamsuddin, A. M. (2005) · Oxidative stress and disease · doi:10.1201/9781420028096.ch19 · Cited by 2

Sequence and functional differences in the ATPase domains of CHD3 and SNF2H promise potential for selective regulability and drugability

Hoffmeister, H., Fuchs, A., Komives, E. A., Gröbner-Ferreira, R., Strobl, L., Nazet, J., Heizinger, L., Merkl, R., Dove, S., & Längst, G. (2021) · FEBS Journal · doi:10.1111/febs.15699 · Cited by 2

Nucleosome remodeling

TRAVERS, A. A., & Owen‐Hughes, T. (2004) · New comprehensive biochemistry · doi:10.1016/s0167-7306(03)39016-7 · Cited by 2

Dual-Specificity Protein Kinases

Thiriet, M. (2012) · Biomathematical and biomechanical modeling of the circulatory and ventilatory systems · doi:10.1007/978-1-4614-4370-4_7 · Cited by 2

Bioprospecting for enzymes in bryophytes: Extraction of L-Myo-inositol-1-phosphate synthase from Sphagnum junghuhnianum Doz. et Molk. and its characterization

Chhetri, D. R., Yonzone, S., & Mukhia, R. (2023) · South African Journal of Botany · doi:10.1016/j.sajb.2023.11.022 · Cited by 1

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

Signal to reshape

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

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

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

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