Anne K. Voss - Publications

Development and Neurobiology The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia 

61 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Gan L, Sun J, Yang S, Zhang X, Chen W, Sun Y, Wu X, Cheng C, Yuan J, Li A, Corbett MA, Dixon MP, Thomas T, Voss AK, Gécz J, et al. Chromatin-Binding Protein PHF6 Regulates Activity-Dependent Transcriptional Networks to Promote Hunger Response. Cell Reports. 30: 3717-3728.e6. PMID 32187544 DOI: 10.1016/j.celrep.2020.02.085  1
2020 Priebbenow DL, Leaver D, Nguyen N, Cleary B, Lagiakos HR, Sanchez J, Xue L, Huang F, Sun Y, Mujumdar P, Mudududdla R, Varghese S, Teguh SC, Charman SA, White KL, ... ... Voss AK, et al. Discovery of Acylsulfonohydrazide-Derived Lysine Acetyltransferase (KAT6A) Inhibitors as Potent Senescence-Inducing Anti-Cancer Agents. Journal of Medicinal Chemistry. PMID 32118427 DOI: 10.1021/acs.jmedchem.9b02071  1
2019 MacPherson L, Anokye J, Yeung MM, Lam EYN, Chan YC, Weng CF, Yeh P, Knezevic K, Butler MS, Hoegl A, Chan KL, Burr ML, Gearing LJ, Willson T, Liu J, ... ... Voss AK, et al. HBO1 is required for the maintenance of leukaemia stem cells. Nature. PMID 31827282 DOI: 10.1038/s41586-019-1835-6  1
2019 Lalaoui N, Boyden SE, Oda H, Wood GM, Stone DL, Chau D, Liu L, Stoffels M, Kratina T, Lawlor KE, Zaal KJM, Hoffmann PM, Etemadi N, Shield-Artin K, Biben C, ... ... Voss AK, et al. Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease. Nature. PMID 31827281 DOI: 10.1038/s41586-019-1828-5  0.64
2019 Kueh AJ, Eccles S, Tang L, Garnham AL, May RE, Herold MJ, Smyth GK, Voss AK, Thomas T. HBO1(KAT7) does not have an essential role in cell proliferation, DNA replication or histone 4 acetylation in human cells. Molecular and Cellular Biology. PMID 31767635 DOI: 10.1128/MCB.00506-19  1
2019 Klein BJ, Jang SM, Lachance C, Mi W, Lyu J, Sakuraba S, Krajewski K, Wang WW, Sidoli S, Liu J, Zhang Y, Wang X, Warfield BM, Kueh AJ, Voss AK, et al. Histone H3K23-specific acetylation by MORF is coupled to H3K14 acylation. Nature Communications. 10: 4724. PMID 31624313 DOI: 10.1038/s41467-019-12551-5  1
2019 Vanyai HK, Garnham A, May RE, McRae HM, Collin C, Wilcox S, Smyth GK, Thomas T, Voss AK. MOZ directs the distal-less homeobox gene expression program during craniofacial development. Development (Cambridge, England). 146. PMID 31340933 DOI: 10.1242/dev.175042  1
2019 McRae HM, Voss AK, Thomas T. Are transplantable stem cells required for adult hematopoiesis? Experimental Hematology. PMID 31175894 DOI: 10.1016/j.exphem.2019.05.007  1
2019 Delbridge ARD, Kueh AJ, Ke F, Zamudio NM, El-Saafin F, Jansz N, Wang GY, Iminitoff M, Beck T, Haupt S, Hu Y, May RE, Whitehead L, Tai L, Chiang W, ... ... Voss AK, et al. Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects. Cell Reports. 27: 442-454.e5. PMID 30970248 DOI: 10.1016/j.celrep.2019.03.048  1
2019 Urdinguio RG, Lopez V, Bayón GF, Diaz de la Guardia R, Sierra MI, García-Toraño E, Perez RF, García MG, Carella A, Pruneda PC, Prieto C, Dmitrijeva M, Santamarina P, Belmonte T, Mangas C, ... ... Voss AK, et al. Chromatin regulation by Histone H4 acetylation at Lysine 16 during cell death and differentiation in the myeloid compartment. Nucleic Acids Research. PMID 30923829 DOI: 10.1093/nar/gkz195  1
2019 McRae HM, Garnham AL, Hu Y, Witkowski MT, Corbett MA, Dixon MP, May RE, Sheikh BN, Chiang W, Kueh AJ, Nguyen TA, Man K, Gloury R, Aubrey BJ, Policheni A, ... ... Voss AK, et al. PHF6 regulates hematopoietic stem and progenitor cells and its loss synergizes with expression of TLX3 to cause leukemia. Blood. PMID 30755422 DOI: 10.1182/blood-2018-07-860726  1
2018 Aubrey BJ, Janic A, Chen Y, Chang C, Lieschke EC, Diepstraten ST, Kueh AJ, Bernardini JP, Dewson G, O'Reilly LA, Whitehead L, Voss AK, Smyth GK, Strasser A, Kelly GL. Mutant TRP53 exerts a target gene-selective dominant-negative effect to drive tumor development. Genes & Development. PMID 30366906 DOI: 10.1101/gad.314286.118  0.64
2018 Grabow S, Kueh AJ, Ke F, Vanyai HK, Sheikh BN, Dengler MA, Chiang W, Eccles S, Smyth IM, Jones LK, de Sauvage FJ, Scott M, Whitehead L, Voss AK, Strasser A. Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities. Cell Reports. 24: 3285-3295.e4. PMID 30232009 DOI: 10.1016/j.celrep.2018.08.048  0.72
2018 Voss AK, Thomas T. Histone Lysine and Genomic Targets of Histone Acetyltransferases in Mammals. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e1800078. PMID 30144132 DOI: 10.1002/bies.201800078  1
2018 Baell JB, Leaver DJ, Hermans SJ, Kelly GL, Brennan MS, Downer NL, Nguyen N, Wichmann J, McRae HM, Yang Y, Cleary B, Lagiakos HR, Mieruszynski S, Pacini G, Vanyai HK, ... ... Voss AK, et al. Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth. Nature. PMID 30069049 DOI: 10.1038/s41586-018-0387-5  1
2018 Ke FFS, Vanyai HK, Cowan AD, Delbridge ARD, Whitehead L, Grabow S, Czabotar PE, Voss AK, Strasser A. Embryogenesis and Adult Life in the Absence of Intrinsic Apoptosis Effectors BAX, BAK, and BOK. Cell. 173: 1217-1230.e17. PMID 29775594 DOI: 10.1016/j.cell.2018.04.036  0.6
2018 El-Saafin F, Curry C, Ye T, Garnier JM, Kolb-Cheynel I, Stierle M, Downer NL, Dixon MP, Negroni L, Berger I, Thomas T, Voss AK, Dobyns W, Devys D, Tora L. Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA Polymerase II transcription. Human Molecular Genetics. PMID 29648665 DOI: 10.1093/hmg/ddy126  1
2016 Sheikh BN, Metcalf D, Voss AK, Thomas T. MOZ and BMI1 act synergistically to maintain Hematopoietic Stem Cells. Experimental Hematology. PMID 27773671 DOI: 10.1016/j.exphem.2016.10.006  1
2016 Newman DM, Voss AK, Thomas T, Allan RS. Essential role for the histone acetyltransferase KAT7 in T cell development, fitness, and survival. Journal of Leukocyte Biology. PMID 27733580 DOI: 10.1189/jlb.1MA0816-338R  1
2016 Sheikh BN, Yang Y, Schreuder J, Nilsson SK, Bilardi R, Carotta S, McRae HM, Metcalf D, Voss AK, Thomas T. MOZ (KAT6A) is essential for the maintenance of classically defined adult hematopoietic stem cells. Blood. PMID 27663673 DOI: 10.1182/blood-2015-10-676072  1
2016 Newman DM, Sakaguchi S, Lun A, Preston S, Pellegrini M, Khamina K, Bergthaler A, Nutt SL, Smyth GK, Voss AK, Thomas T, Ellmeier W, Belz GT, Allan RS. Acetylation of the Cd8 Locus by KAT6A Determines Memory T Cell Diversity. Cell Reports. 16: 3311-21. PMID 27653692 DOI: 10.1016/j.celrep.2016.08.056  1
2015 Lawrenson ID, Krebs DL, Linossi EM, Zhang JG, McLennan TJ, Collin C, McRae HM, Kolesnik TB, Koh K, Britto JM, Kueh AJ, Sheikh BN, El-Saafin F, Nicola NA, Tan SS, ... ... Voss AK, et al. Cortical Layer Inversion and Deregulation of Reelin Signaling in the Absence of SOCS6 and SOCS7. Cerebral Cortex (New York, N.Y. : 1991). PMID 26503265 DOI: 10.1093/cercor/bhv253  1
2015 Moulin M, Voss AK, Thomas T, Wong WW, Cook WD, Koentgen F, Vince J, Silke J, Vaux DL. Response to Heard et al. The Embo Journal. 34: 2396-7. PMID 26427759 DOI: 10.15252/embj.201592761  1
2015 Sheikh BN, Downer NL, Phipson B, Vanyai HK, Kueh AJ, McCarthy DJ, Smyth GK, Thomas T, Voss AK. MOZ and BMI1 play opposing roles during Hox gene activation in ES cells and in body segment identity specification in vivo. Proceedings of the National Academy of Sciences of the United States of America. 112: 5437-42. PMID 25922517 DOI: 10.1073/pnas.1422872112  1
2015 Vanyai HK, Thomas T, Voss AK. Mesodermal expression of Moz is necessary for cardiac septum development. Developmental Biology. 403: 22-9. PMID 25912687 DOI: 10.1016/j.ydbio.2015.04.011  1
2015 Sheikh BN, Lee SC, El-Saafin F, Vanyai HK, Hu Y, Pang SH, Grabow S, Strasser A, Nutt SL, Alexander WS, Smyth GK, Voss AK, Thomas T. MOZ regulates B-cell progenitors and, consequently, Moz haploinsufficiency dramatically retards MYC-induced lymphoma development. Blood. 125: 1910-21. PMID 25605372 DOI: 10.1182/blood-2014-08-594655  0.64
2014 Sheikh BN, Downer NL, Kueh AJ, Thomas T, Voss AK. Excessive versus physiologically relevant levels of retinoic acid in embryonic stem cell differentiation. Stem Cells (Dayton, Ohio). 32: 1451-8. PMID 25099890 DOI: 10.1002/stem.1604  1
2014 Good-Jacobson KL, Chen Y, Voss AK, Smyth GK, Thomas T, Tarlinton D. Regulation of germinal center responses and B-cell memory by the chromatin modifier MOZ. Proceedings of the National Academy of Sciences of the United States of America. 111: 9585-90. PMID 24979783 DOI: 10.1073/pnas.1402485111  1
2014 Carpinelli MR, Voss AK, Manning MG, Perera AA, Cooray AA, Kile BT, Burt RA. A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination. Disease Models & Mechanisms. 7: 649-57. PMID 24682784 DOI: 10.1242/dmm.014605  0.64
2013 Puccini J, Shalini S, Voss AK, Gatei M, Wilson CH, Hiwase DK, Lavin MF, Dorstyn L, Kumar S. Loss of caspase-2 augments lymphomagenesis and enhances genomic instability in Atm-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 110: 19920-5. PMID 24248351 DOI: 10.1073/pnas.1311947110  0.64
2012 Voss AK, Vanyai HK, Collin C, Dixon MP, McLennan TJ, Sheikh BN, Scambler P, Thomas T. MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome. Developmental Cell. 23: 652-63. PMID 22921202 DOI: 10.1016/j.devcel.2012.07.010  0.64
2012 Leong DW, Komen JC, Hewitt CA, Arnaud E, McKenzie M, Phipson B, Bahlo M, Laskowski A, Kinkel SA, Davey GM, Heath WR, Voss AK, Zahedi RP, Pitt JJ, Chrast R, et al. Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene. The Journal of Biological Chemistry. 287: 20652-63. PMID 22535952 DOI: 10.1074/jbc.M111.327601  0.64
2012 Yip YP, Thomas T, Voss AK, Yip JW. Migration of sympathetic preganglionic neurons in the spinal cord of a C3G-deficient mouse suggests that C3G acts in the reelin signaling pathway Journal of Comparative Neurology. 520: 3194-3202. PMID 22351125 DOI: 10.1002/cne.23086  0.64
2012 Sheikh BN, Dixon MP, Thomas T, Voss AK. Querkopf is a key marker of self-renewal and multipotency of adult neural stem cells. Journal of Cell Science. 125: 295-309. PMID 22331353 DOI: 10.1242/jcs.077271  1
2012 Moulin M, Anderton H, Voss AK, Thomas T, Wong WW, Bankovacki A, Feltham R, Chau D, Cook WD, Silke J, Vaux DL. IAPs limit activation of RIP kinases by TNF receptor 1 during development. The Embo Journal. 31: 1679-91. PMID 22327219 DOI: 10.1038/emboj.2012.18  1
2012 Voss AK, Dixon MP, McLennan T, Kueh AJ, Thomas T. Chromatin immunoprecipitation of mouse embryos. Methods in Molecular Biology (Clifton, N.J.). 809: 335-52. PMID 22113287 DOI: 10.1007/978-1-61779-376-9_23  1
2011 Clayton-Smith J, O'Sullivan J, Daly S, Bhaskar S, Day R, Anderson B, Voss AK, Thomas T, Biesecker LG, Smith P, Fryer A, Chandler KE, Kerr B, Tassabehji M, Lynch SA, et al. Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndrome. American Journal of Human Genetics. 89: 675-81. PMID 22077973 DOI: 10.1016/j.ajhg.2011.10.008  1
2011 Taoudi S, Bee T, Hilton A, Knezevic K, Scott J, Willson TA, Collin C, Thomas T, Voss AK, Kile BT, Alexander WS, Pimanda JE, Hilton DJ. ERG dependence distinguishes developmental control of hematopoietic stem cell maintenance from hematopoietic specification. Genes & Development. 25: 251-62. PMID 21245161 DOI: 10.1101/gad.2009211  0.64
2011 Kueh AJ, Dixon MP, Voss AK, Thomas T. HBO1 is required for H3K14 acetylation and normal transcriptional activity during embryonic development. Molecular and Cellular Biology. 31: 845-60. PMID 21149574 DOI: 10.1128/MCB.00159-10  1
2010 Hewitt CA, Ling KH, Merson TD, Simpson KM, Ritchie ME, King SL, Pritchard MA, Smyth GK, Thomas T, Scott HS, Voss AK. Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome. Plos One. 5: e11561. PMID 20661276 DOI: 10.1371/journal.pone.0011561  0.64
2009 Voss AK, Collin C, Dixon MP, Thomas T. Moz and retinoic acid coordinately regulate H3K9 acetylation, Hox gene expression, and segment identity. Developmental Cell. 17: 674-86. PMID 19922872 DOI: 10.1016/j.devcel.2009.10.006  0.64
2009 Voss AK, Thomas T. MYST family histone acetyltransferases take center stage in stem cells and development. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 31: 1050-61. PMID 19722182 DOI: 10.1002/bies.200900051  1
2009 Sharma S, Koh KS, Collin C, Dave A, McMellon A, Sugiyama Y, McAvoy JW, Voss AK, Gécz J, Craig JE. NHS-A isoform of the NHS gene is a novel interactor of ZO-1. Experimental Cell Research. 315: 2358-72. PMID 19447104 DOI: 10.1016/j.yexcr.2009.05.008  0.64
2008 Thomas T, Dixon MP, Kueh AJ, Voss AK. Mof (MYST1 or KAT8) is essential for progression of embryonic development past the blastocyst stage and required for normal chromatin architecture. Molecular and Cellular Biology. 28: 5093-105. PMID 18541669 DOI: 10.1128/MCB.02202-07  1
2008 Voss AK, Britto JM, Dixon MP, Sheikh BN, Collin C, Tan SS, Thomas T. C3G regulates cortical neuron migration, preplate splitting and radial glial cell attachment. Development (Cambridge, England). 135: 2139-49. PMID 18506028 DOI: 10.1242/dev.016725  0.64
2008 Loughran SJ, Kruse EA, Hacking DF, de Graaf CA, Hyland CD, Willson TA, Henley KJ, Ellis S, Voss AK, Metcalf D, Hilton DJ, Alexander WS, Kile BT. The transcription factor Erg is essential for definitive hematopoiesis and the function of adult hematopoietic stem cells. Nature Immunology. 9: 810-9. PMID 18500345 DOI: 10.1038/ni.1617  0.64
2007 Voss AK, Gamble R, Collin C, Shoubridge C, Corbett M, Gécz J, Thomas T. Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity. Gene Expression Patterns : Gep. 7: 858-71. PMID 17698420 DOI: 10.1016/j.modgep.2007.06.007  0.64
2007 Thomas T, Loveland KL, Voss AK. The genes coding for the MYST family histone acetyltransferases, Tip60 and Mof, are expressed at high levels during sperm development. Gene Expression Patterns : Gep. 7: 657-65. PMID 17517537 DOI: 10.1016/j.modgep.2007.03.005  1
2007 Thomas T, Voss AK. The diverse biological roles of MYST histone acetyltransferase family proteins. Cell Cycle (Georgetown, Tex.). 6: 696-704. PMID 17374998 DOI: 10.4161/cc.6.6.4013  1
2006 Merson TD, Dixon MP, Collin C, Rietze RL, Bartlett PF, Thomas T, Voss AK. The transcriptional coactivator Querkopf controls adult neurogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 11359-70. PMID 17079664 DOI: 10.1523/JNEUROSCI.2247-06.2006  0.64
2006 Voss AK, Krebs DL, Thomas T. C3G regulates the size of the cerebral cortex neural precursor population. The Embo Journal. 25: 3652-63. PMID 16858399 DOI: 10.1038/sj.emboj.7601234  1
2006 Thomas T, Corcoran LM, Gugasyan R, Dixon MP, Brodnicki T, Nutt SL, Metcalf D, Voss AK. Monocytic leukemia zinc finger protein is essential for the development of long-term reconstituting hematopoietic stem cells. Genes & Development. 20: 1175-86. PMID 16651658 DOI: 10.1101/gad.1382606  1
2006 Hirst CE, Ng ES, Azzola L, Voss AK, Thomas T, Stanley EG, Elefanty AG. Transcriptional profiling of mouse and human ES cells identifies SLAIN1, a novel stem cell gene. Developmental Biology. 293: 90-103. PMID 16546155 DOI: 10.1016/j.ydbio.2006.01.023  1
2006 Forrai A, Boyle K, Hart AH, Hartley L, Rakar S, Willson TA, Simpson KM, Roberts AW, Alexander WS, Voss AK, Robb L. Absence of suppressor of cytokine signalling 3 reduces self-renewal and promotes differentiation in murine embryonic stem cells. Stem Cells (Dayton, Ohio). 24: 604-14. PMID 16123385 DOI: 10.1634/stemcells.2005-0323  0.64
2004 Krebs DL, Metcalf D, Merson TD, Voss AK, Thomas T, Zhang JG, Rakar S, O'bryan MK, Willson TA, Viney EM, Mielke LA, Nicola NA, Hilton DJ, Alexander WS. Development of hydrocephalus in mice lacking SOCS7. Proceedings of the National Academy of Sciences of the United States of America. 101: 15446-51. PMID 15494444 DOI: 10.1073/pnas.0406870101  0.64
2004 Katschinski DM, Le L, Schindler SG, Thomas T, Voss AK, Wenger RH. Interaction of the PAS B domain with HSP90 accelerates hypoxia-inducible factor-1alpha stabilization. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 14: 351-60. PMID 15319539 DOI: 10.1159/000080345  1
2004 Thomas T, Voss AK. Querkopf, a histone acetyltransferase, is essential for embryonic neurogenesis. Frontiers in Bioscience : a Journal and Virtual Library. 9: 24-31. PMID 14766340  1
2003 Ting SB, Wilanowski T, Auden A, Hall M, Voss AK, Thomas T, Parekh V, Cunningham JM, Jane SM. Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3 Nature Medicine. 9: 1513-1519. PMID 14608380 DOI: 10.1038/nm961  0.64
2003 Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, ... ... Voss AK, et al. Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation. American Journal of Human Genetics. 73: 1120-30. PMID 14564667 DOI: 10.1086/379381  0.64
2003 Voss AK, Gruss P, Thomas T. The guanine nucleotide exchange factor C3G is necessary for the formation of focal adhesions and vascular maturation. Development (Cambridge, England). 130: 355-67. PMID 12466202 DOI: 10.1242/dev.00217  0.64
2002 Stecca B, Nait-Oumesmar B, Kelley KA, Voss AK, Thomas T, Lazzarini RA. Gcm1 expression defines three stages of chorio-allantoic interaction during placental development. Mechanisms of Development. 115: 27-34. PMID 12049764 DOI: 10.1016/S0925-4773(02)00095-3  0.64
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