Journal Articles
Magor, Graham William, Gillinder, Kevin R., Huang, Stephen, Ilsley, Melissa D., Bell, Charles and Perkins, Andrew Charles (2022). KLF1 Acts As a Pioneer Transcription Factor Via SMARCA4 to Open Chromatin and Facilitate Redeployment of an Enhancer Complex Containing GATA1 and SCL. Blood, 140 (Supplement 1), 696-697. doi: 10.1182/blood-2022-157901
Lam, Charlene, Gillinder, Kevin, Carvajal, Natalia, Mitchell, Helen Lorraine, Magor, Graham William and Perkins, Andrew Charles (2022). Novel Immediate Direct Targets of EPO Signalling in Human Erythropoiesis. Blood, 140 (Supplement 1), 1238-1238. doi: 10.1182/blood-2022-168671
Tuong, Zewen K., Lukowski, Samuel W., Nguyen, Quan H., Chandra, Janin, Zhou, Chenhao, Gillinder, Kevin, Bashaw, Abate A., Ferdinand, John R., Stewart, Benjamin J., Teoh, Siok Min, Hanson, Sarah J., Devitt, Katharina, Clatworthy, Menna R., Powell, Joseph E. and Frazer, Ian H. (2021). A model of impaired Langerhans cell maturation associated with HPV induced epithelial hyperplasia. iScience, 24 (11) 103326, 103326. doi: 10.1016/j.isci.2021.103326
Carmichael, Catherine L., Wang, Jueqiong, Nguyen, Thao, Kolawole, Oluseyi, Benyoucef, Aissa, De Mazière, Charlotte, Milne, Anna R., Samuel, Sona, Gillinder, Kevin, Hediyeh-zadeh, Soroor, Vo, Anh N. Q., Huang, Yizhou, Knezevic, Kathy, McInnes, William R. L., Shields, Benjamin J., Mitchell, Helen, Ritchie, Matthew E., Lammens, Tim, Lintermans, Beatrice, Van Vlierberghe, Pieter, Wong, Nicholas C., Haigh, Katharina, Thoms, Julie A. I., Toulmin, Emma, Curtis, David J., Oxley, Ethan P., Dickins, Ross A., Beck, Dominik, Perkins, Andrew ... Haigh, Jody J. (2020). The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1. Blood, 136 (8), 957-973. doi: 10.1182/blood.2019002548
Cheung Tung Shing, Karen S., Broughton, Sophie E., Nero, Tracy L., Gillinder, Kevin, Ilsley, Melissa D., Ramshaw, Hayley, Lopez, Angel F., Griffin, Michael D. W., Parker, Michael W., Perkins, Andrew C. and Dhagat, Urmi (2019). Author Correction: EPO does not promote interaction between the erythropoietin and beta-common receptors (Scientific Reports, (2018), 8, 1, (12457), 10.1038/s41598-018-29865-x). Scientific Reports, 9 (1) 7851, 7851. doi: 10.1038/s41598-019-43988-9
Ilsley, Melissa D., Huang, Stephen, Magor, Graham W., Landsberg, Michael J., Gillinder, Kevin R. and Perkins, Andrew C. (2019). Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors. BMC Genomics, 20 (1) 417, 417. doi: 10.1186/s12864-019-5805-z
Nébor, Danitza, Graber, Joel H., Ciciotte, Steven L., Robledo, Raymond F., Papoin, Julien, Hartman, Emily, Gillinder, Kevin R., Perkins, Andrew C., Bieker, James J., Blanc, Lionel and Peters, Luanne L. (2018). Mutant KLF1 in adult anemic Nan mice leads to profound transcriptome changes and disordered erythropoiesis. Scientific Reports, 8 (1) 12793. doi: 10.1038/s41598-018-30839-2
Cheung Tung Shing, Karen S., Broughton, Sophie E., Nero, Tracy L., Gillinder, Kevin, Ilsley, Melissa D., Ramshaw, Hayley, Lopez, Angel F., Griffin, Michael D. W., Parker, Michael W., Perkins, Andrew C. and Dhagat, Urmi (2018). EPO does not promote interaction between the erythropoietin and beta-common receptors. Scientific Reports, 8 (1) 12457, 12457. doi: 10.1038/s41598-018-29865-x
Gillinder, Kevin, Magor, Graham and Perkins, Andrew (2018). Variable serologic and other phenotypes due to KLF1 mutations. Transfusion, 58 (5), 1324-1325. doi: 10.1111/trf.14529
Gillinder, Kevin R., Tuckey, Hugh, Bell, Charles C., Magor, Graham W., Huang, Stephen, Ilsley, Melissa D. and Perkins, Andrew C. (2017). Direct targets of pStat5 signalling in erythropoiesis. PLoS One, 12 (7) e0180922, e0180922. doi: 10.1371/journal.pone.0180922
Ilsley, Melissa D., Gillinder, Kevin R., Magor, Graham W., Huang, Stephen, Bailey, Timothy L., Crossley, Merlin and Perkins, Andrew C. (2017). Kruppel-like factors compete for promoters and enhancers to fine-tune transcription. Nucleic Acids Research, 45 (11), 6572-6588. doi: 10.1093/nar/gkx441
Planutis, Antanas, Xue, Li, Trainor, Cecelia D., Dangeti, Mohan, Gillinder, Kevin, Siatecka, Miroslawa, Nebor, Danitza, Peters, Luanne L., Perkins, Andrew C. and Bieker, James J. (2017). Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development. Development, 144 (3), 430-440. doi: 10.1242/dev.145656
Gillinder, Kevin R., Ilsley, Melissa D., Nébor, Danitza, Sachidanandam, Ravi, Lajoie, Mathieu, Magor, Graham W., Tallack, Michael R., Bailey, Timothy, Landsberg, Michael J., Mackay, Joel P., Parker, Michael W., Miles, Luke A., Graber,Joel H., Peters, Luanne L., Bieker, James J. and Perkins, Andrew C. (2016). Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability. Nucleic Acids Research, 45 (3), 1130-1143. doi: 10.1093/nar/gkw1014
He, Jingjing, Chen, Daniel L. , Samocha-Bonet, Dorit, Gillinder, Kevin R. , Barclay, Johanna L. , Magor, Graham W. , Perkins, Andrew C. , Greenfield, Jerry R. , Yang, Gongshe and Whitehead, Jonathan P. (2016). Fibroblast growth factor-1 (FGF-1) promotes adipogenesis by downregulation of carboxypeptidase A4 (CPA4)–a negative regulator of adipogenesis implicated in the modulation of local and systemic insulin sensitivity. Growth Factors, 34 (5-6), 210-216. doi: 10.1080/08977194.2017.1285764
Bell, Charles C., Amaral, Paulo P., Kalsbeek, Anton, Magor, Graham W., Gillinder, Kevin R., Tangermann, Pierre, di Lisio, Lorena, Cheetham, Seth W., Gruhl, Franziska, Frith, Jessica, Tallack, Michael R., Ru, Ke-Lin, Crawford, Joanna, Mattick, John S., Dinger, Marcel E. and Perkins, Andrew C. (2016). The Evx1/Evx1as gene locus regulates anterior-posterior patterning during gastrulation. Scientific Reports, 6 (1) 26657, 26657. doi: 10.1038/srep26657
Magor, Graham W., Tallack, Michael R., Gillinder, Kevin R., Bell, Charles C., McCallum, Naomi, Williams, Bronwyn and Perkins, Andrew C. (2015). KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome. Blood, 125 (15), 2405-2417. doi: 10.1182/blood-2014-08-590968
Bell, Charles C., Magor, Graham W., Gillinder, Kevin R. and Perkins, Andrew C. (2014). A high-throughput screening strategy for detecting CRISPR-Cas9 induced mutations using next-generation sequencing. BMC Genomics, 15 (1) 1002, 1002. doi: 10.1186/1471-2164-15-1002
Narytnyk, Alla, Gillinder, Kevin, Verdon, Bernard, Clewes, Oliver and Sieber-Blum, Maya (2014). Neural crest stem cell-specific deletion of the Pygopus2 gene modulates hair follicle development. Stem Cell Reviews and Reports, 10 (1), 60-68. doi: 10.1007/s12015-013-9466-z
Clewes, Oliver, Narytnyk, Alla, Gillinder, Kevin R., Loughney, Andrew D., Murdoch, Alison P. and Sieber-Blum, Maya (2011). Human epidermal neural crest stem cells (hEPI-NCSC)-Characterization and directed differentiation into osteocytes and melanocytes. Stem Cell Reviews and Reports, 7 (4), 799-814. doi: 10.1007/s12015-011-9255-5
Pennisi, David J., Wilkinson, Lorine, Kolle, Gabriel, Sohaskey, Michael L., Gillinder, Kevin, Piper, Michael J., McAvoy, John W., Lovicu, Frank J. and Little, Melissa H. (2007). Crim1(KST264/KST264) mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems. Developmental Dynamics, 236 (2), 502-511. doi: 10.1002/dvdy.21015
Rae, F. K., Martinez, G., Gillinder, K. R., Smith, A., Shooter, G., Forrest, A. R., Grimmond, S. M. and Little, M. H. (2004). Anlaysis of complementary expression profiles following WT1 induction versus repression reveals the cholesterol/fatty acid synthetic pathways as a possible major target of WT1. Oncogene, 23 (17), 3067-3079. doi: 10.1038/sj.onc.1207360
Conference Papers
Gillinder, Kevin R., Magor, Graham, Bell, Charles, Ilsley, Melissa D., Huang, Stephen and Perkins, Andrew (2018). KLF1 acts as a pioneer transcription factor to open chromatin and facilitate recruitment of GATA1. 60th Annual Meeting of the American-Society-of-Hematology (ASH), San Diego, CA, United States, 1-4 December 2018. Washington, DC, United States: American Society of Hematology. doi: 10.1182/blood-201/1-99-11960/1
Huang, Stephen, Gillinder, Kevin R., Ilsley, Melissa, Magor, Graham, Tallack, Michael, Sorolla, Anabel, Oey, Harald, Harten, Sarah, Clemens-Daxinger, Lucia, Whitelaw, Emma and Perkins, Andrew C. (2015). Characterisation of novel hypomorphic and null mutations in klf1 derived from a genetic screen for modifiers of a-globin transgene variegation. 57th Annual Meeting of the American Society of Hematology, Orlando, FL, United States, 5-8 December 2015. Washington, DC, United States: American Society of Hematology.
Nebor, Danitza, Robledo, Raymond F., Graber, Joel H., Aighewi, Omorose, Blanc, Lionel, Perkins, Andrew C., Gillinder, Kevin R., Bieker, James J. and Peters, Luanne L. (2015). Degenerate DNA Binding By Mutant (E339D) KLF1 Dramatically Alters the Erythroid Transcriptome in the Nan Mouse Model. 57th Annual Meeting of the American-Society-of-Hematology, Orlando Fl, Dec 05-08, 2015. WASHINGTON: AMER SOC HEMATOLOGY.
Perkins, Andrew C., Gillinder, Kevin R., Magor, Graham, Lajoie, Mathieu, Bailey, Timothy L., Tallack, Michael R., Ilsley, Melissa, Landsberg, Michael, Mackay, Joel P., Bieker, James J. and Peters, Luanne L. (2014). New Insights into the Mechanism of Dominant Anemia Caused By Zinc Finger Mutations in KLF1. 56th Annual Meeting of the American Society of Hematology, San Francisco, CA United States, 06-09 December 2014. Washington, DC United States: American Society of Hematology.
Gillinder, Kevin R., Lajoie, Mathieu, Ilsley, Melissa, Tallack, Michael R., Magor, Graham, Landsberg, Michael, Bailey, Timothy L. and Perkins, Andrew C. (2013). Mutations In The Zinc Finger Domain Of Human and Mouse KLF1 Cause Congenital Dyserythropoietic Anemia (CDA) Via Promiscuous DNA Binding and Ectopic Target Gene Expression. 55th Annual Meeting of the American-Society-of-Hematology, New Orleans La, Dec 07-10, 2013. WASHINGTON: AMER SOC HEMATOLOGY.
Gillinder, Kevin R., Hughes, Jim R., Tallack, Michael R., Magor, Graham, Ilsley, Melissa, Davies, James, Higgs, Douglas and Perkins, Andrew C. (2013). Dynamics and Mechanics Of KLF1 Regulation In Erythropoiesis. 55th Annual Meeting of the American-Society-of-Hematology, New Orleans La, Dec 07-10, 2013. WASHINGTON: AMER SOC HEMATOLOGY.
Rajan, N., Gillinder, K., Lord, C., Langtry, J. A. A., Burn, J., Ashworth, A., Chaudhury, B. and Sieber-Blum, M. (2010). Unravelling cylindromas: insights into appendageal tumour patterning from patients with truncating CYLD mutations. 90th Annual Meeting of the British-Association-of-Deermatologists, Manchester United Kingdom, Jul 06-08, 2010. MALDEN: WILEY-BLACKWELL PUBLISHING, INC.
Gillinder, Kevin, Rajan, Neil, Loughney, Andrew, Murdoch, Alison and Sieber-Blum, Maya (2009). Characterization of human epidermal neural crest stem cell (hEPI-NCSC) candidate cells. BETHESDA: FEDERATION AMER SOC EXP BIOL.
Pennisi, D., Wilkinson, L., Kolle, G., Gillinder, K. and Little, M. (2005). A hypomorphic mutant of Crim1 reveals a requirement on Crim1 for proper development. AMSTERDAM: ELSEVIER SCIENCE BV.
Wilkinson, Lorine, Gillinder, K., Kolle, G., Kinna, G., Seow, J., Pennis, P. and Little, M. (2005). Towards Elucidating the Role of Crim1 in Kidney Development. HOBOKEN: WILEY-BLACKWELL.
Kett, MM, Ruta, LAM, Gillinder, K, Anderson, WP and Little, MH (2005). Role of Crim1, a novel TGF beta superfamily modulator, in renal development. Experimental Biology 2005 Meeting/35th International Congress of Physiological Sciences, San Diego Ca, Mar 31-Apr 06, 2005. BETHESDA: FEDERATION AMER SOC EXP BIOL.
Dataset Collection
Gillinder, Kevin Robert (2013). Genetic regulation of red blood cell formation in mice. Mater Medical Research Institute. (Collection) doi: 10.14264/uql.2017.88