Esther Camp-Dotlic
Adelaide Medical School
Faculty of Health and Medical Sciences
Eligible to supervise Masters and PhD - email supervisor to discuss availability.
Esther has a research background in progenitor cell biology, migration and differentiation during development and tissue remodelling in vertebrates. She joined the Mesenchymal Stem Cell Research Group in 2013 after having worked as a post-doctoral scientist in Australia, Spain and the UK. Her work at SAHMRI is focused on understanding the molecular mechanisms that control mesenchymal stem/progenitor cell (MSC) proliferation and differentiation during cranial development. The projects she is developing include; investigating the role of the transcription factor Twist-1 and microRNAs in skeletal bone derived MSC and cranial cells, in addition to how these factors can lead to cranial defects in children. She also leads a number of pre-clinical trials that look at the efficiency and safety of drugs to prevent abnormal cranial suture fusion. A better understanding of how cranial defects occur will enable the development of new therapeutic strategies to alleviate abnormal cranial bone formation in children.
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Language Competencies
Language Competency English Can read, write, speak, understand spoken and peer review Spanish; Castilian Can read, write, speak and understand spoken -
Education
Date Institution name Country Title — The University of Adelaide Australia PhD
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Journals
Year Citation 2018 Camp, E., Anderson, P., Zannettino, A., Glackin, C., & Gronthos, S. (2018). Tyrosine kinase receptor c-ros-oncogene 1 inhibition alleviates aberrant bone formation of TWIST-1 haploinsufficient calvarial cells from Saethre-Chotzen syndrome patients. Journal of Cellular Physiology, 233(9), 7320-7332.
Scopus2 WoS2 Europe PMC22018 Camp-Dotlic, E., Pribadi, C., Anderson, P., Zannettino, A., & Gronthos, S. (2018). miRNA-376c-3p mediates TWIST-1 inhibition of BMSC osteogenesis and can reduce aberrant bone formation of TWIST-1 haploinsufficient calvarial cells. Stem Cells and Development, 27(23), 1621-1633.
Scopus2 WoS22017 Camp, E., Anderson, P., Zannettino, A., & Gronthos, S. (2017). Tyrosine kinase receptor c-ros-oncogene 1 mediates TWIST-1 regulation of human mesenchymal stem cell lineage commitment. Bone, 94, 98-107.
Scopus6 WoS6 Europe PMC52017 Tomokiyo, A., Hynes, K., Ng, J., Menicanin, D., Camp, E., Arthur, A., . . . Mark Bartold, P. (2017). Generation of Neural Crest-Like Cells From Human Periodontal Ligament Cell-Derived Induced Pluripotent Stem Cells. Journal of Cellular Physiology, 232(2), 402-416.
Scopus5 WoS4 Europe PMC12015 Cakouros, D., Isenmann, S., Hemming, S., Menicanin, D., Camp, E., Zannetinno, A., & Gronthos, S. (2015). Novel basic helix-loop-helix transcription factor hes4 antagonizes the function of twist-1 to regulate lineage commitment of bone marrow stromal/stem cells. Stem Cells and Development, 24(11), 1297-1308.
Scopus13 WoS13 Europe PMC122014 Song, J., McColl, J., Camp, E., Kennerley, N., Mok, G., McCormick, D., . . . Münsterberg, A. (2014). Smad1 transcription factor integrates BMP2 and Wnt3a signals in migrating cardiac progenitor cells. Proceedings of the National Academy of Sciences of the United States of America, 111(20), 7337-7342.
Scopus22 Europe PMC192012 Camp, E., Dietrich, S., & Münsterberg, A. (2012). Fate mapping identifies the origin of SHF/AHF progenitors in the chick primitive streak. PLoS One, 7(12), e51948-1-e51948-13.
Scopus11 Europe PMC92011 Camp, E., & Munsterberg, A. (2011). Ingression, migration and early differentiation of cardiac progenitors. Frontiers in Bioscience (Landmark Edition), 16(7), 2416-2426.
Scopus5 Europe PMC42011 Sánchez-Sánchez, A., Camp, E., & Mullor, J. (2011). Fishing pluripotency mechanisms in vivo. International Journal of Biological Sciences, 7(4), 410-417.
Scopus112010 Sánchez-Sánchez, A., Camp, E., Leal-Tassias, A., & Mullor, J. (2010). Wnt signaling has different temporal roles during retinal development. Developmental Dynamics, 239(1), 297-310.
Scopus9 Europe PMC52010 Sánchez-Sánchez, A., Camp, E., García-España, A., Leal-Tassias, A., & Mullor, J. (2010). Medaka Oct4 is expressed during early embryo development, and in primordial germ cells and adult gonads. Developmental Dynamics, 239(2), 680-687.
Scopus252010 Newman, M., Wilson, L., Camp-Dotlic, E., Verdile, G., Martins, R., & Lardelli, M. (2010). A zebrafish melanophore model of amyloidβ toxicity. Zebrafish, 7(2), 155-159.
Scopus16 WoS16 Europe PMC102010 Sánchez-Sánchez, A., Camp, E., Leal-Tassias, A., Atkinson, S., Armstrong, L., Díaz-Llopis, M., & Mullor, J. (2010). Nanog regulates primordial germ cell migration through Cxcr4b. Stem Cells, 28(9), 1457-1464.
Scopus14 Europe PMC112010 Sánchez-Sánchez, A., Camp, E., García-España, A., Leal-Tassias, A., & Mullor, J. (2010). Medaka Oct4 is expressed during early embryo development, and in primordial germ cells and adult gonads.. Developmental dynamics : an official publication of the American Association of Anatomists, 239(2), 672-679.
Scopus17 Europe PMC262009 Camp, E., Sánchez-Sánchez, A., García-España, A., DeSalle, R., Odqvist, L., O'Connor, J., & Mullor, J. (2009). Nanog regulates proliferation during early fish development. Stem Cells, 27(9), 2081-2091.
Scopus44 Europe PMC352003 Camp-Dotlic, E., Badhwar, P., Mann, G., & Lardelli, M. (2003). Expression analysis of a Tyrosinase promoter sequence in zebrafish. Pigment Cell Research, 16(2), 117-126.
Scopus12 WoS13 Europe PMC72003 Camp-Dotlic, E., Hope, R., Kortschak, R., Cox, T., & Lardelli, M. (2003). Expression of three spalt (sal) gene homologues in zebrafish embryos. Development Genes and Evolution, 213(1), 35-43.
Scopus20 WoS19 Europe PMC172003 Nornes, S., Groth, C., Camp-Dotlic, E., Ey, P., & Lardelli, M. (2003). Developmental control of Presenilin1 expression, endoproteolysis, and interaction in zebrafish embryos. Experimental Cell Research, 289(1), 124-132.
Scopus39 WoS35 Europe PMC242001 Camp-Dotlic, E., & Lardelli, M. (2001). Tyrosinase gene expression in zebrafish embryos. Development Genes and Evolution, 211(3), 150-153.
Scopus46 WoS44 Europe PMC312000 Tamme, R., Camp-Dotlic, E., Kortschak, R., & Lardelli, M. (2000). Non-specific, nested suppression PCR method for isolation of unknown flanking DNA. Biotechniques, 28(5), 895-902.
Scopus9 WoS8 Europe PMC6 -
Conference Papers
Year Citation 2018 Camp, E., Anderson, P., Zannettino, A., & Gronthos, S. (2018). Inhibition of tyrosine kinase receptor C-ROS-1 as a novel treatment for patients with TWIST haploinsufficiency induced craniosynostosis. In JOURNAL OF BONE AND MINERAL RESEARCH Vol. 33 (pp. 424). Montreal, CANADA: WILEY. 2005 Camp-Dotlic, E., Froiland, D., Kind, K., Irving-Rodgers, H., Thompson, J., & Russell, D. (2005). Murine HIF-1a localisation by immunohistochemistry in a mouse reproductive tissue. In Reproduction Fertility and Development Vol. 17 (pp. 129). C S I R O Publishing.
National Health and Medical Research Council- Histone Demethylase KDM6 is a novel target for treating craniosynostosis in children with Saethre-Chotzen Syndrome(2018-2020).
National Health and Medical Research Council- Tyrosine Kinase receptor c-ros-oncogene 1 mediates TWIST-1 haploinsufficiency induced craniosynostosis in children: A novel therapeutic target (2017-2019).
Channel 7 Children's Research Foundation of SA Inc, Identification of TWIST-1 regulated microRNAs which control cranial bone development in children (2015).
British Society of Developmental Biology Travel Grant (2011).
John and Pamela Salter Charitable Trust Grant UK (2010).
MYORES Exchange Fund grant. MYORES: European Muscle Development Network (2009).
Cellular and Systems Neurobiology
Physiology 2A, 2B
Principles of Human Health and Disease
Biology of Disease
Dental Science and Practice 1 Part 1
Human Biology IOH Part 2
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Current Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2018 Co-Supervisor KDM6A, a Histone Demethylase, as a Novel Therapeutic Target for Treating Craniosynostosis in Children with Saethre-Chotzen Syndrome (SCS) Doctor of Philosophy Doctorate Full Time Miss Clara Pribadi -
Past Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2016 - 2019 Co-Supervisor Identification of Molecular Mechanisms Mediating TWIST-1 Regulation of Mesenchymal Stem Cell Proliferation and Differentiation Doctor of Philosophy Doctorate Full Time Mr Chee Ho H'ng -
Other Supervision Activities
Date Role Research Topic Location Program Supervision Type Student Load Student Name 2017 - 2017 Co-Supervisor Targeting Tyrosinase Kinase Receptor C-ROS-Oncogene 1 to reduce aberrant osteogenesis in Twist-1 haploinsufficiency induced craniosynostosis The University of Adelaide — Honours Full Time Gabrielle Fusco-Allison
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