Graham LieschkeSummaryAffiliation: The Walter and Eliza Hall Institute of Medical Research Country: Australia Publications
Research Grants
| Collaborators
|
Detail Information
Publications
Animal models of human disease: zebrafish swim into viewGraham J Lieschke
Cancer and Haematology Division, Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria, 3050, Australia
Nat Rev Genet 8:353-67. 2007..This Review surveys the achievements and potential of zebrafish for modelling human diseases and for drug discovery and development...
The zebrafish as a model system for human diseaseAlister C Ward
Centre for Cellular and Molecular Biology, School of Biological and Chemical Sciences, Deakin University, Burwood, Victoria, Australia
Front Biosci 7:d827-33. 2002..This review aims to describe several representative examples of how the zebrafish can be successfully used to identify novel genes and assign gene function, providing invaluable clues to human pathophysiology...
Hematopoietic perturbation in zebrafish expressing a tel-jak2a fusionSara M N Onnebo
Centre for Cellular and Molecular Biology, School of Biological and Chemical Sciences, Deakin University, Burwood, Victoria, Australia
Exp Hematol 33:182-8. 2005..Such fusions can mediate factor-independent growth of hematopoietic cell lines and induction of malignancy in mouse models...
Zebrafish in hematology: sushi or science?Duncan Carradice
Walter and Eliza Hall Institute of Medical Reserch, Department of Medical Biology, University of Melbourne, and Department of Clinical Haematology and Medical Oncology, Royal Melbourne Hospital, Parkville, Australia
Blood 111:3331-42. 2008..Despite some limitations and challenges, their successes and discovery potential mean that zebrafish are here to stay in hematology research...
CREB activity modulates neural cell proliferation, midbrain-hindbrain organization and patterning in zebrafishSebastian Dworkin
Differentiation and Transcription Laboratory, Trescowthick Laboratories, Peter MacCallum Cancer Centre, Victoria, 3002, Australia
Dev Biol 307:127-41. 2007..These findings reveal broader and stage-specific physiological roles of CREB function during vertebrate neural development and proliferation...
Zebrafish SPI-1 (PU.1) marks a site of myeloid development independent of primitive erythropoiesis: implications for axial patterningGraham J Lieschke
Ludwig Institute for Cancer Research, The Royal Melbourne Hospital, Parkville, Victoria, 3050, Australia
Dev Biol 246:274-95. 2002....
Characterization of the zebrafish matrix metalloproteinase 9 gene and its developmental expression patternSimon Yoong
Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, Vic, Australia
Gene Expr Patterns 7:39-46. 2007..In the adult, mmp9 expression was most prominent in the splenic cords, a site occupied by mature myeloid cells in other species. These results suggest that mmp9 will serve as a useful marker of mature myeloid cells in the zebrafish...
Characterisation of duplicate zinc finger like 2 erythroid precursor genes in zebrafishBenjamin M Hogan
Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Victoria, Australia
Dev Genes Evol 216:523-9. 2006..The production of loss-of-function models for znfl2, znfl2b and znfl2/znfl2b together suggested that these erythrocyte specific zinc finger genes are dispensible for erythropoiesis...
Specification of the primitive myeloid precursor pool requires signaling through Alk8 in zebrafishBenjamin M Hogan
Ludwig Institute for Cancer Research, Post Office Box 2008, Royal Melbourne Hospital, Parkville, Victoria 3050, Australia
Curr Biol 16:506-11. 2006..1 expression, but the role of alk8 was independent of the scl-dependent cell-fate pathway. Furthermore, the role of Alk8 in myelopoiesis was genetically separable from its earlier role in dorsal-ventral embryonic patterning...
Knockdown of zebrafish crim1 results in a bent tail phenotype with defects in somite and vascular developmentGenevieve Kinna
Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia
Mech Dev 123:277-87. 2006..Hence, the primary role of zebrafish crim1 is likely to be the regulation of somitic and vascular development...
Developmental biology of zebrafish myeloid cellsMeredith O Crowhurst
Ludwig Institute for Cancer Research, The Royal Melbourne Hospital, Victoria, Australia
Int J Dev Biol 46:483-92. 2002....
Zebrafish gcm2 is required for gill filament budding from pharyngeal ectodermBenjamin M Hogan
Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Victoria 3050, Australia
Dev Biol 276:508-22. 2004..This study identifies yet another role for a GCM gene in embryonic development and indicates a role for gcm2 during the evolution of divergent pharyngeal morphologies...
Duplicate zebrafish pth genes are expressed along the lateral line and in the central nervous system during embryogenesisBenjamin M Hogan
Ludwig Institute for Cancer Research, P O Box 2008, The Royal Melbourne Hospital, Victoria 3050, Australia
Endocrinology 146:547-51. 2005..These temporally and anatomically restricted expression patterns imply a novel role for PTH family hormones during embryonic development of the zebrafish and allow for the genetic dissection of PTH function in this model organism...
The Netrin receptor Neogenin is required for neural tube formation and somitogenesis in zebrafishDavid J Mawdsley
Colon Molecular and Cell Biology Laboratory, Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Parkville, Victoria 3050, Australia
Dev Biol 269:302-15. 2004..These observations suggest a role for Neogenin in determining cell polarity or migrational directionality of both neuroectodermal and mesodermal cells during early embryonic development...
The zebrafish spi1 promoter drives myeloid-specific expression in stable transgenic fishAlister C Ward
Centre for Cellular and Molecular Biology, School of Biological and Chemical Sciences, Deakin University, Burwood, Victoria, Australia
Blood 102:3238-40. 2003..These TG(spi1:EGFP)pA301 transgenic zebrafish represent a valuable tool for further studies of myeloid development and its perturbation...
Research Grants
- Congenital myeloid failure syndromes in mutant zebrafishGraham Lieschke; Fiscal Year: 2007..A better understanding of normal myeloid cell development will also help understand the basis for the dysregulation of these processes in myeloproliferative and leukemic diseases. ..
