Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yvette Hoade"'
Autor:
Oscar A. Peña, Alexandra Lubin, Jasmine Rowell, Yvette Hoade, Noreen Khokhar, Hanna Lemmik, Christopher Mahony, Phoebe Dace, Chianna Umamahesan, Elspeth M. Payne
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Germline loss or mutation of one copy of the transcription factor GATA2 in humans leads to a range of clinical phenotypes affecting hematopoietic, lymphatic and vascular systems. GATA2 heterozygous mice show only a limited repertoire of the features
Externí odkaz:
https://doaj.org/article/024e03d57978457a9084fb5f7643a44d
Autor:
Alexandra Lubin, Jason Otterstrom, Yvette Hoade, Ivana Bjedov, Eleanor Stead, Matthew Whelan, Gaia Gestri, Yael Paran, Elspeth Payne
Publikováno v:
Biology Open, Vol 10, Iss 9 (2021)
Zebrafish provide a unique opportunity for drug screening in living animals, with the fast-developing, transparent embryos allowing for relatively high-throughput, microscopy-based screens. However, the limited availability of rapid, flexible imaging
Externí odkaz:
https://doaj.org/article/dbe9a58d3e134c6e8b6b6f9413ca06f5
Autor:
Arief S. Gunawan, Donal P. McLornan, Bridget Wilkins, Katherine Waghorn, Yvette Hoade, Nicholas C. P. Cross, Claire N. Harrison
Publikováno v:
Haematologica, Vol 102, Iss 6 (2017)
Externí odkaz:
https://doaj.org/article/1b2eb367507b4fa1861c4b11f2ccec2e
Autor:
Jasmine Rowell, Chianna Umamahesan, Oscar A Peña, Phoebe Dace, Hanna Lemmik, Yvette Hoade, Alexandra Lubin, Christopher B. Mahony, Elspeth Payne, Noreen Khokhar
Publikováno v:
Peña, O A, Lubin, A, Rowell, J, Hoade, Y, Khokhar, N, Lemmik, H, Mahony, C, Dace, P, Umamahesan, C & Payne, E M 2021, ' Differential Requirement of Gata2a and Gata2b for Primitive and Definitive Myeloid Development in Zebrafish ', Frontiers in Cell and Developmental Biology, vol. 9, 708113 . https://doi.org/10.3389/fcell.2021.708113
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Germline loss or mutation of one copy of the transcription factor GATA2 in humans leads to a range of clinical phenotypes affecting hematopoietic, lymphatic and vascular systems. GATA2 heterozygous mice show only a limited repertoire of the features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1de74ce600599b2703d09134c1bc007c
https://hdl.handle.net/1983/ba9a5231-fe2f-46e5-9819-5c45098d1762
https://hdl.handle.net/1983/ba9a5231-fe2f-46e5-9819-5c45098d1762
Autor:
Yael Paran, Gaia Gestri, Yvette Hoade, Matthew Whelan, Jason Otterstrom, Alexandra Lubin, Ivana Bjedov, Elspeth Payne, Eleanor R. Stead
Publikováno v:
Biology Open, Vol 10, Iss 9 (2021)
Biology Open
article-version (VoR) Version of Record
Biology Open
article-version (VoR) Version of Record
Zebrafish provide a unique opportunity for drug screening in living animals, with the fast-developing, transparent embryos allowing for relatively high-throughput, microscopy-based screens. However, the limited availability of rapid, flexible imaging
Autor:
Philip George, Yvette Hoade, Sahra Ali, Simon Watt, Varun Mehra, Catherine Cargo, Fergus Jack, Paul Evans, Tiziana Fanelli, William J. Tapper, Alastair Whiteway, Gabriela Sciuccati, Iwo Pieniak, Jamie Cavenagh, Emma Das-Gupta, Andres Virchis, Nicole Naumann, Kavita Patel, Rowena Thomas-Dewing, Patrick Thornton, Kris Zegocki, Louise Wallis, Charlotte Grimley, Gonzalo Carreño-Tarragona, Peter Forsyth, Andreas Reiter, Nicholas C.P. Cross, Laura Munro, Kaljit Bhuller, Andrew S Duncombe, Andrew Chase, Barbara J. Bain, Mohamad Jawhar, Johannes Lübke, Ali Rismani, Sonja Burgstaller
Publikováno v:
Leukemia
Cross, N C P, Hoade, Y, Tapper, W J, Carreno-tarragona, G, Fanelli, T, Jawhar, M, Naumann, N, Pieniak, I, Lübke, J, Ali, S, Bhuller, K, Burgstaller, S, Cargo, C, Cavenagh, J, Duncombe, A S, Das-gupta, E, Evans, P, Forsyth, P, George, P, Grimley, C, Jack, F, Munro, L, Mehra, V, Patel, K, Rismani, A, Sciuccati, G, Thomas-dewing, R, Thornton, P, Virchis, A, Watt, S, Wallis, L, Whiteway, A, Zegocki, K, Bain, B J, Reiter, A & Chase, A 2018, ' Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia ', Leukemia . https://doi.org/10.1038/s41375-018-0342-3
Cross, N C P, Hoade, Y, Tapper, W J, Carreno-tarragona, G, Fanelli, T, Jawhar, M, Naumann, N, Pieniak, I, Lübke, J, Ali, S, Bhuller, K, Burgstaller, S, Cargo, C, Cavenagh, J, Duncombe, A S, Das-gupta, E, Evans, P, Forsyth, P, George, P, Grimley, C, Jack, F, Munro, L, Mehra, V, Patel, K, Rismani, A, Sciuccati, G, Thomas-dewing, R, Thornton, P, Virchis, A, Watt, S, Wallis, L, Whiteway, A, Zegocki, K, Bain, B J, Reiter, A & Chase, A 2018, ' Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia ', Leukemia . https://doi.org/10.1038/s41375-018-0342-3
Determining the underlying cause of persistent eosinophilia is important for effective clinical management but remains a diagnostic challenge in many cases. We identified STAT5B N642H, an established oncogenic mutation, in 27/1715 (1.6%) cases referr
Autor:
Toshiko Tanaka, Gabriella Galatà, William J. Tapper, Sigurd Broesby-Olsen, Yvette Hoade, Ahmed A. Z. Dawoud, Carsten Bindslev-Jensen, Alessandro M. Vannucchi, Christian Gieger, Theresia M. Schnurr, Manja Meggendorfer, Javier I. Muñoz-González, Andreas Reiter, Paola Guglielmelli, Andrés C. García-Montero, Torsten Haferlach, Luigi Ferrucci, Iván Álvarez-Twose, Hanne Vestergaard, Michael Boe Møller, Nicholas C.P. Cross, Konstantin Strauch, Andrew Chase, Stefania Bandinelli, Alberto Orfao, Thomas Kielsgaard Kristensen, Deepti Radia
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Am J Hum Genet
Am. J. Hum. Genet. 108, 284-294 (2021)
Galatà, G, García-Montero, A C, Kristensen, T, Dawoud, A A Z, Muñoz-González, J I, Meggendorfer, M, Guglielmelli, P, Hoade, Y, Alvarez-Twose, I, Gieger, C, Strauch, K, Ferrucci, L, Tanaka, T, Bandinelli, S, Schnurr, T M, Haferlach, T, Broesby-Olsen, S, Vestergaard, H, Møller, M B, Bindslev-Jensen, C, Vannucchi, A M, Orfao, A, Radia, D, Reiter, A, Chase, A J, Cross, N C P & Tapper, W J 2021, ' Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis ', American Journal of Human Genetics, vol. 108, no. 2, pp. 284-294 . https://doi.org/10.1016/j.ajhg.2020.12.007
instname
Am J Hum Genet
Am. J. Hum. Genet. 108, 284-294 (2021)
Galatà, G, García-Montero, A C, Kristensen, T, Dawoud, A A Z, Muñoz-González, J I, Meggendorfer, M, Guglielmelli, P, Hoade, Y, Alvarez-Twose, I, Gieger, C, Strauch, K, Ferrucci, L, Tanaka, T, Bandinelli, S, Schnurr, T M, Haferlach, T, Broesby-Olsen, S, Vestergaard, H, Møller, M B, Bindslev-Jensen, C, Vannucchi, A M, Orfao, A, Radia, D, Reiter, A, Chase, A J, Cross, N C P & Tapper, W J 2021, ' Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis ', American Journal of Human Genetics, vol. 108, no. 2, pp. 284-294 . https://doi.org/10.1016/j.ajhg.2020.12.007
Mastocytosis is a rare myeloid neoplasm characterized by uncontrolled expansion of mast cells, driven in >80% of affected individuals by acquisition of the KIT D816V mutation. To explore the hypothesis that inherited variation predisposes to mastocyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::376183914627f9d20406cb384313e20b
http://hdl.handle.net/10261/261456
http://hdl.handle.net/10261/261456
Autor:
Yael Paran, Alexandra Lubin, Elspeth Payne, Gaia Gestri, Yvette Hoade, Eleanor R. Stead, Matthew V. X. Whelan, Ivana Bjedov, Jason Otterstrom
Zebrafish provide a unique opportunity for drug screening in living animals, with the fast developing, transparent embryos allowing for relatively high throughput, microscopy-based screens. However, the limited availability of rapid, flexible imaging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a1508a072668b914b7ab9bcbc947491
https://doi.org/10.1101/2020.12.16.423108
https://doi.org/10.1101/2020.12.16.423108
Autor:
Charlotta Böiers, Oscar A Peña, Alexandra Lubin, Simon Richardson, Elspeth Payne, Maria Virgilio, Catherine Hockings, Youngrock Jung, Jasmine Rowell, Yvette Hoade, Karin Tuschl, Leonardo E Valdivia, Phoebe Dace
Publikováno v:
Peña, O A, Lubin, A, Hockings, C, Rowell, J, Jung, Y, Hoade, Y, Dace, P, Valdivia, L E, Tuschl, K, Böiers, C, Virgilio, M C, Richardson, S & Payne, E M 2021, ' TLR7 ligation augments hematopoiesis in Rps14 (uS11) deficiency via paradoxical suppression of inflammatory signaling ', Blood Advances, vol. 5, no. 20, pp. 4112-4124 . https://doi.org/10.1182/bloodadvances.2020003055
Myelodysplastic syndrome (MDS) is a hematological malignancy characterized by blood cytopenias and predisposition to acute myeloid leukemia (AML). Therapies for MDS are lacking, particularly those that have an impact in the early stages of disease. W
Autor:
Maria Virgilio, Phoebe Dace, Simon Richardson, Oscar A Peña, Catherine Hockings, Yvette Hoade, Jasmine Rowell, Alexandra Lubin, Leonardo E Valdivia, Charlotta Böiers, Elspeth Payne, Karin Tuschl, Youngrock Jung
Myelodysplastic syndrome (MDS) is a haematological malignancy characterised by blood cytopenias and predisposition to acute myeloid leukaemia (AML). Therapies for MDS are lacking, particularly those that impact the early stages of disease. We develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c867196a0b78926d7eb3e6e4119a00c6
https://doi.org/10.1101/2020.07.06.175000
https://doi.org/10.1101/2020.07.06.175000