3D human liver tissue from pluripotent stem cells displays stable phenotype in vitro and supports compromised liver function in vivo
Rashidi, Hassan, Luu, Nguyet-Thin, Alwahsh, Salamah M., Ginai, Maaria, Alhaque, Sharmin, Dong, Hua, Tomaz, Rute A., Vernay, Bertrand, Vigneswara, Vasanthy, Hallett, John M., Chandrashekran, Anil, Dhawan, Anil, Vallier, Ludovic, Bradley, Mark, Callanan, Anthony, Forbes, Stuart J., Newsome, Philip N., Hay, David C.
Published in Archives of toxicology (01.10.2018)
Published in Archives of toxicology (01.10.2018)
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Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans
Gaston-Massuet, Carles, Andoniadou, Cynthia Lilian, Signore, Massimo, Jayakody, Sujatha A, Charolidi, Nicoletta, Kyeyune, Roger, Vernay, Bertrand, Jacques, Thomas S, Taketo, Makoto Mark, Le Tissier, Paul, Dattani, Mehul T, Martinez-Barbera, Juan Pedro
Published in Proceedings of the National Academy of Sciences - PNAS (12.07.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (12.07.2011)
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Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure
Escuin, Sarah, Vernay, Bertrand, Savery, Dawn, Gurniak, Christine B, Witke, Walter, Greene, Nicholas D E, Copp, Andrew J
Published in Journal of cell science (15.07.2015)
Published in Journal of cell science (15.07.2015)
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The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
Waters, Aoife M, Asfahani, Rowan, Carroll, Paula, Bicknell, Louise, Lescai, Francesco, Bright, Alison, Chanudet, Estelle, Brooks, Anthony, Christou-Savina, Sonja, Osman, Guled, Walsh, Patrick, Bacchelli, Chiara, Chapgier, Ariane, Vernay, Bertrand, Bader, David M, Deshpande, Charu, O’ Sullivan, Mary, Ocaka, Louise, Stanescu, Horia, Stewart, Helen S, Hildebrandt, Friedhelm, Otto, Edgar, Johnson, Colin A, Szymanska, Katarzyna, Katsanis, Nicholas, Davis, Erica, Kleta, Robert, Hubank, Mike, Doxsey, Stephen, Jackson, Andrew, Stupka, Elia, Winey, Mark, Beales, Philip L
Published in Journal of medical genetics (01.03.2015)
Published in Journal of medical genetics (01.03.2015)
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Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
Thomas, Anna C., Williams, Hywel, Setó-Salvia, Núria, Bacchelli, Chiara, Jenkins, Dagan, O’Sullivan, Mary, Mengrelis, Konstantinos, Ishida, Miho, Ocaka, Louise, Chanudet, Estelle, James, Chela, Lescai, Francesco, Anderson, Glenn, Morrogh, Deborah, Ryten, Mina, Duncan, Andrew J., Pai, Yun Jin, Saraiva, Jorge M., Ramos, Fabiana, Farren, Bernadette, Saunders, Dawn, Vernay, Bertrand, Gissen, Paul, Straatmaan-Iwanowska, Anna, Baas, Frank, Wood, Nicholas W., Hersheson, Joshua, Houlden, Henry, Hurst, Jane, Scott, Richard, Bitner-Glindzicz, Maria, Moore, Gudrun E., Sousa, Sérgio B., Stanier, Philip
Published in American journal of human genetics (06.11.2014)
Published in American journal of human genetics (06.11.2014)
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Protein deiminases: New players in the developmentally regulated loss of neural regenerative ability
Lange, Sigrun, Gögel, Stefanie, Leung, Kit-Yi, Vernay, Bertrand, Nicholas, Anthony P., Causey, Corey P., Thompson, Paul R., Greene, Nicholas D.E., Ferretti, Patrizia
Published in Developmental biology (15.07.2011)
Published in Developmental biology (15.07.2011)
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An essential function of the mitogen-activated protein kinase Erk2 in mouse trophoblast development
Saba-El-Leil, Marc K, Vella, Francis D J, Vernay, Bertrand, Voisin, Laure, Chen, Lan, Labrecque, Nathalie, Ang, Siew-Lan, Meloche, Sylvain
Published in EMBO reports (01.10.2003)
Published in EMBO reports (01.10.2003)
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Otx2 Regulates Subtype Specification and Neurogenesis in the Midbrain
Vernay, Bertrand, Koch, Muriel, Vaccarino, Flora, Briscoe, James, Simeone, Antonio, Kageyama, Ryoichiro, Ang, Siew-Lan
Published in The Journal of neuroscience (11.05.2005)
Published in The Journal of neuroscience (11.05.2005)
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Injection of embryonic stem cell derived macrophages ameliorates fibrosis in a murine model of liver injury
Haideri, Sharmin S., McKinnon, Alison C., Taylor, A. Helen, Kirkwood, Phoebe, Starkey Lewis, Philip J., O’Duibhir, Eoghan, Vernay, Bertrand, Forbes, Stuart, Forrester, Lesley M.
Published in npj Regenerative medicine (23.05.2017)
Published in npj Regenerative medicine (23.05.2017)
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Disease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration
Worth, Austen J.J., Metelo, Joao, Bouma, Gerben, Moulding, Dale, Fritzsche, Marco, Vernay, Bertrand, Charras, Guillaume, Cory, Giles O.C., Thrasher, Adrian J., Burns, Siobhan O.
Published in Blood (03.01.2013)
Published in Blood (03.01.2013)
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AimSeg
Carrillo-Barberà, Pau, Rondelli, Ana Maria, Morante-Redolat, Jose Manuel, Vernay, Bertrand, Williams, Anna, Bankhead, Peter
Published in PLoS computational biology (01.11.2023)
Published in PLoS computational biology (01.11.2023)
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Human γδ T lymphocytes are licensed for professional antigen presentation by interaction with opsonized target cells
Himoudi, Nourredine, Morgenstern, Daniel A, Yan, Mengyong, Vernay, Bertrand, Saraiva, Luisa, Wu, Yin, Cohen, Cyrille J, Gustafsson, Kenth, Anderson, John
Published in The Journal of immunology (1950) (15.02.2012)
Published in The Journal of immunology (1950) (15.02.2012)
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Human gamma delta T Lymphocytes Are Licensed for Professional Antigen Presentation by Interaction with Opsonized Target Cells
Himoudi, Nourredine, Morgenstern, Daniel A, Yan, Mengyong, Vernay, Bertrand, Saraiva, Luisa, Wu, Yin, Cohen, Cyrille J, Gustafsson, Kenth, Anderson, John
Published in The Journal of immunology (1950) (15.02.2012)
Published in The Journal of immunology (1950) (15.02.2012)
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Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
Jackson, Andrew P, Griffith, Elen, Walker, Sarah, Martin, Carol-Anne, Vagnarelli, Paola, Stiff, Tom, Vernay, Bertrand, Sanna, Nouriya Al, Saggar, Anand, Hamel, Ben, Earnshaw, William C, Jeggo, Penny A, O'Driscoll, Mark
Published in Nature genetics (01.02.2008)
Published in Nature genetics (01.02.2008)
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CoNIC Challenge: Pushing the frontiers of nuclear detection, segmentation, classification and counting
Graham, Simon, Vu, Quoc Dang, Jahanifar, Mostafa, Weigert, Martin, Schmidt, Uwe, Zhang, Wenhua, Zhang, Jun, Yang, Sen, Xiang, Jinxi, Wang, Xiyue, Rumberger, Josef Lorenz, Baumann, Elias, Hirsch, Peter, Liu, Lihao, Hong, Chenyang, Aviles-Rivero, Angelica I, Jain, Ayushi, Ahn, Heeyoung, Hong, Yiyu, Azzuni, Hussam, Xu, Min, Yaqub, Mohammad, Blache, Marie-Claire, Piégu, Benoît, Vernay, Bertrand, Scherr, Tim, Böhland, Moritz, Löffler, Katharina, Li, Jiachen, Ying, Weiqin, Wang, Chixin, Snead, David, Raza, Shan E Ahmed, Minhas, Fayyaz, Rajpoot, Nasir M
Published in Medical image analysis (01.02.2024)
Published in Medical image analysis (01.02.2024)
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Analysis of Coronary Vessels in Cleared Embryonic Hearts
Ivins, Sarah, Roberts, Catherine, Vernay, Bertrand, Scambler, Peter J.
Published in Journal of visualized experiments (07.12.2016)
Published in Journal of visualized experiments (07.12.2016)
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Journal Article
Analysis of Coronary Vessels in Cleared Embryonic Hearts
Ivins, Sarah, Roberts, Catherine, Vernay, Bertrand, Scambler, Peter J
Published in Journal of visualized experiments (07.12.2016)
Published in Journal of visualized experiments (07.12.2016)
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