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554 results on '"Kaufmann, Kerstin"'

1. Best practices for the execution, analysis, and data storage of plant single-cell/nucleus transcriptomics.

Author

Grones, Carolin, Eekhout, Thomas, Shi, Dongbo, Neumann, Manuel, Berg, Lea, Ke, Yuji, Shahan, Rachel, Cox, Kevin, Gomez-Cano, Fabio, Nelissen, Hilde, Lohmann, Jan, Giacomello, Stefania, Martin, Olivier, Wang, Jia-Wei, Kaufmann, Kerstin, Raissig, Michael, Palfalvi, Gergo, Greb, Thomas, Libault, Marc, De Rybel, Bert, and Cole, Benjamin

Subjects
Reproducibility of Results, Gene Expression Profiling, Plants, Stress, Physiological, Information Storage and Retrieval
Abstract

Single-cell and single-nucleus RNA-sequencing technologies capture the expression of plant genes at an unprecedented resolution. Therefore, these technologies are gaining traction in plant molecular and developmental biology for elucidating the transcriptional changes across cell types in a specific tissue or organ, upon treatments, in response to biotic and abiotic stresses, or between genotypes. Despite the rapidly accelerating use of these technologies, collective and standardized experimental and analytical procedures to support the acquisition of high-quality data sets are still missing. In this commentary, we discuss common challenges associated with the use of single-cell transcriptomics in plants and propose general guidelines to improve reproducibility, quality, comparability, and interpretation and to make the data readily available to the community in this fast-developing field of research.

Published
2024

3. Adaptation to ex vivo culture reduces human hematopoietic stem cell activity independently of the cell cycle

Author

Johnson, Carys S., Williams, Matthew, Sham, Kendig, Belluschi, Serena, Ma, Wenjuan, Wang, Xiaonan, Lau, Winnie W. Y., Kaufmann, Kerstin B., Krivdova, Gabriela, Calderbank, Emily F., Mende, Nicole, McLeod, Jessica, Mantica, Giovanna, Li, Juan, Grey-Wilson, Charlotte, Drakopoulos, Michael, Basheer, Shaaezmeen, Sinha, Shubhankar, Diamanti, Evangelia, Basford, Christina, Wilson, Nicola K., Howe, Steven J., Dick, John E., Göttgens, Berthold, Green, Anthony R., Francis, Natalie, and Laurenti, Elisa

Published
2024
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6. Vision, challenges and opportunities for a Plant Cell Atlas.

Author

Plant Cell Atlas Consortium, Jha, Suryatapa Ghosh, Borowsky, Alexander T, Cole, Benjamin J, Fahlgren, Noah, Farmer, Andrew, Huang, Shao-Shan Carol, Karia, Purva, Libault, Marc, Provart, Nicholas J, Rice, Selena L, Saura-Sanchez, Maite, Agarwal, Pinky, Ahkami, Amir H, Anderton, Christopher R, Briggs, Steven P, Brophy, Jennifer An, Denolf, Peter, Di Costanzo, Luigi F, Exposito-Alonso, Moises, Giacomello, Stefania, Gomez-Cano, Fabio, Kaufmann, Kerstin, Ko, Dae Kwan, Kumar, Sagar, Malkovskiy, Andrey V, Nakayama, Naomi, Obata, Toshihiro, Otegui, Marisa S, Palfalvi, Gergo, Quezada-Rodríguez, Elsa H, Singh, Rajveer, Uhrig, R Glen, Waese, Jamie, Van Wijk, Klaas, Wright, R Clay, Ehrhardt, David W, Birnbaum, Kenneth D, and Rhee, Seung Y

Subjects
Plant Cell Atlas Consortium, 4D imaging, A. thaliana, Plant Cell Atlas, cell biology, chlamydomonas reinhardtii, location-to-function, maize, science forum, single-cell omics, translational research, Biochemistry and Cell Biology
Abstract

With growing populations and pressing environmental problems, future economies will be increasingly plant-based. Now is the time to reimagine plant science as a critical component of fundamental science, agriculture, environmental stewardship, energy, technology and healthcare. This effort requires a conceptual and technological framework to identify and map all cell types, and to comprehensively annotate the localization and organization of molecules at cellular and tissue levels. This framework, called the Plant Cell Atlas (PCA), will be critical for understanding and engineering plant development, physiology and environmental responses. A workshop was convened to discuss the purpose and utility of such an initiative, resulting in a roadmap that acknowledges the current knowledge gaps and technical challenges, and underscores how the PCA initiative can help to overcome them.

Published
2021

10. SEPALLATA-driven MADS transcription factor tetramerization is required for inner whorl floral organ development

Author

Hugouvieux, Veronique, primary, Blanc-Mathieu, Romain, additional, Janeau, Aline, additional, Paul, Michel, additional, Lucas, Jeremy, additional, Xu, Xiaocai, additional, Ye, Hailong, additional, Lai, Xuelei, additional, LeHir, Sarah, additional, Guillotin, Audrey, additional, Galien, Antonin, additional, Yan, Wenhao, additional, Nanao, Max, additional, Kaufmann, Kerstin, additional, Parcy, François, additional, and Zubieta, Chloe, additional

Published
2024
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12. The metabolic enzyme hexokinase 2 localizes to the nucleus in AML and normal haematopoietic stem and progenitor cells to maintain stemness

Author

Thomas, Geethu Emily, Egan, Grace, García-Prat, Laura, Botham, Aaron, Voisin, Veronique, Patel, Parasvi S., Hoff, Fieke W., Chin, Jordan, Nachmias, Boaz, Kaufmann, Kerstin B., Khan, Dilshad H., Hurren, Rose, Wang, Xiaoming, Gronda, Marcela, MacLean, Neil, O’Brien, Cristiana, Singh, Rashim P., Jones, Courtney L., Harding, Shane M., Raught, Brian, Arruda, Andrea, Minden, Mark D., Bader, Gary D., Hakem, Razq, Kornblau, Steve, Dick, John E., and Schimmer, Aaron D.

Published
2022
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18. Arabidopsis BBX14 is involved in high light acclimation and seedling development.

Author

Atanasov, Vasil, Schumacher, Julia, Muiño, Jose M., Larasati, Catharina, Wang, Liangsheng, Kaufmann, Kerstin, Leister, Dario, and Kleine, Tatjana

Subjects
ACCLIMATIZATION (Plants), ACCLIMATIZATION, ARABIDOPSIS, SEEDLINGS, TRANSCRIPTION factors, PLANT development
Abstract

SUMMARY: The development of photosynthetically competent seedlings requires both light and retrograde biogenic signaling pathways. The transcription factor GLK1 functions at the interface between these pathways and receives input from the biogenic signal integrator GUN1. BBX14 was previously identified, together with GLK1, in a core module that mediates the response to high light (HL) levels and biogenic signals, which was studied by using inhibitors of chloroplast development. Our chromatin immunoprecipitation‐Seq experiments revealed that BBX14 is a direct target of GLK1, and RNA‐Seq analysis suggests that BBX14 may function as a regulator of the circadian clock. In addition, BBX14 plays a role in chlorophyll biosynthesis during early onset of light. Knockout of BBX14 results in a long hypocotyl phenotype dependent on a retrograde signal. Furthermore, the expression of BBX14 and BBX15 during biogenic signaling requires GUN1. Investigation of the role of BBX14 and BBX15 in GUN‐type biogenic (gun) signaling showed that the overexpression of BBX14 or BBX15 caused de‐repression of CA1 mRNA levels, when seedlings were grown on norflurazon. Notably, transcripts of the LHCB1.2 marker are not de‐repressed. Furthermore, BBX14 is required to acclimate plants to HL stress. We propose that BBX14 is an integrator of biogenic signals and that BBX14 is a nuclear target of retrograde signals downstream of the GUN1/GLK1 module. However, we do not classify BBX14 or BBX15 overexpressors as gun mutants based on a critical evaluation of our results and those reported in the literature. Finally, we discuss a classification system necessary for the declaration of new gun mutants. Significance Statement: A picture is emerging in which BBX proteins have multifaceted functions in plant development, acting as receivers of chloroplast signals as well as playing a role in responses to acute stress. [ABSTRACT FROM AUTHOR]

Published
2024
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19. Distinct routes of lineage development reshape the human blood hierarchy across ontogeny

Author

Notta, Faiyaz, Zandi, Sasan, Takayama, Naoya, Dobson, Stephanie, Gan, Olga I, Wilson, Gavin, Kaufmann, Kerstin B, McLeod, Jessica, Laurenti, Elisa, Dunant, Cyrille F, McPherson, John D, Stein, Lincoln D, Dror, Yigal, and Dick, John E

Subjects
Regenerative Medicine, Stem Cell Research - Nonembryonic - Non-Human, Stem Cell Research, Stem Cell Research - Nonembryonic - Human, Hematology, Underpinning research, 1.1 Normal biological development and functioning, Adult, Antigens, CD34, Cell Lineage, Cell Separation, Cells, Cultured, Erythroid Cells, Fetal Blood, Gene Expression Profiling, Hematopoiesis, Humans, Liver, Megakaryocyte Progenitor Cells, Megakaryocytes, Multipotent Stem Cells, Myeloid Cells, Transcription, Genetic, General Science & Technology
Abstract

In a classical view of hematopoiesis, the various blood cell lineages arise via a hierarchical scheme starting with multipotent stem cells that become increasingly restricted in their differentiation potential through oligopotent and then unipotent progenitors. We developed a cell-sorting scheme to resolve myeloid (My), erythroid (Er), and megakaryocytic (Mk) fates from single CD34(+) cells and then mapped the progenitor hierarchy across human development. Fetal liver contained large numbers of distinct oligopotent progenitors with intermingled My, Er, and Mk fates. However, few oligopotent progenitor intermediates were present in the adult bone marrow. Instead, only two progenitor classes predominate, multipotent and unipotent, with Er-Mk lineages emerging from multipotent cells. The developmental shift to an adult "two-tier" hierarchy challenges current dogma and provides a revised framework to understand normal and disease states of human hematopoiesis.

Published
2016

23. Figure S7 from Distinct Assemblies of Heterodimeric Cytokine Receptors Govern Stemness Programs in Leukemia

Author

Kan, Winnie L., primary, Dhagat, Urmi, primary, Kaufmann, Kerstin B., primary, Hercus, Timothy R., primary, Nero, Tracy L., primary, Zeng, Andy G.X., primary, Toubia, John, primary, Barry, Emma F., primary, Broughton, Sophie E., primary, Gomez, Guillermo A., primary, Benard, Brooks A., primary, Dottore, Mara, primary, Cheung Tung Shing, Karen S., primary, Boutzen, Héléna, primary, Samaraweera, Saumya E., primary, Simpson, Kaylene J., primary, Jin, Liqing, primary, Goodall, Gregory J., primary, Begley, C. Glenn, primary, Thomas, Daniel, primary, Ekert, Paul G., primary, Tvorogov, Denis, primary, D'Andrea, Richard J., primary, Dick, John E., primary, Parker, Michael W., primary, and Lopez, Angel F., primary

Published
2023
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24. Supplementary Table S2 from Distinct Assemblies of Heterodimeric Cytokine Receptors Govern Stemness Programs in Leukemia

Author

Kan, Winnie L., primary, Dhagat, Urmi, primary, Kaufmann, Kerstin B., primary, Hercus, Timothy R., primary, Nero, Tracy L., primary, Zeng, Andy G.X., primary, Toubia, John, primary, Barry, Emma F., primary, Broughton, Sophie E., primary, Gomez, Guillermo A., primary, Benard, Brooks A., primary, Dottore, Mara, primary, Cheung Tung Shing, Karen S., primary, Boutzen, Héléna, primary, Samaraweera, Saumya E., primary, Simpson, Kaylene J., primary, Jin, Liqing, primary, Goodall, Gregory J., primary, Begley, C. Glenn, primary, Thomas, Daniel, primary, Ekert, Paul G., primary, Tvorogov, Denis, primary, D'Andrea, Richard J., primary, Dick, John E., primary, Parker, Michael W., primary, and Lopez, Angel F., primary

Published
2023
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25. Data from Distinct Assemblies of Heterodimeric Cytokine Receptors Govern Stemness Programs in Leukemia

Author

Kan, Winnie L., primary, Dhagat, Urmi, primary, Kaufmann, Kerstin B., primary, Hercus, Timothy R., primary, Nero, Tracy L., primary, Zeng, Andy G.X., primary, Toubia, John, primary, Barry, Emma F., primary, Broughton, Sophie E., primary, Gomez, Guillermo A., primary, Benard, Brooks A., primary, Dottore, Mara, primary, Cheung Tung Shing, Karen S., primary, Boutzen, Héléna, primary, Samaraweera, Saumya E., primary, Simpson, Kaylene J., primary, Jin, Liqing, primary, Goodall, Gregory J., primary, Begley, C. Glenn, primary, Thomas, Daniel, primary, Ekert, Paul G., primary, Tvorogov, Denis, primary, D'Andrea, Richard J., primary, Dick, John E., primary, Parker, Michael W., primary, and Lopez, Angel F., primary

Published
2023
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30. SEPALLATA-driven MADS transcription factor tetramerization is required for inner whorl floral organ development

Author

Hugouvieux, Veronique Genevieve, primary, Blanc-Mathieu, Romain, additional, Paul, Michel, additional, Janeau, Aline, additional, Xu, Xiaocai, additional, Lucas, Jeremy, additional, Lai, Xuelei, additional, Galien, Antonin, additional, Yan, Wenhao, additional, Nanao, Max H, additional, Kaufmann, Kerstin, additional, Parcy, Francois, additional, and Zubieta, Chloë, additional

Published
2023
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32. Distinct Assemblies of Heterodimeric Cytokine Receptors Govern Stemness Programs in Leukemia

Author

Kan, Winnie L., primary, Dhagat, Urmi, additional, Kaufmann, Kerstin B., additional, Hercus, Timothy R., additional, Nero, Tracy L., additional, Zeng, Andy G.X., additional, Toubia, John, additional, Barry, Emma F., additional, Broughton, Sophie E., additional, Gomez, Guillermo A., additional, Benard, Brooks A., additional, Dottore, Mara, additional, Cheung Tung Shing, Karen S., additional, Boutzen, Héléna, additional, Samaraweera, Saumya E., additional, Simpson, Kaylene J., additional, Jin, Liqing, additional, Goodall, Gregory J., additional, Begley, C. Glenn, additional, Thomas, Daniel, additional, Ekert, Paul G., additional, Tvorogov, Denis, additional, D'Andrea, Richard J., additional, Dick, John E., additional, Parker, Michael W., additional, and Lopez, Angel F., additional

Published
2023
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34. Supplementary Data from Sphingosine-1-Phosphate Receptor 3 Potentiates Inflammatory Programs in Normal and Leukemia Stem Cells to Promote Differentiation

Author

Xie, Stephanie Z., primary, Kaufmann, Kerstin B., primary, Wang, Weijia, primary, Chan-Seng-Yue, Michelle, primary, Gan, Olga I., primary, Laurenti, Elisa, primary, Garcia-Prat, Laura, primary, Takayanagi, Shin-ichiro, primary, Ng, Stanley W.K., primary, Xu, ChangJiang, primary, Zeng, Andy G.X., primary, Jin, Liqing, primary, McLeod, Jessica, primary, Wagenblast, Elvin, primary, Mitchell, Amanda, primary, Kennedy, James A., primary, Liu, Qiang, primary, Boutzen, Héléna, primary, Kleinau, Melissa, primary, Jargstorf, Joseph, primary, Holmes, Gareth, primary, Zhang, Yang, primary, Voisin, Veronique, primary, Bader, Gary D., primary, Wang, Jean C.Y., primary, Hannun, Yusuf A., primary, Luberto, Chiara, primary, Schroeder, Timm, primary, Minden, Mark D., primary, and Dick, John E., primary

Published
2023
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35. Data from Sphingosine-1-Phosphate Receptor 3 Potentiates Inflammatory Programs in Normal and Leukemia Stem Cells to Promote Differentiation

Author

Xie, Stephanie Z., primary, Kaufmann, Kerstin B., primary, Wang, Weijia, primary, Chan-Seng-Yue, Michelle, primary, Gan, Olga I., primary, Laurenti, Elisa, primary, Garcia-Prat, Laura, primary, Takayanagi, Shin-ichiro, primary, Ng, Stanley W.K., primary, Xu, ChangJiang, primary, Zeng, Andy G.X., primary, Jin, Liqing, primary, McLeod, Jessica, primary, Wagenblast, Elvin, primary, Mitchell, Amanda, primary, Kennedy, James A., primary, Liu, Qiang, primary, Boutzen, Héléna, primary, Kleinau, Melissa, primary, Jargstorf, Joseph, primary, Holmes, Gareth, primary, Zhang, Yang, primary, Voisin, Veronique, primary, Bader, Gary D., primary, Wang, Jean C.Y., primary, Hannun, Yusuf A., primary, Luberto, Chiara, primary, Schroeder, Timm, primary, Minden, Mark D., primary, and Dick, John E., primary

Published
2023
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36. Supplementary Tables from Sphingosine-1-Phosphate Receptor 3 Potentiates Inflammatory Programs in Normal and Leukemia Stem Cells to Promote Differentiation

Author

Xie, Stephanie Z., primary, Kaufmann, Kerstin B., primary, Wang, Weijia, primary, Chan-Seng-Yue, Michelle, primary, Gan, Olga I., primary, Laurenti, Elisa, primary, Garcia-Prat, Laura, primary, Takayanagi, Shin-ichiro, primary, Ng, Stanley W.K., primary, Xu, ChangJiang, primary, Zeng, Andy G.X., primary, Jin, Liqing, primary, McLeod, Jessica, primary, Wagenblast, Elvin, primary, Mitchell, Amanda, primary, Kennedy, James A., primary, Liu, Qiang, primary, Boutzen, Héléna, primary, Kleinau, Melissa, primary, Jargstorf, Joseph, primary, Holmes, Gareth, primary, Zhang, Yang, primary, Voisin, Veronique, primary, Bader, Gary D., primary, Wang, Jean C.Y., primary, Hannun, Yusuf A., primary, Luberto, Chiara, primary, Schroeder, Timm, primary, Minden, Mark D., primary, and Dick, John E., primary

Published
2023
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37. Supplementary figures merged from Sphingosine-1-Phosphate Receptor 3 Potentiates Inflammatory Programs in Normal and Leukemia Stem Cells to Promote Differentiation

Author

Xie, Stephanie Z., primary, Kaufmann, Kerstin B., primary, Wang, Weijia, primary, Chan-Seng-Yue, Michelle, primary, Gan, Olga I., primary, Laurenti, Elisa, primary, Garcia-Prat, Laura, primary, Takayanagi, Shin-ichiro, primary, Ng, Stanley W.K., primary, Xu, ChangJiang, primary, Zeng, Andy G.X., primary, Jin, Liqing, primary, McLeod, Jessica, primary, Wagenblast, Elvin, primary, Mitchell, Amanda, primary, Kennedy, James A., primary, Liu, Qiang, primary, Boutzen, Héléna, primary, Kleinau, Melissa, primary, Jargstorf, Joseph, primary, Holmes, Gareth, primary, Zhang, Yang, primary, Voisin, Veronique, primary, Bader, Gary D., primary, Wang, Jean C.Y., primary, Hannun, Yusuf A., primary, Luberto, Chiara, primary, Schroeder, Timm, primary, Minden, Mark D., primary, and Dick, John E., primary

Published
2023
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38. Identification of leukemia stem cell subsets with distinct transcriptional, epigenetic and functional properties

Author

Boutzen, Héléna, Murison, Alex, Oriecuia, Alexa, Bansal, Suraj, Arlidge, Christopher, Wang, Jean C. Y., Lupien, Mathieu, Kaufmann, Kerstin B., and Dick, John E.

Abstract

The leukemia stem cell (LSC) compartment is a complex reservoir fueling disease progression in acute myeloid leukemia (AML). The existence of heterogeneity within this compartment is well documented but prior studies have focused on genetic heterogeneity without being able to address functional heterogeneity. Understanding this heterogeneity is critical for the informed design of therapies targeting LSC, but has been hampered by LSC scarcity and the lack of reliable cell surface markers for viable LSC isolation. To overcome these challenges, we turned to the patient-derived OCI-AML22 cell model. This model includes functionally, transcriptionally and epigenetically characterized LSC broadly representative of LSC found in primary AML samples. Focusing on the pool of LSC, we used an integrated approach combining xenograft assays with single-cell analysis to identify two LSC subtypes with distinct transcriptional, epigenetic and functional properties. These LSC subtypes differed in depth of quiescence, differentiation potential, repopulation capacity, sensitivity to chemotherapy and could be isolated based on CD112 expression. A majority of AML patient samples had transcriptional signatures reflective of either LSC subtype, and some even showed coexistence within an individual sample. This work provides a framework for investigating the LSC compartment and designing combinatorial therapeutic strategies in AML.

Published
2024
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40. Transcriptional Activation of Regenerative Hematopoiesis via Vascular Niche Sensing

Author

Itkin, Tomer, primary, Houghton, Sean, additional, Schreiner, Ryan, additional, Lin, Yang, additional, Badwe, Chaitanya R., additional, Voisin, Veronique, additional, Murison, Alex, additional, Seyedhassantehrani, Negar, additional, Kaufmann, Kerstin B., additional, Garcia-Prat, Laura, additional, Booth, Gregory T., additional, Geng, Fuqiang, additional, Liu, Ying, additional, Gomez-Salinero, Jesus M., additional, Shieh, Jae-Hung, additional, Redmond, David, additional, Xiang, Jenny Z., additional, Josefowicz, Steven Z., additional, Trapnell, Cole, additional, Spencer, Joel A., additional, Zangi, Lior, additional, Hadland, Brandon, additional, Dick, John E., additional, Xie, Stephanie Z., additional, and Rafii, Shahin, additional

Published
2023
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42. Auxin Dependent Post-Translational Regulation of MONOPTEROS in the Arabidopsis Root

Author

Cavalleri, Alex, primary, Astori, Chiara, additional, Truskina, Jekaterina, additional, Cucinotta, Mara, additional, Farcot, Etienne, additional, Chrysanthou, Elina, additional, Xu, Xiaocai, additional, Muino, Jose M., additional, Kaufmann, Kerstin, additional, Kater, Martin M., additional, Vernoux, Teva, additional, Weijers, Dolf, additional, Bennett, Malcolm J., additional, Bhosale, Rahul, additional, Bishopp, Anthony, additional, and Colombo, Lucia, additional

Published
2023
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44. Transcriptional Activation of Regenerative Hematopoiesis via Vascular Niche Sensing

Author

Itkin, Tomer, Houghton, Sean, Schreiner, Ryan, Lin, Yang, Badwe, Chaitanya R., Voisin, Veronique, Murison, Alex, Seyedhassantehrani, Negar, Kaufmann, Kerstin B., Garcia-Prat, Laura, Booth, Gregory T., Geng, Fuqiang, Liu, Ying, Gomez-Salinero, Jesus M., Shieh, Jae-Hung, Redmond, David, Xiang, Jenny Z., Josefowicz, Steven Z., Trapnell, Cole, Spencer, Joel A., Zangi, Lior, Hadland, Brandon, Dick, John E., Xie, Stephanie Z., and Rafii, Shahin

Subjects
Article
Abstract

Transition between activation and quiescence programs in hematopoietic stem and progenitor cells (HSC/HSPCs) is perceived to be governed intrinsically and by microenvironmental co-adaptation. However, HSC programs dictating both transition and adaptability, remain poorly defined. Single cell multiome analysis divulging differential transcriptional activity between distinct HSPC states, indicated for the exclusive absence of Fli-1 motif from quiescent HSCs. We reveal that Fli-1 activity is essential for HSCs during regenerative hematopoiesis. Fli-1 directs activation programs while manipulating cellular sensory and output machineries, enabling HSPCs co-adoptability with a stimulated vascular niche. During regenerative conditions, Fli-1 presets and enables propagation of niche-derived Notch1 signaling. Constitutively induced Notch1 signaling is sufficient to recuperate functional HSC impairments in the absence of Fli-1. Applying FLI-1 modified-mRNA transduction into lethargic adult human mobilized HSPCs, enables their vigorous niche-mediated expansion along with superior engraftment capacities. Thus, decryption of stem cell activation programs offers valuable insights for immune regenerative medicine.

Published
2023

49. Adaptation toex vivoculture drives human haematopoietic stem cell loss of repopulation capacity in a cell cycle independent manner

Author

Johnson, Carys S., primary, Sham, Kendig, additional, Belluschi, Serena, additional, Wang, Xiaonan, additional, Lau, Winnie, additional, Kaufmann, Kerstin B., additional, Krivdova, Gabriela, additional, Calderbank, Emily F., additional, Mende, Nicole, additional, McLeod, Jessica, additional, Mantica, Giovanna, additional, Williams, Matthew J., additional, Grey-Wilson, Charlotte, additional, Drakopoulos, Michael, additional, Sinha, Shubhankar, additional, Diamanti, Evangelia, additional, Basford, Christina, additional, Green, Anthony R., additional, Wilson, Nicola K., additional, Howe, Steven J., additional, Dick, John E., additional, Göttgens, Bertie, additional, Francis, Natalie, additional, and Laurenti, Elisa, additional

Published
2022
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