In this SciArt profile, we meet Kathryn Garner, whose passion for art and science has been linked throughout her life as she discovered her passion for science through her art.
Can you tell us about your background and what you work on now?
I discovered a fascination with intracellular signalling pathways early on in my BSc (Hons) Molecular Cell Biology studies at University College London (UCL), UK, which led to a PhD investigating some novel lipid transfer proteins in the heart. After UCL, I held several postdoctoral positions at the University of Bristol, first working on signalling pathways in the cardiovascular system, then, learning to use High Content Imaging (HCI) to study Gonadotropin-releasing hormone (GnRH) signalling dynamics before settling on the kidney. I was awarded a Kidney Research UK Intermediate Fellowship in 2017 to study signalling at the interface between inflammation and blood pressure regulation. HCI generates a huge amount of data, and during my research on GnRH, I worked with mathematicians and statisticians to develop mathematical models. I was able to apply some of this understanding to my fellowship research.
I began working as a Senior Lecturer at Northumbria University, UK, as the first lockdown engulfed us in 2020. I lasted a full academic year of teaching online and homeschooling before being headhunted to join Newcells Biotech as Head of Kidney Development in 2021. I led a Research & Development team developing primary kidney models for testing new drug molecules for pharmaceutical companies. I discovered that I am particularly good at establishing relationships with new clients, making connections, and helping to develop programmes of work to suit their needs. For the last year, I have been working as a consultant contributing to a wide range of projects with different types of companies, from providing advice on developing kidney models to a pharmaceutical company to helping to place cardiac organoid technology in the market for a biotech company, as well as helping a management consultancy navigate microphysiological systems (MPS), including organ-on-a-chip. I recently partnered with a software company to help my clients find custom IT solutions for connecting lab equipment, automate data analysis, or analyse tricky images – which I’m really excited about.
Orange Cell Drawing (1999). Ink and oil pastel on paper (59 x 84 cm).
Purple Cell Drawing (1999). Ink and emulsion paint on paper (59 x 84 cm).
Were you always going to be a scientist?
No, quite the opposite! The art room was where I felt I belonged at school. I was good at art and my dad is an artist. But there were a couple of things that happened early in secondary school that made me wonder whether art was everything for me. In year 10, we learnt about cell biology for the first time, and I found it came so naturally to me, like it was something I had always known. I was the only one in the class to get full marks on the cell biology test. A few months later, we were dissecting a frog, and while my lab partner had long lost interest and was off talking to a boy, I remember being captivated by the frog’s insides and wondering about the connection between what we think and the physical matter of the body. I decided then and there that I wanted to study Neuroscience and I switched my A-level choices from art to four sciences. Only, somewhere along the way, I changed my mind, and no one seemed surprised when I asked to change back to Art & Design. After finishing school, I took an Art Foundation course in High Wycombe, UK, and then moved to Cornwall, UK, to study BA(Hons) Fine Art at Falmouth College of Arts.
Ear (2004). Oil on canvas (60 x 90 cm).
Unlike at school, the curriculum at Falmouth was completely unstructured – we were given a studio space and a tutor to check in with, but other than that it was important we searched out our own inspiration to find our voice. While the other students were making etchings from drawings of shells on the beach, or painting stormy oil paintings, my curiosity took me to the biology textbooks in the library. In my first year, I made a collection of Cell Paintings inspired by brightly-coloured histology images, including Purple Cell Drawing (1999) and Orange Cell Drawing (1999). These works were fresh and vibrant but something niggled at me. It felt like I was copying – I wanted to know more. I wanted to understand the images that I was copying, and I wanted to be able to put more of myself into them. In my final year show, I displayed portraits that were complex, close-up and abstracted – teetering on the edge between what is known and what is unknown. A couple of years later, I exhibited a collection of oil paintings including Ear (2004) in a group show in a gallery in Hammersmith, UK. At this time, I was working as a Cryobank Scientist at an infertility clinic, finally studying those science A-levels in evening classes. The following year, I enrolled at UCL.
Compartmentalisation (2012). (detail) Pencil, watercolour and acrylic paint on paper (84 x 59 cm).
And what about art – have you always enjoyed it?
All of my earliest memories included art, whether it was sitting for one of my dad’s paintings in his studio or hiding in our loft with a big piece of paper drawing an imagined village with roads and buildings. Going to galleries still fills me with that sense of wide-eyed childlike wonder that I had– what treasures would be waiting for me around the next corner? Would I find something new from an artist I’d not heard of before or an old love I’d forgotten about? On a Saturday, we might have reason to drive up to London to submit one of my dad’s paintings for an exhibition, and afterwards visit the Tate or the Royal Academy or the National Gallery.
Emergent Properties (2022-23). Oil on canvas (90 x 90 cm).
What or who are your most important artistic influences?
I love to be enveloped by art, and Terry Winters, Roberto Matta, and Sarah Sze, are artists whose work I come back to repeatedly. All three create other worlds in their art, works that you can spend ages looking at with your mind getting lost in them. Terry Winters seems to layer up graphs and other visualisations of data to create large complex paintings. In 1999, I travelled around the United States by myself on Greyhound buses, stopping in at the art galleries in the big cities. In the San Francisco Museum of Modern Art, I first saw ‘Invasion of the Night’ by Roberto Matta and was compelled to be absorbed by it – a safe refuge from all that was outside and unfamiliar. In the giftshop, I came across a little book of Sarah Sze’s installations, eventually able to see some in person in London several years later. Sze creates elegant miniature worlds from everyday objects – cotton buds, tape measures, pencils – and spending time with them you find yourself wishing you could shrink down to climb the tiny matchstick ladders.
Kidney slice + water treatment plant (2025). Acrylic paint on paper (42 x 59.4 cm).
How do you make your art?
As I came to the end of my PhD, I started to think about art again and how I could join everything up. I was now thinking about cells as tiny cities with highways, or as houses with compartments tailored to different functions – like in a home the bedroom is for sleeping in, the kitchen for preparing food, and so on. I made Compartmentalisation (2012) combining different types of images that had a similar level of complexity as the histology images I copied at art school, only this time with meaning. Here are compartments from a settlement of the Dogon people, who live in the central plateau region of Mali, next to plans of villages in Chad and Cameroon. At the bottom is a drawing of a circuit board, with its connected elements and flows of information. Over the years, I have tried lots of different ways of putting images together. In Emergent Properties (2022-23), I layered up the emergency evacuation plan of Cramlington Children’s Hospital in Northumberland, a children’s playground, and a circuit board, and then added the layer of green to help edit parts out to create something new. In Kidney slice + water treatment plant (2025), I returned to a histology image as a starting point and added an aerial view of a water treatment plant. The circular sediment tanks ground the abstract nature of the kidney slice and directly talk about the function of the kidney in the body.
Brain Art, illustration for the competition promotional materials (2016). Watercolour and pencil on paper (30 x 42 cm).
Does your background in science influence your art?
Art and science have tended to come together for me through public engagement activities, such as running a ‘Brain Art’ competition for local school children at Bristol Neuroscience Festival. A selection of work was presented in the Wills Memorial Building at the top of Park Street in Bristol, which is very grand, before being displayed at the Royal West of England Academy (RWA). This event was fantastic in encouraging children who are usually more interested in art to think about science for a change. It was an opportunity I think I would have loved as a child.
Sometimes, it was the process of carrying out scientific research that I found interesting from an artistic point of view, rather than the subject of the work itself. Groynes and Keys was a piece I made that directly came from my activities in the lab. I was doing a lot of cell culture at the time, and I found a good way to introduce regular drawing into my day was to draw a flask of cells under the microscope while another was being incubated with trypsin for 5 mins. This piece is an amalgamation of several drawings of HEK-293 cells and was exhibited at a SciArt exhibition at Royal United Hospital, Bath (2016-17), organised by the Bristol and Bath branch of the British Science Association. I named this piece, Groynes and Keys, because whenever I’m drawing pictures of cells, I find it difficult not to think of maps of waterways and inlets.
Groynes and Keys (2014). Watercolour and pencil on paper (30 x 42 cm).
What are you thinking of working on next?
All of my original Cell Paintings have new homes – Purple Cell Drawing can be found in a seminar room in the Learning and Research Building of Southmead Hospital, Bristol, and Compartmentalisation hangs in the foyer of the Dorothy Hodgkin Building at the University of Bristol. I am currently growing a new body of work, and I am keen to see more of it in universities, institutions and life science companies, potentially through commissions or other opportunities. I love being sent microscopy images to look at so I would be keen to work closely with scientists to make new paintings.
The 13 August 2025 webinar featured three early-career researchers working on stem cells and organoids. Here, we share the talks from Toshi Yamada (University of California San Francisco) and Daniel Medina-Cano (MSKCC).
We are delighted to bring you the return of our image competition in collaboration with the MBL Embryology course at Woods Hole. We’d like you to vote for your favourite image from the stunning submissions from the students that attended the 2025 course. The winning image will be published on the front cover of Development later this year.
Please vote for your favourite image using the poll at the bottom of the page. The voting will close on Wednesday 3 September.
Thank you and good luck to the following researchers for their contributions:
Virginia Panara, Shirley Ee Shan Liau, Sonoko Mizuno, Ignacio Casanova-Maldonado, Max Makem, Johnny Vertiz, Arthur Boutillon, Anthony Wokasch, Aria Zheyuan Huang, Amartya Tashi Mitra, Nathanial Sweet, Paul Maier, Shivangi Pandey, Marie Lebel, Chloe Kuebler, Nicole Roos
Browse through the gallery (click to view full image)
1. Longfin squid chromatophore Sonoko Mizumo, Virginia Panara, Shirley Ee Shan Liau Fluorescent imaging of the muscle ring surrounding a Longfin Squid chromatophore2. Melanocytes in a Zebrafish larva Sonoko Mizuno Bright field imaging of melanocytes in a Zebrafish larva3. Octopus embryo tentacles Ignacio Casanova-Maldonado, Max Makem & Johnny Vertiz Mitochondria (Magenta), Cell membrane (Cyan). Olympus FV4000 Confocal microscope, 10X (N.A: 0,4).4. Squid embryos Ignacio Casanova-Maldonado, Max Makem & Johnny Vertiz Nuclei (Cyan), Actin (Red). Olympus FV4000 Confocal microscope, 4X (N.A: 0.8)5. Squid head Ignacio Casanova-Maldonado, Max Makem & Johnny Vertiz Actin (magenta), circulatory system (red) mitochondria (green) and nuclei (cyan). Olympus FV4000 Confocal microscope, 10X (N.A: 0,4)6. Amphioxus larva Arthur Boutillon Amphioxus larva (stage L1) stained for nuclei (DAPI, blue) and phosphorylated myosin II (orange), imaged by point scanning confocal microscopy and prossessed using ImageJ.7. Embryonic eye of an Anole lizard Arthur Boutillon Embryonic eye of an Anole lizard stained for nuclei (DAPI, blue) and F-actin (Phalloidin, orange), imaged by spinning disc confocal microscopy and prossessed using ImageJ.8. Butterfly wing disc Arthur Boutillon Wing disc of the butterfly Vanessa cardui stained for F-actin (SiR-Actin, orange) and membrane (PKmem555, magenta), imaged by point scanning confocal microscopy and prossessed using ImageJ.9. Mouse pancreas Anthony Wokasch Ductal branching of an E15.5 mouse pancreas. E15.5 whole-mount pancreas labeled with Mucin-1. Imaged on the Olympus FV4000 Confocal Laser Scanning Microscope (20X) and processed using FIJI Max projection. 10. Red eared slider turtle Anthony Wokasch, Aria Zheyuan Huang, Amartya Tashi Mitra, Nathanial Sweet, Paul Maier Close-up of a Red eared slider turtle (Stage 14), Trachemys scripta, optically cleared and stained with acetylated tubulin. Imaged on the LifeCanvas MegaSPIM Light Sheet. 11. Turtle embryo Amartya Tashi Mitra, Aria Zheyuan Huang, Nathaniel Sweet, Anthony Wokasch, Paul Maier Red-eared slider (Trachemys scripta) embryo stained with acetyl-alpha tubulin, labelling neurons. Optically cleared and imaged on LifeCanvas technologies MegaSPIM light sheet microscope.12. Skate embryo Amartya Tashi Mitra Skeletal preparation of little skate (Leucoraja erinacea) embryo labelling cartilaginous tissue in blue and calcified tissue in red. Imaged on Leica MZ10F stereomicroscope, assembled using focus stacking and tile stitching.13. Squid embryo Amartya Tashi Mitra Longfin inshore squid (Doryteuthis pealei) embryo with plasma membrane (CellMask Green) and nuclear (Hoechst) labelling in blue and orange respectively. Imaged on Nikon AXR laser scanning microscope.14. Mouse embryo – Light-sheet Aria Zheyuan Huang, Amartya Tashi Mitra, Nathanial Sweet, Anthony Wokasch, Paul Maier CD-1 mouse embryo at embryonic day 10.5, optically cleared and stained with acetylated tubulin (yellow), imaged on a LifeCanvas MegaSPIM Light Sheet.15. Zebrafish embryo Shivangi Pandey 24hpf Zebrafish embryo stained for Acetylated tubulin (red), Prox1(green) and DAPI(blue). The image was acquired using a Yokogawa W1 (Eclipse) Spinning Disk microscope. The image was processed using ImageJ.16. Skate embryo Shirley Ee Shan Liau and Shivangi Pandey An early-stage skate embryo stained for DAPI (cyan) and Tuj1 (Magenta). The image was acquired using a Yokogawa W1 (Eclipse) Spinning Disk microscope. The image was processed using ImageJ.17. Capitella teleta juvenile Marie Lebel, Shivangi Pandey Regenerating posterior end of a Capitella teleta juvenile seen from the ventral side, 3 days post amputation imaged with a scanning confocal microscope (Nikon AXR NSPARC; 20x, NA 0.8 objective). Nuclei are in blue, neurons in yellow, and serotonergic neurons in red.18. Late squid embryo Marie Lebel, Shivangi Pandey Late squid embryo, with a tentacle amputated 3 days prior, imaged with a spinning disk confocal microscope ( Andor BC43; 10x, NA 0.45 objective) . TRITC (yellow) and CFSE (magenta) were injected in the vasculature a day before amputation. The cyan signal corresponds to the inverted brightfield, highlighting the eyes and chromatophores.19. Squid HCR Amartya Tashi Mitra, Chloe Kuebler, Shirley Ee Shan Liau Longfin inshore squid (Doryteuthis pealei) embryo HCR in-situ. mRNAs for elav, optix, and pcdh17 mRNAs represented in red, blue and orange respectively. Imaged on Olympus FV4000 laser scanning microscope.20. Mouse embryo – confocal Nicole Roos and Anthony Wokasch Mouse E10.5 embryo immunofluorescent staining of Sox9 (cyan), alpha-tubulin (yellow), and endomucin (magenta) protein. Image captured on Evident FV4000 point scanning confocal, lens UPLXAPO4X, na = 0.16, zoom = 1.04. Image processing conducted on Fiji.
In a series of interviews published in Development, we learn more about each fellow’s career path, research interests and aspirations when they start their own lab.
Meet our 2025 PI fellows
Ethan Ewe
Ethan earned his PhD in Molecular, Cellular, and Developmental Biology from the University of California, Santa Barbara. Under the mentorship of Prof. Joel Rothman, he investigated the gene regulatory network that controls the specification and differentiation of the C. elegans endoderm. He is currently a postdoctoral fellow in Prof. Oded Rechavi’s lab at Tel Aviv University, where he explores how small RNAs regulate stress responses and govern germline development. Ethan is passionate about uncovering how epigenetic mechanisms – particularly those involving small RNAs and Argonaute proteins – mediate phenotypic plasticity and may facilitate adaptation to environmental change. You can follow Ethan on Bluesky at @ethanewe.bsky.social.
Max earned his PhD at the University of Göttingen, Germany, under the supervision of Prof. Gregor Bucher, where he explored how heterochrony shapes the evolution and development of insect brains. He was then awarded a Walter Benjamin Fellowship by the German Research Foundation to investigate how two enigmatic brain regions co-evolve to support novel behaviours, using neotropical butterflies as a model system. He pursued this research in the lab of Dr Stephen Montgomery at the University of Bristol. Currently, Max is a Senior Research Associate developing new tools to study the evolution of neural circuits. He is broadly fascinated by how brains evolve and how neural circuits are shaped and rewired through developmental processes. You can follow Max on Bluesky at @maxfarnworth.bsky.social and find more information at https://linktr.ee/max.farnworth.
Anzy completed her PhD with Brian Hendrich at the Stem Cell Institute at the University of Cambridge. She then joined the lab of Nancy Papalopulu at the University of Manchester and was awarded the Wellcome Trust Sir Henry Wellcome postdoctoral fellowship. Anzy is interested in how dynamic protein expression is decoded by cells and its impact on cell fate decisions in the developing embryo. You can follow Anzy on Bluesky @anzymiller.bsky.social.
Joaquín obtained his PhD in Biology at the Stowers Institute for Medical Research in Kansas City MO, USA. In the laboratory of Dr Piotrowski, he focused on dissecting the role that two signaling pathways – Wnt and Planar Cell Polarity – have during the development of the lateral line in zebrafish, using a combination of mutant analysis, live imaging and immunostaining. Currently, he is a postdoc at the Schier lab at the Biozentrum of the University of Basel, Switzerland, where he studies the Rohon-Beard neurons, a population of neurons that for around 150 years were thought to disappear during early development but Joaquín discovered remain until at least juvenile stages. He is interested in leveraging Rohon-beard neurons to study a fundamental question in biology: what are the mechanisms behind the acquisition of the different layers of neuron diversity? You can follow Joaquín on Bluesky at @mads100tist.bsky.social and Mastodon at https://mastodon.social/@mads100tist. Joaquín also helps managing the popular zebrafish-oriented resource ZebrafishRock! @zebrafishrock.bsky.social.
Marlies is a postdoctoral fellow in the laboratory of Maria-Elena Torres-Padilla at Helmholtz Munich, Germany. She completed her PhD research in the lab of Job Dekker at the University of Massachusetts Medical School, USA, where she studied chromosome organization and epigenetic characteristics of mitotic chromosomes. Marlies’ current research focuses on the transcriptional and epigenetic regulation of and by transposable elements in mammalian preimplantation development and stem cells. You can follow Marlies on Bluesky at @marliesoomen.bsky.social.
Giulia is an EMBO postdoctoral fellow in Yanlan Mao’s group at the Laboratory for Molecular Cell Biology, University College London (UK). Prior to this, she completed her PhD at EMBL Heidelberg (Germany), working with Edward Lemke. A physicist by training, Giulia investigates organism resilience to external perturbations during development and homeostasis, with a focus on mechanical stresses. She combines high-resolution imaging with the development of novel mechanical perturbation tools in Drosophila. You can follow Giulia on Bluesky at @giuliapaci.bsky.social.
Sonya obtained her PhD in molecular biology and genetics from the University of Alberta in Canada, where she used zebrafish to study early vertebrate eye development and disease under the guidance of Dr Andrew Waskiewicz. She is currently a postdoctoral fellow at the Institute of Molecular Biotechnology (IMBA) in Vienna, Austria working with Dr Alejandro Burga, using nematodes as a model system to understand the role of mobile and selfish DNA elements in driving the evolution of genomes. Sonya’s research interests lie in understanding the complex relationship between mobile genetic elements and their host genomes in shaping development and evolution. You can follow Sonya on Bluesky at @sonyawiden.bsky.social.
Toshi earned his PhD in Chemistry from the University of Tokyo, Japan, where he studied regulatory mechanisms controlling RNA dynamics and stability, specifically how RNA localization and mRNA decay influence gene expression. He is currently a postdoctoral fellow in Wendell Lim’s lab at University of California, San Francisco, UCSF. His research focuses on uncovering the design principles of mammalian embryogenesis and reconstituting developmental processes in vitro.
From the nitty-gritty aspects of research to the practice of science communication activities, creativity is an essential part of science. The aim of this webinar is to show that creativity lies at the heart of the practice of science communication and to explore how an explicitly creative approach may help you reach the goals of your science communication project.
In the first part of the webinar, Anatolii will give a conceptual overview of how we might understand creativity in science communication. To that end, he will draw on some parallels between science and art, to unpack several dimensions of creativity relevant to science communication.
The second part will involve practical work, where each of the participants will be given exercises and tools to ideate what their creative science communication project might look like. The webinar will conclude with a facilitated group discussion, through which the participants will join in sharing their insights and try to articulate some practical lessons.
This workshop will be limited to 20 participants working in academic settings. The invitations will be sent out on a first-come-first-served basis.
Anatolii Kozlov is a scientist-turned-philosopher of science and science communicator.
Join us to hear two of Development’s PI fellows speaking on the topic of gene regulation, chaired by James Gahan. One of Development’s first PI fellows, James is an Associate Professor in the Centre for Chromosome Biology at the University of Galway. His research focuses on understanding early animal evolution with a particular interest in gene regulation and chromatin biology.
Wednesday 27 August – 15:00 BST
Anzy Miller (University of Manchester) ‘NGN3 oscillatory expression controls the timing of human pancreatic endocrine differentiation’
Marlies Oomen (Helmholtz Munich, Institute of Epigenetics and Stem Cells) ‘Jumping through evolution; Genome regulation of and by transposable elements during mammalian preimplantation development’
At the speakers’ discretion, the webinar will be recorded to view on demand. To see the other webinars scheduled in our series, and to catch up on previous talks, please visit: thenode.biologists.com/devpres
Development has been organising regular meetings on human development for over a decade. For 2026, the journal has teamed up with the Wellcome-funded consortium the Human Developmental Biology Initiative (HDBI) to co-organise this event, which will bring together researchers from around the world, united by an interest in understanding human developmental biology. Topics covered will range from lineage specification, patterning and morphogenesis through to bioengineering and disease modelling.
Organisers: Paula Alexandre, James Briscoe, Emily Calderbank, Claudio Cortes Rodriguez, Muzz Haniffa, Paul Riley, Liz Robertson, Peter Rugg-Gunn, John Russell, Ben Simons, Shankar Srinivas and Pilar Vazquez Arango
Spotted a preprint in this list that you love? If you’re keen to gain some science writing experience and be part of a friendly, diverse and international community, consider joining preLights and writing a preprint highlight article.
Genetic lineage tracing identifies intermediate mesoderm as a novel contributor to mammalian kidney lymphatics Daniyal J Jafree, Lauren G Russell, Athanasia Stathopoulou, Christopher J Rowan, Andrew T White, Charlotte O’Riordan, Maria Kolatsi-Joannou, Karen L Price, Sarah Ivins, Liam A Ridge, Catherine Roberts, Jennie C Chandler, Laura Wilson, Dale Moulding, Julie Siegenthaler, Adrian S Woolf, Paul R Riley, Christiana Ruhrberg, Peter J Scambler, Norman D Rosenblum, David A Long
Loss of CTLH component MAEA impairs DNA repair and replication and leads to developmental delay Soren H. Hough, Satpal S. Jhujh, Samah W. Awwad, Simon Lam, John C. Thomas, Oliver Lewis, Thorsten Mosler, Aldo S. Bader, Lauren E. Bartik, Shane McKee, Shivarajan M. Amudhavalli, Estelle Colin, Nadirah Damseh, Emma Clement, Pilar Cacheiro, Anirban Majumdar, Damian Smedley, Isabelle Thiffault, Guido Zagnoli Vieira, Rimma Belotserkovskaya, Stephen J. Smerdon, Petra Beli, Yaron Galanty, Christopher J. Carnie, Grant S. Stewart, Stephen P. Jackson
Genetics of growth rate in induced pluripotent stem cells Brian N. Lee, Henry J. Taylor, Filippo Cipriani, Narisu Narisu, Catherine C. Robertson, Amy J. Swift, Neelam Sinha, Tingfen Yan, Lori L. Bonnycastle, Nathan Dale, Annie Butt, Hemant Parsaud, Stefan Semrau, NYSCF Global Stem Cell Array Team, GENESiPS Consortium, iPSCORE Consortium, Joshua W. Knowles, Ivan Carcamo-Orive, Agnieszka D’Antonio-Chronowska, Kelly A. Frazer, Leslie G. Biesecker, Scott Noggle, Michael R. Erdos, Daniel Paull, Francis S. Collins, D. Leland Taylor
Two parallel lineage-committed progenitors contribute to the developing brain Carolyn E. Dundes, Rayyan T. Jokhai, Hadia Ahsan, Rachel S. Kang, Rachel E.A. Salomon-Shulman, Arjun Rajan, Yoon Seok Kim, Liam J. Stanton, Christine Xu, Stephanie Do, Brennan D. McDonald, José Miguel Andrade López, Hugo A. Urrutia, Hannah Greenfeld, Alicia Wong, Yimiao Qu, Andrew S. Petkovic, Yi Miao, K. Christopher Garcia, Michelle Monje, Daniel E. Wagner, Marianne E. Bronner, Christopher J. Lowe, Kyle M. Loh
Stem cells actively suppress regenerative plasticity in human colon Joris H. Hageman, Defne Yalcin, Julian R. Buissant des Amorie, Sascha R. Brunner, Thomas A. Kluiver, Aleksandra Balwierz, Franziska L. Langner, Maria C. Puschhof, Yannik Bollen, Thanasis Margaritis, Hugo J.G. Snippert
Fibroblast depletion reveals mammalian epithelial resilience across neonatal and adult stages Isabella M. Gaeta, Shuangshuang Du, Clémentine Villeneuve, David G. Gonzalez, Catherine Matte-Martone, Smirthy Ganesan, Deandra Simpson, Jessica L Moore, Chen Yuan Kam, Sara Gallini, Haoyang Wei, Fabien Bertillot, Dagmar Zeuschner, Lauren E. Gonzalez, Kaelyn D Sumigray, Sara A Wickström, Valentina Greco
Two Spag6 genes control sperm formation and male fertility in mice Yunhao Liu, Wei Li, Tao Li, Cheng Zheng, Changmin Niu, Alain Schmitt, Yi Tian Yap, Mohammad Abdulghani, Shuiqiao Yuan, Christian Melander, Jerome F Strauss III, Aminata Toure, Ling Zhang, Zhibing Zhang
Microtubule curling as an efficient readout to uncover fundamental concepts of axonal cell biology André Voelzmann, Milli Owens, Robin Beaven, William Cairns, Abigail Elliot, Sheng-Hui Feng, Catarina Goncalves-Pimentel, Ines Hahn, Ella Jones, Kodie Norris, Thomas Murphy, Yu-Ting Liew, Lydia Lorenzo-Cisneros, Judith Fuelle, Liliana M. Pinho-Correia, Yue Qu, Natalia, Tarunima Sharma, Sánchez-Soriano, Andreas Prokop
The Company of Biologists is recruiting a new Community Manager for the Node – a community site hosted by Development for developmental and stem cell biologists.
Why are we hiring?
Since the Node was launched 15 years ago, we’ve had five fantastic Community Managers who support the day-to-day running and long-term development of the site. We’ve found that a full-time Community Manager is really instrumental to keeping the site running smoothly, securing a regular stream of content and developing new features. Last month, we said goodbye to Joyce, our most recent Community Manager, as she took on a new challenge in her career, so now, we are recruiting a new Community Manager to lead the site.
Former Community Managers for the Node.
Who are we looking for?
We’re looking for a passionate science communicator with research experience in developmental or stem cell biology, interested in working in a not-for-profit publishing environment, and eager to bring new ideas to the Node. Experience in science communication, using social media to disseminate research and using the WordPress platform makes for a competitive candidate. Knowledge of technical web development is not a requirement since external IT partners support the Node, but some basic coding skills are a plus.
What does the role involve?
From supporting Node users (mostly research-active scientists), to writing posts and commissioning content, there’s variation and opportunity to try new things as a Community Manager. For more details on the tasks that come with the role, including working with the other Community Managers at the Company to help develop early-career researchers, read this recent breakdown from Joyce. The successful candidate will work within the Development journal team, where they will also contribute non-peer-reviewed content to the journal and manage the social media accounts for both the Node and Development.
Where is the job based?
This is a permanent, full-time position. The role requires being able to work from The Company of Biologists’ offices in Cambridge, UK, at least 50% of the working week. The role also requires national and international travel to attend meetings and conferences.
Interested?
Please see the full job description and apply before Friday 5 September 2025. If you have any questions about the role or the recruitment process, feel welcome to contact me informally at alex.eve@biologists.com.
Summary: It is difficult to predict whether newborns will develop autism, but autism can occur alongside congenital heart disease, which is identifiable at birth. Scientists from University of California, San Francisco, USA, are working to understand the shared biology of autism and congenital heart disease to predict the risk that a child has autism earlier. Their latest study, published in Development, shows that hair-like cell structures (cilia) found on all cells link autism and congenital heart disease.
The skin of a frog embryo, with cilia (in magenta and cyan) and the outline of cells (in grey) highlighted. Image credit: James Schmidt
Press release: Autism spectrum disorders are complex neurodevelopmental conditions affecting about 1 in 100 children worldwide. Early diagnosis would allow timely intervention to improve the development and quality of life for children with autism. Scientists have identified over 200 genes associated with autism, but predicting the risk of developing autism based on genetic information is not straightforward. Autism can co-occur with congenital heart disease, which affects the structure, growth and function of the heart. Because congenital heart disease can be readily identified in newborns, a congenital heart disease diagnosis could help identify children at higher risk of developing autism earlier. Scientists have been trying to understand why the two conditions, which affect the development of the brain and the heart respectively, occur together. A team of scientists, led by Dr Helen Willsey from University of California, San Francisco, USA, discovered that tiny hair-like structures called cilia, found on the surface of almost every cell, underlie the shared biology of autism and congenital heart disease, taking us a step closer to early prediction of children at risk of developing autism. This study is published in the journal Development on 24 June 2025.
‘Understanding how autism and congenital heart disease intersect biologically has been technically challenging just due to the sheer number of risk genes involved in both disorders,’ said Willsey. Previous evidence had shown that mutations in 361 genes increased the risk of individuals developing either autism, congenital heart disease, or both. The scientists wondered whether genes linked to congenital heart disease that directly affect nerve cells may be genes that also increase the risk of autism. ‘Here, we looked at how these risk genes function in the development of both the brain and heart and contribute to disease,’ said Willsey.
Nia Teerikorpi, who performed most of the experiments in this study, grew immature human nerve cells that had been mutated to lack one of the 361 key genes in the lab and monitored how well the cells grew. She found 45 genes that affected the growth of the nerve cells. Looking more closely, Teerikorpi and the team found that all 45 genes function in tiny hair-like protrusions (cilia) extending from our cells that are involved in movement, sensation and communication between cells. Willsey explained why one gene in this group – taok1 – caught their attention: ‘Patients with mutations in the taok1 gene appear to have a higher risk of developing autism, and we previously identified taok1 as a predicted congenital heart disease risk gene, but we had not yet tested whether it functions in heart development. So, seeing this gene come up again in this work looking at the shared biology of the two conditions motivated us to study it more closely.’
To study the role of taok1 in the heart and brain, the team altered the gene in frog embryos and then monitored their growth and development. They found that cilia could not form properly on cell surfaces, and they observed defects developing in the heart and brain. This suggests that the other 44 genes identified could also be relevant for the development of the brain and heart, contributing to autism and congenital heart disease.
Building on this work, the team is now actively pursuing the extent to which genes involved in cilia overlap with genes associated with autism and congenital heart disease, ‘what we discovered is the tip of the iceberg for the intersection of autism and congenital heart disease,’ said Willsey, ‘Our findings offer the opportunity to prioritize people with genes associated with both conditions for early monitoring and intervention.’
![](https://thenode.biologists.com/wp-content/uploads/2025/08/Groynes-and-Keys.png")
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