Join Melanie Chan’s Renal Genomics group at the MRC Laboratory of Medical Sciences on Imperial’s Hammersmith campus. The project investigates gene-regulatory networks in kidney and urinary-tract development and how their disruption causes congenital anomalies. Establish iPSC-derived kidney and ureteric-bud organoids, perturb candidate regulatory elements using CRISPR interference, and profile effects with single-nucleus multiomics, CUT&RUN and low-input chromosome-conformation capture. Work combines experimental testing with collaboration with bioinformaticians and clinicians and offers training in organoid models and single-cell analysis. The appointment is full-time and fixed-term for three years, with a flexible start around 1 December 2026. It is based on site; salary is £50,733–£59,484 annually. Applications close on 13 October 2026.
Developmental Biology
This week
Cell-Cell Interactions
Max Planck Institute for Molecular Biomedicine · Münster, Germany
Postdoctoral research with Stefanie Grosswendt’s group at the Max Planck Institute for Molecular Biomedicine, Münster, Germany. The laboratory investigates how neighbouring cells communicate and how these interactions influence gene regulation, cell fate and tissue function. Experimental and computational approaches combine single-cell genomics, CellMate-seq ligand–receptor measurements and imaging-based spatial transcriptomics. Projects examine neural crest development in mouse embryos and neuroblastoma, with complex in-vitro systems and bottom-up reconstruction used to connect communication patterns with their consequences. The group is recruiting postdocs with experimental or computational expertise, or both, for the September 2026 Max Planck Postdoc Program. The programme guarantees a contract of at least three years. Apply through the official programme portal by 13 October 2026 at 12:00 Europe/Berlin (CEST). An account is required; the Apply action appears after registration. Upload a CV including publications, previous-research summary, statement of interest, academic transcript and contact details for three referees.
AASCRM Webinar Series October 2026
Yun Xia, Minoru Takasato · A*STAR Institute of Molecular and Cell Biology, Singapore; RIKEN Center for Biosystems Dynamics Research, Japan
Tue, Oct 13 · 03:00 UTC · Online
Yun Xia presents macrophage–kidney assembloids that address missing immune and vascular components in stem-cell organoids. Directed differentiation, self-organization, genetic perturbation, xenotransplantation and single-cell analysis reveal immune–epithelial interactions. Macrophages from the same parental cells acquire resident phenotypes; diabetic and polycystic kidney models show context-dependent effects on inflammation, epithelial injury and disease progression. Minoru Takasato addresses kidney organoids’ missing urinary outflow by generating bladder tissue from human pluripotent cells. Stepwise differentiation passes through endoderm, hindgut and cloaca; FGF4 posteriorization and growth-factor screening promote urothelial identity. The resulting sacs contain stratified urothelial cell types, stretch and form a barrier, supporting developmental, disease and future therapeutic studies. Online via Zoom. Tuesday 13 October, 11:00–12:30 SGT (Asia/Singapore). Both talks share this session; individual start times are unspecified. Register through the organizer page. Professional, trainee or student status in stem cells, regenerative medicine or an adjacent field is required; organizer approval and recording restrictions apply.
Opportunities
Assistant Professor - Genetics, Genomics, Evolution, and Development - Molecular and Cell Biology
University of California, Berkeley · Berkeley, USA
Closes
Establish a tenure-track research programme in the Genetics, Genomics, Evolution, and Development division at UC Berkeley. Research may address molecular, cellular or quantitative genetics, genomic technologies, comparative and evolutionary biology, or developmental patterning and organismal form. The department seeks new conceptual or technical directions, with opportunities to collaborate with genomics, bioimaging, developmental biology and computational biology groups. The appointment includes research, teaching, mentoring and service. The anticipated start is 1 July 2027. The advertised nine-month salary is USD 84,100–132,900, with possible additional compensation. Applications close on 19 October 2026 at 23:59 Pacific Time.
The Company of Biologists Travelling Fellowships — October 2026 Round
The Company of Biologists
Closes
Graduate students and postdoctoral researchers can seek up to GBP 3,000 for a research visit to another laboratory. Apply to the participating journal that best matches the work: Development, Journal of Cell Science or Journal of Experimental Biology. The next deadline is 23 October 2026 for travel after 7 December 2026. This recurring fellowship supports research collaboration; it is not a training-course bursary.
Loke Centre for Trophoblast Research PhD Studentship (Fixed Term)
University of Cambridge Department of Physiology, Development and Neuroscience
Closes
The Loke Centre for Trophoblast Research (CTR) provides a dynamic environment for PhD training in placental biology and reproductive science. Founded in 2007, it brings together over 30 Principal Investigators with a shared interest in the scientific study of the placenta, early development and maternal-fetal interactions during pregnancy. Our PIs are recognized international experts in their fields based across Cambridge in the Departments of Physiology, Development, and Neuroscience, Obstetrics and Gynaecology, Pathology, Genetics, and allied institutes, including the Institute of Metabolic Science, Cambridge Stem Cell Institute, Cambridge Institute of Therapeutic Immunology and Infectious Disease, the LMB, Babraham, and Wellcome Sanger Institute. A Loke CTR Studentship will be held within the relevant department or Institute, where an internal Departmental Postgraduate Educational Committee is responsible for administering your degree. Our PhD students have access to unique training opportunities to prepare them for successful careers in research. Students will present their research by giving seminars at our annual Away Days and international conferences, and attend a variety of seminars given by distinguished scientists with the Loke CTR and affiliated Department or Institute. There are also opportunities to participate and present in interdisciplinary seminars hosted by Cambridge Reproduction of which the Loke CTR is a founding member. Students will gain training in our Placental Biology Course and receive support from them to attend international meetings. Loke CTR PhD students will also become members of the Postgraduate School of the Life Sciences, which organises and promotes many further training opportunities. We are pleased to consider applications for fully funded, full-time study over four years or part-time over five years. Application Procedure Please investigate research projects on offer for the 2026/2027 application cycle (https://www.trophoblast.cam.ac.uk/opportunities/projects) and contact potential supervisors in advance of applying. Once you have identified a potential supervisor(s) and project(s), please make a formal application following the instructions and requirements detailed on our website https://www.trophoblast.cam.ac.uk/phd-studentships/selection-process. The application deadline is 3 November 2026. We will hold an initial round of Zoom interviews with potential PhD supervisors in late November (2026). Shortlisted candidates will be invited to a second round of interviews in early January (2027). Finance Loke CTR PhD Studentships will cover all University and College fees at home or international rates, along with a stipend of £22,000 per year. Awarded studentships also include a justified research consumables/equipment of £15,000 and up to £750 funds for conference travel over the duration of the studentship. Key experience and competencies Applicants for this course should have achieved a UK Good II.i Honours Degree. If your degree is not from the UK, please check International Qualifications (https://www.postgraduate.study.cam.ac.uk/international/international-qualifications) to find the equivalent in your country. We are looking for strong candidates that will contribute to the science in the Loke CTR and have potential as researchers. During the admissions process, we will consider the academic record and the comments from referees as well as the research experience and achievements of the applicants. We are mindful that the extent of research opportunity and publications can vary substantially depending on background and undergraduate training, for example some countries have longer undergraduate courses, different master requirements, offer short courses and practical research, etc, and all these are put into context when evaluating potential. Please refer to the University of Cambridge Entry (https://www.postgraduate.study.cam.ac.uk/apply/before/entry-requirements) requirements for further detail. Research projects available for 2026/27 entry Endometrial-trophoblast interactions in the regulation of placental invasion into the uterus, supervised by Irving Aye and Naomi McGovern Epigenetic mechanisms linking maternal choline supply and one-carbon metabolism during early perinatal development, supervised by Geula Hanin and Erica Watson GLP-1receptor agonists effects on the placenta and maternal vasculature in an obese pregnancy model, supervised by Sue Ozanne and Wei Li Imaging the dynamics of human implantation, supervised by Kathy Niakan and Naomi McGovern Investigating the role of transcription factors in regulating trophectoderm specification during human embryogenesis, supervised by Peter Rugg-Gunn and Kathy Niakan Questions If you have any queries regarding the selection process, please refer to our website (https://www.trophoblast.cam.ac.uk/phd-studentships) or email phd.lokectr@pdn.cam.ac.uk. The University actively supports equality, diversity and inclusion and encourages applications from all sections of society. The University has a responsibility to ensure that all employees are eligible to live and work in the UK.
Senior Research Scientist, Research Scientist or Postdoctoral Researcher — BDR–RISE Program (26-750)
RIKEN Center for Biosystems Dynamics Research · Kobe, Japan
Closes
The BDR–RISE programme offers one or two appointments for collaborative research spanning at least two participating RIKEN laboratories. Areas include development, cell systems, brain organoids, neural stem cells, regeneration, AI biology and quantitative biology. Candidates propose the collaboration and must first confirm participation with prospective host and partner laboratory heads. Employment is initially annual and renewable for up to three years. Each project receives JPY 3 million per year through the host laboratories. Senior scientist, scientist and postdoctoral categories have distinct experience requirements; postdoctoral applicants must be within five years of their PhD or complete it before starting. Applications are due 30 November 2026, normally for an April or October 2027 start. Use the official upload form with the coordinated proposal and required documents.
Conferences
2026 Lake Conference - Comparative and Evolutionary Neurobiology
Renton, United States
Oct 25–29, 2026
This Lake Conference is a 3.5-day forum on comparative and evolutionary approaches to nervous-system function. The program includes invited and selected talks, poster sessions, comparative genomics and genetics, evolutionary and developmental mechanisms, and evolutionary neuroscience systems biology.
Annual meeting of the International Society for Stem Cell Research at the Moscone West Convention Center, San Francisco, recognizing 25 years of discovery, collaboration, and progress in stem cell science.
- Minoru Takasato
A*STAR Institute of Molecular and Cell Biology, Singapore; RIKEN Center for Biosystems Dynamics Research, Japan · on a talk, Oct 2026
Next: AASCRM Webinar Series October 2026 · Oct 13
- Yun Xia
A*STAR Institute of Molecular and Cell Biology, Singapore; RIKEN Center for Biosystems Dynamics Research, Japan · on a talk, Oct 2026
Next: AASCRM Webinar Series October 2026 · Oct 13
- Ertuğrul M. Özbudak
Northwestern University · on a talk, Oct 2026
Next: Two distinct timers control vertebrate embryo segmentation · Oct 20
- Alex Pollen
University of California, San Francisco · on a talk, Nov 2021
Next: 2026 Lake Conference - Comparative and Evolutionary Neurobiology · Oct 25
- Barbara Treutlein
ETH Zurich · on a talk, Jun 2021
Next: 2026 Lake Conference - Comparative and Evolutionary Neurobiology · Oct 25
- Detlev Arendt
Next: 2026 Lake Conference - Comparative and Evolutionary Neurobiology · Oct 25
The Roles of Distinct Functions of SynGAP1 in SYNGAP1-Related Disorders
Richard Huganir · Johns Hopkins Medicine
Wed, May 15, 2024 · 00:00 UTC
The asymmetric brain: Utilizing hyper-gravity to manipulate developmental symmetries
Felix Graf, Robin Hiesinger
The evolution and development of all organisms on earth relies on near-constant gravity. Experimental manipulations can create developmental conditions that have never been encountered during evolution, yet reveal developmental mechanisms based on informative phenotypic outcomes; classically, such experiments include transplantation of developing organs as well as pushing boundaries of environmental conditions.Here, we explore the outcome of Drosophila melanogaster brain development at hyper-gravity 10^2 to 10^3 times greater than conventional gravity on earth. Remarkably, Drosophila pupae fully develop when exposed to 300g throughout the period of brain wiring (P50 - P100). The adult brains of such flies exhibit an asymmetric phenotype: synaptic neuropils exhibit a reduction in volume only on the side pointed to by the gravity vector, while the other side appears morphologically normal. Analysis of single cell morphology revealed largely unaltered neuronal branching patterns. However, the investigation of synaptic connectivity with the trans-synaptic tracer trans-tango, revealed a surprisingly dramatic change of synaptic partners to R7 photoreceptor neurons; these changes include a substantial loss of synapses with the main postsynaptic partner Dm8, despite largely unaltered neuronal morphologies. Since the control side of the brain had experienced the same hyper-gravity, yet exhibited normal connectivity, we conclude that hyper-gravity does not directly affect molecular or sub-cellular processes, but caused these effects by a redistribution of resources in the fly pupa.The extent and nature of these synaptic changes reveal the plasticity and principles of how the genetically encoded developmental program leads to specific connectivity during brain wiring.
Transplanted human brain-tissue takes root in mice without a cortex
Nature Podcast
Published Wed, Sep 16
This Nature Podcast episode examines human brain organoids transplanted into mice lacking a cerebral cortex, where extensive cellular integration could create an in-vivo platform for testing therapies and studying human neurobiology. It also covers research highlights and Paper2Agent, an AI system that turns research papers into interactive virtual corresponding authors able to answer questions and support complex scientific tasks.
Cellular and genetic mechanisms of cerebral cortex folding
Víctor Borrell · Instituto de Neurociencias, Alicante
Wed, Jan 17, 2024 · 18:00 UTC
One of the most prominent features of the human brain is the fabulous size of the cerebral cortex and its intricate folding, both of which emerge during development. Over the last few years, work from my lab has shown that specific cellular and genetic mechanisms play central roles in cortex folding, particularly linked to neural stem and progenitor cells. Key mechanisms include high rates of neurogenesis, high abundance of basal Radial Glia Cells (bRGCs), and neuron migration, all of which are intertwined during development. We have also shown that primary cortical folds follow highly stereotyped patterns, defined by a spatial-temporal protomap of gene expression within germinal layers of the developing cortex. I will present recent findings from my laboratory revealing novel cellular and genetic mechanisms that regulate cortex expansion and folding. We have uncovered the contribution of epigenetic regulation to the establishment of the cortex folding protomap, modulating the expression levels of key transcription factors that control progenitor cell proliferation and cortex folding. At the single cell level, we have identified an unprecedented diversity of cortical progenitor cell classes in the ferret and human embryonic cortex. These are differentially enriched in gyrus versus sulcus regions and establish parallel cell lineages, not observed in mouse. Our findings show that genetic and epigenetic mechanisms in gyrencephalic species diversify cortical progenitor cell types and implement parallel cell linages, driving the expansion of neurogenesis and patterning cerebral cortex folds.
New and updated
Research Assistant (Fixed Term)
University of Cambridge Department of Physiology, Development and Neuroscience
Deadline not stated
The Research Luke Harland is establishing a new research group based in the Loke Centre for Trophoblast Research within the Department of Physiology, Development and Neuroscience at the University of Cambridge. The group investigates how specialised blood and vascular cell types arise during mammalian development and uses this knowledge to generate defined cell populations from pluripotent stem cells for mechanistic studies and tissue modelling. We aim to understand how developmental history shapes blood and vascular cell identity and function, and to apply this knowledge to build improved vascularised tissue models. By recreating the developmental processes that generate specialised blood vessels, we hope to build more physiologically relevant models for studying human development and disease. Our initial focus is on reconstructing the fetal placental exchange interface, which enables the transfer of oxygen and nutrients required for fetal growth and development. Our research combines embryology, stem cell biology, single-cell genomics, genome engineering, advanced imaging and computational biology. Further information about Luke Harland and key publications relevant to the ongoing research programme can be found on the Loke Centre for Trophoblast Research website (https://www.trophoblast.cam.ac.uk/people/luke-harland) The Opportunity We are seeking an enthusiastic and motivated Research Assistant to join our growing Wellcome-funded research programme. This is an exciting opportunity to become one of the founding members of a new research group and contribute to its development and culture. The successful candidate will contribute to research spanning developmental and stem cell biology, with opportunities to work with pluripotent stem cell culture and directed differentiation, molecular biology, flow cytometry, microscopy, mouse developmental models and single-cell genomics. About You Applicants should hold a BSc or Master's degree in a relevant biological discipline and have practical laboratory experience in cell biology, developmental biology, stem cell biology, molecular biology or a related field. We are particularly interested in candidates with experience in the culture and directed differentiation of mouse and/or human pluripotent stem cells. Experience with R or Python is desirable, and previous analysis of single-cell RNA-sequencing data would be an advantage. Experience with flow cytometry, microscopy or mouse developmental biology would also be beneficial. Training will be provided, and experience across all of these areas is not expected. We are looking for an organised, enthusiastic and collaborative individual with excellent attention to detail and an interest in combining experimental and computational biology. For more information please see the further particulars. Fixed-term: The funds for this post are available for 2 years in the first instance. Due to the nature of the work, you will be required to work on site. Click the 'Apply' button below to register an account with our recruitment system (if you have not already) and apply online. Applications should include a current CV, a cover letter outlining your interest in the position and relevant experience, and contact details for two professional referees. Informal enquiries can be made to Dr Luke Harland (ltgh2@cam.ac.uk). Please quote reference PM51164 on your application and in any correspondence about this vacancy. The University actively supports equality, diversity and inclusion and encourages applications from all sections of society. The University has a responsibility to ensure that all employees are eligible to live and work in the UK.
Two distinct timers control vertebrate embryo segmentation
Ertuğrul M. Özbudak · Northwestern University
Tue, Oct 20 · 16:00 UTC · Hybrid
Vertebrate embryos form repeated body-axis segments, yet the segmentation-clock period does not always match the timing of somite formation. Real-time clock imaging combined with pharmacological and surgical perturbations identifies two timers: a clock that establishes an initial commitment and a subsequent self-organizing hourglass process. Hourglass duration scales with somite size and depends on cytoskeletal regulation. Changing this timer can turn regular zebrafish segmentation into irregular patterns resembling the anterior chicken embryo and alter the number of predetermined compartments and somite sizes. The findings separate commitment from segmentation as interacting modules. QLS–CAMBAM hybrid seminar with Ertuğrul M. Özbudak (Northwestern University), 2026-10-20, 12:00–13:00 Montréal time. Attend in person at 550 Sherbrooke, Room 189, McGill University, or follow the public Zoom link on the official event page. Open to the university community, including faculty, graduate and undergraduate students.
The Surprising Molecular Changes in Eggs, Sperm, and Females that Mediate Fertility
Mariana Wolfner · Cornell University
Wed, Sep 23 · 18:00 UTC
Mariana Wolfner presents research on the molecular changes in eggs, sperm, and females that coordinate successful reproduction, drawing on genetic and physiological studies of fertilization. This NIH Wednesday Afternoon Lecture Series event is offered in person and through NIH VideoCast.
Recent advances in organoid production and drug discovery
Hideya Sakaguchi, Thomas Mitchell · National Center for Child Health and Development
Thu, Sep 10 · 07:00 UTC
This English-language webinar examines advances in organoid research, production, and drug discovery. Hideya Sakaguchi covers the developmental-biology origins of neural organoid research and its potential for drug discovery, followed by a keynote from Thomas Mitchell of The Organoid Company and a live question session.