Sort by
Refine Your Search
-
Listed
-
Category
-
Country
-
Employer
- CNRS
- Amsterdam UMC
- University of Exeter
- Baylor College of Medicine
- Duke University
- Newcastle University
- University of Pittsburgh
- Aalborg University
- Biofyzikální ústav Akademie věd ČR, v. v. i.
- Deutsches Zentrum für Neurodegenerative Erkrankungen
- ETH Zürich
- Fundació Hospital Universitari Vall d'Hebron- Institut de recerca
- German Cancer Research Center in the Helmholtz Association (DKFZ)
- Harvard University
- Heidelberg University
- Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt
- Institut Pasteur
- Institute of Human Genetics of the Polish Academy of Sciences
- Institute of Neurosciences
- KU LEUVEN
- Purdue University
- Technical University of Munich
- The Ohio State University
- The University of Iowa
- University of Alabama at Birmingham
- University of Amsterdam (UvA)
- University of Bergen
- University of Cambridge
- University of Cambridge;
- University of Florida
- University of Maryland, Baltimore
- University of Oslo
- University of Surrey
- Université Paris Cité
- VIB
- 25 more »
- « less
-
Field
-
reConnect, Institut Pasteur in Paris. The project will develop next-generation AAV gene therapy and precision genome editing for Usher syndrome, building on unique humanized mouse models and strong in vivo
-
science field Flow cytometry experience Mouse handling experience Basic molecular technique experience Job Description: Design and execute experiments across mouse and human systems, including primary cell
-
therapy resistance has already been observed in both patients and pre-clinical mouse models, highlighting the urgent need to define the mechanisms that drive resistance and to identify rational combination
-
van Til at the Amsterdam Leukodystrophy Center (ALC). This doctoral project focuses on the preclinical assessment of gene therapy approaches in leukodystrophy mouse models for vanishing white matter
-
of Pittsburgh School of Medicine, is looking for a candidate to conduct basic and translational interdisciplinary research of dermatological diseases. Maintain existing transgenic mouse colonies and generate new
-
environment and receive training in complementary experimental approaches in cellular and synaptic neuroscience. The project combines primary neuronal cultures, mouse models, advanced fluorescence imaging
-
project focuses on characterising leukodystrophy mouse models and evaluating promising proof-of-concept interventions. You will conduct longitudinal studies in mouse models, with a particular focus on
-
create mouse chronic kidney disease. Works on high throughput data analysis that includes data from single cell sequence, CHIP-Seq, and proteomics. Conducts molecular assays such as real time RT-PCR
-
, functional and metabolic analyses, and co-culture models with tumour microenvironment cells. In vivo experiments using orthotopic mouse models will enable the study of their role in tumour formation and
-
assess their effects on myelination and oligodendrocyte survival. The most promising oligodendrocyte-targeting AAV variants will subsequently be tested in a PMLD1 mouse model to determine their therapeutic