Masaryk University
Max Planck Society
or
Continue with FacebookLooking to list your PhD opportunities? Log in here.
We have 33 developmental genetics PhD Projects, Programmes & Scholarships
developmental genetics PhD Projects, Programmes & Scholarships
We have 33 developmental genetics PhD Projects, Programmes & Scholarships
(BBSRC NWD) The developmental origin of accelerated aging
Aging is an inevitable aspect of human life that is associated with a gradual decline in physiological function. However, the rate of biological aging varies substantially between different individuals and populations. Read more
Understanding psychiatric outcomes in children born with cleft lip and/or palate using genetics
Rationale. Cleft of the lip and/or palate is a common birth defect worldwide and occurs at a rate of one in 650 live births in the UK. Read more
MSc by Research: Jasmonate control of barley development
Description . From the earliest farmers to modern plant breeders, humans have bred and selected for cereals that develop to produce higher grain yields. Read more
(BBSRC NWD) Investigating how dynamic signalling cytonemes enable cell-cell signalling in developing neural tissues
During embryonic nervous system development, neural stem cells must balance decisions between proliferation to allow growth, and differentiation, to generate neurons. Read more
BBSRC NWD: Identifying gene regulatory variants underlying vertebrate neural crest pathologies
Are you passionate about unravelling the mysteries of embryonic development and its impact on vertebrate evolutionary traits and pathologies? Apply for this PhD to explore the fascinating world of neural crest development and its role in vertebrate pathologies. Read more
Last chance to apply
Investigating the origins of the co-occurrence of neurodevelopmental and disruptive behaviour disorders in youth
Primary Supervisor: Dr Margherita Malanchini. Co-Supervisor(s): Dr Giorgia Michelini and Dr Jessica Agnew-Blais. Read more
Last chance to apply
Deciphering morphogenesis of early human brain development in health and disease
Primary Supervisor: Dr Isabel Palacios. Co-Supervisor(s): Dr Julien Gautrot (SEMS). Funding: China Scholarship Council (CSC). Read more
Faculty of Science, Masaryk University
Embark on an enriching academic journey with our esteemed doctoral degree programs in various scientific fields. Read more
Join our graduate school at the interface of biology and computation: IMPRS-BAC in Berlin
We are looking for outstanding graduates from all over the world – whether you have a degree in biology, biochemistry, bioinformatics, computer science or mathematics, as long as you have a passion for working at the interface between molecular life sciences and computational sciences, this may be the place for you. Read more
Drug repurposing in HNRNP-related disorders: towards developing novel therapies.
Rare diseases affect over 3.5 million people in the UK and recent medical advances have provided the means to generate potential treatments for several rare diseases that have been studied to-date but have no treatment. Read more
Durham Doctoral Teaching Fellow: Optogenetic Manipulation of Signalling Pathways in vivo
BACKGROUND. Precise regulation of cell fate in time and space is critical for normal development and adult homeostasis. Read more
PhD position in Medical Science with orientation towards Molecular Biology
Umeå University is one of Sweden’s largest higher education institutions with over 37,000 students and about 4,700 employees. The University offers a diversity of high-quality education and world-leading research in several fields. Read more
Last chance to apply
Thylakoid membrane generation in cyanobacteria
Primary Supervisor: Prof Conrad Mullineaux. Co-Supervisor(s): Dr Vidya Darbari. Funding: China Scholarship Council (CSC). Read more
Developing targeted treatments for HNRNPU-related neurodevelopmental disorder using drug repurposing strategies
Project Title. Developing targeted treatments for HNRNPU-related neurodevelopmental disorder using drug repurposing strategies. Read more
Investigating Epilepsy Molecular Mechanisms in Patient-Specific Stem Cell Models of SLC6A1 Deficiency
SLC6A1 encodes GAT-1, a voltage-dependent gamma-aminobutyric acid (GABA) transporter that is responsible for the reuptake of GABA from the synapse. Read more