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Leaver's feedback form - confidential

Leaver's form - Part 2 (confidential feedback)

The information you provide in this second part of the leaver's form will be received only by the Business Operations Manager and the Grants/HR Manager, and will be anonymised before any further use. Your honest feedback will help us to improve all Institute services and to encourage change within the Institute where appropriate, and may be useful in support of applications to funding agencies, Athena SWAN etc. The information will be valuable for statistical analysis, and we may also use anonymised quotes in reports or promotional material. Thank you very much in advance for your help, and for your contribution to the Institute.

Apologies for duplicating the email/fullname fields - this is required for each independent form on the site. It won't affect the confidentiality of the responses you provide, and this data will be stripped out before inclusion in any analysis or publication.

Studying development to understand disease

The Gurdon Institute is funded by Wellcome and Cancer Research UK to study the biology of development, and how normal growth and maintenance go wrong in cancer and other diseases.

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Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48

The developmental origin of brain tumours: a cellular and molecular framework

Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing

ATM orchestrates the DNA-damage response to counter toxic non-homologous end-joining at broken replication forks

Extracellular Forms of Aβ and Tau from iPSC Models of Alzheimer's Disease Disrupt Synaptic Plasticity

Combinational Treatment of Trichostatin A and Vitamin C Improves the Efficiency of Cloning Mice by Somatic Cell Nuclear Transfer

Predominant Asymmetrical Stem Cell Fate Outcome Limits the Rate of Niche Succession in Human Colonic Crypts

G9a regulates temporal preimplantation developmental program and lineage segregation in blastocyst

Validating the concept of mutational signatures with isogenic cell models

A PAX5-OCT4-PRDM1 developmental switch specifies human primordial germ cells

Targeting NAT10 enhances healthspan and lifespan in a mouse model of human accelerated aging syndrome

An alternative mode of epithelial polarity in the Drosophila midgut

Detection of functional protein domains by unbiased genome-wide forward genetic screening

Fank1 and Jazf1 promote multiciliated cell differentiation in the mouse airway epithelium

Genome organization at different scales: nature, formation and function

Mouse Model of Alagille Syndrome and Mechanisms of Jagged1 Missense Mutations


Link to full list on PubMed