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A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

Journal article

Issler N. et al, (2022), J Am Soc Nephrol

Phenotype of a transient neonatal diabetes point mutation (SUR1-R1183W) in mice

Journal article

Sachse G. et al, (2021), Wellcome Open Research, 5, 15 - 15

RNAseq reveals mechanisms of cardiomyopathy in Mlp-C58G knock-in mice

Conference paper

Ehsan M. et al, (2020), JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 140, 53 - 53

Phenotype of a transient neonatal diabetes point mutation (SUR1-R1183W) in mice

Journal article

Sachse G. et al, (2020), Wellcome Open Research, 5, 15 - 15

The technical risks of human gene editing

Journal article

Davies B., (2019), Human Reproduction

Loss of ZnT8 function protects against diabetes by enhanced insulin secretion

Journal article

Dwivedi OP. et al, (2019), Nature Genetics, 51, 1596 - 1606

Genetic diversity and its unexpected impacts on recombination, genome evolution, speciation and sterility in mammals

Conference paper

Li R. et al, (2019), EUROPEAN JOURNAL OF HUMAN GENETICS, 27, 1073 - 1073

Systemic silencing of Phd2 causes reversible immune regulatory dysfunction

Journal article

Yamamoto A. et al, (2019), Journal of Clinical Investigation, 129, 3640 - 3656

Gene editing - past, present and future

Conference paper

Davies B., (2019), HUMAN REPRODUCTION, 34, 1 - 1

Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm

Journal article

Hinch AG. et al, (2019), Science, 363, eaau8861 - eaau8861

An essential role for the Zn2+ transporter ZIP7 in B cell development

Journal article

Anzilotti C. et al, (2019), Nature Immunology, 20, 350 - 361

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