JOURN

Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice';

Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice

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Beyond genomic studies of congenital heart defects through systematic modelling and phenotyping';

Beyond genomic studies of congenital heart defects through systematic modelling and phenotyping

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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines';

Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines

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Improving laboratory animal genetic reporting: LAG-R guidelines';

Improving laboratory animal genetic reporting: LAG-R guidelines

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Pleiotropic brain function of whirlin identified by a novel mutation';

Pleiotropic brain function of whirlin identified by a novel mutation

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An unbiased ranking of murine dietary models based on their proximity to human metabolic dysfunction-associated steatotic liver disease (MASLD)';

An unbiased ranking of murine dietary models based on their proximity to human metabolic dysfunction-associated steatotic liver disease (MASLD)

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Naturally sterile Mus spretus hybrids are suitable for the generation of pseudopregnant embryo transfer recipients';

Naturally sterile Mus spretus hybrids are suitable for the generation of pseudopregnant embryo transfer recipients

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Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)';

Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)

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Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult Cerebellum';

Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult Cerebellum

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Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes';

Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes

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